WO2014071686A1 - 一种加氢处理催化剂,其制造方法及其应用 - Google Patents
一种加氢处理催化剂,其制造方法及其应用 Download PDFInfo
- Publication number
- WO2014071686A1 WO2014071686A1 PCT/CN2013/001319 CN2013001319W WO2014071686A1 WO 2014071686 A1 WO2014071686 A1 WO 2014071686A1 CN 2013001319 W CN2013001319 W CN 2013001319W WO 2014071686 A1 WO2014071686 A1 WO 2014071686A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- active metal
- metal component
- concentration
- cross
- section
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 448
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 68
- 238000005984 hydrogenation reaction Methods 0.000 title abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 532
- 239000002184 metal Substances 0.000 claims abstract description 532
- 239000002245 particle Substances 0.000 claims abstract description 263
- 238000009826 distribution Methods 0.000 claims abstract description 101
- 230000000694 effects Effects 0.000 claims abstract description 57
- 238000000034 method Methods 0.000 claims description 101
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 84
- 229910052698 phosphorus Inorganic materials 0.000 claims description 76
- 229910052750 molybdenum Inorganic materials 0.000 claims description 73
- 238000005470 impregnation Methods 0.000 claims description 69
- 238000001035 drying Methods 0.000 claims description 62
- 239000003463 adsorbent Substances 0.000 claims description 53
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 51
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 44
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 42
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 39
- 239000011574 phosphorus Substances 0.000 claims description 39
- 230000000737 periodic effect Effects 0.000 claims description 36
- 239000003921 oil Substances 0.000 claims description 33
- 229910052799 carbon Inorganic materials 0.000 claims description 32
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 30
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 28
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 27
- 229910052731 fluorine Inorganic materials 0.000 claims description 25
- 239000011737 fluorine Substances 0.000 claims description 25
- 238000001354 calcination Methods 0.000 claims description 24
- 101100189913 Caenorhabditis elegans pept-1 gene Proteins 0.000 claims description 23
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 23
- 238000011068 loading method Methods 0.000 claims description 23
- 101100243399 Caenorhabditis elegans pept-2 gene Proteins 0.000 claims description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 21
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 21
- 239000000377 silicon dioxide Substances 0.000 claims description 21
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 20
- 229920006395 saturated elastomer Polymers 0.000 claims description 20
- 229910052721 tungsten Inorganic materials 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 16
- 239000000395 magnesium oxide Substances 0.000 claims description 16
- 150000002739 metals Chemical class 0.000 claims description 16
- -1 VIB metals Chemical class 0.000 claims description 15
- 150000003863 ammonium salts Chemical class 0.000 claims description 14
- 235000015165 citric acid Nutrition 0.000 claims description 14
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 14
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 14
- 229910021480 group 4 element Inorganic materials 0.000 claims description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 11
- 239000002202 Polyethylene glycol Substances 0.000 claims description 11
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 11
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 11
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 11
- 229910052796 boron Inorganic materials 0.000 claims description 11
- 229920001223 polyethylene glycol Polymers 0.000 claims description 11
- 229910052710 silicon Inorganic materials 0.000 claims description 11
- 239000010703 silicon Substances 0.000 claims description 11
- 239000010936 titanium Substances 0.000 claims description 11
- 229910052719 titanium Inorganic materials 0.000 claims description 11
- 229910052726 zirconium Inorganic materials 0.000 claims description 11
- 235000006408 oxalic acid Nutrition 0.000 claims description 10
- 150000005846 sugar alcohols Polymers 0.000 claims description 10
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 9
- 238000004438 BET method Methods 0.000 claims description 9
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 9
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 9
- 235000011054 acetic acid Nutrition 0.000 claims description 9
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 9
- 239000001630 malic acid Substances 0.000 claims description 9
- 235000011090 malic acid Nutrition 0.000 claims description 9
- 229920005862 polyol Polymers 0.000 claims description 9
- 150000003077 polyols Chemical class 0.000 claims description 9
- 239000011975 tartaric acid Substances 0.000 claims description 9
- 235000002906 tartaric acid Nutrition 0.000 claims description 9
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 8
- 230000003247 decreasing effect Effects 0.000 claims description 8
- 150000002009 diols Chemical class 0.000 claims description 8
- 229920000570 polyether Polymers 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002283 diesel fuel Substances 0.000 claims description 7
- 239000004310 lactic acid Substances 0.000 claims description 7
- 235000014655 lactic acid Nutrition 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 7
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 claims description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 6
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 6
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 6
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 6
- 239000011148 porous material Substances 0.000 claims description 6
- 239000000811 xylitol Substances 0.000 claims description 6
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 6
- 235000010447 xylitol Nutrition 0.000 claims description 6
- 229960002675 xylitol Drugs 0.000 claims description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 150000001735 carboxylic acids Chemical class 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000391 magnesium silicate Substances 0.000 claims description 5
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 5
- 235000019792 magnesium silicate Nutrition 0.000 claims description 5
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 claims description 5
- GSWGDDYIUCWADU-UHFFFAOYSA-N aluminum magnesium oxygen(2-) Chemical compound [O--].[Mg++].[Al+3] GSWGDDYIUCWADU-UHFFFAOYSA-N 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 229910000510 noble metal Inorganic materials 0.000 claims description 3
- XNSPQPOQXWCGKC-UHFFFAOYSA-N C(C)(=O)O.C(C)(=O)O.C(C)(=O)O.[N] Chemical compound C(C)(=O)O.C(C)(=O)O.C(C)(=O)O.[N] XNSPQPOQXWCGKC-UHFFFAOYSA-N 0.000 claims description 2
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 claims description 2
- 229940106681 chloroacetic acid Drugs 0.000 claims description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 2
- 239000004575 stone Substances 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 10
- HSLKFDVLUCDISN-UHFFFAOYSA-N [N].CC(O)=O Chemical compound [N].CC(O)=O HSLKFDVLUCDISN-UHFFFAOYSA-N 0.000 claims 1
- VYTBPJNGNGMRFH-UHFFFAOYSA-N acetic acid;azane Chemical compound N.N.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O VYTBPJNGNGMRFH-UHFFFAOYSA-N 0.000 claims 1
- GSJMPHIKYICTQX-UHFFFAOYSA-N magnesium;oxosilicon Chemical compound [Mg].[Si]=O GSJMPHIKYICTQX-UHFFFAOYSA-N 0.000 claims 1
- 229920000151 polyglycol Polymers 0.000 claims 1
- 239000010695 polyglycol Substances 0.000 claims 1
- 239000002594 sorbent Substances 0.000 claims 1
- 239000000969 carrier Substances 0.000 abstract description 3
- 239000000047 product Substances 0.000 description 133
- 239000000243 solution Substances 0.000 description 81
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 74
- 239000000523 sample Substances 0.000 description 59
- 239000007788 liquid Substances 0.000 description 40
- 230000000052 comparative effect Effects 0.000 description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- 238000011156 evaluation Methods 0.000 description 27
- 238000007654 immersion Methods 0.000 description 26
- 229910052759 nickel Inorganic materials 0.000 description 26
- 239000002243 precursor Substances 0.000 description 23
- 238000009736 wetting Methods 0.000 description 23
- 238000006243 chemical reaction Methods 0.000 description 20
- 150000001875 compounds Chemical class 0.000 description 19
- 238000005507 spraying Methods 0.000 description 19
- 238000001723 curing Methods 0.000 description 18
- 238000006477 desulfuration reaction Methods 0.000 description 16
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 15
- 230000023556 desulfurization Effects 0.000 description 15
- 239000000203 mixture Substances 0.000 description 13
- 239000011265 semifinished product Substances 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000012298 atmosphere Substances 0.000 description 12
- 238000005259 measurement Methods 0.000 description 12
- 229910052717 sulfur Inorganic materials 0.000 description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 11
- 238000010521 absorption reaction Methods 0.000 description 11
- 239000012530 fluid Substances 0.000 description 11
- 239000011555 saturated liquid Substances 0.000 description 11
- 239000011593 sulfur Substances 0.000 description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000000843 powder Substances 0.000 description 9
- 238000007598 dipping method Methods 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 6
- 239000003929 acidic solution Substances 0.000 description 6
- 230000003750 conditioning effect Effects 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000000465 moulding Methods 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- OBWXQDHWLMJOOD-UHFFFAOYSA-H cobalt(2+);dicarbonate;dihydroxide;hydrate Chemical compound O.[OH-].[OH-].[Co+2].[Co+2].[Co+2].[O-]C([O-])=O.[O-]C([O-])=O OBWXQDHWLMJOOD-UHFFFAOYSA-H 0.000 description 5
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 description 5
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 description 5
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical class C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 3
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000004453 electron probe microanalysis Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000000691 measurement method Methods 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 230000003020 moisturizing effect Effects 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003464 sulfur compounds Chemical class 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 2
- 239000004353 Polyethylene glycol 8000 Substances 0.000 description 2
- 241000219793 Trifolium Species 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 210000002196 fr. b Anatomy 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910000480 nickel oxide Inorganic materials 0.000 description 2
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 2
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229940113116 polyethylene glycol 1000 Drugs 0.000 description 2
- 235000019446 polyethylene glycol 8000 Nutrition 0.000 description 2
- 229940085678 polyethylene glycol 8000 Drugs 0.000 description 2
- 239000008213 purified water Substances 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 239000002210 silicon-based material Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229930192474 thiophene Natural products 0.000 description 2
- 150000003577 thiophenes Chemical class 0.000 description 2
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 2
- 238000004846 x-ray emission Methods 0.000 description 2
- DGUACJDPTAAFMP-UHFFFAOYSA-N 1,9-dimethyldibenzo[2,1-b:1',2'-d]thiophene Natural products S1C2=CC=CC(C)=C2C2=C1C=CC=C2C DGUACJDPTAAFMP-UHFFFAOYSA-N 0.000 description 1
- MYAQZIAVOLKEGW-UHFFFAOYSA-N 4,6-dimethyldibenzothiophene Chemical compound S1C2=C(C)C=CC=C2C2=C1C(C)=CC=C2 MYAQZIAVOLKEGW-UHFFFAOYSA-N 0.000 description 1
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- QLFRWUVLCRCBBG-UHFFFAOYSA-N C1=CC2=C(C(=C1)S)SC3=C2C=CC=C3S Chemical compound C1=CC2=C(C(=C1)S)SC3=C2C=CC=C3S QLFRWUVLCRCBBG-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241000736305 Marsilea quadrifolia Species 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- XSKZHDYMDAQAMO-UHFFFAOYSA-N [W].[Cl-].[NH4+] Chemical compound [W].[Cl-].[NH4+] XSKZHDYMDAQAMO-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910021446 cobalt carbonate Inorganic materials 0.000 description 1
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 1
- 229910001981 cobalt nitrate Inorganic materials 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- ZOTKGJBKKKVBJZ-UHFFFAOYSA-L cobalt(2+);carbonate Chemical compound [Co+2].[O-]C([O-])=O ZOTKGJBKKKVBJZ-UHFFFAOYSA-L 0.000 description 1
- MULYSYXKGICWJF-UHFFFAOYSA-L cobalt(2+);oxalate Chemical compound [Co+2].[O-]C(=O)C([O-])=O MULYSYXKGICWJF-UHFFFAOYSA-L 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000005261 decarburization Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940104869 fluorosilicate Drugs 0.000 description 1
- 210000003918 fraction a Anatomy 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- RIAJLMJRHLGNMZ-UHFFFAOYSA-N triazanium;trioxomolybdenum;phosphate Chemical compound [NH4+].[NH4+].[NH4+].O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.[O-]P([O-])([O-])=O RIAJLMJRHLGNMZ-UHFFFAOYSA-N 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
- B01J27/19—Molybdenum
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/002—Mixed oxides other than spinels, e.g. perovskite
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/881—Molybdenum and iron
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/882—Molybdenum and cobalt
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/88—Molybdenum
- B01J23/883—Molybdenum and nickel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/04—Sulfides
- B01J27/047—Sulfides with chromium, molybdenum, tungsten or polonium
- B01J27/051—Molybdenum
- B01J27/0515—Molybdenum with iron group metals or platinum group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/185—Phosphorus; Compounds thereof with iron group metals or platinum group metals
- B01J27/1853—Phosphorus; Compounds thereof with iron group metals or platinum group metals with iron, cobalt or nickel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/0009—Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst
- B01J37/0018—Addition of a binding agent or of material, later completely removed among others as result of heat treatment, leaching or washing,(e.g. forming of pores; protective layer, desintegrating by heat)
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
- B01J37/082—Decomposition and pyrolysis
- B01J37/088—Decomposition of a metal salt
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/20—Sulfiding
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
- C10G45/06—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
- C10G45/08—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof in combination with chromium, molybdenum, or tungsten metals, or compounds thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/34—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of chromium, molybdenum or tungsten
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1037—Hydrocarbon fractions
- C10G2300/1048—Middle distillates
- C10G2300/1055—Diesel having a boiling range of about 230 - 330 °C
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/107—Atmospheric residues having a boiling point of at least about 538 °C
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1074—Vacuum distillates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1077—Vacuum residues
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
- C10G45/06—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
Definitions
- This invention relates to a hydrotreating catalyst, and more particularly to a hydrotreating catalyst suitable for hydrodesulfurization of heavy distillates, particularly diesel.
- the invention further relates to a process for the manufacture of the hydrotreating catalyst and its use as a hydrodesulfurization catalyst in heavy distillate hydrodesulfurization, particularly deep hydrodesulfurization. Background technique
- the sulfur-containing compounds in diesel oil mainly include aliphatic sulfides, thioethers, dibenzothiophenes, alkylbenzothiophenes and alkyldibenzothiophenes, among which dibenzothiophene and alkylbenzene are more difficult to remove.
- Thiophene compounds such as thiophene and alkyl dibenzothiophene (hereinafter collectively referred to as difficult-to-desulfurous compounds), especially 4,6-dimethyldibenzothiophene and 2,4,6-trimethyldiphenyl Thiophene compounds with complex structures and steric hindrance effects such as thiophene are the most difficult to remove.
- diesel deep hydrodesulfurization The main purpose of diesel deep hydrodesulfurization is to remove such difficult sulfur-containing compounds, which are difficult to remove even under high temperature and high pressure if they are passed through conventional hydrodesulfurization technology. Therefore, hydrodesulfurization of diesel oil (especially deep hydrodesulfurization) is inevitably significantly different from conventional hydrodesulfurization in the reaction mechanism, which requires special requirements in the design of diesel hydrodesulfurization catalyst.
- Chinese patent CN99103007.9 discloses a hydrotreating catalyst comprising tungsten oxide and/or molybdenum oxide, nickel oxide and cobalt oxide supported on an alumina support.
- the catalyst has a low metal content but a high low temperature activity, and is particularly suitable for the hydrogenation of light oils.
- Chinese Patent No. CN 991 13281.5 discloses a hydrotreating catalyst which uses alumina or silica-containing alumina as a carrier, W, Mo and Ni as active components, and a phosphorus assistant.
- the catalyst showed a significantly high hydrodenitrogenation activity.
- the inventors have conducted painstaking research on the basis of the prior art and found that when the concentration distribution of certain active metal components in the catalyst particles satisfies specific requirements, the obtained hydrotreating catalyst can exhibit a markedly increased weight.
- the above problem can be solved by the distillate (depth) hydrodesulfurization activity, and thus the present invention has been completed.
- the present invention relates to the following aspects.
- a hydrotreating catalyst characterized by being in the form of particles and comprising a porous refractory support (preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic resistant)
- a porous refractory support preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic resistant
- One or more of the molten oxides more preferably one or more selected from the group consisting of oxides of Group II, Group III, and Group IV elements of the Periodic Table of the Elements, more preferably selected from the group consisting of silica, One or more of alumina, magnesia, silica alumina, silica magnesia and alumina alumina, further preferably alumina
- active metal component A active metal supported on the porous refractory support a component B, an active metal component C and an optional auxiliary component, wherein the active metal component A is Ni, and the active metal component B is selected from the group VIII
- the metals preferably selected from one or more of Group VIII non-noble metals other than Ni in the periodic table, more preferably Co, the active metal component C being selected from the periodic table of elements One of the Group VIB metals or Preferably, one or more selected from the group consisting of Mo and W, more preferably Mo, the auxiliary component is selected from one or more of fluorine, silicon, phosphorus, titanium, zirconium and boron, preferably selected from the group consisting of One or more of fluorine and phosphorus, more preferably phosphorus,
- the concentration distribution of the active metal component A satisfies one of the following conditions (I) or ( ⁇ ),
- C A . ut of the active metal component A is the concentration at an arbitrary position of the point P A with the active metal component A at the center point of the cross-section of catalyst particles on the outermost edge of the cross section of the catalyst particles a ratio of a straight line segment connecting the center point to the position point P A in a cross section of the catalyst particle is L A
- C A 1/2 is the active metal component A in the straight line the position of a point on a line segment distance P a L a at the concentration of the active metal component ratio of the concentration at the center point a of the cross section of the catalyst particle is (1/2)
- C a 1/4 is the active metal component on the a line segment from the position of the point P a is (1/4) L a at a concentration of the active metal component a and the center point in the cross section of the catalyst particle
- C A 3/4 is the concentration of the active metal component A on the straight line segment from the position point P A (3/4) L A and the active metal component A
- the concentration distribution of the active metal component B satisfies one of the following conditions (III) or (IV)
- C B . Ut is the concentration of the active metal component B at any position P B on the outermost edge of the cross section of the catalyst particle and the concentration of the active metal component B at the center point of the cross section of the catalyst particle a ratio of a straight line segment connecting the center point to the position point P B in a cross section of the catalyst particle is L B
- C B i /2 is the activity
- C B 1/4 is a concentration of the active metal component B on the straight line segment from the position point P B of (1/4) L B and the active metal component B at the catalyst a ratio of the concentration at the center point of the cross section of the particle
- C B 3/4 is the concentration of the active metal component B at the position point P B of the active metal component B at (3/4) L B
- concentration distribution of the active metal component A and the concentration distribution of the active metal component B satisfy the aforementioned conditions (I) and (III),
- the concentration distribution of the active metal component A satisfies the aforementioned condition ( ⁇ ), and the concentration distribution of the active metal component B satisfies the aforementioned condition (IV).
- the hydrotreating catalyst according to any of the preceding aspects which has a specific surface area (BET method) of from 100 to 260 m 2 /g, preferably from 120 to 220 m 2 /g, and a pore volume (BET method) of from 0.20 to 0.60. Ml/g, preferably 0.20 to 0.50 ml/g.
- the content of the porous refractory carrier is 45 to 89 wt%, 46 to 87 wt% or 55 to 85 wt%, based on the weight of the catalyst, a preferred balance;
- the active metal component A in terms of NiO
- the active metal component B in terms of its corresponding oxide, such as Co in terms of CoO
- the content is at least 0.5 wt%, lwt% or 1.5 wt%, up to 6 wt% or 8 wt%;
- the content of the active metal component C (in terms of its corresponding oxide) is 6 to 60 wt%, preferably 6 ⁇ 40% by weight, in particular Mo (in terms of Mo0 3 ), is at least 6 wt%, 8 wt% or 10 wt%, up to 26 wt%, 32 wt% or 40 wt%, and/or W (in terms of W0 3 )
- the content is 45 to 89 wt%, 46 to 87 wt% or 55 to
- C M °. Ut is the point P M of the active metal component Mo at any position on the outermost edge of the cross section of the catalyst particle.
- the ratio of the concentration at which the concentration of the active metal component Mo at the center point of the cross section of the catalyst particle is set is such that the central point of the catalyst particle is connected to the center point and the position point P M .
- the length of the straight line segment is L M .
- C M ° 1/2 is the distance from the position point P M of the active metal component Mo on the straight line segment. Is (1/2) L M .
- a concentration of the active metal component Mo at a concentration at a center point of the cross section of the catalyst particle, C M ° 1/4 is the distance of the active metal component Mo on the straight line segment Location point P M .
- Is (1/4) L M a concentration at a ratio of a concentration of the active metal component Mo at a center point of a cross section of the catalyst particle, C M ° 3/4 is a distance from the active metal component Mo on the straight line segment Location point P M .
- Is (3/4) L M The concentration at which the ratio of the concentration of the active metal component Mo at the center point of the cross section of the catalyst particle, C M °. Pt is the concentration of the active metal component Mo at any position on the straight line segment (excluding the center point and the position point P M . . . ) and the active metal component Mo at the catalyst particle The ratio of the concentration at the center point of the cross section,
- the active metal component C is a combination of Mo and W, wherein the concentration distribution of Mo satisfies one of the following conditions (V) or (VI), and the concentration distribution of the W satisfies the following condition (VII) or (VIII) One of them,
- C M °. ut is the concentration of the active metal components Mo concentration at an arbitrary position of the point ⁇ ⁇ with the active metal component Mo at the center point of the cross-section of catalyst particles on the outermost edge of the cross section of the catalyst particles Ratio, based on the cross section of the catalyst particles
- the center point is connected to the position point P M .
- the length of the straight line segment is L M .
- C M ° 1/2 is the distance from the position point P M of the active metal component Mo on the straight line segment. Is (1/2) L M .
- a concentration at a concentration of the active metal component Mo at a center point of the cross section of the catalyst particle, C M ° 1/4 is the distance of the active metal component Mo on the straight line segment Location point P M .
- the active metal component ut W is the concentration at an arbitrary position of the point P w of the active metal component W at the center point of the cross-section of catalyst particles on the outermost edge of the cross section of the catalyst particles a ratio of a straight line segment connecting the center point to the position point P w in a cross section of the catalyst particle is L w
- C w 1/2 is the active metal component W at the straight line
- the distance from the position point P w at the line segment is (1/2) L W to the concentration of the active metal component W at the center point of the cross section of the catalyst particle
- C w 1/4 is a concentration of the active metal component W at (1/4) L W from the position point P w on the straight line segment and a center point of the active metal component W at a cross section of the catalyst particle a ratio of the concentration
- C W 3 /4 is the concentration of the active metal component W on the straight line segment from the position point Pw of (3/4) L w and the active metal component W a ratio of the concentration at the
- C ⁇ pw is the concentration of the active metal component A at any position on the straight line segment opt-1 (excluding the center point and the position point P A ) and the active metal component
- the concentration of the active metal component B is gradually increased along the straight line segment, preferably satisfying the following relationship (3'), provided that (d2 B - dl B ) /
- L B is 5% or less (preferably 2% or less, more preferably 1% or less, more preferably 0.5% or less)
- C B is used .
- Pt-2 (preferably C B . pt-1 ⁇ 105% C B . pt-2 , more preferred
- the relation (3) is a relationship (3') and a relation (3'): C B . Ut ⁇ C B . Pt- i ⁇ C opt-2 ⁇ l,
- C B 0 pt-i is the concentration and the activity of the active metal component B at any position on the straight line segment Opt-1 (excluding the center point and the position point P B )
- the ratio of the concentration of the metal component B at the center point of the cross section of the catalyst particle, C B opt , 2 is the point opt-2 of the active metal component B at any position on the straight line segment (excluding the a ratio of a concentration at a center point and the position point P B ) to a concentration of the active metal component B at a center point of a cross section of the catalyst particle, and the position point P B and the position point opt
- the straight line distance between -1 is dl B
- the linear distance between the position point P B and the position point opt-2 is d2 B , then dl B /d2 B ⁇ l.
- a ratio of a concentration of the active metal component A to a concentration of the active metal component C on the outermost surface of the particle preferably a ratio of a concentration of Ni to a concentration of Mo, a ratio of a concentration of Ni to a concentration of W or
- the ratio of the concentration of Ni to the concentration of (W+Mo) is 0.22 to 0.80, preferably 0.30 to 0.70, and/or the concentration of the active metal component B at the center point of the catalyst particles is
- the ratio of the concentration of the active metal component C (preferably the ratio of the concentration of Co to the concentration of Mo) is 0.20 to 0.78, preferably 0.25 to 0.65.
- a method for producing a hydrotreating catalyst comprising at least the following steps:
- a particulate porous refractory support preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic refractory oxides
- a particulate porous refractory support preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic refractory oxides
- adsorbent I is loaded with adsorbent I, and optionally, an organic alcohol having a carbon number of 1 to 5 (especially a monohydric or polyhydric alcohol, preferably selected from one or more of ethylene glycol, propylene glycol, glycerol, pentaerythritol, and xylitol, wherein the adsorbent I is
- step (1-1) supporting, on the product obtained in the step (1-1), an active metal component B, an optional active metal component C, and an optional auxiliary component, wherein the active metal component B is selected from the group consisting of One or more of the Group VIII metals other than Ni in the periodic table, preferably Co, and the active metal component C is selected from one or more of the Group VIB metals of the periodic table, preferably One or more selected from the group consisting of Mo and W, more preferably Mo, the auxiliary component is selected from one or more of fluorine, silicon, phosphorus, titanium, zirconium and boron, preferably selected from the group consisting of fluorine and phosphorus. One or more, more preferably phosphorus, and
- the premise is to pass at least one of step (1-2) and step (1-3) (preferably by step) a combination of step (1-2) and step (1-3)) to load the active metal component C, or
- a saturated impregnation method or an excessive impregnation method in a particulate porous refractory support (preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic refractory)
- a particulate porous refractory support preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic refractory
- One or more of the oxides more preferably one or more selected from the group consisting of oxides of Group II, Group III and Group IV elements of the periodic table, more preferably selected from the group consisting of silica, oxidation
- aluminum, magnesium oxide, aluminum oxide oxide, magnesium oxide, and aluminum oxide magnesium, further preferably alumina is supported on the adsorbent II, wherein the adsorbent II is selected from the number average molecular weight Mn (GPC method)
- the polyol having a measurement of 400 to 10,000 is preferably selected from the group consisting of a number average
- the active metal component C is selected from one or more of the metals of Group VIB of the periodic table, preferably selected from one or more of Mo and W, more preferably Mo, the auxiliary component One or more selected from the group consisting of fluorine, silicon, phosphorus, titanium, zirconium and boron, preferably one or more selected from the group consisting of fluorine and phosphorus, more preferably phosphorus, and
- step (2-2) before the start of step (2-1) and/or after the end of step (2-2), supporting the active metal component B, optionally the active, on the porous refractory carrier a metal component C and optionally the auxiliary component, wherein the active metal component B is selected from one or more of the Group VIII metals other than Ni in the periodic table, preferably Co,
- the active metal component C is supported by at least one of the step (2-2) and the step (2-3), preferably by a combination of the step (2-2) and the step (2-3),
- alumina is loaded with an adsorbent I, and optionally an organic alcohol having a carbon number of 1 to 5 (particularly a monohydric or polyhydric alcohol, preferably selected from the group consisting of ethylene glycol, propylene glycol, glycerol, pentaerythritol and xylose) One or more of the alcohols, wherein the adsorbent I is selected from the group consisting of organic carboxylic acids
- step (3-2) supporting, on the product obtained in the step (3-1), an active metal component B, an optional active metal component C, and an optional auxiliary component, wherein the active metal component B is selected from the group consisting of One or more of the Group VIII metals other than Ni in the periodic table, preferably Co, and the active metal component C is selected from one or more of the Group VIB metals of the periodic table, preferably One or more selected from the group consisting of Mo and W, more preferably Mo, the auxiliary component is selected from one or more of fluorine, silicon, phosphorus, titanium, zirconium and boron, preferably selected from the group consisting of fluorine and phosphorus. One or more of them, more preferably phosphorus,
- the adsorbent II is supported on the product obtained in the step (3-2) by a saturated impregnation method or an excessive impregnation method, wherein the adsorbent II is selected from the number average molecular weight Mn (measured by a GPC method) of 400 ⁇
- the polyol of 10,000 is preferably selected from polyhydric alcohols having a number average molecular weight Mn (measured by GPC method) of from 1,000 to 8,000, more preferably selected from polyether diols having a number average molecular weight Mn (measured by GPC method) of from 1,000 to 8,000 (especially a polyethylene glycol), the adsorbent II is used in an amount of 0.1 to 10% by weight of the porous refractory support;
- step (3-4) supporting, on the product obtained in the step (3-3), an active metal component A, optionally the active metal component C, and optionally the auxiliary component, wherein the active metal group A is Ni, and
- step (3-5) optionally before the start of step (3-1), after the end of step (3-2) but before the start of step (3-3) and/or after the end of step (3-4), Supporting the active metal component C and optionally the auxiliary component on the porous refractory support,
- a particulate porous refractory support preferably selected from one or more of porous refractory oxides, more preferably selected from porous inorganic refractory
- One or more of the oxides more preferably one or more selected from the group consisting of oxides of Group II, Group III and Group IV elements of the periodic table, more preferably selected from the group consisting of silica, oxidation
- One or more of aluminum, magnesium oxide, aluminum oxide oxide, magnesium oxide, and aluminum oxide magnesium, further preferably alumina is supported on the adsorbent, wherein the adsorbent II is selected from the number average molecular weight Mn (GPC method)
- the polyol having a basis weight of 400 to 10,000 is preferably selected from the group consisting of a number average molecular weight Mn (measured by GPC method) of from 1,000 to 8,000, more preferably from a polyether having a number average molecular weight Mn (GPC method)
- the active metal component A is N i
- the active metal component C is selected from one or more of the metals of Group VIB of the periodic table, preferably selected from one or more of Mo and W, more preferably Mo
- the auxiliary group One or more selected from the group consisting of fluorine, silicon, phosphorus, titanium, zirconium and boron, preferably one or more selected from the group consisting of fluorine and phosphorus, more preferably phosphorus,
- the adsorbent I is supported on the product obtained in the step (4-2), and optionally an organic alcohol having a carbon number of 1 to 5 (particularly a monohydric or polyhydric alcohol, Preferably, one or more selected from the group consisting of ethylene glycol, propylene glycol, glycerol, pentaerythritol, and xylitol, wherein the adsorbent I is selected from the group consisting of organic carboxylic acids having 2 to 15 carbon atoms (especially one yuan) Or one or more of a polycarboxylic acid, preferably a dicarboxylic acid) and an ammonium salt thereof, preferably selected from the group consisting of acetic acid, oxalic acid, lactic acid, malonic acid, tartaric acid, malic acid, citric acid, trichloroacetic acid, monochloro One or more of acetic acid, thioglycolic acid,
- an active metal component B supporting, on the product obtained in the step (4-3), an active metal component B, optionally the active metal component C, and optionally the auxiliary component, wherein the active metal group Sub-B is selected from one or more of Group VIII metals other than Ni in the periodic table, preferably Co, and
- step (44-5) optionally before the start of step (4-1), after the end of step (4- 2 ) but
- the active metal component C and optionally the auxiliary component are supported on the porous refractory support before the start of the step (4_3) and/or after the end of the step (4-4),
- step (I) curing the obtained product after the end of the step (1-1) but before the start of the step (1-2) 0.5 ⁇ 8h (preferably 0.5 ⁇ 6h) or without curing, and / or drying at a temperature of 60 ⁇ 250 ° C (preferably 100 ⁇ 200 ° C) for 0.5 ⁇ 20h (preferably 1 ⁇ 6h);
- step (II) After the end of step (1-2) but before the start of step (1-3), the obtained product is cured for 0.5 ⁇ 6h (preferably 0.5 ⁇ 4h) or without health, at a temperature of 70 ⁇ 200 °C (preferably 100 ⁇ Drying at 160 ° C for 0.5 ⁇ 20h (preferably 1 ⁇ 6h) and calcining at a temperature of 300 ⁇ 750 ° C (preferably 400 - 650 ⁇ ) for 0.5 ⁇ 20h (preferably l ⁇ 6h);
- step (III) After the end of step (1-3), the obtained product is maintained for 0.5 to 6 hours (preferably 0.5 to 4 hours) or without health, at a temperature of 70 to 200. a step of drying 0.5 to 20 hours (preferably 1 to 6 hours) at C (preferably 100 to 160 ° C) and 0.5 to 20 hours (preferably 1 to 6 hours) at a temperature of 300 to 750 ° C (preferably 400 to 650 ° C);
- step (IV) After the end of step (2-1) but before the start of step (2-2), the obtained product is cured for 1 to 12 h (preferably 4 to 12 h), and then at a temperature of 60 to 250 ° C (preferably, the step of drying for 0.5 to 20 hours (preferably 1 to 6 hours) is carried out at 100 to 200 ° C;
- step (V) After the end of step (2-2) but before the start of step (2-3), the obtained product is maintained for 0.5 to 6 hours (preferably 0.5 to 4 hours) or without health, at a temperature of 70 to 200 °C. (preferably 100 ⁇ 160V) drying 0.5 ⁇ 20h (preferably 1 ⁇ 6h) and calcining at a temperature of 300 ⁇ 750 ° C (preferably 400 ⁇ 650 ° C) 0.5 ⁇ 20h (preferably 1 ⁇ 6h);
- step (2-3) After the end of step (2-3), the obtained product is cured for 0.5 - 6h (preferably 0.5 ⁇ 4h) or dried without treatment, at a temperature of 70 to 20 (TC (preferably 100 ⁇ 160 ° C) 0.5 to 20 h (preferably 1 to 6 h) and calcination at a temperature of 300 to 750 ° C (preferably 400 to 650 ° C) for 0.5 to 20 h (preferably 1 to 6 h);
- TC preferably 100 ⁇ 160 ° C
- 0.5 to 20 h preferably 1 to 6 h
- calcination at a temperature of 300 to 750 ° C (preferably 400 to 650 ° C) for 0.5 to 20 h (preferably 1 to 6 h);
- step (3-1) After the end of step (3-1) but before the start of step (3-2), the obtained product is maintained for 0.5 to 8 hours (preferably 0.5 to 6 hours) or without curing, and then at temperature 60 ⁇ a step of drying for 0.5 to 20 hours (preferably 1 to 6 hours) at 250 ° C (preferably 100 to 200 ° C);
- step (VIII) After the end of step (3-2) but before the start of step (3-3), the obtained product is cured for 0.5-6 h (preferably 0.5 ⁇ 4 h) or without curing at a temperature of 70 ⁇ 200 °C.
- step (3-3) drying 0.5 ⁇ 20h (preferably 1 ⁇ 6h) and calcined at a temperature of 300 ⁇ 750 ° C (preferably 400 ⁇ 650 ° C) 0.5 ⁇ 20h (preferably l ⁇ 6h);
- step (3-4) After the end of step (3-3) but before the start of step (3-4), the obtained product is cured for 1 to 12 h (preferably 4 to 12 h), and then at a temperature of 60 to 250 ° C (preferred) 100 ⁇ 200°C) drying step of 0.5 ⁇ 20h (preferably 1 ⁇ 6h);
- step (X) After the end of step (3-4) but before the start of step (3-5), the obtained product is maintained for 0.5 ⁇ 6h (preferably 0.5 ⁇ 4h) or without health, at a temperature of 70 ⁇ 200 °C (preferably 100 ⁇ 160 ° C) drying 0.5 ⁇ 20h (preferably 1 ⁇ 6h) and baking at a temperature of 300 ⁇ 750 ° C (preferably 400 ⁇ 650 ° C) 0.5 ⁇ 20h (preferably l ⁇ 6h);
- step (XI) After the end of step (3-5), the obtained product is cured for 0.5 to 6 hours (preferably 0.5 to 4 hours) or dried without treatment, at a temperature of 70 to 200 ° C (preferably 100 to 160 ° C). 0.5 to 20h (preferably 1 to 6h) and calcination at a temperature of 300 to 750 ° C (preferably 400 to 650 ° C) for 0.5 to 20 h (preferably 1 to 6 h),
- step (4-1) After the end of step (4-1) but before the start of step (4-2), the obtained product is cured for 1 to 12 h (preferably 4 to 12 h), and then at a temperature of 60 to 250 ° C (preferably, the step of drying for 0.5 to 20 hours (preferably 1 to 6 hours) is carried out at 100 to 200 ° C;
- step (4-2) After the end of step (4-2) but before the start of step (4-3), the obtained product is maintained for 0.5 to 6 hours (preferably 0.5 to 4 hours) or without health, at a temperature of 70 ⁇
- step (4-3) After the end of step (4-3) but before the start of step (4-4), the obtained product is cured for 0.5 ⁇ 8h (preferably 0.5 ⁇ 6h) or without health, and then / at temperature 60 ⁇ a step of drying at 0.5 ° C (preferably 1 ⁇ 6 h) at 250 ° C (preferably 100 ⁇ 200 ° C);
- step (4-4) After the end of step (4-4) but before the start of step (4-5), the obtained product is cured for 0.5 to 6 hours (preferably 0.5 to 4 hours) or without health, at a temperature of 70 to 200 °C. (preferably 100 ⁇ 160 ° C) drying 0.5 ⁇ 20h (preferably 1 ⁇ 6h) and baking at a temperature of 300 ⁇ 750 ° C (preferably 400 ⁇ 650 ° C) 0.5 ⁇ 20h (preferably 1 ⁇ 6h);
- step (XVI) After the end of step (4-5), the obtained product is maintained for 0.5-6 h (preferably 0.5-4 h) or without curing, at a temperature of 70-200 ° C (preferably 100-160) Dry for 0.5 ⁇ 20h (preferably l ⁇ 6h) and at temperatures of 300 ⁇ 750.
- the active metal component C comprises Mo
- the active metal component C comprises Mo
- the molar ratio of the Mo load in the previous step to the Mo loading in the latter step is 0.4 ⁇ 2.5 : 1 , and the optimum it is 0.4 ⁇ 2.0: 1.
- a hydrodesulfurization process for heavy distillate oil, especially diesel comprising feeding the heavy distillate oil with a hydrotreating catalyst according to any of the preceding aspects or according to any of the foregoing The step of contacting the hydrotreating catalyst produced by the manufacturing method under hydrodesulfurization conditions.
- the more highly concentrated active metal component such as Ni, in combination with Mo, W or Mo+W
- the more relatively high concentration distribution in the catalyst particles or
- the higher the hydrodesulfurization activity of the active metal component (such as Co, with Mo) in the catalyst particles closer to the center, the relatively high concentration distribution, or the combination of the two distribution modes, can show a significantly improved heavy distillate (depth) ) Hydrogenation of L-L activity.
- a hydrodearomatization reaction and a hydrodesulfurization reaction (hereinafter sometimes referred to as a relay hydrogenation reaction) of a hard-to-desulfurization compound are sequentially performed on one (each) catalyst particle, thereby extracting it from the heavy distillate oil Quickly remove.
- the reaction sequence of the relay hydrogenation reaction is followed by the active metal having a higher hydrodearomatic activity.
- the hydrotreating catalysts of the present invention exhibit higher potency especially when such difficult to remove sulfur compounds are removed.
- Figure 1 illustrates the manner of dicing the hydrotreating catalyst particles of the present invention. among them.
- Figure 1 (a) shows the cutting pattern of the spherical catalyst particles
- Figure 1 (b) shows the cutting pattern of the columnar catalyst particles
- Figure 1 (c) shows the cross-section obtained by the cutting method and the cross-section
- the out represents the arbitrary position point on the outermost edge of the cross section
- 1/4 represents the 1/4 position point
- 1/2 represents the 1/2 position point
- 3/4 represents the 3/4 position point.
- center represents the center point.
- FIG. 2 to 5 are graphs showing the concentration distribution of the active metal component A (Ni ) and the active metal component B (Co ) in the cross section of the catalyst particles obtained in the examples of the specification of the present application.
- the abscissa is the position point of the cross section
- the ordinate is the ratio of the concentration value at a certain point to the concentration value at the center point of the cross section of the particle.
- FIG. 2 corresponds to the catalyst C4 obtained in Example 1-2
- FIG. 3 corresponds to the catalyst C1 obtained in Example II-1
- FIG. 4 corresponds to the catalyst C3 obtained in Example 1-1
- FIG. 5 corresponds to Example IV-2.
- the obtained catalyst C6 The obtained catalyst C6. detailed description
- the term "unsaturated impregnation method” applies to the most conventional understanding in the art, meaning that the volume of the wetting fluid for dipping (also known as the impregnating solution or wetting fluid) is less than that when impregnating.
- the saturated liquid absorption of the object to be impregnated such as carrier particles, etc.
- the ratio of the volume of the dampening solution to the saturated liquid absorption (converted to volume) of the object to be impregnated is generally 0.01 0.6: 1 , preferably 0.02 to 0.4: 1.
- the unsaturated impregnation method is generally carried out under normal temperature and normal pressure, but may be carried out under heating, reduced pressure or under pressure as needed, and is not particularly limited.
- the term "saturated impregnation method" (also referred to as an equal volume impregnation method) is applied in the most conventional manner of understanding in the art, and refers to a dampening fluid for dipping (also referred to as an impregnation liquid) when impregnating.
- the volume of the wetting fluid (substantially) is equal to the saturated liquid absorption of the object to be impregnated (such as carrier particles, etc.).
- the ratio of the volume of the dampening solution to the saturated liquid absorption (converted to volume) of the object to be impregnated is generally 0.9 to 1.1. : 1 , preferably 0.95 to 1.05: 1.
- the saturated dipping method is generally carried out under normal temperature and normal pressure, but may be carried out under heating, reduced pressure or under pressure as needed, and is not particularly limited.
- the term "excessive impregnation” applies to the most conventional understanding in the art, meaning that the volume of the wetting fluid (also referred to as the impregnation or wetting fluid) for impregnation is greater than the The saturated liquid absorption of the impregnated object (such as carrier particles, etc.).
- the ratio of the volume of the dampening solution to the saturated liquid absorption (converted to volume) of the object to be impregnated is generally 1.5 to 15 : 1 , preferably 5 to 10: 1.
- the excessive impregnation method is generally carried out under normal temperature and normal pressure, but may be carried out under heating, reduced pressure or under pressure as needed, and is not particularly limited.
- the hydrotreating catalyst is in the form of pellets and comprises a porous refractory support and an active metal component VIII supported on the porous refractory support, an active metal component B and an active metal component (:.
- the refractory support is optionally further loaded with an auxiliary component.
- the porous refractory support, the active metal component A, the active metal component B, and the active metal component C are simultaneously contained in one of the catalyst particles, and The adjuvant component, if any, is selected.
- the hydrotreating catalyst is (solid) granular, rather than an amorphous state such as a powder.
- shape of the particles various shapes conventionally used in the hydrotreating catalysts of the art may be mentioned, and for example, spherical and columnar may be further mentioned.
- the spherical shape include a spherical shape and an ellipsoidal shape; and the columnar shape may be, for example, a columnar shape, a square column shape, and a profiled cross section (e.g., clover, four-leaf clover, etc.).
- cross section of catalyst particles refers to the entire surface that is exposed after being cut through the geometric center of its shape along the smallest dimension of a catalyst particle.
- the cross section refers to the entire surface exposed through the center of the sphere along the radius or short axis of the sphere (see, for example, Fig. 1 (a)).
- the cross section refers to a vertical surface (see, for example, Figure 1 '(b)°). ' , mouth '
- the outer circumference of the exposed surface is referred to as the outermost edge of the cross section, and the geometric center (such as the aforementioned center point of the center or length dimension) is referred to as the center of the cross section. point.
- the active metal component A is Ni.
- the active metal component A is generally present on the support in the form of a nickel oxide such as ⁇ .
- the active metal component B is selected from one or more of the Group VIII metals other than Ni in the periodic table, preferably one of the Group VIII non-noble metals other than Ni or A variety, most preferred Co.
- the active metal component B is typically present on the support in the form of its corresponding metal oxide (e.g., CoO).
- the active metal component C is selected from one or more of the metals of Group VIB of the Periodic Table of the Elements, preferably one or more selected from the group consisting of Mo and W, more preferably Mo.
- the live The metal component C is generally present on the support in the form of its corresponding metal oxides, such as MoO 3 and W0 3 .
- the auxiliary component is optional and is selected from one or more of fluorine, silicon, phosphorus, titanium, zirconium and boron, preferably one or more selected from the group consisting of fluorine and phosphorus. More preferably, phosphorus (P).
- the porous refractory support is preferably one or more selected from the group consisting of porous refractory oxides, more preferably one or more selected from the group consisting of porous inorganic refractory oxides, more preferably selected.
- One or more of the oxides of the Group II, Group III and Group IV elements of the periodic table more preferably selected from the group consisting of silica, alumina, magnesia, silica alumina, magnesium silicate and One or more of alumina magnesium, most preferably alumina.
- the porous refractory support preferably contains alumina as an essential component.
- the specific surface area (BET method) of the hydrotreating catalyst is generally from 100 to 260 m 2 /g, preferably from 120 to 220 m 2 /g, and the pore volume (BET method) is generally from 0.20 to 0.60 ml / g, preferably 0.20 to 0.50 ml/g.
- the content of the active metal component A (in terms of ⁇ ) is generally from 1 to 8 wt% based on the weight of the catalyst,
- the active metal component B in terms of its corresponding oxide, such as Co in terms of CoO is the lowest in terms of the weight of the catalyst. It is 0.5 wt%, 1% or 1.5%, and the highest is generally 6 wt% or 8 wt%.
- the content (total content) of the active metal component C is generally 6 to 60 wt% based on the weight of the catalyst. %, preferably 6 to 40% by weight.
- the content of the Mo in terms of Mo0 3
- the content of W is generally 6 to 28% by weight, preferably 8 to 26% by weight based on the weight of the catalyst.
- the content of the auxiliary component is usually 30% by weight or less, preferably 20% by weight or less based on the weight of the catalyst.
- the content of the phosphorus in terms of P 2 0 5
- the fluorine in terms of F
- the fluorine is usually from 1 to 6 wt%, preferably from 1 to 5 wt%, based on the weight of the catalyst.
- the content of the porous refractory support is generally 45 to 89 wt% or 46 to 87 wt%, and sometimes 55 to 85 wt%, based on the weight of the catalyst. , the balance is preferred.
- the aforementioned contents of these active metal components A, B and C and the auxiliary component can be measured by a method conventional in the art, such as X-ray fluorescence spectrometry or the like.
- the concentration distribution of the active metal component A satisfies one of the following conditions (I) or (II).
- Condition (I) substantially uniformly distributed in a cross section of each of the catalyst particles.
- C A is the concentration of the active metal component A at any position on the outermost edge of the cross section of the catalyst particle, P A (randomly arbitrarily selected position point), and the active metal component A in the catalyst particle
- the ratio of the concentration at the center point of the cross section, the length of the straight line segment connecting the center point to the position point P A on the cross section of the catalyst particle is L A (no specific unit of measurement is required)
- C A 1/2 is the concentration of the active metal component A on the straight line segment from the position point P A at (1/2) L A (also referred to as 1/2 position point, similarly understood below) a ratio of the concentration of the active metal component A at a center point of the cross section of the catalyst particle
- C A 1/4 is the active metal component A on the straight line segment from the position point P A (1/4) the ratio of the concentration at the L A (also referred to as the 1/4 position point, similarly understood below) to the concentration of the active metal component A at the center point of the cross section of the catalyst particle
- C A 3/4 is that
- Pi is an arbitrary position point of the active metal component A on the straight line segment (ie, a randomly selected position point on the straight line segment, but not including the center point and the position point P A )
- the concentration is the ratio of the concentration of the active metal component A at the center point of the cross section of the catalyst particle.
- the so-called "crossing of each of the catalyst particles means that the concentration distribution of the active metal component A over the entire cross section of each of the catalyst particles is uniform, but allows the presence of those skilled in the art.
- Tolerance or negligible or unavoidable concentration distribution fluctuations (deviations) for the state of the art for example, for example, C A . ut is in the range of 1 ⁇ 5% and C A . pt is at 1 in the range of ⁇ 5%, preferably C a. ut is in the range of 1 ⁇ 2% and C a. pt in the range of 1 ⁇ 2%.
- the fluctuation does not affect the concentration profile of the intended purpose of the present invention, is acceptable, It is also included in the scope of protection of the present invention.
- C A is preferred.
- C A 0Ut /C A 1/2 1.5 - 2.6 , preferably 1.7 - 2.5 is more preferable.
- C A is more preferable.
- Ut / C A 1/4 1.2-1.8, preferably 1.3-1.7.
- C A 1/4 /C A 1/2 l .1-1.7, preferably 1.2-1.6 is more preferable.
- C A is preferred in accordance with the invention. o u u t t ⁇ —2 ⁇ .-0 ⁇ , better select ⁇ C A . o u u t t ⁇ ; 2.4.
- the active metal group preferably in the cross section of each of the catalyst particles, from the position point P A to the center point, the active metal group The concentration of the fraction A gradually decreases substantially along the straight line segment.
- the concentration of the active metal component A is substantially gradually decreased along the straight line segment means that the concentration distribution of the active metal component A is along the straight line segment from the position point P A to the entire interval of the center point (in general) exhibits a gradual decreasing trend, but one or more local intervals are allowed to exist; in the local interval, the concentration distribution of the active metal component A is along Straight line segments exhibit different trends (such as maintaining a constant and/or gradual increase and/or disordered state).
- the premise is that the existence of such local intervals can be tolerated or negligible to those skilled in the art, or is inevitable for the state of the art, and the existence of these local intervals does not affect the technology in the field.
- the concentration distribution of the active metal component A in the entire interval was still judged as "(in general) a tendency to gradually decrease".
- the existence of the local interval does not affect the implementation of the intended purpose of the present invention, is acceptable, and is also included in the scope of the present invention.
- the relation (1) for example, it is preferable to satisfy the following relationship (1'), provided that the position point opt-1 and the position point opt-2 When sufficiently close, for example, the calculated value of (d2 A - dl A ) / L A is very small, for example, 5% or less, preferably 2% or less, more preferably 1% or less, more preferably 0.5% or less, allowing the relationship C A .
- Pt _ 2 (preferably C A . pt- ] > 95% C A . pt-2 , more preferably C A . pt-1 >98% C A . pt-2 ) holds, and does not necessarily satisfy the relationship C A . Pt-1 >C A . Pt-2 .
- C A . p w is a point opt-1 of the active metal component A at any position on the straight line segment (ie, a randomly selected position point opt-1 on the straight line segment, but excluding the center point and the The ratio of the concentration at the position point P A ) to the concentration of the active metal component A at the center point of the cross section of the catalyst particle, C A .
- Pt - 2 is a point opt-2 of the active metal component A at any position on the straight line segment (ie, a randomly selected position point opt-2 on the straight line segment, but excluding the center point and a ratio of a concentration at the position point P A ) to a concentration of the active metal component A at a center point of a cross section of the catalyst particle, and the position point P A and the position point opt-1
- the straight line distance between them is dl A
- the linear distance between the position point P A and the position point opt-2 is d2 A , then dl A /d2 A ⁇ l.
- the relationship (1) is more preferably the relationship ((), ie C A . Ut >C A . Pt -]>C A . Pt-2 >l.
- the concentration distribution of the active metal component B satisfies one of the following conditions (III) or (IV).
- Condition (III) substantially uniformly distributed on the cross section of each of the catalyst particles.
- C B is the concentration of the active metal component B at any position on the outermost edge of the cross section of the catalyst particle P B (randomly arbitrarily selected point) and the active metal component B in the catalyst particle
- the ratio of the concentration at the center point of the cross section, the length of the straight line segment connecting the center point and the position point PB on the cross section of the catalyst particle is L B (no specific unit of measurement is required)
- C B 1 /2 is the concentration of the active metal component B at the linear line segment from the position point PB at (1 /2) L B and the active gold
- the ratio of the concentration of the component B at the center point of the cross section of the catalyst particle, C B is the active metal component B on the straight line segment from the position point P B is (1/4)
- the ratio of the concentration at B to the concentration of the active metal component B at the center point of the cross section of the catalyst particle, C B 3/4 is the distance of the active metal component B on the straight line segment
- the position point P B is the ratio of the concentration at (3/4) L
- Pt is the position of the active metal component B at any position on the straight line segment (ie, a randomly selected position point on the straight line segment, but not including the center point and the position point P B )
- the concentration is the ratio of the concentration of the active metal component B at the center point of the cross section of the catalyst particle.
- the phrase "substantially hook-like distribution in the cross section of each of the catalyst particles” means the entire cross-section of the active metal component B in each of the catalyst particles.
- the concentration profiles on the cross-section are uniformly consistent, but allow for the presence of concentration distribution fluctuations (deviations) that can be tolerated or negligible to one skilled in the art or unavoidable for the state of the art.
- C B at this time Ut is in the range of 5% soil and C B .
- Pt is in the range of 1 5%, preferably C B .
- pt is in the range of 1 ⁇ 2%.
- This concentration distribution fluctuation does not affect the realization of the intended purpose of the present invention, is acceptable, and is also included in the scope of protection of the present invention. within.
- C B is preferred.
- the relationship (3) It is preferably from 0.3 to 0.85.
- C B 1/4 /C B 1/2 0.4-0.9, preferably 0.4-0.87 is more preferable.
- C B is preferred. ut ⁇ 0.70, preferably C B. ut ⁇ 0.68, more preferably C B. Ut ⁇ 0.60.
- C B out >0. 10 preferably C B . ut ⁇ 0.20.
- the active metal group preferably in the cross section of each of the catalyst particles, from the position point P B to the center point, the active metal group The concentration of the fraction B gradually increases substantially along the straight line segment.
- the concentration of the active metal component B is gradually increased substantially along the straight line segment means that the concentration distribution of the active metal component B is along the straight line segment In the entire interval from the position point P B to the center point (in general), a gradual increase trend is exhibited, but one or more partial intervals are allowed to exist; in the local interval, the active metal component B
- the concentration profile exhibits different trends along the straight line segments (eg, maintaining a constant and/or progressively decreasing and/or disordered state).
- the premise is that the existence of such local intervals is tolerable or negligible to those skilled in the art, or is unavoidable for the state of the art, and the existence of these local intervals does not affect the field.
- the concentration distribution of the active metal component B in the entire interval is still "(in general) a tendency to gradually increase".
- the existence of the local interval does not affect the implementation of the intended purpose of the present invention, is acceptable, and is also included in the scope of the present invention.
- the relation (3) for example, it is preferable to satisfy the following relation (3'), provided that the position point opt-1 and the position point opt-2 When sufficiently close, for example, the calculated value of (d2 B - dl B ) / L B is very small, for example, 5% or less, preferably 2% or less, more preferably 1% or less, more preferably 0.5% or less, allowing the relationship C B o pt-1 ⁇ 110%C B opt- 2 (preferably C B . pt-1 ⁇ 105% C B . pt-2 , more preferably C B op t- i ⁇ 102% C B O p t-2 ) At this time, the relationship C B is not necessarily satisfied. Pt-1 ⁇ C B . Pt _ 2 .
- C B opt- i is the point opt-1 of the active metal component B at any position on the straight line segment (ie, a randomly selected position point opt-l on the straight line segment, but not The ratio of the concentration at the center point and the position point P B ) to the concentration of the active metal component B at the center point of the cross section of the catalyst particle, C B .
- Pt _ 2 is the point opt- 2 of the active metal component B at any position on the straight line segment (ie, a randomly selected position point opt-2 on the straight line segment, but excluding the center point and a ratio of a concentration at the position point P B ) to a concentration of the active metal component B at a center point of a cross section of the catalyst particle, and the position point P B and the position point opt-1
- the straight line distance between them is dl B
- the linear distance between the position point P B and the position point opt-2 is d2 B
- dl B /d2 B ⁇ l The straight line distance between them.
- the relation (3) is more preferably the relationship (3'), that is, C B . Ut ⁇ C B . Pt-1 ⁇ C B . Pt-2 ⁇ l.
- the concentration distribution of the active metal component A and the concentration distribution of the active metal component B do not simultaneously satisfy the aforementioned conditions (I) and (III), which may lead to the intended purpose of the invention. can not achieve.
- the concentration distribution of the active metal component A satisfies the aforementioned condition (11), while the concentration distribution of the active metal component B satisfies the aforementioned condition (IV), thereby making the present invention
- the hydrotreating catalyst exhibits a further significantly improved heavy distillate (depth) hydrodesulfurization activity.
- the active metal component C Mo or a combination of Mo and W is preferred.
- the concentration distribution of the active metal component C (such as Mo or a combination of Mo and W) in the catalyst particles is not particularly limited, for example, in the cross section of each of the catalyst particles, Basically, the distribution is hooked, distributed according to a specific law or randomly distributed.
- the concentration distribution of the active metal component C in the catalyst is such that the concentration of the active metal component C is at any point on the cross section of each of the catalyst particles. Sufficient to meet the requirements of these hydrogenation reactions. For example, at any point in the cross section of each of the catalyst particles, the concentration of Mo is sufficient to be combined with Ni and/or Co at the point of the point to achieve the desired hydrodesulfurization activity, or the concentration of W is sufficient The desired hydrodearomatization activity can be achieved in combination with this position.
- the concentration distribution of Mo preferably satisfies one of the following conditions (V) or (VI).
- Condition (V) substantially uniformly branched across the cross section of each of the catalyst particles.
- the condition (Vl) satisfies the following relations (5) and (6) in the cross section of each of the catalyst particles.
- C M °. Ut is the point P M of the active metal component Mo at any position on the outermost edge of the cross section of the catalyst particle. a ratio of a concentration at a (randomly arbitrarily selected position point) to a concentration of the active metal component Mo at a center point of a cross section of the catalyst particle, which is disposed on a cross section of the catalyst particle to connect the center point with The position point P M .
- the length of the straight line segment is L M . (Specific unit of measurement is not required), C M ° 1/2 is the distance from the position point P M of the active metal component Mo on the straight line segment.
- Pt is the position of the active metal component Mo at any position on the straight line segment (ie, a randomly selected position point on the straight line segment, but not including the center point and the position point PMO)
- the ratio of the concentration to the concentration of the active metal component Mo at the center point of the cross section of the catalyst particle is the position of the active metal component Mo at any position on the straight line segment (ie, a randomly selected position point on the straight line segment, but not including the center point and the position point PMO)
- the phrase "substantially hook-shaped distribution in the cross section of each of the catalyst particles” means that the concentration distribution of Mo over the entire cross section of each of the catalyst particles is Both are consistent, but allow for concentration distribution fluctuations (deviations) that can be tolerated or negligible to those skilled in the art or are unavoidable for the state of the art.
- Ut is in the range of 1 ⁇ 5% and C M °.
- Pt is in the range of 1 5%, preferably C M °.
- Ut is at 1 ⁇ 2. /.
- Within the range and C M °. Pt is at 1 ° 2 ° /.
- Fluctuations in the concentration distribution do not affect the achievement of the intended purpose of the invention, are acceptable, and are also included within the scope of the invention.
- C M is preferred. . Ut ⁇ C M . 1/4 ⁇ C M . 1/2 ⁇ C M . 3/4 ⁇ l , more preferably c M . . Ut ⁇ c M v ⁇ i.
- the concentration of the active metal component Mo gradually increases substantially along the straight line segment.
- the entire interval to the center point exhibits a gradually increasing trend, but one or more local intervals are allowed to exist; within the local interval, the concentration distribution of the active metal component Mo follows the straight line Line segments exhibit different trends (such as maintaining a constant and/or decreasing and/or disordered state).
- the premise is that the existence of such local intervals is tolerable or negligible to those skilled in the art, or is unavoidable for the state of the art, and the existence of these local intervals does not affect the field.
- the concentration distribution of the active metal component Mo in the entire interval is "(in general) a gradually increasing tendency".
- the existence of the local interval does not affect the implementation of the intended purpose of the present invention, and is acceptable. It is also included in the scope of protection of the present invention.
- the relation (5) for example, it is preferable to satisfy the following relation (5'), provided that the position point opt-1 and the position point opt-2 When close enough, for example (d2 M .- dl M .) / L M .
- the calculated value is very small, for example, 5% or less, preferably 2% or less, more preferably 1% or less, and even more preferably 0.5% or less, the relationship c M ° is allowed.
- Pt-1 ⁇ no%c M °. Pt-2 (preferably c M °. pt-I ⁇ i 05% c M °. pt-2 , more preferred
- C M °. p w is a point opt-1 of the active metal component Mo at any position on the straight line segment (ie, a randomly selected position point opt-1 on the straight line segment, but does not include the center point and the The ratio of the concentration at the position point P M . ) to the concentration of the active metal component Mo at the center point of the cross section of the catalyst particle
- C M ° . Pt . 2 is the point opt- 2 of the active metal component Mo at any position on the straight line segment (ie, a randomly selected position point opt-2 on the straight line segment, but excluding the center point and The ratio of the concentration at the position point P M .
- the relationship (5) is more preferably the relationship (5'), that is, C Mo out ⁇ C Mo opt-1 ⁇ C Mo opt-2 ⁇ l.
- the concentration distribution of the Mo preferably satisfies one of the conditions (V) or (VI)
- the concentration distribution of W preferably satisfies one of the following conditions (VII) or (VIII).
- Condition (VII) a substantially uniform distribution of the cross section of each of the catalyst particles.
- C w is the concentration of the active metal component W at any position on the outermost edge of the cross section of the catalyst particle, Pw (randomly arbitrarily selected point), and the active metal component W in the cross section of the catalyst particle.
- the length of the straight line segment is L w (no specific unit of measurement is required), and C w 1/2 is that the active metal component W is at (1/2) L W from the position point P w on the straight line segment a concentration of the active metal component W at a concentration at a center point of the cross section of the catalyst particle, C w 1/4 is the active metal component W on the straight line segment from the position P w is the ratio of the concentration at (1/4) L W to the concentration of the active metal component W at the center point of the cross section of the catalyst particle, and C w 3 /4 is the active metal component W a ratio of a concentration at the position point P w of (3/4) L w to a concentration of the active metal component W at a center point of a cross section of the catalyst particle on the straight line segment, C w .
- Pt is the position of the active metal component W at any position on the straight line segment (ie, a randomly selected position point on the straight line segment, but not including the center point and the position point P w )
- the concentration is the ratio of the concentration of the active metal component W at the center point of the cross section of the catalyst particle.
- the phrase "substantially hook-shaped distribution in the cross section of each of the catalyst particles” means the entire cross-section of the active metal component W in each of the catalyst particles.
- the concentration distribution on the cross section is uniform, but allows concentration distribution fluctuations (deviations) that are unavoidable for the level.
- Ut is in the range of 1 5% and ⁇ is in the range of 1 5%, preferably Cw .
- Ut is in the range of 1 ⁇ 2% and C w .
- Pt is in the range of 1 ⁇ 2%. Fluctuations in the concentration distribution do not affect the achievement of the intended purpose of the invention, are acceptable, and are also included within the scope of the invention.
- the active metal group preferably in the cross section of each of the catalyst particles, from the position point P w to the center point, the active metal group The concentration of the fraction W gradually decreases substantially along the straight line segment.
- the concentration of the active metal component W is substantially gradually decreased along the straight line segment, and refers to the concentration distribution of the active metal component W along the straight line segment from the position point.
- P w to the entire interval of the center point exhibits a gradually decreasing trend, but one or more local intervals are allowed to exist; in the local interval, the concentration distribution of the active metal component W is along Straight line segments show different trends
- the relation (7) for example, it is preferable to satisfy the following relation (7'), provided that the position point opt-1 and the position point opt-2 When sufficiently close, for example, the calculated value of (d2 w - dl w ) / L w is very small, for example, 5% or less, preferably 2% or less, more preferably 1% or less, more preferably 0.5% or less, allowing the relationship C w . Pt-1 >90%C w . Pt 2 (preferably C w . pt-1 >95% C w . pt-2 , more preferably C w . p w>98. / 0 C w . pt-2 ) holds, and does not necessarily satisfy the relationship C w . Pt-1 ⁇ C w . Pt _ 2 .
- C w . p w is a point opt-1 of the active metal component W at any position on the straight line segment (ie, a randomly selected position point opt-1 on the straight line segment, but excluding the center point and the The ratio of the concentration at the position point P w ) to the concentration of the active metal component W at the center point of the cross section of the catalyst particle, C w .
- Pt-2 is a point opt-2 of the active metal component W at any position on the straight line segment (ie, a randomly selected position point opt-2 on the straight line segment, but does not include the center point and a ratio of a concentration at the position point P w ) to a concentration of the active metal component W at a center point of a cross section of the catalyst particle, and the position point P w and the position point opt-1
- the straight line distance between them is dl w
- the straight line distance between the position point P w and the position point opt-2 is d2 w , then dl w /d2 w ⁇ lo
- the relationship (7) is more preferably the relationship (7'), i.e. Cw . Ut >C w . Pt-1 >C w . Pt-2 >l.
- a ratio of a concentration of the active metal component A to a concentration of the active metal component C (preferably a ratio of a concentration of Ni to a concentration of Mo, a ratio of a concentration of Ni to a concentration of W, or a concentration of Ni and (W+)
- the ratio of the concentration of Mo is generally 0.22 to 0.80, preferably 0.30 to 0.70.
- the active metal group is at a central point of the catalyst particle, that is, at a center point of a cross section of the catalyst particle
- the ratio of the concentration of the fraction B to the concentration of the active metal component C is generally 0.20 to 0.78, preferably 0.25 to 0.65.
- the concentration distribution of the optional auxiliary component in the catalyst particles or the concentration distribution on the cross section of the catalyst particles there is no limitation on the concentration distribution of the optional auxiliary component in the catalyst particles or the concentration distribution on the cross section of the catalyst particles, and those conventionally used in the art may be employed, such as As described above, basically all of them can be distributed.
- the concentration of each active metal component, B and C, and optional auxiliary component at a point on the cross section of the catalyst particle or the concentration distribution on the cross section can be carried out using any known method in a conventional manner in the art.
- the specific value of the concentration (such as its absolute value or unit of measure) is not critical, but more concerned with the relative ratio between the two concentrations (such as the aforementioned C A . ut, etc.), so it is preferred to use EPMA.
- the method Electro Probe Micro-analyzer
- the measurement method and calculation method are known in the art and will not be described herein. At this time, the position point corresponds to a measurement micro-area of the EPMA method.
- the hydrotreated catalyst can be produced by one of the following first to fourth production methods.
- the adsorbent I is loaded on the particulate porous refractory support by an unsaturated impregnation method.
- the porous refractory support is preferably one or more selected from the group consisting of porous refractory oxides, more preferably one or more selected from the group consisting of porous inorganic refractory oxides, more preferably selected.
- One or more of the oxides of the Group II, Group III and Group IV elements of the periodic table more preferably selected from the group consisting of silica, alumina, magnesia, silica alumina, magnesium silicate and One or more of alumina magnesium is more preferably alumina.
- the porous refractory support preferably contains alumina as an essential component.
- alumina for example, one or more of ⁇ -alumina, ⁇ -alumina, lanthanum-alumina, ⁇ -alumina, and yttrium-alumina may be mentioned, and among them, ⁇ -alumina is preferable.
- the porous refractory carrier is (solid) granular, rather than an amorphous state such as powder.
- shape of the particles it is known in the art
- various shapes conventionally used for the carrier of the hydrotreating catalyst for example, a spherical shape, a column shape, a sheet shape and the like can be further exemplified, and among them, a spherical shape or a column shape is preferable.
- the spherical shape include a spherical shape and an ellipsoidal shape.
- Examples of the cylindrical shape include a columnar shape, a square column shape, and a profiled cross section (for example, a clover or the like).
- the porous refractory support can be formed into a pellet form by any method conventionally known in the art, or a commercially available granulated product.
- the molding method include a dropping ball molding method, a ball granulation method, an extrusion molding method, and a compression molding method.
- a dropping ball molding method and an extrusion molding method are preferable.
- the foregoing oxide (including the precursor of the oxide) or a mixture thereof, such as alumina (or its precursor) and/or silicon oxide (or its precursor), etc. may be passed through these molding methods. Molding is carried out and then calcined.
- the precursor of the alumina may be, for example, one or more of various hydrated aluminas and aluminum sols
- the precursor of the silica may be any water-soluble silicon-containing compound or
- the silicon-containing compound which can be hydrolyzed to form a silicone gel or a sol in an aqueous medium may be one or more of water glass, silica sol, and silicate.
- an appropriate amount of a sizing agent and/or an adhesive may be added to the carrier or oxide to be formed, followed by molding.
- the type and amount of the squeezing agent and peptizer are known to those skilled in the art.
- a common squeezing agent may be selected from the group consisting of phthalocyanine powder, methyl cellulose, starch, polyvinyl alcohol, and polyethanol. One or several of them.
- the specific surface area (BET method) of the particulate porous refractory support is generally from 100 to 500 m 2 /g, preferably from 150 to 400 m 2 /g.
- the pore volume (BET method) of the particulate porous refractory carrier is generally 1.0 ml/g, preferably 0.3 to 0.9 1 .
- the bulk density (mechanical knocking method) of the particulate porous refractory carrier is generally 40 to 100 g/100 ml, preferably 50 to 70 g/100 ml.
- the saturated porous refractory carrier of the particulate form generally has a saturated liquid absorption of 40 to 140 ml/100 g, preferably 60 100 ml/100 g.
- 100 g of the granular porous refractory carrier was weighed into a separatory funnel, and then 300 ml of purified water was added to make the water surface exceed the surface of the carrier, and it was left for 30 minutes, and then the excess water was drained. In the graduated cylinder, the volume of excess water is obtained. At this time, the formula for calculating the saturated liquid absorption is (300-L) ⁇ 100 (ml/100g).
- the average particle size (sieving method) of the particulate porous refractory carrier is generally from 3 to 8 mm, preferably from 3 to 5 mm.
- the adsorbent I is selected from the group consisting of organic carboxylic acids having 2 to 15 carbon atoms, and examples thereof include a monovalent or polybasic carboxylic acid according to the specification, and among them, a dicarboxylic acid is preferred, and the organic carboxylic acid can also be used.
- An ammonium salt of an acid is selected from the group consisting of organic carboxylic acids having 2 to 15 carbon atoms, and examples thereof include a monovalent or polybasic carboxylic acid according to the specification, and among them, a dicarboxylic acid is preferred, and the organic carboxylic acid can also be used.
- An ammonium salt of an acid is selected from the group consisting of organic carboxylic acids having 2 to 15 carbon atoms, and examples thereof include a monovalent or polybasic carboxylic acid according to the specification, and among them
- adsorbent I preferably selected from the group consisting of acetic acid, oxalic acid, lactic acid, malonic acid, tartaric acid, malic acid, citric acid, trichloroacetic acid, monochloroacetic acid, thioglycolic acid, mercaptopropionic acid, ethylenediaminetetraacetic acid, nitrogen One or more of triacetic acid, cycloethylenediaminetetraacetic acid, and ammonium salts thereof.
- the adsorbent I is used in an amount of usually 0.1 to 10% by weight, preferably 0.5 to 9.0% by weight based on the total mass of the particulate porous refractory support.
- an organic alcohol having 1 to 5 carbon atoms together with the adsorbent I on the particulate porous refractory support as needed.
- the organic alcohol for example, a monohydric or polyhydric alcohol which meets the requirements may be mentioned, and one or more selected from the group consisting of ethylene glycol, propylene glycol, glycerin, pentaerythritol and xylitol is preferable.
- the amount of the organic alcohol is generally 0.1 to 10% by weight, preferably 0.5 to 9.0% by weight based on the weight of the particulate porous refractory support.
- porate porous refractory carrier is abbreviated as “porous refractory carrier” unless otherwise specified or not in accordance with the conventional understanding of those skilled in the art.
- the adsorbent I and optionally the organic alcohol are preferably a wetting fluid (ie containing the adsorbent I and optionally the organic alcohol) Used in the form of a solution).
- the solvent of the solution may, for example, be water, ethanol or a mixture of water and ethanol in any ratio, but may not be limited thereto.
- the unsaturated impregnation method can be carried out by any means conventionally known in the art, with unsaturated impregnation being preferred.
- the wetting liquid is directly sprayed onto the porous refractory carrier (as a target to be immersed) in a predetermined amount ratio to effect immersion.
- the spraying time is generally lmin ⁇ 40min, preferably 2min ⁇ 20mm.
- a nozzle having a good atomization effect can be selected so that the wetting liquid is uniformly dispersed on the porous refractory carrier.
- the product directly obtained by the step (1-1) can be maintained (i.e., static) after the end of the step (1) or before the start of the following step (1-2), as needed or preferred.
- the health step 0.5 ⁇ 8h (preferably 0.5 ⁇ 6h)
- the product is first subjected to the conditioning step, and then This drying step is carried out again.
- the product thus obtained is collectively referred to as "the product obtained in the step (1-1)" in a non-discriminate manner with the product directly obtained from the step (1-1).
- the description of the active metal component B, the active metal component C and the auxiliary component is as described above.
- the product directly obtained by the step (1-2) can be raised 0.5 after the end of the step (1-2) but before the start of the following step (1-3), as needed or preferred.
- - 6h preferably 0.5 ⁇ 4h or without curing, drying at a temperature of 70 ⁇ 200 ° C (preferably 100 ⁇ 160 ° C) 0.5 ⁇ 20h (preferably 1 ⁇ 6h), then at a temperature of 300 ⁇ 750 ° C (preferred 400 ⁇ 650.
- C) Roasting 0.5 ⁇ 20h (preferably 1 ⁇ 6h).
- the product thus obtained is collectively referred to as "the product obtained in the step (1-2)" indiscriminately with the product directly obtained from the step (1-2).
- the meaning is that before the start of step (1-1), the active metal component A is supported on the (granular) porous refractory support, and the active metal component is optionally loaded beforehand, simultaneously or subsequently C and/or the auxiliary component, wherein preferably the active metal component A and the active metal component C are simultaneously supported, and the auxiliary component is optionally loaded beforehand or simultaneously, thereby obtaining a pretreated a porous refractory support (which is still referred to as a porous refractory support in the present specification); or, after the end of the step (1-2), is loaded on the product obtained in the step (1-2) (substantially still Loading onto the porous refractory support) active metal component A, and optionally loading the active metal component C and/or the auxiliary component in advance, simultaneously or
- the description of the active metal component A is as described above.
- the product directly obtained by the step may be cured for 0.5-6 h (preferably 0.5 4 h) or after the end of the step (1-3), as needed or preferably Drying at a temperature of 70 ⁇ 200 ° C (preferably 100 ⁇ 160 ° C) for 0.5 ⁇ 20h (preferably 1 ⁇ 6h), followed by roasting at a temperature of 300 ⁇ 750 ° C (preferably 400 - 650 ° C) ⁇ 20h (preferably 1 ⁇ 6h), and then carry out the subsequent steps or obtain the hydrotreating catalyst of the present invention.
- any of the aforementioned health, drying or calcination can be carried out in a manner conventionally known in the art, and if necessary, it can also be carried out under an inert atmosphere such as nitrogen or an atmosphere (preferably an air atmosphere). There are no special restrictions.
- the loading method involved in the step (1-2) and the step (1-3) is not particularly limited as long as the active metal component A can be introduced onto the carrier or the product.
- Any method of the active metal component (:, the active metal component B and optionally the auxiliary component may be employed.
- a saturated impregnation method or an excessive impregnation method may be mentioned. These methods are conventionally known in the art, and the technical details of the implementation thereof are not described in detail herein.
- the saturated impregnation method is carried out by a saturated spray immersion method, and the immersion time is generally 5 to 40 minutes, preferably 10 to 20 minutes.
- the active metal component A, the active metal component C, the active metal component B and optionally the auxiliary component are desirably selected as a wetting liquid.
- a solution containing the corresponding component also called an immersion liquid
- the solvent of the solution may, for example, be water, ethanol or a mixture of water and ethanol in any ratio, but may not be limited thereto.
- the active metal component A, the active metal component C, the active metal component B and optionally the auxiliary component are generally soluble compounds.
- Formal use which is conventionally known in the art.
- the soluble compound of the active metal component A for example, (water)-soluble organic or inorganic acid salts, particularly nickel nitrate, nickel carbonate, basic nickel carbonate, nickel chloride, oxalic acid, may be mentioned. Nickel and nickel sulfate.
- the soluble compound of the active metal component A may be used singly or in combination of two or more kinds.
- Examples of the soluble compound of the active metal component B include organic (aqueous) soluble organic or inorganic acid salts, particularly cobalt nitrate, cobalt carbonate, basic cobalt carbonate, cobalt chloride, and cobalt oxalate.
- the soluble compound of the active metal component B may be used singly or in combination of two or more kinds.
- As the soluble compound of the active metal component C for example, (water)-soluble oxyacid salts thereof, particularly ammonium molybdate, ammonium paramolybdate, ammonium phosphomolybdate, ammonium metatungstate and ethyl group can be mentioned. Ammonium tungstate and the like.
- the soluble compound of the active metal component C may be used alone, They can also be used in combination of two or more kinds.
- the soluble compound of the auxiliary component for example, phosphoric acid, phosphorous acid, phosphate, phosphite, trimethyl phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, and ammonium phosphate (phosphorus-containing auxiliary group) may be mentioned. Sub), ammonium fluoroborate, hydrofluoric acid, hydrofluoric acid salt, fluorosilicic acid, fluorosilicate and ammonium fluoride (fluorine-containing auxiliary component).
- the soluble compounds of the auxiliary component may be used singly or in combination of two or more kinds.
- the components i.e., active metal component A, active metal component C, active metal component B, and optional auxiliary group
- the respective amounts or total amounts (when loaded separately by a plurality of steps), including the concentration in the respective dampening liquids and/or the amount of the dampening liquid, are not particularly limited as long as they can be applied to each
- the loading method used in the step and the content of these components (including the porous refractory carrier) in the hydrotreating catalyst finally obtained by the first production method may satisfy the aforementioned specifications of the present specification.
- the two or more components may be in the same wetting fluid, or may be in separate wetting fluids either individually or in any combination.
- the active metal component C (essential component of the present invention) must be supported by at least one of the step (1-2) and the step (1-3), wherein preferably by the step (1) -2) A combination of steps (1-3) to support the active metal component C.
- the active metal component C when the active metal component C includes Mo, it is preferred to carry Mo by a combination of the step (1-2) and the step (1-3). At this time, it is preferred that the molar ratio of the Mo loading in the previous step to the Mo loading in the subsequent step is 0.4 to 2.5:1, preferably 0.4 to 2.0:1, by adjusting the amount of Mo in each of the two steps.
- the adsorbent II is selected from the group consisting of polyols having a number average molecular weight Mn (measured by GPC method) of from 400 to 10,000, preferably selected from polyols having a number average molecular weight Mn (measured by GPC method) of from 1,000 to 8,000.
- polyhydric alcohol for example, polyether two according to the regulation can be cited. Alcohol, polyester diol, and the like.
- the polyether diol include polyethylene glycol, polypropylene glycol, polyglycerin, a copolymer of ethylene oxide and propylene oxide, and among them, polyethylene glycol is preferred.
- the adsorbent II is used in an amount of usually 0.1 to 10% by weight, preferably 0.5 to 9.0% by weight based on the weight of the particulate porous refractory support.
- the adsorbent II is preferably used in the form of a dampening solution (i.e., a solution containing the adsorbent II).
- the solvent of the solution may, for example, be water, ethanol or a mixture of water and ethanol in any ratio, but may not be limited thereto.
- the saturated impregnation method or the excess impregnation method can be carried out by any means conventionally known in the art, and is not particularly limited and will not be further described herein.
- the saturated impregnation method is carried out by a saturated spray immersion method, and the immersion time is generally 5 to 40 minutes, preferably 10 to 20 minutes.
- the product directly obtained in the step (2-1) can be maintained after the end of the step (2-1) but before the start of the following step (2-2), as needed or preferred ( That is, standing still, the same as below) 1 ⁇ 12h (preferably 4 ⁇ 12h) (called the health step), or the product is dried at a temperature of 60 - 250 ° C (preferably 100 ⁇ 200 V) for 0.5 ⁇ 20h (preferably l ⁇ 6h) (referred to as the drying step), or the product is first subjected to the conditioning step, and then the drying step is carried out.
- the product thus obtained is collectively referred to as "the product obtained in the step (2-1)" indiscriminately together with the product directly obtained from the step (2-1).
- the active metal component A is supported on the product obtained in step (2-1), and optionally the active metal component C and/or the auxiliary component are simultaneously and/or subsequently supported.
- the product directly obtained in the step (2-2) can be raised 0.5 after the end of the step (2-2) but before the start of the following step (2-3), as needed or preferred.
- ⁇ 6h preferably 0.5 ⁇ 4h or without curing, drying at a temperature of 70 ⁇ 200 ° C (preferably 100 ⁇ 160 ° C) 0.5 ⁇ 20h (preferably 1 ⁇ 6h), then at a temperature of 300 ⁇ 750 ° C (preferred Roasting at 400 ⁇ 650 °C for 0.5 ⁇ 20h (preferably 1 ⁇ 6h).
- the product thus obtained is collectively referred to as "the product obtained in the step (2-2)" indiscriminately together with the product directly obtained from the step (2-2).
- Step (2-3) Before the start of step (2-1) and/or after the end of step (2-2), The active metal component B, optionally the active metal component C, and optionally the auxiliary component are supported on the porous refractory support.
- the meaning is that before the start of step (2-1), the active metal component B is supported on the (granular) porous refractory support, and the active metal component is optionally loaded beforehand, simultaneously or subsequently And/or the auxiliary component, wherein preferably the active metal component B and the active metal component C are simultaneously supported, and the auxiliary component is optionally loaded before or at the same time, thereby obtaining a pretreated a porous refractory support (which is still referred to as a porous refractory support in the present specification); or, after the end of the step (2-2), is loaded on the product obtained in the step (2-2) (substantially still Loading onto the porous refractory support) the active metal component B, and optionally supporting the active metal component C and/or the auxiliary component in advance
- the product directly obtained from the step can be cured for 0.5 to 6 hours (preferably 0.5 to 4 hours) or without curing at a temperature of 70, as needed or preferably after the end of the step (2-3). Dry at ⁇ 200 ° C (preferably 100 ⁇ 160 ° C) for 0.5 ⁇ 20h (preferably 1 ⁇ 6h), then calcined at a temperature of 300 ⁇ 750 °C (preferably 400 ⁇ 650 °C) for 0.5 ⁇ 20h (preferably l ⁇ 6h) And then proceeding to the subsequent step or obtaining the hydrotreating catalyst of the present invention.
- any of the aforementioned curing, drying or calcining can be carried out in a manner conventionally known in the art, and if necessary, in an inert atmosphere such as nitrogen or an air atmosphere (preferably an air atmosphere), and There is no particular limitation.
- the loading method involved in the step (2-2) and the step (2-3) includes the active metal component A, the active metal component C, and the active metal component B.
- the loading method and dosage of the auxiliary component There is no special requirement for the loading method and dosage of the auxiliary component, and the corresponding regulations or descriptions in the first manufacturing method described above can be directly applied.
- the active metal component C (essential component of the present invention) must be supported by at least one of the step (2-2) and the step ( 2-3 ), wherein preferably by the step (2) -2) in combination with step (2-3) to support the active metal component C.
- the active metal component C includes Mo
- the molar ratio of the Mo loading in the previous step to the Mo loading in the latter step is 0.4 to 2.5:1, preferably 0.4 to 2.0:1, by adjusting the amount of Mo in each of the two steps.
- Step (3-1) The adsorbent I is loaded on the particulate porous refractory support by an unsaturated impregnation method, and optionally an organic alcohol having 1 to 5 carbon atoms is supported. This step directly applies to the provisions and descriptions of step (1-1) in the first manufacturing method.
- the product directly obtained in the step (3-1) can be maintained after the end of the step (3-1) or before the start of the following step (3-2), as needed or preferred ( That is, standing still, the same as below) 0.5 ⁇ 811 (preferably 0.5 ⁇ 611) (called a health step), or drying the product at a temperature of 60-250 ° C (preferably 100 ⁇ 200 ° C) for 0.5 ⁇ 20h (preferably l ⁇ 6h) (referred to as the drying step), or the product is first subjected to the conditioning step, and then the drying step is carried out.
- the product thus obtained is collectively referred to as "the product obtained in the step (3-1)", indiscriminately together with the product directly obtained from the step (3-1).
- the product directly obtained in the step (3-2) can be raised 0.5 after the end of the step (3-2) but before the start of the following step (3-3), as needed or preferred.
- ⁇ 6h preferably 0.5 ⁇ 4h
- the product thus obtained is collectively referred to as "the product obtained in the step (3-2)" indiscriminately together with the product directly obtained from the step (3-2).
- Step (3-3) The adsorbent II is supported on the product obtained in the step (3-2) by a saturated impregnation method or an excessive impregnation method.
- This step is directly applicable to the specification and description of the step (2-1) in the second production method, except that the porous refractory carrier is replaced with the product obtained in the step (3-2).
- the adsorbent II is used in an amount of usually 0.1 to 10% by weight, preferably 0.5 to 9.0% by weight based on the weight of the particulate porous refractory support.
- the step (3-3) may be performed as needed or preferably.
- the product directly obtained in step (3-3) is cured (ie, left, the same below) 1 ⁇ 12h (preferably 4 ⁇ 12h) (referred to as the health step) , or drying the product at a temperature of 60-250 ° C (preferably 100-200 ° C) for 0.5-20 h (preferably l ⁇ 6 h) (referred to as a drying step), or the product is first subjected to the conditioning step, and then This drying step is carried out.
- the product thus obtained is collectively referred to as "the product obtained in the step (3-3)" in a non-discriminate manner with the product directly obtained from the step (3-3).
- the product directly obtained in the step (3-4) can be raised 0.5 after the end of the step (3-4) but before the start of the following step (3-5), as needed or preferred.
- ⁇ 6h preferably 0.5 ⁇ 4h
- drying at a temperature of 70 ⁇ 200 ° C (preferably 100 ⁇ 160V) for 0.5 ⁇ 20h (preferably 1 ⁇ 6h), then at a temperature of 300 ⁇ 750 ° C (preferably 400 ⁇ Calcined at 650 ° C for 0.5 ⁇ 20 h (preferably 1 ⁇ 6 h).
- the product thus obtained is collectively referred to as "the product obtained in the step (3-4)" indiscriminately together with the product directly obtained from the step (3-4).
- the active metal component C and optionally the auxiliary component are supported on the porous refractory support.
- the meaning is that before the start of step (3-1), the active metal component C is supported on the (granular) porous refractory support, and the auxiliary component is optionally pre-, simultaneously or subsequently loaded.
- a pretreated porous refractory support (which is still referred to as a porous refractory support in the present specification); or, after the end of the step (3-2) but at the step (3-3) Previously, the active metal component C is supported (substantially still supported on the porous refractory support) on the product obtained in step (3-2), and optionally the auxiliary component is loaded beforehand, simultaneously or subsequently Thereby obtaining a pretreated product (which is still referred to as the product obtained in the step (3-2) in the present specification); or, after the end of the step (3-4), obtaining in the step (3-4) The product is loaded (substantially still supported on the porous refractory support) with the active metal component C, and optionally the precursor component is supported beforehand, simultaneously or subsequently, thereby obtaining the present The hydrotreating catalyst of the invention; or any combination of the three.
- the product directly obtained by the step may be cured for 0.5 to 6 hours (preferably 0.5 to 4 hours) or not after the end of the step (3-5), as needed or preferably, at a temperature of 70 Dry at ⁇ 200 ° C (preferably 100 ⁇ 160 ° C) for 0.5 ⁇ 20h (preferably 1 ⁇ 6h), then calcined at a temperature of 300 - 750 ° C (preferably 400 ⁇ 650 ° C) for 0.5 ⁇ 20h (preferably l ⁇ 6h) And then proceeding to the subsequent step or obtaining the hydrotreating catalyst of the present invention.
- any of the aforementioned curing, drying or calcining can be carried out in a manner conventionally known in the art, and, if necessary, in an inert atmosphere such as nitrogen or an air atmosphere (preferably an air atmosphere), and There is no particular limitation.
- the loading method involved in the step (3-2), the step (3-4) and the step (3-5) includes the active metal component A and the active metal component
- the loading mode, amount, and the like of the active metal component B and the auxiliary component there is no particular requirement for the loading mode, amount, and the like of the active metal component B and the auxiliary component, and the corresponding regulations or descriptions in the first manufacturing method described above can be directly applied.
- the active metal component C (essential component of the present invention) must be supported by at least one of the step (3-2), the step (3-4), and the step (3-5).
- the active metal component is preferably supported by a combination of the step (3-2) and the step (3-4).
- the active metal component C includes Mo
- the molar ratio of the Mo loading in the previous step to the Mo loading in the subsequent step is 0.4 to 2.5:1, preferably 0.4 to 2.0:1, by adjusting the amount of Mo in each of the two steps.
- Step (4-1) The adsorbent II is supported on a particulate porous refractory support by a saturated impregnation method or an excessive impregnation method. This step directly applies to the specification and description of step (2-1) in the second manufacturing method.
- the product directly obtained in the step (4-1) can be maintained after the end of the step (4-1) or before the start of the following step (4-2), as needed or preferably ( That is, standing still, the same as below) 1 ⁇ 12h (preferably 4 ⁇ 12h) (called the health step), or the product is dried at a temperature of 60 ⁇ 250 ° C (preferably 100 ⁇ 200 ° C) 0.5 - 20h (excellent l ⁇ 6h) (referred to as the drying step), or the product is first subjected to the conditioning step, and then the drying step.
- the product thus obtained is collectively referred to as "the product obtained in the step (4-1)" indiscriminately together with the product directly obtained from the step (4-1).
- Step (4-2) The active metal component A, the optional active metal component C and the optional auxiliary component are supported on the product obtained in the step (4-1). This means that the active metal component A is supported on the product obtained in step (4-1), and optionally the active metal component C and/or the auxiliary component are simultaneously and/or subsequently supported. Among them, it is preferred to simultaneously carry the active metal component A and the active metal component C on the product obtained in the step (4-1), and optionally simultaneously carry the auxiliary component.
- the product directly obtained in the step (4-2) can be raised 0.5 after the end of the step (4-2) but before the start of the following step (4-3), as needed or preferred.
- ⁇ 6h preferably 0.5 ⁇ 4h
- at a temperature of 300 ⁇ 750 ° C preferred Roasting at 400 ⁇ 650 ° C for 0.5 ⁇ 20h (preferably 1 ⁇ 6h).
- the product thus obtained is collectively referred to as "the product obtained in the step (4-2)" indiscriminately together with the product directly obtained from the step (4-2).
- Step (4-3) The adsorbent I is loaded on the product obtained in the step (4-2) by an unsaturated impregnation method, and optionally an organic alcohol having a carbon number of 1 to 5 is supported.
- This step is directly applicable to the specification and description of the step (1-1) in the first production method, except that the porous refractory carrier is replaced with the product obtained in the step (4-2).
- the adsorbent I is used in an amount of usually 0.1 to 10% by weight, preferably 0.5 to 9.0% by weight based on the weight of the particulate porous refractory support.
- the organic alcohol is generally used in an amount of from 0.1 to 10% by weight, preferably from 0.5 to 9.0% by weight, based on the weight of the particulate porous refractory support.
- the product directly obtained in the step (4-3) can be maintained after the end of the step (4-3) but before the start of the following step (4-4), as needed or preferred ( That is, standing still, the same as below) 0.5 ⁇ 8h (preferably 0.5 ⁇ 6h) (called the health step), or the product is dried at a temperature of 60 ⁇ 250 ° C (preferably 100 ⁇ 200 ° C) for 0.5 ⁇ 20h (preferably l ⁇ 6h) (referred to as the drying step), or the product is first subjected to the conditioning step, and then the drying step.
- the product thus obtained is collectively referred to as "the product obtained in the step (4-3)" together with the product directly obtained from the step (4-3).
- Step (4-4) The active metal component B, optionally the active metal component C, and optionally the auxiliary component are supported on the product obtained in the step (4-3). Its meaning is that The product obtained in step (4-3) is supported on the active metal component B, and optionally simultaneously and/or subsequently loaded with the active metal component C and/or the auxiliary component. Among them, it is preferred to simultaneously carry the active metal component B and the active metal component C on the product obtained in the step (4-3), and optionally simultaneously carry the auxiliary component.
- the product directly obtained in the step (4-4) can be raised 0.5 after the end of the step (4-4) but before the start of the following step (4-5), as needed or preferred.
- ⁇ 6h preferably 0.5 ⁇ 4h
- the product thus obtained is collectively referred to as "the product obtained in the step (4-4)" indiscriminately together with the product directly obtained from the step (4-4).
- the active metal component C and optionally the auxiliary component are supported on the porous refractory support.
- the meaning is that before the start of step (4-1), the active metal component C is supported on the (granular) porous refractory support, and the auxiliary component is optionally pre-, simultaneously or subsequently loaded.
- a pretreated porous refractory support (which is still referred to as a porous refractory support in the present specification); or, after the end of the step (4-2) but at the step (4-3) Previously, the active metal component C is supported (substantially still supported on the porous refractory support) on the product obtained in step (4-2), and optionally the auxiliary component is loaded beforehand, simultaneously or subsequently Thereby obtaining a pretreated product (which is still referred to as the product obtained in the step (4-2) in the present specification); or, after the end of the step (4-4), obtaining in the step (4-4) The product is supported (substantially still supported on the porous refractory support) active metal component C, and optionally pre-, simultaneously or subsequently loaded with the auxiliaries component, thereby obtaining the hydrotreating of the present invention Catalyst; or three ways Italian combination.
- the product directly obtained by the step may be cured for 0.5 to 6 hours (preferably 0.5 to 4 hours) or not after the end of the step (4-5), as needed or preferably, at a temperature of 70 5 ⁇ 20 ⁇ Preferably, it is dried at a temperature of 300 ⁇ 750 ° C (preferably 400 ⁇ 650V) 0. 5 ⁇ 20h (preferably l ⁇ 6h) And then proceeding to the subsequent step or obtaining the hydrotreating catalyst of the present invention.
- any of the aforementioned health, drying or baking can be followed It is carried out in a manner conventionally known in the art, and may be carried out under an inert atmosphere such as nitrogen or an air atmosphere (preferably an air atmosphere) as needed, and is not particularly limited.
- the loading method involved in the step (4-2), the step (4-4) and the step ( 4 _ 5 ) includes the active metal component A and the active metal component C.
- the loading method and amount of the active metal component B and the auxiliary component are not particularly required, and the corresponding provisions or descriptions in the first to third manufacturing methods described above can be directly applied.
- the active metal component C (essential component of the present invention) must be supported by at least one of the step (4-2), the step (4-4), and the step (4-5).
- the active metal group is preferably supported by a combination of the step (4-2) and the step (4-4) according to the fourth manufacturing method, and when the active metal component C comprises Mo, preferably by the step (4) -4) Combine with step (4-2) to load Mo.
- the molar ratio of the Mo loading in the previous step to the Mo loading in the subsequent step is 0.4 to 2.5:1, preferably 0.4 to 2.0:1, by adjusting the amount of Mo in each of the two steps.
- the hydrotreating catalyst may be presulfided with sulfur, hydrogen sulfide or a sulfur-containing raw material or the like in the presence of hydrogen gas as needed before use. It can also be vulcanized in situ in the vessel, thereby converting it to a sulfide type. This pre-vulcanization technique is known in the art and will not be described again.
- the present invention also relates to the use of the aforementioned hydrotreating catalyst as a hydrodesulfurization catalyst in hydrodesulfurization (especially deep hydrodesulfurization) of heavy distillates (especially diesel).
- the heavy distillate for example, diesel oil and wax oil can be cited, and among them, diesel oil is preferred. It is known that the heavy distillate has a total sulfur content of generally 0.3 to 3.0% by weight, preferably 0.3 to 2.5% by weight, wherein it is difficult to remove sulfur compounds (4,6-dimercaptodibenzothiophene) The contribution of sulfur is about 0.01 wt% or more, generally 0.0 b 0.05 wt%.
- the total sulfur content of the heavy distillate can be reduced to 0.05 wt% or less, preferably to 0.005 wt% or less, especially It is possible to remove 80% by weight or more (preferably 90% by weight or more) of the hardly-depleted compound.
- the heavy distillate may be mentioned.
- the method of contacting the hydrotreating catalyst of the present invention under hydrodesulfurization conditions is also referred to as a hydrocracking method for heavy distillate.
- the hydrotreating catalyst of the present invention in the application or the hydrodesulfurization method, can be used as a single hydrotreating catalyst, and the hydrotreating catalyst of the present invention can be further hydrotreated.
- Catalysts such as those known in the art, are mixed in any desired ratio and used as a composite hydrotreating catalyst.
- the hydrodesulfurization conditions are not particularly limited, and those conventionally used in the art may be employed, and for example, a reaction temperature of 260 to 400 ° C, preferably 310 to 370 ° C, and a total reaction pressure of 3 may be mentioned.
- a reaction temperature of 260 to 400 ° C, preferably 310 to 370 ° C, and a total reaction pressure of 3 may be mentioned.
- the content (wt%) of each of the active metal component A, the active metal component B, the active metal component C and the auxiliary component in the catalyst particles was measured by X-ray fluorescence spectrometry.
- the content (wt%) of the porous refractory support in the catalyst particles was calculated based on the actual amount of charge.
- the specific surface area (m 2 /g ) and pore volume (ml/g ) of the catalyst particles and the carrier particles were measured by the BET method.
- the bulk density (g/100 ml) of the porous refractory support was measured by mechanical tapping.
- one catalyst particle was randomly selected from the catalyst particles obtained in each of the examples and the comparative examples as a measurement sample, and then cut perpendicularly to the longitudinal dimension of the cylindrical particle by the center point of the length dimension (Fig. 1) (b) shown schematically), obtaining two exposed surfaces. Take one of the exposed surfaces as a cross section for measurement.
- This measurement was performed on the cross section for measurement using an EPMA method in accordance with GB/T 15074-2008 on an electron probe microanalyzer (Model JXA-8230, manufactured by JEOL Ltd.).
- the measurement conditions were: acceleration voltage 15 kV, beam intensity 5 x l (T 8 A, beam spot diameter ⁇ ⁇ , X-ray detection angle: W was 53., Mo was 38., Ni was 24., and Co was 26.
- the calibration method is ZAF correction method.
- the standard used is pure metal oxide standards (NiO, CoO, W0 3 and Mo0 3 respectively ) with an accuracy of less than 1% and a secondary electron image resolution of 3 nm (LaB 6 ).
- Line system W ⁇ for ⁇ line system, Mo ⁇ for L a line system, Co and Ni for ⁇ ⁇ line system.
- the measurement method is: arbitrarily select a position point on the outermost edge of the cross section as out, Taking a center point on the cross section as a center, along a straight line segment connecting the position point out and the position point center (substantially the radius of the cross section, and therefore also referred to as a radial direction), measuring a predetermined position point
- the concentration value of the target active metal component is then calculated by division to obtain a ratio of the respective concentration values (molar ratio in the present invention).
- the concentration distribution maps of FIG. 2 to FIG. 5 are obtained by selecting 21 position points (including a position point out and a position point center) on the straight line segment, and using these position points as the abscissa, the target measured at each position point.
- the ratio of the concentration value of the active metal component (taking Ni and Co as an example) to the concentration value of the corresponding active metal component measured at the center of the position point is the ordinate, thus drawing acquired.
- Relative desulfurization activity [(l/Sci)°' 65 -(l/So) 0 - 65 ] wherein, 8 1 and 8 (: 1 respectively represent the use of the hydrotreating catalyst of the invention and the hydrotreating catalyst of the comparative example for the feedstock oil
- the total sulfur content in the hydrotreated product obtained by hydrotreating, S represents the total sulfur content (in S, in g/g) of the feedstock.
- the total sulfur content S (wt%) in the feedstock oil and hydrotreated product was measured by ultraviolet fluorescence (ASTM D5453-1993).
- the content of the hard-to-de-slag-containing compound (for example, 4,6-BMDBT) in the feedstock oil and hydrotreated product (g/g) was measured by gas chromatography-atomic luminescence spectrometry (GC-AED).
- GC-AED gas chromatography-atomic luminescence spectrometry
- a cylindrical alumina carrier is used as the granular porous refractory carrier, and the preparation method is as follows: 400 g of pseudo-boehmite dry rubber powder, 8 g of citric acid and phthalocyanine powder, and mixing After the hooking, 345 g of the acidic solution was added, and the weight concentration of HN0 3 in the acidic solution was 3.2%, kneaded for 20 minutes, and after rolling for 20 minutes, the cylindrical carrier strip was extruded on the extruder.
- the alumina carrier A used in the present invention has a carrier diameter of about 1.2 mm and a length of about 3 to 5 mm, and its physicochemical properties are shown in Table 1-1.
- Table 1-1 Physicochemical properties of alumina carrier A used in the examples and comparative examples
- the Mo precursor in the Mo, Ni, P and Mo, Co, P impregnation liquid used in this embodiment is Mo0 3
- the Ni precursor is basic nickel carbonate
- the Co precursor is basic cobalt carbonate
- the P precursor is phosphoric acid.
- the obtained semi-finished product is recorded as B1; after the end of the dampening solution, the second sample is cured for 1 h, and after the same post-treatment step as the catalyst B1, the semi-finished product obtained is recorded as B2. After the spraying of the dampening solution, the third sample was cured for 5 h, and after the same post-treatment step as the catalyst B1, the semi-finished product obtained was recorded as B3.
- 0.8 g of oxalic acid was weighed and dissolved in 4 g of ethanol to obtain a dampening solution.
- the alumina carrier Al OOg was taken, and the dampening solution was uniformly sprayed on the alumina carrier A, and the spraying time was 4 min. After the spraying of the dampening solution, it was maintained for 0.5 h.
- the carrier was impregnated with an equal volume of 70 mL of an impregnation liquid containing Mo, Co, and P, and then dried at 120 ° C for 3 hours and calcined at 480 ° C for 2 hours, and the obtained semi-finished product was designated as B4.
- the active metal components Mo, Co gradually increase in concentration from the outermost edge to the center point along the cross section of the catalyst particles, and the concentration of the active metal component Mo, Co in the radial direction at the respective positions of the comparative catalyst C6 Substantially the same, unlike the catalysts prepared according to the invention, there is a distinct gradient distribution. It is found by C l, C2 and C3 that the concentration distribution of the active metal component in the cross-sectional radial direction of the catalyst particles can be adjusted by controlling the curing time after the spraying of the dampening solution; as seen from C2, C4 and C5, by wetting The volume change of the liquid also adjusts the concentration distribution of the active metal components Mo, Co in the radial direction of the cross section of the catalyst particles.
- the preparation method of the catalyst of the present invention can conveniently adjust the concentration distribution of the active metal component in the radial direction of the cross section of the catalyst particles compared with the comparative catalyst, so that Mo and Co having higher hydrodesulfurization activity are at the center of the cross section of the particle.
- the concentration of the point is higher, and the reaction of the reactant molecules to the center point of the cross section of the catalyst particles is firstly subjected to hydrogenation saturation, and then reacted at the active sites of Mo and Co having high direct desulfurization activity, thereby improving the catalyst. Deep desulfurization performance.
- This example is an activity evaluation experiment of a catalyst.
- the catalyst activity evaluation experiment was carried out on a 100 ml small hydrogenation unit before the activity evaluation.
- the catalyst is pre-vulcanized.
- the catalyst evaluation conditions were a total reaction pressure of 6.0 MPa, a liquid hourly space velocity of 2.0 1 -1 , a hydrogen-oil ratio of 500:1, and a reaction temperature of 340 °C.
- the properties of the feedstock oil used in the activity evaluation test are shown in Table 1-7.
- the results of the activity evaluation are shown in Tables 1-8 and 1-9. It can be seen from the data in the table that the desulfurization activity of the catalyst is significantly higher than that of the comparative example.
- C1 represents a hydrotreated product obtained by treating the feedstock oil using the catalyst C1 as a hydrotreating catalyst, and other similar understandings.
- Example II
- a cylindrical alumina carrier is used as the granular porous refractory carrier, and the preparation method is as follows: 400 g of pseudo-boehmite dry rubber powder, 8 g of citric acid and phthalocyanine powder, and mixing After the hooking, add 345g of acidic solution, the weight concentration of HN0 3 in the acidic solution is 3.0%, kneading 20mm, rolling for 20min, then squeezing into a cylinder on the extruder Shaped carrier strip.
- the alumina carrier B used in the present invention has a carrier diameter of about 1.2 mm and a length of about 3 to 5 mm, and its physicochemical properties are shown in Table II-1.
- Table II-1 Physical and chemical properties of alumina carrier B used in the examples
- the Mo precursor in the Mo, Ni, P and Mo, Co, P impregnation liquid used in this embodiment is Mo0 3
- the Ni precursor is basic nickel carbonate
- the Co precursor is basic cobalt carbonate
- the P precursor is phosphoric acid.
- the sample is not cured, dried at 120 ° C for 3 h, calcined at 480 ° C for 2 h, the obtained sample is recorded as B 1 ; the second sample is maintained for 1 h, and the same post-treatment step as the catalyst intermediate B1 is used to prepare the sample. Recorded as B2; the third sample was cured for 3 h, and after the same post-treatment step as the catalyst intermediate B1, the obtained sample was designated as B3.
- polyethylene glycol 2000 i.e., polyethylene glycol having a molecular weight of 2000, the same below
- the samples B l, B2 and B3 were impregnated in equal volumes with dampening solution II, and then cured for 10 h. After drying at 120 ° C for 3 h, the prepared samples were recorded as Zl, Z2 and Z3, respectively.
- the malic acid l.Og was weighed and dissolved in 6 g of ethanol to obtain a wetting solution I.
- the alumina carrier BlOOg was taken, and the dampening solution I was sprayed on the alumina carrier B, and the spraying time was 5 mm.
- the carrier was impregnated with an equal volume of 67.5 mL of an impregnating solution containing Mo, Co, and P. After the immersion, the mixture was maintained for 1 hour, dried at 120 ° C for 3 hours, and calcined at 480 ° C for 2 hours, and the obtained sample was designated as B4.
- the Z4 sample was sprayed with a volume of 52 mL of an immersion liquid containing Mo, Ni, and P, and after the immersion was completed, a sample was obtained.
- the same method obtained three samples.
- the first sample is directly 120.
- the second sample was cured for 1 h, and after the same post-treatment step as the catalyst C4, the obtained catalyst was recorded as C5;
- the third sample was cured for 3 h, and after the same post-treatment step as the catalyst C4, the obtained catalyst was designated as C6.
- Example II-3
- alumina carrier B l OOg was taken, and the dampening solution I was sprayed on the alumina carrier B, and the spraying time was 25 min.
- the carrier was impregnated with a volume of 53 mL of Mo, Co, P impregnating solution, and then immersed for 1 h, dried at 120 ° C for 3 h, and calcined at 480 ° C for 2 h, and the obtained sample was recorded as B7.
- alumina carrier B 100 g was taken, and the carrier was impregnated with 75 mL of an impregnation liquid containing Mo, Co, and P, and then dried at 120 ° C for 3 hours and calcined at 480 ° C for 2 hours, and the obtained sample was designated as B8.
- the concentration distribution of the active metal component Co in the cross-sectional radial direction of the catalyst particles can be adjusted; as seen from C2, C6 and C7,
- the concentration distribution of the active metal component Co in the cross-sectional radial direction of the catalyst particles can also be adjusted by the change in the content of the wetting fluid I; as seen from C4, C5, C6 and C7, the content of the wetting fluid ⁇ and the immersion Mo
- the growth time of the catalyst after Ni, P can adjust the concentration distribution of the active metal component Ni in the radial direction of the cross section of the catalyst particles.
- the method of the invention can conveniently adjust the concentration distribution of the active metal component in the radial direction of the cross section of the catalyst particles, so that the saturation of the aromatic hydrocarbons is better, and the concentration of Mo and Ni at the edge of the catalyst particles is higher, and the hydrodesulfurization activity is further improved.
- High Mo and Co have higher concentrations at the center point of the cross section of the particle, making the opposite In the diffusion process of the reactant molecules to the center point of the cross section of the catalyst particles, the hydrogenation is saturated, and then reacted at the active sites of Mo and Co which have high activity of direct decarburization, thereby improving the deep desulfurization performance of the catalyst.
- Example II-4
- This example is an activity evaluation experiment of a catalyst.
- the catalyst activity evaluation test was carried out on a 100 ml small hydrogenation unit, and the catalyst was pre-vulcanized before the activity evaluation.
- the catalyst evaluation conditions were at a total reaction pressure of 6. OMPa, a volumetric space velocity of 2.0 h, a hydrogen to oil ratio of 500:1, and a reaction temperature of 340 °C.
- the properties of the raw material oil for the activity evaluation experiment are shown in Table ⁇ -7, and the results of the activity evaluation are shown in Tables ⁇ -8 and II-9. It can be seen from the data in the table that the desulfurization activity of the catalyst is significantly higher than that of the comparative example by the preparation of the hydrotreating catalyst of the present invention. catalyst.
- Table II-7 Raw material oil properties
- C1 indicates the use of catalyst C1 as a hydrotreating catalyst.
- the hydrotreated product obtained by treating the feedstock oil is otherwise well understood.
- a cylindrical alumina carrier is used as the granular porous refractory carrier, and the preparation method is as follows: 400 g of pseudo-boehmite dry rubber powder, 8 g of citric acid and phthalocyanine powder, and mixed After the hooking, 345 g of the acidic solution was added, and the weight concentration of HN0 3 in the acidic solution was 3.6%, and the mixture was kneaded by 20 mm, and after rolling for 20 minutes, the cylindrical carrier strip was extruded on the extruder.
- the alumina carrier C used in the present invention has a carrier diameter of about 1.2 mm and a length of about 3 to 5 mm, and its physicochemical properties are shown in Table III-1.
- Table III-1 Physical and chemical properties of alumina carrier C used in the examples and comparative examples
- the Mo precursor in the Mo, Co, and P impregnation liquid used in this embodiment is Mo0 3
- the Co precursor is basic cobalt carbonate
- the P precursor is phosphoric acid
- the W precursor in the W and Ni impregnation liquid is tungsten Ammonium chloride
- Ni precursor is nickel nitrate.
- the second sample is cured for 1 hour after the spraying of the dampening solution, and after the same post-treatment step as the catalyst B1, the semi-finished product is recorded as B2; after the spraying of the dampening solution, the third sample is cured for 5 hours, after The same post-treatment step of Catalyst B 1 was carried out, and the semi-finished product obtained was designated as B3.
- oxalic acid 0.6 g was weighed and dissolved in 4 g of ethanol to obtain a dampening solution.
- the alumina carrier ClOOg was taken, and the dampening solution was uniformly sprayed on the alumina carrier C for 4 minutes. After the spraying of the dampening solution, it was maintained for 0.5 h.
- the carrier was impregnated with an equal volume of 68 mL of an impregnation liquid containing Mo, Co, and P, and then dried at 120 ° C for 3 hours and calcined at 480 ° C for 2 hours, and the obtained semi-finished product was designated as B4.
- the carrier was impregnated with an immersion liquid of 670 ⁇ and Ni, and dried at 120 ° C for 3 hours and calcined at 480 ° C for 2 hours, and the obtained catalyst was designated as C4.
- Example ⁇ -3
- the carrier was impregnated with an immersion liquid containing 670 ⁇ and Ni, and dried at 120 ° C for 3 hours and calcined at 480 ° C for 2 hours, and the obtained catalyst was designated as C5.
- Comparative ratio ⁇ -1 Comparative ratio ⁇ -1
- the alumina carrier Cl OOg was taken, and the carrier was impregnated with 73 mL of an impregnation liquid containing Mo, Co, and P, and dried by 12 CTC for 3 hours, and calcined at 480 ° C for 2 hours, and the obtained semi-finished product was designated as B6.
- the B6 was impregnated with an equal volume of 6711 ⁇ containing ⁇ and Ni, dried at 120 ° C for 3 h, and calcined at 480 ° C for 2 h, and the obtained catalyst was designated as C6.
- Table -6 Concentration distribution of Ni element (active metal component A) in the catalyst in the radial direction of the cross section of the catalyst particles in the examples and comparative examples
- the active metal components Mo, Co are radially from the outermost edge to the center point along the cross section of the catalyst particles.
- the concentration of the active metal component Mo, Co of the comparative catalyst C6 at each position in the radial direction is substantially the same, unlike the catalyst prepared by the present invention, which exhibits a distinct gradient distribution.
- the concentration distribution of the active metal component in the cross-sectional radial direction of the catalyst particles can be adjusted by controlling the curing time after the spraying of the dampening solution; as seen from C2, C4 and C5, by wetting
- the volume change of the liquid also adjusts the concentration distribution of the active metal components Mo, Co in the radial direction of the cross section of the catalyst particles. Therefore, the preparation method of the catalyst of the present invention can conveniently adjust the concentration distribution of the active metal component in the radial direction of the cross section of the catalyst particles compared with the comparative catalyst, so that Mo and Co having higher hydrodesulfurization activity are at the center of the cross section of the particle.
- This example is an activity evaluation experiment of a catalyst.
- the catalyst activity evaluation was carried out on a 100 ml small hydrogenation unit, and the catalyst was pre-vulcanized before the activity evaluation.
- the catalyst evaluation conditions were a total reaction pressure of 6.0 MPa, a volumetric space velocity of 2. 0 h, a hydrogen to oil ratio of 500:1, and a reaction temperature of 340 °C.
- the properties of the raw material oil for the activity evaluation experiment are shown in Table -7, and the results of the activity evaluation are shown in Tables ⁇ -8 and III-9. It can be seen from the data in the table that the desulfurization activity of the catalyst is significantly higher than that of the comparative example. catalyst.
- Table III-7 Raw oil properties
- Example IV The alumina support used in Example IV was the same as in Example I, i.e., alumina carrier A.
- the Mo precursor in the Mo, Ni, P and Mo, Co, P impregnation liquid used in this embodiment is Mo0 3
- the Ni precursor is basic nickel carbonate
- the Co precursor is basic cobalt carbonate
- the P precursor is phosphoric acid.
- polyethylene glycol 2000 i.e., polyethylene glycol having a molecular weight of 2000, the same below
- alumina carrier A was impregnated with the solution I, followed by curing for 10 hours, and after drying at 120 ° C for 3 hours, the obtained sample was designated as B l .
- the above B1 sample was sprayed with a volume of 204 mL of an impregnating solution containing Mo, Ni, P, and the mixture was directly dried at 120 ° C for 3 hours, and calcined at 480 ° C for 2 hours, and the obtained sample was recorded as Z1.
- the obtained sample is recorded as C1; the second sample is cured for lh, and then dried at 120 ° C for 3 h, and calcined at 480 ° C for 2 h, the obtained sample is recorded as C2; the third sample is maintained for 3 h, and then passed through 120 °. After C was dried for 3 h and calcined at 480 ° C for 2 h, the obtained sample was designated as C3.
- the B4 sample was sprayed with a volume of 204 mL of an impregnation liquid containing Mo, Ni, and P, and after the completion of the spray immersion, the obtained sample was equally divided into three portions.
- the first sample was directly dried at 120 °C for 3 hours, and calcined at 480 °C for 2 hours.
- the sample obtained was recorded as Z4.
- the second sample was cured for lh, dried at 120 °C for 3 hours, and calcined at 480 °C for 2 hours.
- the obtained sample was recorded as Z5; the third sample was cured for 3 hours, dried at 120 ° C for 3 h, and calcined at 480 ° C for 2 h, and the obtained sample was recorded as Z6.
- Example IV-3 1.5 g of malic acid was weighed and dissolved in 6 g of ethanol to obtain a dampening solution II. The dampening solution II was evenly sprayed on the Z4, and the spray immersion time was 5 rmn. The sample was immersed in an equal volume of 54 mL of an impregnating solution containing Mo, Co, and P. After the immersion, the mixture was aged for 1 hour, dried at 120 ° C for 3 hours, and calcined at 480 ° C for 2 hours, and the obtained catalyst was designated as C4. The Z5 and Z6 samples were separately treated in the same treatment steps as Z4, and the obtained catalysts were designated as C5 and C6, respectively.
- Example IV-3 1.
- the B7 sample was sprayed with a volume of 69 mL of an impregnation solution containing Mo, Ni, and P, and dried directly at 120 ° C for 3 hours, and calcined at 480 ° C for 2 hours, and the obtained sample was recorded as Z7.
- the alumina carrier AlOOg was taken, and the carrier was immersed in an equal volume of 75 mL of an impregnation liquid containing Mo, Ni, and P, and then dried at 120 ° C for 3 hours and calcined at 480 ° C for 2 hours, and the obtained sample was designated as B8.
- the B8 was impregnated with an equal volume of 70 mL of an impregnating solution containing Mo, Co, and P, dried at 120 ° C for 3 hours, and calcined at 480 ° C for 2 hours, and the obtained catalyst was designated as C8.
- Table IV-1 Examples and Comparative Examples Catalyst Composition
- the concentration of the active metal Co in the radial direction of the catalyst particles can be adjusted by controlling the curing time after the dipping of the dampening solution II; as seen from C2, C6 and C7, by the wetting liquid
- the content variation can also adjust the distribution concentration of the active metal Co in the radial direction of the catalyst particles; as seen from C4, C5, C6 and C7, the content of the wetting agent I and the curing time of the catalyst after spraying Mo, Ni and P,
- the distribution concentration of the active metal Ni in the radial direction of the catalyst particles can be adjusted.
- the method of the invention can conveniently adjust the distribution concentration of the active metal in the radial direction of the catalyst particles, so that the saturation of the aromatic hydrocarbons is better, and the concentration of Mo and Ni at the edge of the catalyst particles is higher, and the Mo, Co having higher hydrodesulfurization activity is obtained.
- High concentration in the center of the particle allowing the diffusion of reactant molecules toward the center of the catalyst particles
- the reaction is further carried out on the Mo and Co active sites with high direct desulfurization activity, thereby improving the deep desulfurization performance of the catalyst.
- This example is an activity evaluation experiment of a catalyst.
- the catalyst activity evaluation test was carried out on a 100 ml small hydrogenation unit, and the catalyst was pre-vulcanized before the activity evaluation.
- the catalyst evaluation conditions were a reaction pressure of 6.0 MPa, a volumetric space velocity S.O h at a liquid state, a hydrogen to oil ratio of 500:1, and a reaction temperature of 340 °C.
- the properties of the feedstock oil for the activity evaluation test are shown in Table IV-6, and the results of the activity evaluation are shown in Tables IV-7 and IV-8. It can be seen from the data in the table that the desulfurization activity of the catalyst is significantly higher than that of the comparative example. catalyst.
- Table IV-6 Raw material oil properties
- C 1 represents a hydrotreated product obtained by treating the feedstock oil using the catalyst C1 as a hydrotreating catalyst, and other similar understandings.
- the embodiments of the present invention have been described in detail with reference to the embodiments of the present invention. It is to be understood that the scope of the present invention is not limited by the specific embodiments, but is defined by the appended claims. A person skilled in the art can appropriately change these embodiments without departing from the spirit and scope of the invention, and such modified embodiments are obviously included in the scope of the present invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Inorganic Chemistry (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020157015198A KR102172384B1 (ko) | 2012-11-08 | 2013-10-31 | 수소 처리 촉매, 그의 제조 방법 및 그의 용도 |
US14/441,806 US9713806B2 (en) | 2012-11-08 | 2013-10-31 | Hydrotreating catalyst, production and use thereof |
AU2013344232A AU2013344232B2 (en) | 2012-11-08 | 2013-10-31 | Hydrogenation catalyst and manufacturing method therefor and use thereof |
CA2890626A CA2890626C (en) | 2012-11-08 | 2013-10-31 | A hydrotreating catalyst, production and use thereof |
DK13853150.4T DK2918339T3 (da) | 2012-11-08 | 2013-10-31 | Hydrogeneringskatalysator og fremgangsmåde til fremstilling deraf og anvendelse deraf |
SG11201503615YA SG11201503615YA (en) | 2012-11-08 | 2013-10-31 | A hydrotreating catalyst, production and use thereof |
RU2015121363A RU2646753C2 (ru) | 2012-11-08 | 2013-10-31 | Катализатор гидропереработки, его получение и применение |
EP13853150.4A EP2918339B1 (en) | 2012-11-08 | 2013-10-31 | Hydrogenation catalyst and manufacturing method therefor and use thereof |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210443119 | 2012-11-08 | ||
CN201210442850 | 2012-11-08 | ||
CN201210442850.8 | 2012-11-08 | ||
CN201210443119.7 | 2012-11-08 | ||
CN201210442653.6 | 2012-11-08 | ||
CN201210442653 | 2012-11-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2014071686A1 true WO2014071686A1 (zh) | 2014-05-15 |
WO2014071686A8 WO2014071686A8 (zh) | 2015-05-28 |
Family
ID=50683985
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2013/001319 WO2014071686A1 (zh) | 2012-11-08 | 2013-10-31 | 一种加氢处理催化剂,其制造方法及其应用 |
Country Status (11)
Country | Link |
---|---|
US (1) | US9713806B2 (zh) |
EP (1) | EP2918339B1 (zh) |
KR (1) | KR102172384B1 (zh) |
CN (1) | CN103801314B (zh) |
AU (1) | AU2013344232B2 (zh) |
CA (1) | CA2890626C (zh) |
DK (1) | DK2918339T3 (zh) |
RU (1) | RU2646753C2 (zh) |
SG (1) | SG11201503615YA (zh) |
TW (1) | TWI604040B (zh) |
WO (1) | WO2014071686A1 (zh) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160008792A1 (en) * | 2014-06-20 | 2016-01-14 | Instituto Mexicano Del Petroleo | Procedimiento de obtencion de una formulacion catalitica para la produccion de diesel de ultrabajo azufre, el producto obtenido y su aplicacion |
CN107597152A (zh) * | 2016-07-11 | 2018-01-19 | 中国石油天然气股份有限公司 | 一种加氢催化剂及其制备方法 |
CN108421548A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 一种加氢保护催化剂及其制备方法和重油加氢处理方法 |
CN108421563A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 加氢异构化催化剂及其制备方法 |
CN108421561A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 一种重油加氢催化剂及其制备方法和重油加氢处理方法 |
CN108421554A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 加氢精制催化剂及其制备方法和应用 |
CN110064405A (zh) * | 2018-01-23 | 2019-07-30 | 中国石油天然气股份有限公司 | 一种具有脱硫活性的加氢处理催化剂的制备方法 |
CN115518663A (zh) * | 2021-06-25 | 2022-12-27 | 中国石油化工股份有限公司 | 一种渣油加氢裂化催化剂的制备方法 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107921413B (zh) * | 2015-05-29 | 2021-07-20 | 先进炼制技术有限公司 | 高加氢脱氮选择性的加氢处理催化剂 |
RU2745607C2 (ru) | 2016-09-12 | 2021-03-29 | Чайна Петролеум Энд Кемикал Корпорейшен | Катализатор гидрирования, его получение и применение |
CN110404578A (zh) | 2019-02-01 | 2019-11-05 | 中国石油大学(北京) | 加氢脱硫耦合异构化的双功能催化剂及其制备方法和应用 |
CN116037218B (zh) * | 2021-10-28 | 2024-07-02 | 中国石油化工股份有限公司 | 一种硼改性氧化铝载体、加氢脱残炭催化剂及其制备方法 |
CN116037176B (zh) * | 2021-10-28 | 2024-06-07 | 中国石油化工股份有限公司 | 一种加氢脱硫催化剂及其制备方法 |
CN116037136B (zh) * | 2021-10-28 | 2024-06-07 | 中国石油化工股份有限公司 | 一种含硼加氢脱氮催化剂及其制备方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4760045A (en) * | 1985-06-05 | 1988-07-26 | Nippon Oil Co., Ltd. | Catalyst for hydrotreatment of heavy oils and method for its preparation |
CN101279289A (zh) * | 2007-04-04 | 2008-10-08 | 中国石油化工股份有限公司 | 一种加氢处理催化剂的制备方法 |
CN101279291A (zh) * | 2007-04-04 | 2008-10-08 | 中国石油化工股份有限公司 | 加氢处理催化剂的制备方法 |
CN101439293A (zh) * | 2007-11-19 | 2009-05-27 | 中国石油天然气集团公司 | 含有介孔分子筛的选择性加氢脱硫催化剂及其制备方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4411824A (en) * | 1981-05-12 | 1983-10-25 | Chevron Research Company | Method of making a catalyst suitable for hydrometalation of hydrocarbonaceous feedstocks |
JPS6115739A (ja) * | 1984-04-25 | 1986-01-23 | Toa Nenryo Kogyo Kk | 水素化処理用触媒 |
CN1072706C (zh) | 1998-03-20 | 2001-10-10 | 中国石油化工集团公司 | 含钼和/或钨的轻质油品加氢处理催化剂及其制备方法 |
CN1083476C (zh) | 1999-09-29 | 2002-04-24 | 中国石油化工集团公司 | 馏分油加氢精制催化剂及其制备方法 |
US7629289B2 (en) * | 2004-06-23 | 2009-12-08 | Uop Llc | Selective naphtha desulfurization process and catalyst |
CA2631703C (en) * | 2005-12-14 | 2012-04-03 | Advanced Refining Technologies Llc | Method of making hydroprocessing catalyst |
JP5508856B2 (ja) * | 2006-12-19 | 2014-06-04 | エクソンモービル リサーチ アンド エンジニアリング カンパニー | 高活性の担持留出油水素処理触媒 |
FR2940143B1 (fr) * | 2008-12-18 | 2015-12-11 | Inst Francais Du Petrole | Catalyseurs d'hydrodemetallation et d'hydrodesulfuration et mise en oeuvre dans un procede d'enchainement en formulation unique |
CN101927176B (zh) * | 2009-06-26 | 2012-05-30 | 中国石油天然气股份有限公司 | 活性金属和酸性助剂浓度呈梯度增加分布的加氢催化剂及制备方法 |
-
2013
- 2013-10-31 CN CN201310533922.4A patent/CN103801314B/zh active Active
- 2013-10-31 CA CA2890626A patent/CA2890626C/en active Active
- 2013-10-31 US US14/441,806 patent/US9713806B2/en active Active
- 2013-10-31 WO PCT/CN2013/001319 patent/WO2014071686A1/zh active Application Filing
- 2013-10-31 EP EP13853150.4A patent/EP2918339B1/en active Active
- 2013-10-31 RU RU2015121363A patent/RU2646753C2/ru active
- 2013-10-31 AU AU2013344232A patent/AU2013344232B2/en active Active
- 2013-10-31 KR KR1020157015198A patent/KR102172384B1/ko active IP Right Grant
- 2013-10-31 TW TW102139559A patent/TWI604040B/zh active
- 2013-10-31 DK DK13853150.4T patent/DK2918339T3/da active
- 2013-10-31 SG SG11201503615YA patent/SG11201503615YA/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4760045A (en) * | 1985-06-05 | 1988-07-26 | Nippon Oil Co., Ltd. | Catalyst for hydrotreatment of heavy oils and method for its preparation |
CN101279289A (zh) * | 2007-04-04 | 2008-10-08 | 中国石油化工股份有限公司 | 一种加氢处理催化剂的制备方法 |
CN101279291A (zh) * | 2007-04-04 | 2008-10-08 | 中国石油化工股份有限公司 | 加氢处理催化剂的制备方法 |
CN101439293A (zh) * | 2007-11-19 | 2009-05-27 | 中国石油天然气集团公司 | 含有介孔分子筛的选择性加氢脱硫催化剂及其制备方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2918339A4 |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160008792A1 (en) * | 2014-06-20 | 2016-01-14 | Instituto Mexicano Del Petroleo | Procedimiento de obtencion de una formulacion catalitica para la produccion de diesel de ultrabajo azufre, el producto obtenido y su aplicacion |
US11097255B2 (en) * | 2014-06-20 | 2021-08-24 | Instituto Mexicano Del Petroleo | Procedure for obtaining a catalytic formulation for the production of ultra low sulfur diesel, obtained product and application thereof |
CN107597152A (zh) * | 2016-07-11 | 2018-01-19 | 中国石油天然气股份有限公司 | 一种加氢催化剂及其制备方法 |
CN108421561B (zh) * | 2017-02-15 | 2020-06-16 | 中国石油化工股份有限公司 | 一种重油加氢催化剂及其制备方法和重油加氢处理方法 |
CN108421561A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 一种重油加氢催化剂及其制备方法和重油加氢处理方法 |
CN108421554A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 加氢精制催化剂及其制备方法和应用 |
CN108421563B (zh) * | 2017-02-15 | 2020-06-12 | 中国石油化工股份有限公司 | 加氢异构化催化剂及其制备方法 |
CN108421548B (zh) * | 2017-02-15 | 2020-06-16 | 中国石油化工股份有限公司 | 一种加氢保护催化剂及其制备方法和重油加氢处理方法 |
CN108421563A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 加氢异构化催化剂及其制备方法 |
CN108421548A (zh) * | 2017-02-15 | 2018-08-21 | 中国石油化工股份有限公司 | 一种加氢保护催化剂及其制备方法和重油加氢处理方法 |
CN110064405A (zh) * | 2018-01-23 | 2019-07-30 | 中国石油天然气股份有限公司 | 一种具有脱硫活性的加氢处理催化剂的制备方法 |
CN115518663A (zh) * | 2021-06-25 | 2022-12-27 | 中国石油化工股份有限公司 | 一种渣油加氢裂化催化剂的制备方法 |
CN115518663B (zh) * | 2021-06-25 | 2024-01-09 | 中国石油化工股份有限公司 | 一种渣油加氢裂化催化剂的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
CN103801314B (zh) | 2016-08-31 |
RU2646753C2 (ru) | 2018-03-07 |
EP2918339A4 (en) | 2016-07-20 |
CN103801314A (zh) | 2014-05-21 |
CA2890626C (en) | 2022-06-28 |
SG11201503615YA (en) | 2015-06-29 |
RU2015121363A (ru) | 2016-12-27 |
AU2013344232A1 (en) | 2015-06-11 |
CA2890626A1 (en) | 2014-05-15 |
TWI604040B (zh) | 2017-11-01 |
US20150306579A1 (en) | 2015-10-29 |
US9713806B2 (en) | 2017-07-25 |
KR20150091085A (ko) | 2015-08-07 |
EP2918339B1 (en) | 2019-05-22 |
AU2013344232B2 (en) | 2016-10-13 |
WO2014071686A8 (zh) | 2015-05-28 |
KR102172384B1 (ko) | 2020-11-02 |
EP2918339A1 (en) | 2015-09-16 |
DK2918339T3 (da) | 2019-08-05 |
TW201422803A (zh) | 2014-06-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2014071686A1 (zh) | 一种加氢处理催化剂,其制造方法及其应用 | |
JP6802806B2 (ja) | ドープされた担体に金属有機硫化物を含有する水素化処理触媒 | |
RU2377067C2 (ru) | Высокоактивный катализатор гидрообессеривания, способ его изготовления и способ получения среднего топливного дистиллята с ультранизким содержанием серы | |
JP5548257B2 (ja) | リンおよびホウ素を含有する水素処理触媒 | |
WO2018161952A1 (zh) | 浸渍法制备加氢处理催化剂的方法 | |
EP3821978B1 (en) | Process for forming a catalyst with concentrated solutions comprising group vi metal, group viii metal, and phosphorus | |
JP2006035051A (ja) | 石油系炭化水素の水素化脱硫触媒および水素化脱硫方法 | |
TW201943457A (zh) | 氫化精製催化劑、其製備方法及應用 | |
JP5013658B2 (ja) | 石油系炭化水素油の水素化脱硫触媒および水素化脱硫方法 | |
CN108435244B (zh) | 一种提高十六烷值加氢改质催化剂、制备方法及其应用 | |
TW202140139A (zh) | 氫化催化劑及其製備方法和用途 | |
CN109718857B (zh) | 加氢精制催化剂及其制备方法和应用以及馏分油的加氢精制方法 | |
CN108404897B (zh) | 一种重油加氢催化剂载体、其制备方法、应用其的催化剂及催化剂的制备方法 | |
CN1508224A (zh) | 一种加氢裂化后处理催化剂及其制备方法 | |
JP4778605B2 (ja) | 軽油留分の水素化脱硫触媒 | |
CN111100691B (zh) | 一种烃油加氢处理方法 | |
CN109718766B (zh) | 加氢精制催化剂及其制备方法和应用以及馏分油的加氢精制方法 | |
JP2006314916A (ja) | 水素化処理触媒、その製造方法および水素化処理方法 | |
CN109718816B (zh) | 加氢精制催化剂及其制备方法和应用以及馏分油的加氢精制方法 | |
CN109718818B (zh) | 加氢精制催化剂及其制备方法和应用以及馏分油的加氢精制方法 | |
CN109772400B (zh) | 一种加氢处理催化剂及其制备方法和应用 | |
JP4519379B2 (ja) | 重質炭化水素油の水素化処理触媒 | |
CN114471630A (zh) | 馏分油加氢脱硫催化剂及其制备方法和在馏分油加氢脱硫反应中的应用 | |
CN106925285B (zh) | 重油加氢催化剂及其制备方法 | |
WO2024012422A1 (zh) | 加氢催化剂、及其制备和应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13853150 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2890626 Country of ref document: CA |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14441806 Country of ref document: US Ref document number: IDP00201502761 Country of ref document: ID |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2013853150 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 20157015198 Country of ref document: KR Kind code of ref document: A Ref document number: 2015121363 Country of ref document: RU Kind code of ref document: A |
|
ENP | Entry into the national phase |
Ref document number: 2013344232 Country of ref document: AU Date of ref document: 20131031 Kind code of ref document: A |