DE69030489T3 - Fester Katalysatorbestandteil für Olefinpolymerisation und Olefinpolymerisationsverfahren unter Anwendung derselben - Google Patents
Fester Katalysatorbestandteil für Olefinpolymerisation und Olefinpolymerisationsverfahren unter Anwendung derselben Download PDFInfo
- Publication number
- DE69030489T3 DE69030489T3 DE69030489T DE69030489T DE69030489T3 DE 69030489 T3 DE69030489 T3 DE 69030489T3 DE 69030489 T DE69030489 T DE 69030489T DE 69030489 T DE69030489 T DE 69030489T DE 69030489 T3 DE69030489 T3 DE 69030489T3
- Authority
- DE
- Germany
- Prior art keywords
- olefin
- catalyst component
- polymerization
- olefin polymerization
- titanium
- 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.)
- Expired - Lifetime
Links
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 124
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 118
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims abstract description 115
- 238000000034 method Methods 0.000 title claims abstract description 80
- 239000011949 solid catalyst Substances 0.000 title claims abstract description 43
- 239000003054 catalyst Substances 0.000 claims abstract description 195
- 239000010936 titanium Substances 0.000 claims abstract description 111
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 85
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 83
- 239000007787 solid Substances 0.000 claims abstract description 61
- 239000004711 α-olefin Substances 0.000 claims abstract description 60
- 229920000098 polyolefin Polymers 0.000 claims abstract description 37
- 150000002902 organometallic compounds Chemical class 0.000 claims abstract description 35
- 230000008569 process Effects 0.000 claims abstract description 20
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 11
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 39
- 239000007788 liquid Substances 0.000 claims description 38
- 229910052736 halogen Inorganic materials 0.000 claims description 37
- 150000002430 hydrocarbons Chemical group 0.000 claims description 37
- 150000002367 halogens Chemical class 0.000 claims description 36
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 36
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 32
- 239000005977 Ethylene Substances 0.000 claims description 30
- 238000007334 copolymerization reaction Methods 0.000 claims description 27
- 239000000725 suspension Substances 0.000 claims description 27
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
- 239000002904 solvent Substances 0.000 claims description 25
- 229930195733 hydrocarbon Natural products 0.000 claims description 24
- 150000002148 esters Chemical class 0.000 claims description 22
- 239000004215 Carbon black (E152) Substances 0.000 claims description 21
- 229910052751 metal Inorganic materials 0.000 claims description 20
- 239000002184 metal Substances 0.000 claims description 20
- 239000011777 magnesium Substances 0.000 claims description 19
- 229910052749 magnesium Inorganic materials 0.000 claims description 17
- 230000000737 periodic effect Effects 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 14
- 150000003961 organosilicon compounds Chemical class 0.000 claims description 11
- 239000007791 liquid phase Substances 0.000 claims description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 8
- 239000012071 phase Substances 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 7
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 3
- 239000002245 particle Substances 0.000 abstract description 62
- 229920000642 polymer Polymers 0.000 abstract description 39
- 238000009826 distribution Methods 0.000 abstract description 10
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical group 0.000 description 40
- 150000002681 magnesium compounds Chemical class 0.000 description 37
- -1 alkylaluminum halide Chemical class 0.000 description 33
- 150000003609 titanium compounds Chemical class 0.000 description 29
- 238000002360 preparation method Methods 0.000 description 26
- 239000007789 gas Substances 0.000 description 24
- 229920001577 copolymer Polymers 0.000 description 23
- 238000006243 chemical reaction Methods 0.000 description 22
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 20
- 125000000217 alkyl group Chemical group 0.000 description 15
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 230000001603 reducing effect Effects 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 11
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 11
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 10
- 230000000704 physical effect Effects 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
- 125000005234 alkyl aluminium group Chemical group 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
- SJJCABYOVIHNPZ-UHFFFAOYSA-N cyclohexyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1CCCCC1 SJJCABYOVIHNPZ-UHFFFAOYSA-N 0.000 description 6
- 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 6
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 6
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- JQCXWCOOWVGKMT-UHFFFAOYSA-N diheptyl phthalate Chemical compound CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 150000003377 silicon compounds Chemical class 0.000 description 5
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 5
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 4
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 150000001733 carboxylic acid esters Chemical class 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 4
- 238000012685 gas phase polymerization Methods 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 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
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 238000010923 batch production Methods 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
- MQHNKCZKNAJROC-UHFFFAOYSA-N dipropyl phthalate Chemical compound CCCOC(=O)C1=CC=CC=C1C(=O)OCCC MQHNKCZKNAJROC-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000002680 magnesium Chemical class 0.000 description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 238000010298 pulverizing process Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 3
- SXNLMXPRYYYOSO-UHFFFAOYSA-N (2,3-dimethylcyclopentyl)-trimethoxysilane Chemical compound CO[Si](OC)(OC)C1CCC(C)C1C SXNLMXPRYYYOSO-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- YQXKUILMUQPCPU-UHFFFAOYSA-N 2,2,2-tricyclopentylethoxysilane Chemical compound C1CCCC1C(C1CCCC1)(CO[SiH3])C1CCCC1 YQXKUILMUQPCPU-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-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
- KCXZNSGUUQJJTR-UHFFFAOYSA-N Di-n-hexyl phthalate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC KCXZNSGUUQJJTR-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 229910010199 LiAl Inorganic materials 0.000 description 2
- YZBOVSFWWNVKRJ-UHFFFAOYSA-N Monobutylphthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(O)=O YZBOVSFWWNVKRJ-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- FYXKZNLBZKRYSS-UHFFFAOYSA-N benzene-1,2-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC=C1C(Cl)=O FYXKZNLBZKRYSS-UHFFFAOYSA-N 0.000 description 2
- DEKYCKZXEQLEEJ-UHFFFAOYSA-N bis(2,3-dimethylcyclopentyl)-dimethoxysilane Chemical compound C1CC(C)C(C)C1[Si](OC)(OC)C1CCC(C)C1C DEKYCKZXEQLEEJ-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- QQHRHLXGCZWTDK-UHFFFAOYSA-L butylaluminum(2+);dibromide Chemical compound [Br-].[Br-].CCCC[Al+2] QQHRHLXGCZWTDK-UHFFFAOYSA-L 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- RTYZQVDVGVAXSW-UHFFFAOYSA-N cyclohexylmethyl(diethoxy)silane Chemical compound CCO[SiH](OCC)CC1CCCCC1 RTYZQVDVGVAXSW-UHFFFAOYSA-N 0.000 description 2
- MGGAITMRMJXXMT-UHFFFAOYSA-N cyclopentyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C1CCCC1 MGGAITMRMJXXMT-UHFFFAOYSA-N 0.000 description 2
- YRMPTIHEUZLTDO-UHFFFAOYSA-N cyclopentyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C1CCCC1 YRMPTIHEUZLTDO-UHFFFAOYSA-N 0.000 description 2
- LITADYQPNQQQCR-UHFFFAOYSA-N cyclopentyl-diethyl-methoxysilane Chemical compound CC[Si](CC)(OC)C1CCCC1 LITADYQPNQQQCR-UHFFFAOYSA-N 0.000 description 2
- NGUKXKTXADXBIB-UHFFFAOYSA-N cyclopentyl-ethoxy-dimethylsilane Chemical compound CCO[Si](C)(C)C1CCCC1 NGUKXKTXADXBIB-UHFFFAOYSA-N 0.000 description 2
- BVNCDRJKUJGGTL-UHFFFAOYSA-N cyclopentyl-methoxy-dimethylsilane Chemical compound CO[Si](C)(C)C1CCCC1 BVNCDRJKUJGGTL-UHFFFAOYSA-N 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- RFUDQCRVCDXBGK-UHFFFAOYSA-L dichloro(propyl)alumane Chemical compound [Cl-].[Cl-].CCC[Al+2] RFUDQCRVCDXBGK-UHFFFAOYSA-L 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
- RUHGCFSYBXWPNF-UHFFFAOYSA-N dicyclopentylmethyl(ethoxy)silane Chemical compound C1CCCC1C([SiH2]OCC)C1CCCC1 RUHGCFSYBXWPNF-UHFFFAOYSA-N 0.000 description 2
- WVEWXPQUQZKPJK-UHFFFAOYSA-N dicyclopentylmethyl(methoxy)silane Chemical compound C1CCCC1C([SiH2]OC)C1CCCC1 WVEWXPQUQZKPJK-UHFFFAOYSA-N 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- ZZNQQQWFKKTOSD-UHFFFAOYSA-N diethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OCC)(OCC)C1=CC=CC=C1 ZZNQQQWFKKTOSD-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
- HJXBDPDUCXORKZ-UHFFFAOYSA-N diethylalumane Chemical compound CC[AlH]CC HJXBDPDUCXORKZ-UHFFFAOYSA-N 0.000 description 2
- JJSGABFIILQOEY-UHFFFAOYSA-M diethylalumanylium;bromide Chemical compound CC[Al](Br)CC JJSGABFIILQOEY-UHFFFAOYSA-M 0.000 description 2
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 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
- OSZVQUZIQCJAPJ-UHFFFAOYSA-N dimethoxy-bis(2-methylcyclopentyl)silane Chemical compound C1CCC(C)C1[Si](OC)(OC)C1CCCC1C OSZVQUZIQCJAPJ-UHFFFAOYSA-N 0.000 description 2
- SZIZIGBTHTUEBU-UHFFFAOYSA-N dimethoxy-bis(4-methylphenyl)silane Chemical compound C=1C=C(C)C=CC=1[Si](OC)(OC)C1=CC=C(C)C=C1 SZIZIGBTHTUEBU-UHFFFAOYSA-N 0.000 description 2
- CVQVSVBUMVSJES-UHFFFAOYSA-N dimethoxy-methyl-phenylsilane Chemical compound CO[Si](C)(OC)C1=CC=CC=C1 CVQVSVBUMVSJES-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 150000002366 halogen compounds Chemical class 0.000 description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 239000004615 ingredient Substances 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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- BDJAEZRIGNCQBZ-UHFFFAOYSA-N methyl-cyclobutane Natural products CC1CCC1 BDJAEZRIGNCQBZ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- OBRKWFIGZSMARO-UHFFFAOYSA-N propylalumane Chemical compound [AlH2]CCC OBRKWFIGZSMARO-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- ASEHKQZNVUOPRW-UHFFFAOYSA-N tert-butyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C(C)(C)C ASEHKQZNVUOPRW-UHFFFAOYSA-N 0.000 description 2
- SGCFZHOZKKQIBU-UHFFFAOYSA-N tributoxy(ethenyl)silane Chemical compound CCCCO[Si](OCCCC)(OCCCC)C=C SGCFZHOZKKQIBU-UHFFFAOYSA-N 0.000 description 2
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 2
- PTCWADDVLPYBBZ-UHFFFAOYSA-N tricyclopentylmethoxysilane Chemical compound C1CCCC1C(C1CCCC1)(O[SiH3])C1CCCC1 PTCWADDVLPYBBZ-UHFFFAOYSA-N 0.000 description 2
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 2
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 2
- IOPAQHDEQBHWEB-UHFFFAOYSA-N trimethoxy-(2-methylcyclopentyl)silane Chemical compound CO[Si](OC)(OC)C1CCCC1C IOPAQHDEQBHWEB-UHFFFAOYSA-N 0.000 description 2
- 238000013022 venting Methods 0.000 description 2
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
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- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- MYEJNNDSIXAGNK-UHFFFAOYSA-N ethyl-tri(propan-2-yloxy)silane Chemical compound CC(C)O[Si](CC)(OC(C)C)OC(C)C MYEJNNDSIXAGNK-UHFFFAOYSA-N 0.000 description 1
- BBIDBFWZMCTRNP-UHFFFAOYSA-N ethylalumane Chemical compound CC[AlH2] BBIDBFWZMCTRNP-UHFFFAOYSA-N 0.000 description 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 1
- SYLAFCZSYRXBJF-UHFFFAOYSA-N furan-3,4-dicarboxylic acid Chemical compound OC(=O)C1=COC=C1C(O)=O SYLAFCZSYRXBJF-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 1
- 229910001623 magnesium bromide Inorganic materials 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- BLQJIBCZHWBKSL-UHFFFAOYSA-L magnesium iodide Chemical compound [Mg+2].[I-].[I-] BLQJIBCZHWBKSL-UHFFFAOYSA-L 0.000 description 1
- 229910001641 magnesium iodide Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- BSGVJBRWDNPHOR-UHFFFAOYSA-M magnesium;butan-1-olate;chloride Chemical compound [Mg+2].[Cl-].CCCC[O-] BSGVJBRWDNPHOR-UHFFFAOYSA-M 0.000 description 1
- KJJBSBKRXUVBMX-UHFFFAOYSA-N magnesium;butane Chemical compound [Mg+2].CCC[CH2-].CCC[CH2-] KJJBSBKRXUVBMX-UHFFFAOYSA-N 0.000 description 1
- QUXHCILOWRXCEO-UHFFFAOYSA-M magnesium;butane;chloride Chemical compound [Mg+2].[Cl-].CCC[CH2-] QUXHCILOWRXCEO-UHFFFAOYSA-M 0.000 description 1
- YJCTUQFSSZSZPO-UHFFFAOYSA-L magnesium;chloride;phenoxide Chemical compound [Cl-].[Mg+]OC1=CC=CC=C1 YJCTUQFSSZSZPO-UHFFFAOYSA-L 0.000 description 1
- BJZBHTNKDCBDNQ-UHFFFAOYSA-L magnesium;dodecanoate Chemical compound [Mg+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O BJZBHTNKDCBDNQ-UHFFFAOYSA-L 0.000 description 1
- DLPASUVGCQPFFO-UHFFFAOYSA-N magnesium;ethane Chemical compound [Mg+2].[CH2-]C.[CH2-]C DLPASUVGCQPFFO-UHFFFAOYSA-N 0.000 description 1
- YCCXQARVHOPWFJ-UHFFFAOYSA-M magnesium;ethane;chloride Chemical compound [Mg+2].[Cl-].[CH2-]C YCCXQARVHOPWFJ-UHFFFAOYSA-M 0.000 description 1
- KRTCPMDBLDWJQY-UHFFFAOYSA-M magnesium;ethanolate;chloride Chemical compound [Mg+2].[Cl-].CC[O-] KRTCPMDBLDWJQY-UHFFFAOYSA-M 0.000 description 1
- RVOYYLUVELMWJF-UHFFFAOYSA-N magnesium;hexane Chemical compound [Mg+2].CCCCC[CH2-].CCCCC[CH2-] RVOYYLUVELMWJF-UHFFFAOYSA-N 0.000 description 1
- GBRJQTLHXWRDOV-UHFFFAOYSA-M magnesium;hexane;chloride Chemical compound [Mg+2].[Cl-].CCCCC[CH2-] GBRJQTLHXWRDOV-UHFFFAOYSA-M 0.000 description 1
- CFXDAHURBQNVFG-UHFFFAOYSA-M magnesium;propan-2-olate;chloride Chemical compound [Mg+2].[Cl-].CC(C)[O-] CFXDAHURBQNVFG-UHFFFAOYSA-M 0.000 description 1
- RYEXTBOQKFUPOE-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].CC[CH2-] RYEXTBOQKFUPOE-UHFFFAOYSA-M 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides 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
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- YWWHKOHZGJFMIE-UHFFFAOYSA-N monoethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(O)=O YWWHKOHZGJFMIE-UHFFFAOYSA-N 0.000 description 1
- RZJSUWQGFCHNFS-UHFFFAOYSA-N monoisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(O)=O RZJSUWQGFCHNFS-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- JHVNMGWNEQGGDU-UHFFFAOYSA-N tert-butyl-diethoxy-methylsilane Chemical compound CCO[Si](C)(C(C)(C)C)OCC JHVNMGWNEQGGDU-UHFFFAOYSA-N 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
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 1
- ALVYUZIFSCKIFP-UHFFFAOYSA-N triethoxy(2-methylpropyl)silane Chemical compound CCO[Si](CC(C)C)(OCC)OCC ALVYUZIFSCKIFP-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- OJAJJFGMKAZGRZ-UHFFFAOYSA-N trimethyl(phenoxy)silane Chemical compound C[Si](C)(C)OC1=CC=CC=C1 OJAJJFGMKAZGRZ-UHFFFAOYSA-N 0.000 description 1
- DFLYRVOWPYSYMZ-UHFFFAOYSA-N tris(3-methylbut-2-enyl)alumane Chemical compound CC(C)=CC[Al](CC=C(C)C)CC=C(C)C DFLYRVOWPYSYMZ-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
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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP340909/89 | 1989-12-29 | ||
| JP1340909A JP2940684B2 (ja) | 1989-12-29 | 1989-12-29 | オレフィン重合用固体状触媒成分およびこの触媒成分を用いたオレフィンの重合方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE69030489D1 DE69030489D1 (de) | 1997-05-22 |
| DE69030489T2 DE69030489T2 (de) | 1997-09-04 |
| DE69030489T3 true DE69030489T3 (de) | 2006-03-16 |
Family
ID=18341422
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69030489T Expired - Lifetime DE69030489T3 (de) | 1989-12-29 | 1990-12-28 | Fester Katalysatorbestandteil für Olefinpolymerisation und Olefinpolymerisationsverfahren unter Anwendung derselben |
| DE199090125706T Pending DE435332T1 (de) | 1989-12-29 | 1990-12-28 | Fester katalysatorbestandteil fuer olefinpolymerisation und olefinpolymerisationsverfahren unter anwendung derselben. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE199090125706T Pending DE435332T1 (de) | 1989-12-29 | 1990-12-28 | Fester katalysatorbestandteil fuer olefinpolymerisation und olefinpolymerisationsverfahren unter anwendung derselben. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5153158A (en:Method) |
| EP (1) | EP0435332B2 (en:Method) |
| JP (1) | JP2940684B2 (en:Method) |
| KR (1) | KR940010963B1 (en:Method) |
| CN (2) | CN1038685C (en:Method) |
| AT (1) | ATE151782T1 (en:Method) |
| CA (1) | CA2033404C (en:Method) |
| CZ (1) | CZ283582B6 (en:Method) |
| DE (2) | DE69030489T3 (en:Method) |
| DK (1) | DK0435332T3 (en:Method) |
| ES (1) | ES2031800T3 (en:Method) |
| GR (2) | GR920300075T1 (en:Method) |
| MY (1) | MY105326A (en:Method) |
| PL (3) | PL167913B1 (en:Method) |
| RU (1) | RU2092495C1 (en:Method) |
| TW (1) | TW201763B (en:Method) |
Families Citing this family (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU648534B2 (en) * | 1989-12-28 | 1994-04-28 | Idemitsu Petrochemical Co., Ltd. | Carrier for olefin polymerization catalyst and process for producing olefins |
| IT1246614B (it) | 1991-06-03 | 1994-11-24 | Himont Inc | Procedimento per la polimerizzazione in fase gas delle olefine |
| US5470812A (en) * | 1991-11-06 | 1995-11-28 | Mobil Oil Corporation | High activity polyethylene catalysts prepared with alkoxysilane reagents |
| US5939348A (en) * | 1991-11-06 | 1999-08-17 | Mobil Oil Corporation | Catalyst for the manufacture of polythylene with a narrow molecular weight distribution |
| US6291384B1 (en) | 1991-11-06 | 2001-09-18 | Mobil Oil Corporation | High activity catalyst prepared with alkoxysilanes |
| FR2689133A1 (fr) * | 1992-03-27 | 1993-10-01 | Atochem Elf Sa | Catalyseur de polymérisation des oléfines, son procédé d'obtention. |
| US5308818A (en) * | 1992-06-08 | 1994-05-03 | Fina Technology, Inc. | Catalyst system for the polymerization of olefins |
| JP3156213B2 (ja) * | 1993-02-23 | 2001-04-16 | 日石三菱株式会社 | ポリオレフィンの製造方法 |
| US5376743A (en) * | 1993-03-11 | 1994-12-27 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the production of sticky polymers |
| US5518973A (en) * | 1993-10-15 | 1996-05-21 | Exxon Chemical Patents Inc. | Titanium trichloride catalyst system for polymerizing olefins |
| ES2126870T3 (es) * | 1993-11-18 | 1999-04-01 | Mobil Oil Corp | Una composicion catalitica para la copolimerizacion de etileno. |
| US6034189A (en) * | 1994-05-19 | 2000-03-07 | Mitsui Petrochemical Industries, Ltd. | Solid titanium catalyst component for olefin polymerization, process for preparation of the same, olefin polymerization catalyst and process for olefin polymerization |
| TW412546B (en) * | 1994-05-19 | 2000-11-21 | Mitsui Petrochemical Ind | Solid titanium catalyst component for olefin polymerization, process for preparation of the same, olefin polymerization catalyst and process for olefin polymerization |
| IT1275867B1 (it) * | 1995-03-07 | 1997-10-24 | Enichem Elastomers | Procedimento per l'ottenimento di copolimeri elastomerici etilene- propilene ad alta purezza e distribuzione dei pesi molecolari |
| US5849655A (en) * | 1996-12-20 | 1998-12-15 | Fina Technology, Inc. | Polyolefin catalyst for polymerization of propylene and a method of making and using thereof |
| US5948720A (en) * | 1997-01-07 | 1999-09-07 | Huntsman Polymers Corporation | Catalyst for the production of flexible polyolefin compositions, methods for making and using same, and products thereof |
| US6100351A (en) * | 1997-01-07 | 2000-08-08 | Huntsman Polymers Corporation | Olefin polymerization process and products thereof |
| US6864207B2 (en) * | 1997-01-28 | 2005-03-08 | Fina Technology, Inc. | Ziegler-Natta catalyst for polyolefins |
| US6930071B2 (en) * | 1997-01-28 | 2005-08-16 | Fina Technology, Inc. | Ziegler-natta catalyst for polyolefins |
| US6080818A (en) * | 1997-03-24 | 2000-06-27 | Huntsman Polymers Corporation | Polyolefin blends used for non-woven applications |
| ES2364330T3 (es) * | 1998-03-23 | 2011-08-31 | Basell Poliolefine Italia S.R.L. | Componentes catalíticos prepolimerizados para la polimerización de olefinas. |
| EP1094083A3 (en) * | 1999-10-19 | 2001-12-12 | Idemitsu Petrochemical Co., Ltd. | Catalyst for olefin polymerization, method for producing olefin polymer, and olefin polymer |
| US6358372B1 (en) | 2000-07-11 | 2002-03-19 | Union Carbide Chemicals & Plastics Technology Corporation | Method of reducing formation of precipitates in solvent recovery system |
| US20030087755A1 (en) | 2001-05-29 | 2003-05-08 | Linfeng Chen | Olefin polymerization catalyst compositions and method of preparation |
| US6825146B2 (en) * | 2001-05-29 | 2004-11-30 | Union Carbide Chemicals & Plastics Technology Corporation | Olefin polymerization catalyst compositions and method of preparation |
| MY136330A (en) * | 2001-12-12 | 2008-09-30 | Basell Poliolefine Spa | Process for the polymerization of olefins |
| KR100530795B1 (ko) * | 2001-12-26 | 2005-11-23 | 삼성토탈 주식회사 | 에틸렌 중합 및 공중합 방법 |
| CN1169845C (zh) * | 2002-02-07 | 2004-10-06 | 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和含该催化剂组分的催化剂及其应用 |
| US7141635B2 (en) * | 2002-06-14 | 2006-11-28 | Union Carbide Chemicals And Plastics Tech | Catalyst composition and polymerization process using mixtures of selectivity control agents |
| US7276463B2 (en) * | 2002-09-11 | 2007-10-02 | Japan Polypropylene Corporation | Polymerization catalyst for α-olefins and process for production of α-olefin polymers therewith |
| CN1788024A (zh) * | 2003-05-12 | 2006-06-14 | 联合碳化化学及塑料技术公司 | 控制气相聚合反应中聚合物粉末的方法 |
| JP5073291B2 (ja) * | 2003-05-29 | 2012-11-14 | 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 | 触媒成分の製造方法およびそれから得られる成分 |
| DE602004024994D1 (de) * | 2003-06-24 | 2010-02-25 | Union Carbide Chem Plastic | Katalysatorzusammensetzung und Polymerisationsverfahren mit einer Mischung von Silane Elektrondonoren |
| CN1845940A (zh) * | 2003-08-29 | 2006-10-11 | 陶氏环球技术公司 | 用于制造部分干燥的易分散的烯烃聚合前催化剂的方法 |
| US20060223956A1 (en) * | 2003-09-23 | 2006-10-05 | Linfeng Chen | Catalyst composition with mixed sca and propylene polymerization process |
| WO2005030815A1 (en) | 2003-09-23 | 2005-04-07 | Dow Global Technologies Inc. | Self limiting catalyst composition and propylene polymerization process |
| KR101146472B1 (ko) * | 2003-09-23 | 2012-05-21 | 유니온 카바이드 케미칼즈 앤드 플라스틱스 테크날러지 엘엘씨 | 모노카르복실산 에스테르 내부 공여체를 갖는 자가-소멸촉매 조성물 및 프로필렌 중합 방법 |
| EP2261268B1 (en) * | 2003-09-23 | 2020-04-29 | Dow Global Technologies LLC | Ethylene polymerization using ziegler-natta catalyst compositions |
| JP5248774B2 (ja) | 2003-09-23 | 2013-07-31 | ダウ グローバル テクノロジーズ エルエルシー | ジカルボン酸エステル内部供与体を有する自己制限性触媒組成物及びプロピレン重合方法 |
| US7135531B2 (en) * | 2004-01-28 | 2006-11-14 | Basf Catalysts Llc | Spherical catalyst for olefin polymerization |
| RU2006139061A (ru) * | 2004-04-07 | 2008-05-20 | Юнион Карбайд Кемикалз энд Пластикс Текнолоджи Корпорейшн (US) | Композиции прокатализаторов для полимеризации олефинов и способ получения |
| JP4846714B2 (ja) | 2004-06-16 | 2011-12-28 | ダウ グローバル テクノロジーズ エルエルシー | チーグラー・ナッタ共触媒の同定方法 |
| DE602005017627D1 (de) * | 2004-06-16 | 2009-12-24 | Dow Global Technologies Inc | Vorrichtung und verfahren für die ziegler-natta-forschung |
| CN1993391A (zh) * | 2004-08-09 | 2007-07-04 | 联合碳化化学及塑料技术公司 | 强喷雾干燥的齐格勒－纳塔前催化剂及使用其的聚合方法 |
| WO2006020623A1 (en) | 2004-08-09 | 2006-02-23 | Union Carbide Chemicals & Plastics Technology Corporation | Robust spray-dried ziegler-natta procatalyst and polymerization process employing same |
| KR100640275B1 (ko) * | 2004-10-14 | 2006-11-01 | 대한유화공업 주식회사 | 에틸렌 중합 및/또는 에틸렌 공중합용 고체 촉매의 제조방법 |
| US7776979B2 (en) * | 2007-01-26 | 2010-08-17 | Lg Chem, Ltd. | Prepolymerized catalyst for olefin polymerization, process for polymerizing olefin by using the catalyst and polyolefin produced by the process |
| US7817819B1 (en) * | 2007-04-03 | 2010-10-19 | Nanostellar, Inc. | Characterization of metal particle distributions in a supported catalyst |
| ATE509967T1 (de) * | 2007-06-14 | 2011-06-15 | Borealis Tech Oy | Verfahren zur herstellung von propylen- copolymeren mit hilfe eines vorpolymerisierten katalysators |
| US7981517B2 (en) * | 2007-08-28 | 2011-07-19 | Dow Global Technologies Inc. | Bituminous compositions and methods of making and using same |
| US8003741B2 (en) | 2008-02-07 | 2011-08-23 | Fina Technology, Inc. | Ziegler-Natta catalyst |
| US8003559B2 (en) * | 2008-05-13 | 2011-08-23 | Basf Corporation | Internal donor for olefin polymerization catalysts |
| US7638585B2 (en) | 2008-05-13 | 2009-12-29 | Basf Catalysts, Llc | Catalyst flow |
| US8003558B2 (en) * | 2008-07-29 | 2011-08-23 | Basf Corporation | Internal donor for olefin polymerization catalysts |
| WO2010021768A1 (en) * | 2008-08-19 | 2010-02-25 | Dow Global Technologies, Inc. | Classified catalyst composition, apparatus, and method |
| US10125200B2 (en) | 2008-09-26 | 2018-11-13 | Basell Poliolefine Italia S.R.L. | Catalyst components for the polymerization of olefins |
| RU2497834C2 (ru) * | 2008-11-25 | 2013-11-10 | Юнион Карбайд Кемикалз Энд Пластикс Текнолоджи Ллс | Композиция прокатализатора с многокомпонентным внутренним донором, содержащим сложный эфир, и способ |
| US8088872B2 (en) * | 2008-11-25 | 2012-01-03 | Dow Global Technologies Llc | Procatalyst composition including silyl ester internal donor and method |
| RU2553475C2 (ru) | 2008-12-31 | 2015-06-20 | У.Р.Грейс эед Ко.-Конн. | Получение замещенных фенилен ароматических сложных диэфиров |
| SG172447A1 (en) * | 2008-12-31 | 2011-08-29 | Dow Global Technologies Llc | Procatalyst composition with substituted 1,2-phenylene aromatic diester internal donor and method |
| CN101864008B (zh) * | 2009-04-17 | 2011-11-02 | 中国石油化工股份有限公司 | 一种用于烯烃聚合反应的催化剂 |
| US8247341B2 (en) * | 2009-04-17 | 2012-08-21 | Dow Global Technologies Llc | Procatalyst composition with silyl glutarate and method |
| BRPI1006623A2 (pt) * | 2009-04-23 | 2016-04-19 | Dow Global Technologies Llc | composição de catalisador e processo para produzir um polímero a case de olefina |
| EA021841B1 (ru) | 2009-11-10 | 2015-09-30 | Тотал Ресерч Энд Текнолоджи Фелюи | Бимодальный полиэтилен для использований в литье под давлением с раздувом и вытяжкой |
| CN102712704B (zh) * | 2009-12-02 | 2015-01-07 | 陶氏环球技术有限责任公司 | 作为用于聚丙烯制造的催化剂中的内部给体的三个和四个原子桥接的二碳酸酯化合物 |
| WO2011068770A1 (en) | 2009-12-02 | 2011-06-09 | Dow Global Technologies Inc. | Two atom bridged dicarbonate compounds as internal donors in catalysts for polypropylene manufacture |
| FI2531533T4 (fi) | 2010-02-05 | 2025-06-10 | Totalenergies Onetech Belgium | Menetelmä polyolefiinien valmistamiseksi |
| KR101906621B1 (ko) | 2010-12-21 | 2018-10-10 | 더블유.알. 그레이스 앤드 캄파니-콘. | 고 용융 유동 프로필렌-기재 중합체의 생산 공정 및 이로부터의 생산물 |
| EP2681274B1 (en) | 2011-03-04 | 2017-10-04 | Total Research & Technology Feluy | Process for preparing polyolefin blends in a device for continuously physically melting and blending the blends |
| WO2012119953A1 (en) | 2011-03-04 | 2012-09-13 | Total Research & Technology Feluy | Process for preparing ziegler-natta produced polyethylene blends |
| CN103958593A (zh) | 2011-09-30 | 2014-07-30 | 道达尔研究技术弗吕公司 | 用于帽和封闭件的高密度聚乙烯 |
| EP2607387A1 (en) | 2011-12-23 | 2013-06-26 | Basell Poliolefine Italia S.r.l. | Pre-polymerized catalyst components for the polymerization of olefins |
| EP2607386A1 (en) * | 2011-12-23 | 2013-06-26 | Basell Poliolefine Italia S.r.l. | Pre-polymerized catalyst components for the polymerization of olefins |
| EA032252B1 (ru) | 2013-08-12 | 2019-04-30 | Тотал Ресерч & Технолоджи Фелай | Изделие, полученное из полиэтилена посредством литья под давлением с раздувом и ориентированием |
| HRP20170727T1 (hr) | 2014-07-10 | 2017-09-22 | Total Research & Technology Feluy | Postupak izrade polietilena visoke gustoće, otpornog na puknuća zbog visokih okolišnih pritisaka, od otpada koji stvaraju potrošači (post consumer resin, pcr) i predmeta izrađenih od spomenutog sastava |
| EP3507312A4 (en) | 2016-08-30 | 2020-06-03 | W.R. Grace & Co.-Conn. | LOW ASH POLYOLEFINS AND PROCESS FOR PRODUCING THE SAME |
| CN109206547B (zh) * | 2017-07-03 | 2021-02-05 | 中国石化扬子石油化工有限公司 | 一种Ziegler－Natta型的丙烯聚合催化剂的外给电子体及包含它的催化剂 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5634709A (en) † | 1979-08-31 | 1981-04-07 | Mitsui Petrochem Ind Ltd | Gas phase polymerization or copolymerization of olefin |
| JPS6042806B2 (ja) * | 1979-12-26 | 1985-09-25 | 日石三菱株式会社 | 共重合体の製造方法 |
| JPS56133303A (en) * | 1980-03-22 | 1981-10-19 | Chisso Corp | Production of alpha-olefin polymer |
| US4325837A (en) * | 1980-08-12 | 1982-04-20 | Phillips Petroleum Company | Catalyst, method of producing the catalyst, and polymerization process employing the catalyst |
| US4410671A (en) * | 1980-08-12 | 1983-10-18 | Phillips Petroleum Company | Catalyst, method of producing the catalyst, and polymerization process employing the catalyst |
| US4326988A (en) * | 1980-08-12 | 1982-04-27 | Phillips Petroleum Company | Catalyst, method of producing the catalyst, and polymerization process employing the catalyst |
| JPS5898315A (ja) * | 1981-12-07 | 1983-06-11 | Chisso Corp | ポリオレフイン共重合体の粉体流動性改良法 |
| DE3366573D1 (en) * | 1982-06-24 | 1986-11-06 | Bp Chimie Sa | Process for the polymerization and copolymerization of alpha-olefins in a fluidized bed |
| FR2541683B1 (fr) * | 1983-02-28 | 1986-05-09 | Ato Chimie | Procede pour la preparation d'un solide hydrocarbone actif utilisable pour polymeriser des olefines, et procede de synthese d'un polymere ou copolymere olefinique faisant appel audit solide hydrocarbone actif comme systeme |
| CA1284549C (en) † | 1986-09-26 | 1991-05-28 | Fathi David Hussein | Process for the polymerization of propylene |
| EP0588277B1 (en) † | 1987-02-02 | 2001-05-16 | Fina Technology, Inc. | Process for increasing the efficiency of a pre-polymerized catalyst |
| FR2629461B1 (fr) * | 1988-03-31 | 1993-05-07 | Bp Chimie Sa | Catalyseur de (co)polymerisation du propylene, supporte sur des particules spheriques de chlorure de magnesium et enrobe par du polypropylene, et procedes de preparation |
| FR2651234B1 (fr) * | 1989-08-29 | 1993-03-12 | Bp Chem Int Ltd | Procede de fabrication en phase gazeuse de copolymeres du propylene a l'aide d'un systeme catalytique de haute activite. |
-
1989
- 1989-12-29 JP JP1340909A patent/JP2940684B2/ja not_active Expired - Lifetime
-
1990
- 1990-12-27 MY MYPI90002271A patent/MY105326A/en unknown
- 1990-12-27 TW TW079110903A patent/TW201763B/zh active
- 1990-12-27 US US07/634,737 patent/US5153158A/en not_active Expired - Lifetime
- 1990-12-28 DE DE69030489T patent/DE69030489T3/de not_active Expired - Lifetime
- 1990-12-28 AT AT90125706T patent/ATE151782T1/de not_active IP Right Cessation
- 1990-12-28 PL PL90300679A patent/PL167913B1/pl unknown
- 1990-12-28 PL PL90288512A patent/PL167899B1/pl unknown
- 1990-12-28 EP EP90125706A patent/EP0435332B2/en not_active Expired - Lifetime
- 1990-12-28 RU SU904894186A patent/RU2092495C1/ru not_active IP Right Cessation
- 1990-12-28 PL PL90300678A patent/PL167905B1/pl unknown
- 1990-12-28 CA CA002033404A patent/CA2033404C/en not_active Expired - Fee Related
- 1990-12-28 ES ES90125706T patent/ES2031800T3/es not_active Expired - Lifetime
- 1990-12-28 DK DK90125706.3T patent/DK0435332T3/da active
- 1990-12-28 DE DE199090125706T patent/DE435332T1/de active Pending
- 1990-12-29 CZ CS906942A patent/CZ283582B6/cs not_active IP Right Cessation
- 1990-12-29 CN CN90110256A patent/CN1038685C/zh not_active Expired - Lifetime
- 1990-12-29 KR KR1019900022415A patent/KR940010963B1/ko not_active Expired - Fee Related
-
1992
- 1992-10-08 GR GR92300075T patent/GR920300075T1/el unknown
-
1997
- 1997-05-02 GR GR970400965T patent/GR3023309T3/el unknown
- 1997-07-04 CN CN97113747A patent/CN1174204A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP0435332B1 (en) | 1997-04-16 |
| JPH03203908A (ja) | 1991-09-05 |
| CZ283582B6 (cs) | 1998-05-13 |
| PL167899B1 (pl) | 1995-12-30 |
| TW201763B (en:Method) | 1993-03-11 |
| GR920300075T1 (en) | 1992-10-08 |
| CA2033404A1 (en) | 1991-06-30 |
| EP0435332A3 (en) | 1992-02-26 |
| RU2092495C1 (ru) | 1997-10-10 |
| KR940010963B1 (ko) | 1994-11-21 |
| PL167905B1 (pl) | 1995-12-30 |
| ES2031800T3 (es) | 1997-09-16 |
| ATE151782T1 (de) | 1997-05-15 |
| JP2940684B2 (ja) | 1999-08-25 |
| CN1052870A (zh) | 1991-07-10 |
| DE435332T1 (de) | 1992-09-03 |
| PL167913B1 (pl) | 1995-12-30 |
| EP0435332B2 (en) | 2005-08-10 |
| KR910011920A (ko) | 1991-08-07 |
| DE69030489D1 (de) | 1997-05-22 |
| DK0435332T3 (da) | 1997-05-12 |
| DE69030489T2 (de) | 1997-09-04 |
| CZ694290A3 (en) | 1996-07-17 |
| CA2033404C (en) | 1995-09-05 |
| ES2031800T1 (es) | 1993-01-01 |
| EP0435332A2 (en) | 1991-07-03 |
| US5153158A (en) | 1992-10-06 |
| CN1038685C (zh) | 1998-06-10 |
| GR3023309T3 (en) | 1997-08-29 |
| MY105326A (en) | 1994-09-30 |
| PL288512A1 (en) | 1991-09-09 |
| CN1174204A (zh) | 1998-02-25 |
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