IL101246A - Components of catalysts for olefin polymerization - Google Patents

Components of catalysts for olefin polymerization

Info

Publication number: IL101246A
Authority: IL; Israel
Prior art keywords: compound; weight; catalyst component; component; electron
Prior art date: 1991-03-27

Application number

IL10124692A

Other languages

English (en)

Hebrew (he)

Original Assignee

Himont Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1991-03-27

Filing date

1992-03-16

Publication date

1994-12-29

1992-03-16 Application filed by Himont Inc filed Critical Himont Inc

1994-12-29 Publication of IL101246A publication Critical patent/IL101246A/en

Links

239000003054 catalyst Substances 0.000 title claims abstract description 71
238000006116 polymerization reaction Methods 0.000 title claims abstract description 20
150000001336 alkenes Chemical class 0.000 title claims abstract description 10
150000001875 compounds Chemical class 0.000 claims abstract description 40
239000010936 titanium Substances 0.000 claims abstract description 35
-1 titanium halide Chemical class 0.000 claims abstract description 33
229920000642 polymer Polymers 0.000 claims abstract description 30
229910052719 titanium Inorganic materials 0.000 claims abstract description 19
238000006243 chemical reaction Methods 0.000 claims abstract description 17
229910052736 halogen Inorganic materials 0.000 claims abstract description 9
150000002367 halogens Chemical class 0.000 claims abstract description 9
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims description 6
229910003074 TiCl4 Inorganic materials 0.000 claims description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
239000011148 porous material Substances 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
239000011777 magnesium Substances 0.000 abstract description 46
229910052749 magnesium Inorganic materials 0.000 abstract description 11
150000002681 magnesium compounds Chemical class 0.000 abstract description 11
150000003609 titanium compounds Chemical class 0.000 abstract description 8
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
239000011347 resin Substances 0.000 description 23
229920005989 resin Polymers 0.000 description 23
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
239000000203 mixture Substances 0.000 description 19
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 17
238000000034 method Methods 0.000 description 17
239000011949 solid catalyst Substances 0.000 description 15
239000000243 solution Substances 0.000 description 14
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 12
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
QUXHCILOWRXCEO-UHFFFAOYSA-M magnesium;butane;chloride Chemical compound [Mg+2].[Cl-].CCC[CH2-] QUXHCILOWRXCEO-UHFFFAOYSA-M 0.000 description 11
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 10
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 10
150000002148 esters Chemical class 0.000 description 9
239000004615 ingredient Substances 0.000 description 9
239000007787 solid Substances 0.000 description 9
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
239000005977 Ethylene Substances 0.000 description 8
230000000694 effects Effects 0.000 description 8
239000000178 monomer Substances 0.000 description 8
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 7
150000002170 ethers Chemical class 0.000 description 7
229910052757 nitrogen Inorganic materials 0.000 description 7
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
229910001629 magnesium chloride Inorganic materials 0.000 description 6
229910044991 metal oxide Inorganic materials 0.000 description 6
150000004706 metal oxides Chemical class 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
239000000377 silicon dioxide Substances 0.000 description 6
238000011282 treatment Methods 0.000 description 6
239000004215 Carbon black (E152) Substances 0.000 description 5
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 5
239000004743 Polypropylene Substances 0.000 description 5
239000012298 atmosphere Substances 0.000 description 5
229930195733 hydrocarbon Natural products 0.000 description 5
239000007788 liquid Substances 0.000 description 5
229920001155 polypropylene Polymers 0.000 description 5
239000000047 product Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
239000012265 solid product Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
239000004711 α-olefin Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
150000005840 aryl radicals Chemical class 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000009826 distribution Methods 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000005470 impregnation Methods 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
230000000877 morphologic effect Effects 0.000 description 3
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
239000002245 particle Substances 0.000 description 3
150000003377 silicon compounds Chemical class 0.000 description 3
CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000001569 carbon dioxide Substances 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000003247 decreasing effect Effects 0.000 description 2
150000001993 dienes Chemical class 0.000 description 2
MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 2
AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
239000007789 gas Substances 0.000 description 2
230000002140 halogenating effect Effects 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
239000012071 phase Substances 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
150000003623 transition metal compounds Chemical class 0.000 description 2
HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-N 0.000 description 1
125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 description 1
LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
RFONJRMUUALMBA-UHFFFAOYSA-N 2-methanidylpropane Chemical compound CC(C)[CH2-] RFONJRMUUALMBA-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229910003910 SiCl4 Inorganic materials 0.000 description 1
229910010066 TiC14 Inorganic materials 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
159000000032 aromatic acids Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
LJWBIAMZBJWAOW-UHFFFAOYSA-N benzhydryloxysilane Chemical compound C=1C=CC=CC=1C(O[SiH3])C1=CC=CC=C1 LJWBIAMZBJWAOW-UHFFFAOYSA-N 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000004653 carbonic acids Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
150000001923 cyclic compounds Chemical class 0.000 description 1
SJJCABYOVIHNPZ-UHFFFAOYSA-N cyclohexyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1CCCCC1 SJJCABYOVIHNPZ-UHFFFAOYSA-N 0.000 description 1
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
230000007423 decrease Effects 0.000 description 1
JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 1
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
DWNAQMUDCDVSLT-UHFFFAOYSA-N diphenyl phthalate Chemical compound C=1C=CC=C(C(=O)OC=2C=CC=CC=2)C=1C(=O)OC1=CC=CC=C1 DWNAQMUDCDVSLT-UHFFFAOYSA-N 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
OANIYCQMEVXZCJ-UHFFFAOYSA-N ditert-butyl(dimethoxy)silane Chemical compound CO[Si](OC)(C(C)(C)C)C(C)(C)C OANIYCQMEVXZCJ-UHFFFAOYSA-N 0.000 description 1
HHEIMYAXCOIQCJ-UHFFFAOYSA-N ethyl 2,2-dimethylpropanoate Chemical compound CCOC(=O)C(C)(C)C HHEIMYAXCOIQCJ-UHFFFAOYSA-N 0.000 description 1
YCNSGSUGQPDYTK-UHFFFAOYSA-N ethyl phenyl carbonate Chemical compound CCOC(=O)OC1=CC=CC=C1 YCNSGSUGQPDYTK-UHFFFAOYSA-N 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002431 hydrogen Chemical group 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N malonic acid group Chemical group C(CC(=O)O)(=O)O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
150000002905 orthoesters Chemical class 0.000 description 1
DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 description 1
125000004437 phosphorous atom Chemical group 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
125000005546 pivalic acid group Chemical group 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920005606 polypropylene copolymer Polymers 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
230000000707 stereoselective effect Effects 0.000 description 1
150000003444 succinic acids Chemical class 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
NETBVGNWMHLXRP-UHFFFAOYSA-N tert-butyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C(C)(C)C NETBVGNWMHLXRP-UHFFFAOYSA-N 0.000 description 1
150000003608 titanium Chemical class 0.000 description 1
JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/904—Monomer polymerized in presence of transition metal containing catalyst at least part of which is supported on a polymer, e.g. prepolymerized catalysts

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

IL10124692A 1991-03-27 1992-03-16 Components of catalysts for olefin polymerization IL101246A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
ITMI910813A IT1245249B (it)	1991-03-27	1991-03-27	Componenti e catalizzatori per la polimerizzazione di olefine

Publications (1)

Publication Number	Publication Date
IL101246A true IL101246A (en)	1994-12-29

Family

ID=11359255

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10124692A IL101246A (en)	1991-03-27	1992-03-16	Components of catalysts for olefin polymerization

Country Status (23)

Country	Link
US (1)	US5244855A (ja)
EP (1)	EP0506073B1 (ja)
JP (1)	JP3308589B2 (ja)
KR (1)	KR100204131B1 (ja)
CN (1)	CN1035383C (ja)
AT (1)	ATE137772T1 (ja)
AU (1)	AU645896B2 (ja)
BR (1)	BR9201078A (ja)
CA (1)	CA2064125A1 (ja)
CS (1)	CS91992A3 (ja)
DE (1)	DE69210454T2 (ja)
FI (1)	FI108442B (ja)
HU (1)	HUT62611A (ja)
IL (1)	IL101246A (ja)
IT (1)	IT1245249B (ja)
MX (1)	MX9201352A (ja)
MY (1)	MY106929A (ja)
NO (1)	NO179329C (ja)
PT (1)	PT100311B (ja)
RU (1)	RU2073688C1 (ja)
TW (1)	TW203063B (ja)
YU (1)	YU27892A (ja)
ZA (1)	ZA921926B (ja)

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EP1238990B1 (en) *	2001-02-15	2005-06-08	Saudi Basic Industries Corporation	Supported catalyst composition for polymerization of olefins; method for preparing the same and process for polymerization using the same
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CN1958621B (zh) *	2005-10-31	2010-12-22	中国石油化工股份有限公司	用于烯烃聚合的固体催化剂组分及其催化剂和催化剂应用
CN101412767B (zh) *	2007-10-16	2011-09-21	中国石化扬子石油化工有限公司	一种负载型非茂金属催化剂及其制备方法
CN101412769B (zh) *	2007-10-16	2014-05-07	中国石化扬子石油化工有限公司	一种负载型非茂金属催化剂及其制备方法
CN101412766B (zh) *	2007-10-16	2011-10-19	中国石化扬子石油化工有限公司	一种镁化合物负载型非茂金属催化剂及其制备方法
JP5480148B2 (ja) *	2007-10-16	2014-04-23	中国石化揚子石油化工有限公司	マグネシウム化合物担持非メタロセン触媒およびその製造
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CN103626893B (zh) *	2012-08-23	2016-03-30	中国石油化工股份有限公司	用于烯烃聚合反应的催化剂组分及其催化剂制备方法
CN103626894B (zh) *	2012-08-23	2016-03-30	中国石油化工股份有限公司	用于烯烃聚合反应的催化剂组分及其催化剂制备方法
CN103626895B (zh) *	2012-08-23	2016-03-30	中国石油化工股份有限公司	用于烯烃聚合反应的催化剂组分及其催化剂制备方法
WO2022094508A1 (en) *	2020-10-30	2022-05-05	Exxonmobil Chemical Patents Inc.	Polypropylene produced using modified styrenic internal electron donors

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1991
- 1991-03-27 IT ITMI910813A patent/IT1245249B/it active IP Right Grant
1992
- 1992-03-16 ZA ZA921926A patent/ZA921926B/xx unknown
- 1992-03-16 IL IL10124692A patent/IL101246A/en not_active IP Right Cessation
- 1992-03-19 MY MYPI92000466A patent/MY106929A/en unknown
- 1992-03-19 YU YU27892A patent/YU27892A/sh unknown
- 1992-03-24 US US07/856,773 patent/US5244855A/en not_active Expired - Lifetime
- 1992-03-25 AU AU13197/92A patent/AU645896B2/en not_active Ceased
- 1992-03-26 CA CA002064125A patent/CA2064125A1/en not_active Abandoned
- 1992-03-26 NO NO921185A patent/NO179329C/no unknown
- 1992-03-26 MX MX9201352A patent/MX9201352A/es unknown
- 1992-03-26 CS CS92919A patent/CS91992A3/cs unknown
- 1992-03-26 HU HU9200943A patent/HUT62611A/hu unknown
- 1992-03-26 RU SU925011203A patent/RU2073688C1/ru active
- 1992-03-27 PT PT100311A patent/PT100311B/pt not_active IP Right Cessation
- 1992-03-27 JP JP10195092A patent/JP3308589B2/ja not_active Expired - Fee Related
- 1992-03-27 KR KR1019920005084A patent/KR100204131B1/ko not_active IP Right Cessation
- 1992-03-27 CN CN92102960A patent/CN1035383C/zh not_active Expired - Lifetime
- 1992-03-27 AT AT92105294T patent/ATE137772T1/de not_active IP Right Cessation
- 1992-03-27 EP EP92105294A patent/EP0506073B1/en not_active Expired - Lifetime
- 1992-03-27 FI FI921348A patent/FI108442B/fi not_active IP Right Cessation
- 1992-03-27 DE DE69210454T patent/DE69210454T2/de not_active Expired - Fee Related
- 1992-03-27 BR BR929201078A patent/BR9201078A/pt not_active IP Right Cessation
- 1992-03-28 TW TW081102383A patent/TW203063B/zh active

Also Published As

Publication number	Publication date
JP3308589B2 (ja)	2002-07-29
CN1035383C (zh)	1997-07-09
AU1319792A (en)	1992-10-01
JPH0625338A (ja)	1994-02-01
EP0506073B1 (en)	1996-05-08
MY106929A (en)	1995-08-30
TW203063B (ja)	1993-04-01
DE69210454T2 (de)	1996-10-10
AU645896B2 (en)	1994-01-27
FI921348A0 (fi)	1992-03-27
ITMI910813A0 (it)	1991-03-27
FI108442B (fi)	2002-01-31
ATE137772T1 (de)	1996-05-15
BR9201078A (pt)	1992-11-24
NO179329B (no)	1996-06-10
HU9200943D0 (en)	1992-06-29
US5244855A (en)	1993-09-14
PT100311A (pt)	1993-06-30
ZA921926B (en)	1992-11-25
CN1066274A (zh)	1992-11-18
YU27892A (sh)	1994-06-24
FI921348A (fi)	1992-09-28
HUT62611A (en)	1993-05-28
NO921185D0 (no)	1992-03-26
PT100311B (pt)	1999-06-30
NO179329C (no)	1996-09-18
CS91992A3 (en)	1992-10-14
CA2064125A1 (en)	1992-09-28
ITMI910813A1 (it)	1992-09-27
KR100204131B1 (ko)	1999-06-15
IT1245249B (it)	1994-09-13
NO921185L (no)	1992-09-28
DE69210454D1 (de)	1996-06-13
RU2073688C1 (ru)	1997-02-20
EP0506073A2 (en)	1992-09-30
MX9201352A (es)	1992-10-01
KR920018083A (ko)	1992-10-21
EP0506073A3 (en)	1992-12-02

Legal Events

Date	Code	Title
1997-11-20	HC	Change of name of proprietor(s)
1998-08-16	KB	Patent renewed
2002-12-01	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
AU645896B2 (en)	1994-01-27	Components and catalysts for the polymerization of olefins
US5244854A (en)	1993-09-14	Components and catalysts for the polymerization of olefins
EP1802668B1 (en)	2015-01-07	Method of making a ziegler-natta catalyst
JP2974797B2 (ja)	1999-11-10	オレフィンの重合用成分および触媒
JPH0145485B2 (ja)	1989-10-03
HU202562B (en)	1991-04-29	Process for producing solid catalyst composition and for using it for stereospecific polymerization of propylene
NO176053B (no)	1994-10-17	Katalysatorkomponent og katalysator for polymerisering av olefiner
US5547912A (en)	1996-08-20	Solid catalyst component for polymerizing olefins and catalyst containing the same
CA2148596A1 (en)	1994-05-26	Process for polymerizing alpha-olefin
AU672637B2 (en)	1996-10-10	Process for polymerizing alpha-olefin
US5330949A (en)	1994-07-19	Method for producing polyolefin
JP3399067B2 (ja)	2003-04-21	ポリオレフインの多分散度の制御を行うためのチグラー・ナツタ触媒と組み合わせる電子供与体
US5036147A (en)	1991-07-30	Propylene polymerization method
JPH05247127A (ja)	1993-09-24	オレフィン重合用触媒および当該触媒を用いたオレフィン重合体の製造方法
GB2061978A (en)	1981-05-20	Ethylene polymerisation