JP2006199738A - オレフィン類重合用固体触媒成分および触媒 - Google Patents
オレフィン類重合用固体触媒成分および触媒 Download PDFInfo
- Publication number
- JP2006199738A JP2006199738A JP2005010179A JP2005010179A JP2006199738A JP 2006199738 A JP2006199738 A JP 2006199738A JP 2005010179 A JP2005010179 A JP 2005010179A JP 2005010179 A JP2005010179 A JP 2005010179A JP 2006199738 A JP2006199738 A JP 2006199738A
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- JP
- Japan
- Prior art keywords
- compound
- catalyst component
- succinate
- group
- solid catalyst
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 85
- 239000011949 solid catalyst Substances 0.000 title claims abstract description 80
- 239000003054 catalyst Substances 0.000 title claims abstract description 16
- 230000000379 polymerizing effect Effects 0.000 title abstract description 6
- -1 succinic acid diester Chemical class 0.000 claims abstract description 138
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 47
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000001384 succinic acid Substances 0.000 claims abstract description 28
- 150000002681 magnesium compounds Chemical class 0.000 claims abstract description 21
- 238000006116 polymerization reaction Methods 0.000 claims description 82
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 67
- 239000010936 titanium Substances 0.000 claims description 37
- 239000000725 suspension Substances 0.000 claims description 33
- 229910052719 titanium Inorganic materials 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 238000006243 chemical reaction Methods 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
- 239000007787 solid Substances 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 21
- 150000003609 titanium compounds Chemical class 0.000 claims description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- 150000005690 diesters Chemical class 0.000 claims description 15
- 239000012265 solid product Substances 0.000 claims description 15
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 14
- 239000002685 polymerization catalyst Substances 0.000 claims description 13
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 12
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 6
- XDKQUSKHRIUJEO-UHFFFAOYSA-N magnesium;ethanolate Chemical compound [Mg+2].CC[O-].CC[O-] XDKQUSKHRIUJEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical class Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 abstract description 39
- 238000009826 distribution Methods 0.000 abstract description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 8
- 239000001257 hydrogen Substances 0.000 abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 8
- 229920000098 polyolefin Polymers 0.000 abstract description 6
- 229920001155 polypropylene Polymers 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 23
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 16
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 15
- 239000002245 particle Substances 0.000 description 15
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 14
- 239000011777 magnesium Substances 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 13
- 229910052749 magnesium Inorganic materials 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 11
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 11
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 10
- 150000003961 organosilicon compounds Chemical class 0.000 description 10
- 239000007788 liquid Substances 0.000 description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 9
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 9
- WWIDLUJSQINFMG-UHFFFAOYSA-N diethyl 2,3-dipropylbutanedioate Chemical compound CCOC(=O)C(CCC)C(CCC)C(=O)OCC WWIDLUJSQINFMG-UHFFFAOYSA-N 0.000 description 8
- 229920001296 polysiloxane Polymers 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229960002097 dibutylsuccinate Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000012456 homogeneous solution Substances 0.000 description 4
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 3
- WGFNXLQURMLAGC-UHFFFAOYSA-N diethyl 2,3-di(propan-2-yl)butanedioate Chemical compound CCOC(=O)C(C(C)C)C(C(C)C)C(=O)OCC WGFNXLQURMLAGC-UHFFFAOYSA-N 0.000 description 3
- ADZYAUVCHQDILS-UHFFFAOYSA-N diethyl 2,3-dibromobutanedioate Chemical compound CCOC(=O)C(Br)C(Br)C(=O)OCC ADZYAUVCHQDILS-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical group 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 230000026030 halogenation Effects 0.000 description 3
- 238000005658 halogenation reaction Methods 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 230000037048 polymerization activity Effects 0.000 description 3
- 239000005049 silicon tetrachloride Substances 0.000 description 3
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 3
- FJWGRXKOBIVTFA-UHFFFAOYSA-N 2,3-dibromobutanedioic acid Chemical compound OC(=O)C(Br)C(Br)C(O)=O FJWGRXKOBIVTFA-UHFFFAOYSA-N 0.000 description 2
- BODSXKKAYTVVLU-UHFFFAOYSA-N 2-cyclopentylethyl(diethoxy)silane Chemical compound CCO[SiH](OCC)CCC1CCCC1 BODSXKKAYTVVLU-UHFFFAOYSA-N 0.000 description 2
- BHPDSAAGSUWVMP-UHFFFAOYSA-N 3,3-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(C(C)C)(COC)CCC(C)C BHPDSAAGSUWVMP-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 2
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- XSIFPSYPOVKYCO-UHFFFAOYSA-N butyl benzoate Chemical compound CCCCOC(=O)C1=CC=CC=C1 XSIFPSYPOVKYCO-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 230000001186 cumulative effect Effects 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 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 description 2
- ZYBAWIGLQSTQBP-UHFFFAOYSA-N cyclohexyl-cyclopentyl-diethoxysilane Chemical compound C1CCCCC1[Si](OCC)(OCC)C1CCCC1 ZYBAWIGLQSTQBP-UHFFFAOYSA-N 0.000 description 2
- SJJCABYOVIHNPZ-UHFFFAOYSA-N cyclohexyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1CCCCC1 SJJCABYOVIHNPZ-UHFFFAOYSA-N 0.000 description 2
- QEPVYYOIYSITJK-UHFFFAOYSA-N cyclohexyl-ethyl-dimethoxysilane Chemical compound CC[Si](OC)(OC)C1CCCCC1 QEPVYYOIYSITJK-UHFFFAOYSA-N 0.000 description 2
- RTYZQVDVGVAXSW-UHFFFAOYSA-N cyclohexylmethyl(diethoxy)silane Chemical compound CCO[SiH](OCC)CC1CCCCC1 RTYZQVDVGVAXSW-UHFFFAOYSA-N 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- XDCKEUDKBSSPCB-UHFFFAOYSA-N cyclopentyl-(3,5-dimethylcyclohexyl)-dimethoxysilane Chemical compound C1C(C)CC(C)CC1[Si](OC)(OC)C1CCCC1 XDCKEUDKBSSPCB-UHFFFAOYSA-N 0.000 description 2
- BGNDGZWNHDJSEE-UHFFFAOYSA-N cyclopentyl-dimethoxy-(4-methylcyclohexyl)silane Chemical compound C1CC(C)CCC1[Si](OC)(OC)C1CCCC1 BGNDGZWNHDJSEE-UHFFFAOYSA-N 0.000 description 2
- DFLBJDBDZMNGCW-UHFFFAOYSA-N cyclopentylmethyl(dimethoxy)silane Chemical compound CO[SiH](OC)CC1CCCC1 DFLBJDBDZMNGCW-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- DGPFXVBYDAVXLX-UHFFFAOYSA-N dibutyl(diethoxy)silane Chemical compound CCCC[Si](OCC)(OCC)CCCC DGPFXVBYDAVXLX-UHFFFAOYSA-N 0.000 description 2
- CGYGEZLIGMBRKL-UHFFFAOYSA-N dicyclohexyl(diethoxy)silane Chemical compound C1CCCCC1[Si](OCC)(OCC)C1CCCCC1 CGYGEZLIGMBRKL-UHFFFAOYSA-N 0.000 description 2
- ZVMRWPHIZSSUKP-UHFFFAOYSA-N dicyclohexyl(dimethoxy)silane Chemical compound C1CCCCC1[Si](OC)(OC)C1CCCCC1 ZVMRWPHIZSSUKP-UHFFFAOYSA-N 0.000 description 2
- FVAXOELGJXMINU-UHFFFAOYSA-N dicyclopentyl(diethoxy)silane Chemical compound C1CCCC1[Si](OCC)(OCC)C1CCCC1 FVAXOELGJXMINU-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- RPFNAJGCHRWCRI-UHFFFAOYSA-N diethyl 2,3-dibutylbutanedioate Chemical compound CCCCC(C(=O)OCC)C(CCCC)C(=O)OCC RPFNAJGCHRWCRI-UHFFFAOYSA-N 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- JQCXWCOOWVGKMT-UHFFFAOYSA-N diheptyl phthalate Chemical compound CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 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
- JVUVKQDVTIIMOD-UHFFFAOYSA-N dimethoxy(dipropyl)silane Chemical compound CCC[Si](OC)(OC)CCC JVUVKQDVTIIMOD-UHFFFAOYSA-N 0.000 description 2
- NHYFIJRXGOQNFS-UHFFFAOYSA-N dimethoxy-bis(2-methylpropyl)silane Chemical compound CC(C)C[Si](OC)(CC(C)C)OC NHYFIJRXGOQNFS-UHFFFAOYSA-N 0.000 description 2
- VHPUZTHRFWIGAW-UHFFFAOYSA-N dimethoxy-di(propan-2-yl)silane Chemical compound CO[Si](OC)(C(C)C)C(C)C VHPUZTHRFWIGAW-UHFFFAOYSA-N 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- IPKKHRVROFYTEK-UHFFFAOYSA-N dipentyl phthalate Chemical compound CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCC IPKKHRVROFYTEK-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- MQHNKCZKNAJROC-UHFFFAOYSA-N dipropyl phthalate Chemical compound CCCOC(=O)C1=CC=CC=C1C(=O)OCCC MQHNKCZKNAJROC-UHFFFAOYSA-N 0.000 description 2
- 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 2
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 235000011147 magnesium chloride Nutrition 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- WNJYXPXGUGOGBO-UHFFFAOYSA-N magnesium;propan-1-olate Chemical compound CCCO[Mg]OCCC WNJYXPXGUGOGBO-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229940095102 methyl benzoate Drugs 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- YLYBTZIQSIBWLI-UHFFFAOYSA-N octyl acetate Chemical compound CCCCCCCCOC(C)=O YLYBTZIQSIBWLI-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
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- CMFVMOIFTUDPNL-UHFFFAOYSA-N dimethoxy-bis(4-methylcyclohexyl)silane Chemical compound C1CC(C)CCC1[Si](OC)(OC)C1CCC(C)CC1 CMFVMOIFTUDPNL-UHFFFAOYSA-N 0.000 description 1
- CVQVSVBUMVSJES-UHFFFAOYSA-N dimethoxy-methyl-phenylsilane Chemical compound CO[Si](C)(OC)C1=CC=CC=C1 CVQVSVBUMVSJES-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 238000004090 dissolution Methods 0.000 description 1
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- NWPWRAWAUYIELB-UHFFFAOYSA-N ethyl 4-methylbenzoate Chemical compound CCOC(=O)C1=CC=C(C)C=C1 NWPWRAWAUYIELB-UHFFFAOYSA-N 0.000 description 1
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- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
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- BSGVJBRWDNPHOR-UHFFFAOYSA-M magnesium;butan-1-olate;chloride Chemical compound [Mg+2].[Cl-].CCCC[O-] BSGVJBRWDNPHOR-UHFFFAOYSA-M 0.000 description 1
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- CCLBJCVPJCHEQD-UHFFFAOYSA-N magnesium;ethanolate;propan-1-olate Chemical compound [Mg+2].CC[O-].CCC[O-] CCLBJCVPJCHEQD-UHFFFAOYSA-N 0.000 description 1
- CRGZYKWWYNQGEC-UHFFFAOYSA-N magnesium;methanolate Chemical compound [Mg+2].[O-]C.[O-]C CRGZYKWWYNQGEC-UHFFFAOYSA-N 0.000 description 1
- ZHLDMBMNKCIBQN-UHFFFAOYSA-M magnesium;methanolate;chloride Chemical compound [Cl-].CO[Mg+] ZHLDMBMNKCIBQN-UHFFFAOYSA-M 0.000 description 1
- UYICAKKJLNIPRK-UHFFFAOYSA-M magnesium;propan-1-olate;chloride Chemical compound [Mg+2].[Cl-].CCC[O-] UYICAKKJLNIPRK-UHFFFAOYSA-M 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- POPACFLNWGUDSR-UHFFFAOYSA-N methoxy(trimethyl)silane Chemical compound CO[Si](C)(C)C POPACFLNWGUDSR-UHFFFAOYSA-N 0.000 description 1
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- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- QSSJZLPUHJDYKF-UHFFFAOYSA-N methyl 4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C=C1 QSSJZLPUHJDYKF-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- DDIZAANNODHTRB-UHFFFAOYSA-N methyl p-anisate Chemical compound COC(=O)C1=CC=C(OC)C=C1 DDIZAANNODHTRB-UHFFFAOYSA-N 0.000 description 1
- OLXYLDUSSBULGU-UHFFFAOYSA-N methyl pyridine-4-carboxylate Chemical compound COC(=O)C1=CC=NC=C1 OLXYLDUSSBULGU-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
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- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
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- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
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- AIFMYMZGQVTROK-UHFFFAOYSA-N silicon tetrabromide Chemical compound Br[Si](Br)(Br)Br AIFMYMZGQVTROK-UHFFFAOYSA-N 0.000 description 1
- JHGCXUUFRJCMON-UHFFFAOYSA-J silicon(4+);tetraiodide Chemical compound [Si+4].[I-].[I-].[I-].[I-] JHGCXUUFRJCMON-UHFFFAOYSA-J 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
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- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
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- GJZOQUZYVAYWJH-UHFFFAOYSA-N triethoxy(2-ethylhexyl)silane Chemical compound CCCCC(CC)C[Si](OCC)(OCC)OCC GJZOQUZYVAYWJH-UHFFFAOYSA-N 0.000 description 1
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- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
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- LGROXJWYRXANBB-UHFFFAOYSA-N trimethoxy(propan-2-yl)silane Chemical compound CO[Si](OC)(OC)C(C)C LGROXJWYRXANBB-UHFFFAOYSA-N 0.000 description 1
- IEVQSSVQJPNPJB-UHFFFAOYSA-N tritert-butyl(methoxy)silane Chemical compound CO[Si](C(C)(C)C)(C(C)(C)C)C(C)(C)C IEVQSSVQJPNPJB-UHFFFAOYSA-N 0.000 description 1
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Abstract
【解決手段】 マグネシウム化合物、四塩化チタン、及びコハク酸ジエステル誘導体を芳香族炭化水素化合物中で接触させて調製することを特徴とするオレフィン重合用固体触媒成分および触媒。
【選択図】 図1
Description
(式中、R7は炭素数1〜4のアルキル基を示し、Qは水素原子あるいはハロゲン原子を示し、pは0<p≦3の整数である。)で表される有機アルミニウム化合物、および(C)電子供与性化合物を含有することを特徴とするオレフィン類重合用触媒を提供するものである。
(1)ジアルコキシマグネシウムを芳香族炭化水素化合物溶媒中に懸濁させた後、四塩化チタンと接触させ、その後昇温して成分(c)と接触させて固体生成物を得、該固体生成物を芳香族炭化水素化合物で洗浄した後、芳香族炭化水素化合物の存在下、再度四塩化チタンと接触させてオレフィン類重合用固体触媒成分(A)を調製する方法。なおこの際、該固体成分を、炭化水素化合物溶媒の存在下又は不存在下で加熱処理してオレフィン類重合用固体触媒成分(A)を得ることができる。
R8 qSi(OR9)4-q (2)
(式中、R8は炭素数1〜12のアルキル基、シクロアルキル基、フェニル基、ビニル基、アリル基、アラルキル基を示し、同一または異なっていてもよく、R9は炭素数1〜4の直鎖もしくは分岐を持つアルキル基を示し、同一または異なっていてもよく、qは0≦q≦3の整数である。)で表される化合物が用いられる。このような有機ケイ素化合物としては、フェニルアルコキシシラン、アルキルアルコキシシラン、フェニルアルキルアルコキシシラン、シクロアルキルアルコキシシラン、シクロアルキルアルキルアルコキシシラン等を挙げることができる。
窒素ガスで十分に置換され、撹拌機を具備した容量500mlの丸底フラスコにジエトキシマグネシウム10g、2,3−ジプロピルコハク酸ジエチル2.8gおよびトルエン80mlを装入して、懸濁状態とし、温度を10℃に保持した。次いで該懸濁溶液に四塩化チタン20mlを懸濁液の温度が10℃に保持するようにフラスコを冷却しながら加えて、その後1時間10℃で攪拌した。その後、昇温して90℃とした。その後90℃の温度を保持した状態で、1時間撹拌しながら反応させた。反応終了後、80℃のトルエン100mlで4回洗浄し、新たに四塩化チタン20mlおよびトルエン80mlを加え、100℃に昇温し、1時間撹拌しながら反応させた。反応終了後、40℃のn−ヘプタン100mlで7回洗浄して、固体触媒成分を得た。なお、この固体触媒成分中の固液を分離して、固体分中のチタン含有率を測定したところ、3.1重量%であった。
窒素ガスで完全に置換された内容積2.0リットルの撹拌機付オートクレーブに、トリエチルアルミニウム1.32mmol、ジシクロペンチルジメトキシシラン0.13mmolおよび前記固体触媒成分をチタン原子として0.0026mmol装入し、重合用触媒を形成した。その後、水素ガス1.5リットル、液化プロピレン1.4リットルを装入し、20℃で5分間予備重合を行なった後に昇温し、70℃で1時間重合反応を行った。このときの固体触媒成分1g当たりの重合活性、キシレン溶解成分(XS)、生成重合体のメルトインデックスの値(MI)、多分散性指数(PI)を表1に示した。
重合活性=生成重合体(g)/固体触媒成分(g)
また、キシレン溶解成分(XS)は以下の方法で測定した。
キシレン溶解成分の測定方法:4.0g のポリマーを200mlのパラキシレンに装入し、沸点下(138℃)で2時間かけてポリマーを溶解した。その後23℃まで冷却し、溶解成分と不溶解成分とをろ過分別した。その溶解成分を加熱乾燥し、得られたポリマーをキシレン溶解成分(XS)とした(重量%)。
多分散性指数の値(PI)は、レオメトリクス社製ダイナミックストレスレオメーターで厚さ1.0mmのディスクを用いて測定した。
さらに、生成重合体(a)のメルトインデックスの値(MI)は、ASTM D 1238、 JIS K 7210に準じて測定した。
2,3−ジプロピルコハク酸ジエチル2.8gの代わりに、コハク酸ジエチル1.9gを使用した以外は実施例1と同様に固体成分を調製し、更に重合触媒の形成および重合を行った。その結果固体触媒成分中のチタン含有量は2.2重量%であった。重合結果を表1に示した。
2,3−ジプロピルコハク酸ジエチル2.8gの代わりに、フタル酸ジブチル3.0gを使用した以外は実施例1と同様に固体成分を調製し、更に重合触媒の形成および重合を行った。その結果固体触媒成分中のチタン含有量は3.4重量%であった。重合結果を表1に示した。
無水塩化マグネシウム8.3g、デカン50mlおよび2−エチルヘキシルアルコール40.8mlを混合し130℃で2時間反応させ、均一溶液とした。この溶液中に無水フタル酸1.9gを添加し、130℃で1時間撹拌し均一溶液を得た。この均一溶液を室温に冷却し、−20℃に冷却した四塩化チタン350ml中に1時間かけて加えた。その後、4時間かけて110℃に昇温した。110℃に達したときにイソブチルフタレート4.7mlを添加し、110℃に保持したまま撹拌した。反応後に固液を分離した。固体部に四塩化チタン350mlを加え、110℃で2時間反応させた。反応終了後、固液を分離し固体部を得た。この固体部を60℃のヘプタンで溶液中に遊離のチタン化合物が認められなくなるまで洗浄した。得られた固体触媒成分中のチタン含有量は3.7%であった。重合結果を表1に示した。
Claims (15)
- R3〜R6の少なくとも1個の基がハロゲン原子であることを特徴とする請求項1に記載のオレフィン類重合用固体触媒成分。
- R3〜R6の2個の基がハロゲン原子2個であり、該ハロゲン原子2個が異なる炭素原子に結合していることを特徴とする請求項1又は2に記載のオレフィン類重合用固体触媒成分。
- 前記マグネシウム化合物(a)を前記芳香族炭化水素化合物(d)に懸濁させ懸濁液を形成し、次いで該懸濁液と前記チタン化合物(b)を接触させ、このいずれかの時点で前記コハク酸ジエステル誘導体(c)を接触させて調製されることを特徴とする請求項1〜3のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- 前記マグネシウム化合物(a)および前記コハク酸ジエステル誘導体(c)を前記芳香族炭化水素化合物(d)に懸濁させ懸濁液を形成し、次いで該懸濁液と前記チタン化合物(b)を接触させ調製されることを特徴とする請求項1〜3のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- 前記マグネシウム化合物(a)を前記芳香族炭化水素化合物(d)に懸濁させ懸濁液を形成し、次いで該懸濁液と前記チタン化合物(b)を接触させ、このいずれかの時点で前記コハク酸ジエステル誘導体(c)を接触させて反応させた固体生成物を得た後、該固体生成物を前記芳香族炭化水素(d)で洗浄し、さらに前記チタン化合物(b)を接触させて調製されることを特徴とする請求項1〜3のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- 前記成分(a)マグネシウム化合物がジアルコキシマグネシウムであることを特徴とする請求項1〜6のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- 前記成分(a)マグネシウム化合物がジエトキシマグネシウムであることを特徴とする請求項1〜6のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- 前記成分(a)マグネシウム化合物がジアルコキシマグネシウムであり、且つ前記成分(b)チタン化合物がチタンハロゲン化物であることを特徴とする請求項1〜6のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- 前記芳香族炭化水素化合物(d)がトルエン、キシレン、エチルベンゼンのいずれかであることを特徴とする請求項1〜9のいずれか1項に記載のオレフィン類重合用固体触媒成分。
- ジアルコキシマグネシウムを前記芳香族炭化水素化合物(d)に懸濁させ懸濁液を形成し、次いで該懸濁液とチタンハロゲン化物を接触させた後、発生する反応熱を除去しながらジアルコキシマグネシウムの少なくとも一部をハロゲン化することを特徴とする請求項9に記載のオレフィン類重合用固体触媒成分。
- ジアルコキシマグネシウムを前記芳香族炭化水素化合物(d)に懸濁させ懸濁液を形成し、次いで該懸濁液とチタンハロゲン化物を接触させた後、発生する反応熱を除去しながら−20〜30℃の範囲で30〜150分間ジアルコキシマグネシウムの少なくとも一部をハロゲン化することを特徴とする請求項9に記載のオレフィン類重合用固体触媒成分。
- ジアルコキシマグネシウムを前記芳香族炭化水素化合物(d)に懸濁させ懸濁液を形成し、次いで該懸濁液とチタンハロゲン化物を接触させた後、発生する反応熱を除去しながら−20〜30℃の範囲で30〜150分間ジアルコキシマグネシウムの少なくとも一部をハロゲン化し、その後、70〜120℃に昇温して反応処理することを特徴とする請求項9に記載のオレフィン類重合用固体触媒成分。
- (A)請求項1〜13のいずれか1項に記載のオレフィン類重合用固体触媒成分、(B)下記一般式(1); R7 pAlQ3-p (1)
(式中、R7は炭素数1〜4のアルキル基を示し、Qは水素原子あるいはハロゲン原子を示し、pは0<p≦3の整数である。)で表される有機アルミニウム化合物、および(C)電子供与性化合物を含有することを特徴とするオレフィン類重合用触媒。 - 前記(C)電子供与性化合物が、下記一般式(2);
R8 qSi(OR9)4-q (2)
(式中、R8は炭素数1〜12のアルキル基、シクロアルキル基、フェニル基、ビニル基、アリル基、アラルキル基を示し、同一または異なっていてもよい。R9は炭素数1〜4のアルキル基、シクロアルキル基、フェニル基、ビニル基、またはアリル基又はアラルキル基を示し、同一または異なっていてもよい。qは0≦q≦3の整数である。)で表される有機ケイ素化合物であることを特徴とする請求項14に記載のオレフィン類重合用触媒。
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Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6211706A (ja) * | 1985-07-09 | 1987-01-20 | Mitsubishi Petrochem Co Ltd | オレフイン重合体の製造法 |
JPH09143218A (ja) * | 1995-11-24 | 1997-06-03 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JPH09169808A (ja) * | 1995-09-01 | 1997-06-30 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JPH1129611A (ja) * | 1997-07-08 | 1999-02-02 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JP2002542347A (ja) * | 1999-04-15 | 2002-12-10 | バセル テクノロジー カンパニー ビー.ブイ. | オレフィン重合用の成分および触媒 |
JP2004091513A (ja) * | 2002-08-29 | 2004-03-25 | Toho Catalyst Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
WO2004024785A1 (en) * | 2002-09-16 | 2004-03-25 | Basell Poliolefine Italia S.P.A. | Components and catalysts for the polymerization of olefins |
JP2004107462A (ja) * | 2002-09-18 | 2004-04-08 | Toho Catalyst Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JP2004511590A (ja) * | 2000-10-13 | 2004-04-15 | バセル ポリオレフィン イタリア エス.ピー.エー. | オレフィン重合用触媒成分 |
JP2004210913A (ja) * | 2002-12-27 | 2004-07-29 | Toho Catalyst Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JP2006522186A (ja) * | 2003-04-03 | 2006-09-28 | バセル ポリオレフィン イタリア エス.アール.エル. | 耐衝撃性ポリオレフィン組成物 |
-
2005
- 2005-01-18 JP JP2005010179A patent/JP4688135B2/ja active Active
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6211706A (ja) * | 1985-07-09 | 1987-01-20 | Mitsubishi Petrochem Co Ltd | オレフイン重合体の製造法 |
JPH09169808A (ja) * | 1995-09-01 | 1997-06-30 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JPH09143218A (ja) * | 1995-11-24 | 1997-06-03 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JPH1129611A (ja) * | 1997-07-08 | 1999-02-02 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JP2002542347A (ja) * | 1999-04-15 | 2002-12-10 | バセル テクノロジー カンパニー ビー.ブイ. | オレフィン重合用の成分および触媒 |
JP2004511590A (ja) * | 2000-10-13 | 2004-04-15 | バセル ポリオレフィン イタリア エス.ピー.エー. | オレフィン重合用触媒成分 |
JP2004091513A (ja) * | 2002-08-29 | 2004-03-25 | Toho Catalyst Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
WO2004024785A1 (en) * | 2002-09-16 | 2004-03-25 | Basell Poliolefine Italia S.P.A. | Components and catalysts for the polymerization of olefins |
JP2004107462A (ja) * | 2002-09-18 | 2004-04-08 | Toho Catalyst Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JP2004210913A (ja) * | 2002-12-27 | 2004-07-29 | Toho Catalyst Co Ltd | オレフィン類重合用固体触媒成分および触媒 |
JP2006522186A (ja) * | 2003-04-03 | 2006-09-28 | バセル ポリオレフィン イタリア エス.アール.エル. | 耐衝撃性ポリオレフィン組成物 |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010514905A (ja) * | 2006-12-29 | 2010-05-06 | フイナ・テクノロジー・インコーポレーテツド | ポリプロピレンフィルムグレード樹脂製造用n−ブチルメチルジメトキシシラン使用スクシネート含有重合触媒系 |
JP2011500907A (ja) * | 2007-10-15 | 2011-01-06 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 高流動性プロピレンポリマーの製造方法 |
JP2011508013A (ja) * | 2007-12-21 | 2011-03-10 | ダウ グローバル テクノロジーズ インコーポレイティド | 二座内部供与体を有する自己制限性触媒組成物 |
WO2013125504A1 (ja) * | 2012-02-20 | 2013-08-29 | サンアロマー株式会社 | シート成形用ポリプロピレン系樹脂組成物 |
JPWO2013125504A1 (ja) * | 2012-02-20 | 2015-07-30 | サンアロマー株式会社 | シート成形用ポリプロピレン系樹脂組成物 |
JP2014065816A (ja) * | 2012-09-26 | 2014-04-17 | Toho Titanium Co Ltd | オレフィン類重合用固体触媒成分、オレフィン類重合用触媒及びオレフィン類重合体の製造方法 |
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JP2015000961A (ja) * | 2013-06-17 | 2015-01-05 | サンアロマー株式会社 | 二軸延伸フィルム用ポリプロピレン樹脂組成物 |
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WO2018092805A1 (ja) * | 2016-11-15 | 2018-05-24 | サンアロマー株式会社 | マスターバッチ組成物およびこれを含むポリプロピレン樹脂組成物 |
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