PT97208A - Processo de preparacao de componentes de catalisadores e catalisadores para a polimerizacao de olefinas - Google Patents
Processo de preparacao de componentes de catalisadores e catalisadores para a polimerizacao de olefinas Download PDFInfo
- Publication number
- PT97208A PT97208A PT97208A PT9720891A PT97208A PT 97208 A PT97208 A PT 97208A PT 97208 A PT97208 A PT 97208A PT 9720891 A PT9720891 A PT 9720891A PT 97208 A PT97208 A PT 97208A
- Authority
- PT
- Portugal
- Prior art keywords
- quot
- dimethoxypropane
- ether
- halogen
- compound
- Prior art date
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- 239000003054 catalyst Substances 0.000 title claims abstract description 51
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 17
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims description 19
- 238000002360 preparation method Methods 0.000 title claims description 12
- -1 titanium halide Chemical class 0.000 claims abstract description 92
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000011777 magnesium Substances 0.000 claims abstract description 22
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 20
- 125000005843 halogen group Chemical group 0.000 claims abstract description 19
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 11
- 239000010936 titanium Substances 0.000 claims abstract description 11
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 10
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 9
- 125000001033 ether group Chemical group 0.000 claims abstract description 8
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 8
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 239000011949 solid catalyst Substances 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 6
- 238000000605 extraction Methods 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims 2
- 150000002680 magnesium Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 abstract description 13
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 239000007787 solid Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 8
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 6
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 6
- 229910003074 TiCl4 Inorganic materials 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 150000003609 titanium compounds Chemical class 0.000 description 5
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- 230000000707 stereoselective effect Effects 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052809 inorganic oxide Inorganic materials 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
- PBIJVUVDJZHLFX-UHFFFAOYSA-N 2-chloro-4,4-bis(methoxymethyl)heptane Chemical compound CCCC(COC)(COC)CC(C)Cl PBIJVUVDJZHLFX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000002083 X-ray spectrum Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004799 bromophenyl group Chemical group 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
- 230000000694 effects Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- VNKYTQGIUYNRMY-UHFFFAOYSA-N methoxypropane Chemical compound CCCOC VNKYTQGIUYNRMY-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- KMVFFAABYZVJGG-UHFFFAOYSA-N (2-bromo-1,3-dimethoxypropan-2-yl)benzene Chemical compound COCC(Br)(COC)C1=CC=CC=C1 KMVFFAABYZVJGG-UHFFFAOYSA-N 0.000 description 1
- ZYBDWJYMHMGIRK-UHFFFAOYSA-N (2-chloro-1,3-dimethoxypropan-2-yl)benzene Chemical compound COCC(Cl)(COC)C1=CC=CC=C1 ZYBDWJYMHMGIRK-UHFFFAOYSA-N 0.000 description 1
- YRNAXGKPGUGTAJ-UHFFFAOYSA-N (2-chloro-1,3-dimethoxypropan-2-yl)cyclohexane Chemical compound COCC(Cl)(COC)C1CCCCC1 YRNAXGKPGUGTAJ-UHFFFAOYSA-N 0.000 description 1
- XBCMZQUUCKJLNP-UHFFFAOYSA-N 1,1,1-trifluoro-2,2-bis(methoxymethyl)-3-methylbutane Chemical compound COCC(C(F)(F)F)(C(C)C)COC XBCMZQUUCKJLNP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- KONNYEDMJCUCNO-UHFFFAOYSA-N 1,3-dimethoxypropan-2-yl(trimethyl)silane Chemical compound COCC([Si](C)(C)C)COC KONNYEDMJCUCNO-UHFFFAOYSA-N 0.000 description 1
- BHDSGQOSIWVMJW-UHFFFAOYSA-N 1-(2-chloroethoxy)propane Chemical compound CCCOCCCl BHDSGQOSIWVMJW-UHFFFAOYSA-N 0.000 description 1
- OHTHQIGQSMFIAT-UHFFFAOYSA-N 1-(chloromethyl)-4-[1-ethoxy-2-(ethoxymethyl)-4-methylpentan-2-yl]benzene Chemical compound CCOCC(COCC)(CC(C)C)C1=CC=C(CCl)C=C1 OHTHQIGQSMFIAT-UHFFFAOYSA-N 0.000 description 1
- CTIFSJISEUWEMR-UHFFFAOYSA-N 1-(chloromethyl)-4-[1-methoxy-2-(methoxymethyl)-4-methylpentan-2-yl]benzene Chemical compound COCC(COC)(CC(C)C)C1=CC=C(CCl)C=C1 CTIFSJISEUWEMR-UHFFFAOYSA-N 0.000 description 1
- KFDUWZOUWLGGRD-UHFFFAOYSA-N 1-[1-butoxy-2-(butoxymethyl)-4-methylpentan-2-yl]-4-chlorocyclohexane Chemical compound CCCCOCC(COCCCC)(CC(C)C)C1CCC(Cl)CC1 KFDUWZOUWLGGRD-UHFFFAOYSA-N 0.000 description 1
- DZUDQJYWGJDBLT-UHFFFAOYSA-N 1-[1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]piperidine Chemical compound COCC(COC)(C(C)C)N1CCCCC1 DZUDQJYWGJDBLT-UHFFFAOYSA-N 0.000 description 1
- YVVKXOZBSGCSNM-UHFFFAOYSA-N 1-[1-methoxy-2-(methoxymethyl)pentan-2-yl]-2,6-dimethylpiperidine Chemical compound CCCC(COC)(COC)N1C(C)CCCC1C YVVKXOZBSGCSNM-UHFFFAOYSA-N 0.000 description 1
- LZTLEOBQFVCKDT-UHFFFAOYSA-N 1-butoxy-2-(butoxymethyl)-2-chloropentane Chemical compound CCCCOCC(Cl)(CCC)COCCCC LZTLEOBQFVCKDT-UHFFFAOYSA-N 0.000 description 1
- YIUIBOWABRHDSP-UHFFFAOYSA-N 1-butoxy-2-[butoxy(chloro)methyl]-1-chloro-4-methylpentane Chemical compound CCCCOC(Cl)C(CC(C)C)C(Cl)OCCCC YIUIBOWABRHDSP-UHFFFAOYSA-N 0.000 description 1
- CAMLIDHCMJDBQW-UHFFFAOYSA-N 1-chloro-2,2-bis(methoxymethyl)-4-methylpentane Chemical compound COCC(CCl)(COC)CC(C)C CAMLIDHCMJDBQW-UHFFFAOYSA-N 0.000 description 1
- CAGNICCNRQJQAL-UHFFFAOYSA-N 1-chloro-2,3-dimethoxy-2,3-dimethylbutane Chemical compound COC(C)(C)C(C)(CCl)OC CAGNICCNRQJQAL-UHFFFAOYSA-N 0.000 description 1
- VETOEGANPLEWQH-UHFFFAOYSA-N 1-chloro-4-[1-ethoxy-2-(ethoxymethyl)-4-methylpentan-2-yl]cyclohexane Chemical compound CCOCC(COCC)(CC(C)C)C1CCC(Cl)CC1 VETOEGANPLEWQH-UHFFFAOYSA-N 0.000 description 1
- YAITXWMWRXHHHD-UHFFFAOYSA-N 1-chloro-4-[1-methoxy-2-(methoxymethyl)-4-methylpentan-2-yl]cyclohexane Chemical compound COCC(COC)(CC(C)C)C1CCC(Cl)CC1 YAITXWMWRXHHHD-UHFFFAOYSA-N 0.000 description 1
- WYZNBPDYRFRINI-UHFFFAOYSA-N 1-chloro-4-[2-(4-chlorocyclohexyl)-1,3-dimethoxypropan-2-yl]cyclohexane Chemical compound C1CC(Cl)CCC1C(COC)(COC)C1CCC(Cl)CC1 WYZNBPDYRFRINI-UHFFFAOYSA-N 0.000 description 1
- MONYYIXELXZWSY-UHFFFAOYSA-N 1-chloro-5,5-bis(methoxymethyl)-2,2-dimethylheptane Chemical compound COCC(COC)(CC)CCC(C)(C)CCl MONYYIXELXZWSY-UHFFFAOYSA-N 0.000 description 1
- NVJUHMXYKCUMQA-UHFFFAOYSA-N 1-ethoxypropane Chemical compound CCCOCC NVJUHMXYKCUMQA-UHFFFAOYSA-N 0.000 description 1
- NGMVWDKVVMVTTM-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-3-methylbutane Chemical compound COCC(C(C)C)COC NGMVWDKVVMVTTM-UHFFFAOYSA-N 0.000 description 1
- MUDBTJJLOAEUIQ-UHFFFAOYSA-N 2,2-bis(butoxymethyl)-1,1,1-trifluoro-3-methylbutane Chemical compound CCCCOCC(C(F)(F)F)(C(C)C)COCCCC MUDBTJJLOAEUIQ-UHFFFAOYSA-N 0.000 description 1
- SVCKMYPKGPEVMT-UHFFFAOYSA-N 2,2-bis(ethoxymethyl)-1,1,1-trifluoro-3-methylbutane Chemical compound CCOCC(C(F)(F)F)(C(C)C)COCC SVCKMYPKGPEVMT-UHFFFAOYSA-N 0.000 description 1
- UYTIHLDCHAUOCC-UHFFFAOYSA-N 2-bromo-1-ethoxy-2-(ethoxymethyl)pentane Chemical compound CCOCC(Br)(CCC)COCC UYTIHLDCHAUOCC-UHFFFAOYSA-N 0.000 description 1
- SFRTTYNZLOUXDY-UHFFFAOYSA-N 2-bromo-1-methoxy-2-(methoxymethyl)butane Chemical compound COCC(Br)(CC)COC SFRTTYNZLOUXDY-UHFFFAOYSA-N 0.000 description 1
- KVGOHOUSAWEZMU-UHFFFAOYSA-N 2-bromo-1-methoxy-2-(methoxymethyl)pentane Chemical compound CCCC(Br)(COC)COC KVGOHOUSAWEZMU-UHFFFAOYSA-N 0.000 description 1
- NPTOAUGGHFJJKI-UHFFFAOYSA-N 2-chloro-1,1,1-trifluoro-3-methoxy-2-(methoxymethyl)propane Chemical compound COCC(Cl)(C(F)(F)F)COC NPTOAUGGHFJJKI-UHFFFAOYSA-N 0.000 description 1
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 1
- UASOPPLIIBWACF-UHFFFAOYSA-N 2-chloro-1-(2-chloroethoxy)-2-(2-chloroethoxymethyl)butane Chemical compound ClCCOCC(Cl)(CC)COCCCl UASOPPLIIBWACF-UHFFFAOYSA-N 0.000 description 1
- FKTBPXRDGNRGGU-UHFFFAOYSA-N 2-chloro-1-(2-chloroethoxy)-2-(methoxymethyl)butane Chemical compound COCC(Cl)(CC)COCCCl FKTBPXRDGNRGGU-UHFFFAOYSA-N 0.000 description 1
- WPEWLQUBIZNQOZ-UHFFFAOYSA-N 2-chloro-1-(2-chloroethoxy)-2-(methoxymethyl)pentane Chemical compound CCCC(Cl)(COC)COCCCl WPEWLQUBIZNQOZ-UHFFFAOYSA-N 0.000 description 1
- PHRIVOCGJTWUJH-UHFFFAOYSA-N 2-chloro-1-ethoxy-2-(ethoxymethyl)-4-methylpentane Chemical compound CCOCC(Cl)(CC(C)C)COCC PHRIVOCGJTWUJH-UHFFFAOYSA-N 0.000 description 1
- LUNLOCROVVZMJE-UHFFFAOYSA-N 2-chloro-1-ethoxy-2-(ethoxymethyl)-5-methylhexane Chemical compound CCOCC(Cl)(CCC(C)C)COCC LUNLOCROVVZMJE-UHFFFAOYSA-N 0.000 description 1
- DXUOLTNRPNROAU-UHFFFAOYSA-N 2-chloro-1-ethoxy-2-(ethoxymethyl)butane Chemical compound CCOCC(Cl)(CC)COCC DXUOLTNRPNROAU-UHFFFAOYSA-N 0.000 description 1
- FJNQDUQMJIRLCD-UHFFFAOYSA-N 2-chloro-1-ethoxy-2-(ethoxymethyl)pentane Chemical compound CCOCC(Cl)(CCC)COCC FJNQDUQMJIRLCD-UHFFFAOYSA-N 0.000 description 1
- RKIWMOPVJOELEL-UHFFFAOYSA-N 2-chloro-1-methoxy-2-(methoxymethyl)-4,4-dimethylpentane Chemical compound COCC(Cl)(COC)CC(C)(C)C RKIWMOPVJOELEL-UHFFFAOYSA-N 0.000 description 1
- WKCALFPSVUHMFA-UHFFFAOYSA-N 2-chloro-1-methoxy-2-(methoxymethyl)-4-methylpentane Chemical compound COCC(Cl)(COC)CC(C)C WKCALFPSVUHMFA-UHFFFAOYSA-N 0.000 description 1
- FXBHBAHSCISCHP-UHFFFAOYSA-N 2-chloro-1-methoxy-2-(methoxymethyl)-5-methylhexane Chemical compound COCC(Cl)(COC)CCC(C)C FXBHBAHSCISCHP-UHFFFAOYSA-N 0.000 description 1
- BJCIGNGOLCYMTH-UHFFFAOYSA-N 2-chloro-1-methoxy-2-(methoxymethyl)hexane Chemical compound CCCCC(Cl)(COC)COC BJCIGNGOLCYMTH-UHFFFAOYSA-N 0.000 description 1
- FCAZHKLWGAPKHF-UHFFFAOYSA-N 2-ethylsulfonyl-1-methoxy-2-(methoxymethyl)-3-methylbutane Chemical compound CCS(=O)(=O)C(COC)(COC)C(C)C FCAZHKLWGAPKHF-UHFFFAOYSA-N 0.000 description 1
- IPWZXDDVIQBHDA-UHFFFAOYSA-N 2-tert-butylsulfanyl-1-methoxy-2-(methoxymethyl)butane Chemical compound COCC(CC)(COC)SC(C)(C)C IPWZXDDVIQBHDA-UHFFFAOYSA-N 0.000 description 1
- KIXDNQJIHLYASL-UHFFFAOYSA-N 3-chloro-1-methoxy-2-(methoxymethyl)-2,4,4-trimethylpentane Chemical compound COCC(C)(COC)C(Cl)C(C)(C)C KIXDNQJIHLYASL-UHFFFAOYSA-N 0.000 description 1
- ZDJPOZOCPVDEQQ-UHFFFAOYSA-N 3-chloro-2-methoxy-3-(methoxymethyl)-4-methylpentane Chemical compound COCC(Cl)(C(C)C)C(C)OC ZDJPOZOCPVDEQQ-UHFFFAOYSA-N 0.000 description 1
- JGWVEAHCBFJTLD-UHFFFAOYSA-N 3-iodo-4,4-bis(methoxymethyl)-2,2-dimethylhexane Chemical compound COCC(CC)(COC)C(I)C(C)(C)C JGWVEAHCBFJTLD-UHFFFAOYSA-N 0.000 description 1
- QQRHEESVOJHCMN-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-3,6-dimethylhept-2-ene Chemical compound COCC(COC)(CC(C)C)C(C)=CC QQRHEESVOJHCMN-UHFFFAOYSA-N 0.000 description 1
- 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 1
- CTTCFVZEPXFEIY-UHFFFAOYSA-N 5,5-bis(methoxymethyl)-3,7-dimethyloct-2-ene Chemical compound COCC(COC)(CC(C)C)CC(C)=CC CTTCFVZEPXFEIY-UHFFFAOYSA-N 0.000 description 1
- JKZUPYLLIBBVDS-UHFFFAOYSA-N 5,5-bis(methoxymethyl)-8-methylnon-2-ene Chemical compound CC(C)CCC(COC)(COC)CC=CC JKZUPYLLIBBVDS-UHFFFAOYSA-N 0.000 description 1
- WBGZDMPKFKDOGR-UHFFFAOYSA-N 5,5-bis(methoxymethyl)bicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(COC)(COC)CC1C=C2 WBGZDMPKFKDOGR-UHFFFAOYSA-N 0.000 description 1
- FJNORHVWZOSHSE-UHFFFAOYSA-N 5-[1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]bicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C(COC)(C(C)C)COC)CC1C=C2 FJNORHVWZOSHSE-UHFFFAOYSA-N 0.000 description 1
- WQKHERPPDYPMNX-UHFFFAOYSA-N 6-chloro-3,4-dihydro-2h-naphthalen-1-one Chemical compound O=C1CCCC2=CC(Cl)=CC=C21 WQKHERPPDYPMNX-UHFFFAOYSA-N 0.000 description 1
- LVAORLDGEVSYMC-UHFFFAOYSA-N C(CC)C(COCC)COCC Chemical compound C(CC)C(COCC)COCC LVAORLDGEVSYMC-UHFFFAOYSA-N 0.000 description 1
- QKFJCTXQICYNSL-UHFFFAOYSA-N COCC1=C(C2CCC1C2)COC Chemical compound COCC1=C(C2CCC1C2)COC QKFJCTXQICYNSL-UHFFFAOYSA-N 0.000 description 1
- DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical class CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical class CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000007818 Grignard reagent Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 229910010068 TiCl2 Inorganic materials 0.000 description 1
- 238000007239 Wittig reaction Methods 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- KSCPOLMSSJBNEC-UHFFFAOYSA-N [1-butoxy-2-(butoxymethyl)pentan-2-yl]oxy-trimethylsilane Chemical compound CCCCOCC(CCC)(O[Si](C)(C)C)COCCCC KSCPOLMSSJBNEC-UHFFFAOYSA-N 0.000 description 1
- ASEWPBADLVFWHO-UHFFFAOYSA-N [1-ethoxy-2-(ethoxymethyl)-3-methylbutan-2-yl]oxy-trimethylsilane Chemical compound CCOCC(C(C)C)(O[Si](C)(C)C)COCC ASEWPBADLVFWHO-UHFFFAOYSA-N 0.000 description 1
- FPKFTJQSFRHCHU-UHFFFAOYSA-N [1-ethoxy-2-(ethoxymethyl)hexan-2-yl]cyclohexane Chemical compound CCCCC(COCC)(COCC)C1CCCCC1 FPKFTJQSFRHCHU-UHFFFAOYSA-N 0.000 description 1
- OUROMMVNKZOPGL-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]oxy-trimethylsilane Chemical compound COCC(COC)(O[Si](C)(C)C)C(C)C OUROMMVNKZOPGL-UHFFFAOYSA-N 0.000 description 1
- NVGULOOULKEAMK-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)-4-methylpentan-2-yl] benzoate Chemical compound COCC(COC)(CC(C)C)OC(=O)C1=CC=CC=C1 NVGULOOULKEAMK-UHFFFAOYSA-N 0.000 description 1
- JNUJMVLLVXORBR-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)butan-2-yl]-trimethylsilane Chemical compound COCC(CC)(COC)[Si](C)(C)C JNUJMVLLVXORBR-UHFFFAOYSA-N 0.000 description 1
- UNHYSYXXWUMXMV-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)pentan-2-yl] 2,2-dimethylpropanoate Chemical compound CCCC(COC)(COC)OC(=O)C(C)(C)C UNHYSYXXWUMXMV-UHFFFAOYSA-N 0.000 description 1
- XMPMICXLFQZGAS-UHFFFAOYSA-N [2,2-bis(methoxymethyl)-3-trimethylsilylpropyl]-trimethylsilane Chemical compound COCC(COC)(C[Si](C)(C)C)C[Si](C)(C)C XMPMICXLFQZGAS-UHFFFAOYSA-N 0.000 description 1
- ZXBHLFGEGWGQHK-UHFFFAOYSA-N [2-chloro-1,3-bis(2-chloroethoxy)propan-2-yl]benzene Chemical compound ClCCOCC(Cl)(COCCCl)C1=CC=CC=C1 ZXBHLFGEGWGQHK-UHFFFAOYSA-N 0.000 description 1
- VYPCYIBDGZSHSE-UHFFFAOYSA-N [2-methoxy-3-(methoxymethyl)pentan-3-yl]-trimethylsilane Chemical compound COCC(CC)(C(C)OC)[Si](C)(C)C VYPCYIBDGZSHSE-UHFFFAOYSA-N 0.000 description 1
- DTRQQCWSHYFUPQ-UHFFFAOYSA-N [4-[1,3-dimethoxy-2-(4-trimethylsilylphenyl)propan-2-yl]phenyl]-trimethylsilane Chemical compound C=1C=C([Si](C)(C)C)C=CC=1C(COC)(COC)C1=CC=C([Si](C)(C)C)C=C1 DTRQQCWSHYFUPQ-UHFFFAOYSA-N 0.000 description 1
- VJGPAPFCEZGWDR-UHFFFAOYSA-N [4-[2-(4-diphenylphosphanylphenyl)-1,3-dimethoxypropan-2-yl]phenyl]-diphenylphosphane Chemical compound C=1C=C(P(C=2C=CC=CC=2)C=2C=CC=CC=2)C=CC=1C(COC)(COC)C(C=C1)=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 VJGPAPFCEZGWDR-UHFFFAOYSA-N 0.000 description 1
- REDBPKFBXLDWAM-UHFFFAOYSA-N [4-[2-[4-(2,2-dimethylpropanoyloxy)phenyl]-1,3-dimethoxypropan-2-yl]phenyl] 2,2-dimethylpropanoate Chemical compound C=1C=C(OC(=O)C(C)(C)C)C=CC=1C(COC)(COC)C1=CC=C(OC(=O)C(C)(C)C)C=C1 REDBPKFBXLDWAM-UHFFFAOYSA-N 0.000 description 1
- AQUOBFFOTBPJLL-UHFFFAOYSA-N [4-methoxy-3-(methoxymethyl)butyl]-trimethylsilane Chemical compound COCC(COC)CC[Si](C)(C)C AQUOBFFOTBPJLL-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- UXXXZMDJQLPQPH-UHFFFAOYSA-N bis(2-methylpropyl) carbonate Chemical compound CC(C)COC(=O)OCC(C)C UXXXZMDJQLPQPH-UHFFFAOYSA-N 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 229940071221 dihydroxybenzoate Drugs 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 class 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 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
- 239000004744 fabric Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- NDMWNXVHZWMKJC-UHFFFAOYSA-N methyl 1-methoxy-2-(methoxymethyl)butane-2-sulfonate Chemical compound COCC(CC)(COC)S(=O)(=O)OC NDMWNXVHZWMKJC-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000005049 silicon tetrachloride 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
- 239000012798 spherical particle Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- ZWYDDDAMNQQZHD-UHFFFAOYSA-L titanium(ii) chloride Chemical compound [Cl-].[Cl-].[Ti+2] ZWYDDDAMNQQZHD-UHFFFAOYSA-L 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- C08F4/06—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen
- C08F4/10—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen of alkaline earth metals, zinc, cadmium, mercury, copper or silver
-
- 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
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT19891A IT1241093B (it) | 1990-03-30 | 1990-03-30 | Componenti e catalizzatori per la polimerizzazione di olefine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT97208A true PT97208A (pt) | 1992-01-31 |
Family
ID=11162104
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT97208A PT97208A (pt) | 1990-03-30 | 1991-03-28 | Processo de preparacao de componentes de catalisadores e catalisadores para a polimerizacao de olefinas |
Country Status (24)
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69127220T2 (de) * | 1990-04-13 | 1998-01-02 | Mitsui Petrochemical Ind | Festes Titan enthaltendes Katalysatorbestandteil und Katalysator für Olefinpolymerisation, vorpolymerisierte Olefinpolymerisationskatalysator und Verfahren für Olefinpolymerisation |
| US5726262A (en) * | 1990-04-13 | 1998-03-10 | Mitsui Petrochemical Industries, Ltd. | Solid titanium catalyst component for olefin polymerization, olefin polymerization catalyst, prepolymerized polyolefin-containing catalyst and method of olefin polymerization |
| IT1246614B (it) | 1991-06-03 | 1994-11-24 | Himont Inc | Procedimento per la polimerizzazione in fase gas delle olefine |
| IT1255523B (it) * | 1992-09-24 | 1995-11-09 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
| TW354792B (en) * | 1993-08-13 | 1999-03-21 | Mitsui Petrochemical Ind | Olefin polymerization catalyst and process for preparing polypropylene and propylene block copolymer |
| IT1270842B (it) * | 1993-10-01 | 1997-05-13 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
| CA2142748C (en) * | 1994-02-18 | 1999-02-23 | Shin-Ichi Kojoh | Ethylene polymer and process for preparing the same |
| FI96214C (fi) * | 1994-05-31 | 1996-05-27 | Borealis As | Olefiinien polymerointiin tarkoitettu stereospesifinen katalyyttisysteemi |
| IT1270125B (it) * | 1994-10-05 | 1997-04-28 | Spherilene Srl | Processo per la ( co) polimerizzazione di olefine |
| US7049377B1 (en) * | 1995-02-21 | 2006-05-23 | Basell Poliolefine Italia S.R.L. | 1,3-diethers and components and catalysts for the polymerization of olefins, containing said diethers |
| IT1274253B (it) * | 1995-02-21 | 1997-07-15 | Himont Inc | Processo per la preparazione di componenti catalitici solidi per la polimerizzazione di olefine |
| IL117114A (en) * | 1995-02-21 | 2000-02-17 | Montell North America Inc | Components and catalysts for the polymerization ofolefins |
| IT1274469B (it) | 1995-05-11 | 1997-07-17 | Spherilene Spa | Composizioni poliolefiniche vulcanizzabili dinamicamente |
| US5747407A (en) * | 1996-08-29 | 1998-05-05 | Phillips Petroleum Company | Method of making a Ziegler-Natta olefin polymerization catalyst |
| KR20000068886A (ko) * | 1997-09-03 | 2000-11-25 | 간디 지오프레이 에이치. | 올레핀 중합용 성분 및 촉매 |
| ES2198098T3 (es) | 1998-03-09 | 2004-01-16 | Basell Poliolefine Italia S.P.A. | Procedimiento multietapas para la polimerizacion de olefinas. |
| ES2208301T3 (es) | 1999-03-09 | 2004-06-16 | Basell Polyolefine Gmbh | Procedimiento multietapa para la (co)polimerizacion de olefinas. |
| US6436864B1 (en) | 1999-10-06 | 2002-08-20 | Sri International | Unsaturated nitrogenous compounds as electron donors for use with ziegler-natta catalysts |
| CN1367184A (zh) | 2001-01-12 | 2002-09-04 | 弗纳技术股份有限公司 | 生产超高熔体流动聚丙烯树脂的方法 |
| US7365137B2 (en) | 2001-07-17 | 2008-04-29 | Basell Polyolefine Gmbh | Multistep process for the (co) polymerization of olefins |
| CN100498383C (zh) | 2001-11-21 | 2009-06-10 | 株式会社大真空 | 光学滤波器及其制造方法和收纳结构、以及光学装置 |
| JP4780958B2 (ja) | 2002-06-26 | 2011-09-28 | 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 | 耐衝撃性ポリオレフィン組成物 |
| RU2308470C2 (ru) | 2002-06-26 | 2007-10-20 | Базелль Полиолефин Италия С.П.А. | Ударопрочные полиолефиновые композиции |
| BRPI0416282A (pt) | 2003-11-06 | 2007-01-23 | Basell Poliolefine Srl | composição de polipropileno |
| WO2005077990A1 (en) * | 2004-02-16 | 2005-08-25 | Reliance Industries Limited | Catalytic system for polymerisation of lower alpha alkene. |
| CA2569656A1 (en) | 2004-06-08 | 2005-12-22 | Basell Poliolefine Italia S.R.L. | Polyolefin composition having a high balance of stiffness, impact strength and elongation at break and low thermal shrinkage |
| CN100389133C (zh) * | 2004-10-29 | 2008-05-21 | 中国石油化工股份有限公司 | 一种用于烯烃聚合的催化剂及其应用 |
| CN101153062B (zh) * | 2006-09-29 | 2010-09-22 | 中国石油化工股份有限公司 | 一种烯烃聚合固体催化剂组分及制备方法与应用 |
| JP5419871B2 (ja) | 2007-06-29 | 2014-02-19 | 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 | 非フェノール系安定剤を含む照射ポリオレフィン組成物 |
| KR101580849B1 (ko) | 2008-02-29 | 2015-12-30 | 바셀 폴리올레핀 이탈리아 에스.알.엘 | 폴리올레핀 조성물 |
| US7935740B2 (en) | 2008-12-30 | 2011-05-03 | Basell Poliolefine Italia S.R.L. | Process for producing high melt strength polypropylene |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL258907A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1958-09-17 | |||
| DE1445225B2 (de) * | 1960-09-24 | 1971-11-18 | Badische Anilin & Soda Fabrik AG, 6700 Ludwigshafen | Verfahren zur polymerisation von monoalpha olefinen mit drei oder mehr kohlenstoffatomen |
| US4098976A (en) * | 1971-07-13 | 1978-07-04 | Imperial Chemical Industries Limited | Process for the production of olefin polymers using an organo-phosphorus catalyst compound |
| US4397763A (en) * | 1977-12-13 | 1983-08-09 | Phillips Petroleum Company | Catalyst and process of polymerization of alpha-monoolefins |
| GB2097411B (en) * | 1981-04-23 | 1985-07-03 | Showa Denko Kk | Catalyst for ethylene polymerisation |
| IT1190683B (it) * | 1982-02-12 | 1988-02-24 | Montedison Spa | Componenti e catalizzatori per la polimerizzazione di olefine |
| DE3247919A1 (de) * | 1982-12-24 | 1984-06-28 | Basf Ag, 6700 Ludwigshafen | Verfahren zum herstellen von homo- und copolymerisaten von (alpha)-monoolefinen mittels einer ziegler-natta-katalysatorsystems |
| JPS60130607A (ja) * | 1983-12-19 | 1985-07-12 | Mitsubishi Petrochem Co Ltd | α−オレフイン重合用触媒成分の製造法 |
| US4701505A (en) * | 1984-09-26 | 1987-10-20 | Mitsubishi Petrochemical Company Limited | Process for production of olefin polymers |
| IT1227259B (it) * | 1988-09-30 | 1991-03-28 | Himont Inc | Catalizzatori per la polimerizzazione di olefine. |
| IT1227258B (it) * | 1988-09-30 | 1991-03-28 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
| DE69127220T2 (de) * | 1990-04-13 | 1998-01-02 | Mitsui Petrochemical Ind | Festes Titan enthaltendes Katalysatorbestandteil und Katalysator für Olefinpolymerisation, vorpolymerisierte Olefinpolymerisationskatalysator und Verfahren für Olefinpolymerisation |
-
1990
- 1990-03-30 IT IT19891A patent/IT1241093B/it active IP Right Grant
-
1991
- 1991-03-26 NO NO911238A patent/NO178153C/no not_active IP Right Cessation
- 1991-03-26 US US07/675,234 patent/US5068213A/en not_active Expired - Lifetime
- 1991-03-26 IL IL9767991A patent/IL97679A/en not_active IP Right Cessation
- 1991-03-26 ZA ZA912288A patent/ZA912288B/xx unknown
- 1991-03-27 FI FI911507A patent/FI106382B/fi active
- 1991-03-27 PH PH42220A patent/PH27575A/en unknown
- 1991-03-27 AU AU73860/91A patent/AU633712B2/en not_active Ceased
- 1991-03-28 ES ES91105043T patent/ES2132075T3/es not_active Expired - Lifetime
- 1991-03-28 EP EP98119781A patent/EP0891988B1/en not_active Expired - Lifetime
- 1991-03-28 CN CN91102627A patent/CN1019580B/zh not_active Expired
- 1991-03-28 EP EP91105043A patent/EP0451645B1/en not_active Expired - Lifetime
- 1991-03-28 PT PT97208A patent/PT97208A/pt not_active Application Discontinuation
- 1991-03-28 DK DK91105043T patent/DK0451645T3/da active
- 1991-03-28 YU YU56391A patent/YU56391A/sh unknown
- 1991-03-28 DE DE69131219T patent/DE69131219T2/de not_active Expired - Fee Related
- 1991-03-28 CA CA002039443A patent/CA2039443A1/en not_active Abandoned
- 1991-03-28 ES ES98119781T patent/ES2200252T3/es not_active Expired - Lifetime
- 1991-03-28 AT AT91105043T patent/ATE179996T1/de active
- 1991-03-28 DE DE69133274T patent/DE69133274T2/de not_active Expired - Fee Related
- 1991-03-29 RU SU914895116A patent/RU2087485C1/ru active
- 1991-03-29 CS CS91878A patent/CS87891A2/cs unknown
- 1991-03-29 HU HU911057A patent/HUT57800A/hu unknown
- 1991-03-30 KR KR1019910005149A patent/KR0169489B1/ko not_active Expired - Fee Related
- 1991-03-30 JP JP09326391A patent/JP3307658B2/ja not_active Expired - Fee Related
- 1991-04-01 BR BR919101279A patent/BR9101279A/pt not_active IP Right Cessation
- 1991-04-25 TW TW080102405A patent/TW198043B/zh active
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| Date | Code | Title | Description |
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| BB1A | Laying open of patent application |
Effective date: 19910912 |
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| FC3A | Refusal |
Effective date: 19971202 |