SI8711789A8 - Method of titanium three-chlorides containing catalyt's solid component production for application during alpha-olefines polymerisation. - Google Patents
Method of titanium three-chlorides containing catalyt's solid component production for application during alpha-olefines polymerisation. Download PDFInfo
- Publication number
- SI8711789A8 SI8711789A8 SI8711789A SI8711789A SI8711789A8 SI 8711789 A8 SI8711789 A8 SI 8711789A8 SI 8711789 A SI8711789 A SI 8711789A SI 8711789 A SI8711789 A SI 8711789A SI 8711789 A8 SI8711789 A8 SI 8711789A8
- Authority
- SI
- Slovenia
- Prior art keywords
- solid
- compound
- polymerization
- tert
- butyl
- Prior art date
Links
- 239000007787 solid Substances 0.000 title claims abstract description 96
- 238000000034 method Methods 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title description 4
- 239000010936 titanium Substances 0.000 title description 4
- 229910052719 titanium Inorganic materials 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 74
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 claims abstract description 24
- 239000004711 α-olefin Substances 0.000 claims abstract description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 54
- -1 di-tert-alkylated monocyclic phenols Chemical class 0.000 claims description 46
- 239000003054 catalyst Substances 0.000 claims description 34
- 239000002243 precursor Substances 0.000 claims description 29
- 239000011949 solid catalyst Substances 0.000 claims description 28
- 239000003085 diluting agent Substances 0.000 claims description 20
- 229930195733 hydrocarbon Natural products 0.000 claims description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims description 18
- 150000002430 hydrocarbons Chemical class 0.000 claims description 15
- 230000008569 process Effects 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 12
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
- 150000002367 halogens Chemical group 0.000 claims description 5
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
- 230000007420 reactivation Effects 0.000 claims description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 3
- 239000012190 activator Substances 0.000 claims description 3
- 125000005234 alkyl aluminium group Chemical group 0.000 claims description 3
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 27
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract description 27
- 230000003197 catalytic effect Effects 0.000 abstract description 16
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 150000002899 organoaluminium compounds Chemical class 0.000 abstract 1
- 125000002370 organoaluminium group Chemical group 0.000 abstract 1
- 230000000707 stereoselective effect Effects 0.000 abstract 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 76
- 229920001155 polypropylene Polymers 0.000 description 28
- 239000004743 Polypropylene Substances 0.000 description 27
- 239000000725 suspension Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 17
- 239000007788 liquid Substances 0.000 description 15
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 13
- 239000008139 complexing agent Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 238000011282 treatment Methods 0.000 description 11
- 239000012071 phase Substances 0.000 description 10
- 239000002245 particle Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 239000003638 chemical reducing agent Substances 0.000 description 7
- 150000001993 dienes Chemical class 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical class Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 229910010068 TiCl2 Inorganic materials 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 150000002902 organometallic compounds Chemical class 0.000 description 4
- 238000007669 thermal treatment Methods 0.000 description 4
- ZWYDDDAMNQQZHD-UHFFFAOYSA-L titanium(ii) chloride Chemical compound [Cl-].[Cl-].[Ti+2] ZWYDDDAMNQQZHD-UHFFFAOYSA-L 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000000536 complexating effect Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000007872 degassing Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 239000011859 microparticle Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 229960003742 phenol Drugs 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 2
- ZDWSNKPLZUXBPE-UHFFFAOYSA-N 3,5-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1 ZDWSNKPLZUXBPE-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- AQZGPSLYZOOYQP-UHFFFAOYSA-N Diisoamyl ether Chemical compound CC(C)CCOCCC(C)C AQZGPSLYZOOYQP-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- GCPCLEKQVMKXJM-UHFFFAOYSA-N ethoxy(diethyl)alumane Chemical compound CCO[Al](CC)CC GCPCLEKQVMKXJM-UHFFFAOYSA-N 0.000 description 2
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 2
- 238000012685 gas phase polymerization Methods 0.000 description 2
- 150000002366 halogen compounds Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000012721 stereospecific polymerization Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
- RRGYARNMKLQUFF-UHFFFAOYSA-N 1,3-bis(3-methylbutyl)naphthalen-2-ol Chemical compound C1=CC=C2C(CCC(C)C)=C(O)C(CCC(C)C)=CC2=C1 RRGYARNMKLQUFF-UHFFFAOYSA-N 0.000 description 1
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- YRZOMIQAOVISEV-UHFFFAOYSA-N 1,3-ditert-butylanthracen-2-ol Chemical compound C1=CC=C2C=C(C(=C(C(C(C)(C)C)=C3)O)C(C)(C)C)C3=CC2=C1 YRZOMIQAOVISEV-UHFFFAOYSA-N 0.000 description 1
- MUVQKFGNPGZBII-UHFFFAOYSA-N 1-anthrol Chemical compound C1=CC=C2C=C3C(O)=CC=CC3=CC2=C1 MUVQKFGNPGZBII-UHFFFAOYSA-N 0.000 description 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- GTBXZWADMKOZQJ-UHFFFAOYSA-N 1-phenanthrol Chemical compound C1=CC2=CC=CC=C2C2=C1C(O)=CC=C2 GTBXZWADMKOZQJ-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- UCFIZNITZIGADY-UHFFFAOYSA-N 2,6-ditert-butyl-4-[[3-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]phenyl]methyl]phenol Chemical compound C(C)(C)(C)C=1C=C(CC2=CC=CC(=C2)CC2=CC(=C(C(=C2)C(C)(C)C)O)C(C)(C)C)C=C(C1O)C(C)(C)C UCFIZNITZIGADY-UHFFFAOYSA-N 0.000 description 1
- JAJCQYUAORSGHI-UHFFFAOYSA-N 2,8-ditert-butylnaphthalen-1-ol Chemical compound C1=CC=C(C(C)(C)C)C2=C(O)C(C(C)(C)C)=CC=C21 JAJCQYUAORSGHI-UHFFFAOYSA-N 0.000 description 1
- NMVXHZSPDTXJSJ-UHFFFAOYSA-L 2-methylpropylaluminum(2+);dichloride Chemical class CC(C)C[Al](Cl)Cl NMVXHZSPDTXJSJ-UHFFFAOYSA-L 0.000 description 1
- LZHCVNIARUXHAL-UHFFFAOYSA-N 2-tert-butyl-4-ethylphenol Chemical compound CCC1=CC=C(O)C(C(C)(C)C)=C1 LZHCVNIARUXHAL-UHFFFAOYSA-N 0.000 description 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 1
- YVXZDHMHPCFGGQ-UHFFFAOYSA-N 3-[2,3-bis[3-hydroxy-2,6-bis(2-methylpentan-2-yl)phenyl]phenyl]-2,4-bis(2-methylpentan-2-yl)phenol Chemical compound CCCC(C)(C)C1=CC=C(O)C(C(C)(C)CCC)=C1C1=CC=CC(C=2C(=C(O)C=CC=2C(C)(C)CCC)C(C)(C)CCC)=C1C1=C(C(C)(C)CCC)C=CC(O)=C1C(C)(C)CCC YVXZDHMHPCFGGQ-UHFFFAOYSA-N 0.000 description 1
- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-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
- BFZOTKYPSZSDEV-UHFFFAOYSA-N 4-butan-2-yl-2,6-ditert-butylphenol Chemical compound CCC(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BFZOTKYPSZSDEV-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- 241001103870 Adia Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- ONJXMLOOLFUVAT-UHFFFAOYSA-N C(=CC(C)=C)[AlH2] Chemical compound C(=CC(C)=C)[AlH2] ONJXMLOOLFUVAT-UHFFFAOYSA-N 0.000 description 1
- MXRPRLNAHDRHLQ-UHFFFAOYSA-N CCCC(C)(C)C1C2=C(C=CC1(C(C)(C)CCC)O)C3=CC=CC=C3C=C2 Chemical compound CCCC(C)(C)C1C2=C(C=CC1(C(C)(C)CCC)O)C3=CC=CC=C3C=C2 MXRPRLNAHDRHLQ-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 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
- 125000004104 aryloxy group Chemical group 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- KMGBZBJJOKUPIA-UHFFFAOYSA-N butyl iodide Chemical compound CCCCI KMGBZBJJOKUPIA-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- VJRUISVXILMZSL-UHFFFAOYSA-M dibutylalumanylium;chloride Chemical class CCCC[Al](Cl)CCCC VJRUISVXILMZSL-UHFFFAOYSA-M 0.000 description 1
- UZVQWTNJZQZICK-UHFFFAOYSA-L dichloro(2-methylpropoxy)alumane Chemical class [Cl-].[Cl-].CC(C)CO[Al+2] UZVQWTNJZQZICK-UHFFFAOYSA-L 0.000 description 1
- DLRHRQTUCJTIIV-UHFFFAOYSA-N diethoxy(ethyl)alumane Chemical compound CC[O-].CC[O-].CC[Al+2] DLRHRQTUCJTIIV-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 125000002734 organomagnesium group Chemical group 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 229920006301 statistical copolymer Polymers 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- GBECUEIQVRDUKB-UHFFFAOYSA-M thallium monochloride Chemical compound [Tl]Cl GBECUEIQVRDUKB-UHFFFAOYSA-M 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000005406 washing Methods 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
- C08F4/16—Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen of silicon, germanium, tin, lead, titanium, zirconium or hafnium
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/901—Monomer polymerized in vapor state in presence of transition metal containing catalyst
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8613649A FR2604439B1 (fr) | 1986-09-26 | 1986-09-26 | Solide catalytique utilisable pour la polymerisation stereospecifique des alpha-olefines, procede pour le preparer et procede pour polymeriser des alpha-olefines en sa presence |
| YU178987A YU46229B (sh) | 1986-09-26 | 1987-09-28 | Postupak za dobijanje čvrstog katalizatora na bazi kompleksa titan-trihlorida za polimerizaciju alfa olefina specifičnog karaktera |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI8711789A8 true SI8711789A8 (en) | 1996-08-31 |
Family
ID=9339422
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI8711789A SI8711789A8 (en) | 1986-09-26 | 1987-09-28 | Method of titanium three-chlorides containing catalyt's solid component production for application during alpha-olefines polymerisation. |
| SI8811759A SI8811759A8 (en) | 1986-09-26 | 1988-09-19 | Process for polymerization of alpha-olefines |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI8811759A SI8811759A8 (en) | 1986-09-26 | 1988-09-19 | Process for polymerization of alpha-olefines |
Country Status (33)
| Country | Link |
|---|---|
| EP (1) | EP0261727B1 (en)) |
| JP (1) | JP2625126B2 (en)) |
| KR (1) | KR940010961B1 (en)) |
| CN (1) | CN1010781B (en)) |
| AR (1) | AR246277A1 (en)) |
| AT (1) | ATE82986T1 (en)) |
| AU (1) | AU601769B2 (en)) |
| BG (1) | BG60622B1 (en)) |
| BR (1) | BR8704955A (en)) |
| CA (1) | CA1327965C (en)) |
| CZ (2) | CZ509890A3 (en)) |
| DE (1) | DE3782903T2 (en)) |
| DK (1) | DK505187A (en)) |
| ES (1) | ES2052548T3 (en)) |
| FI (1) | FI92834C (en)) |
| FR (1) | FR2604439B1 (en)) |
| GR (1) | GR3006472T3 (en)) |
| HK (1) | HK48893A (en)) |
| HR (2) | HRP920976A2 (en)) |
| HU (1) | HU202562B (en)) |
| IE (1) | IE63110B1 (en)) |
| IN (1) | IN172196B (en)) |
| NO (1) | NO171070C (en)) |
| PH (1) | PH27151A (en)) |
| PL (2) | PL152012B1 (en)) |
| PT (1) | PT85751B (en)) |
| RO (1) | RO103447B1 (en)) |
| SI (2) | SI8711789A8 (en)) |
| SK (2) | SK279077B6 (en)) |
| SU (1) | SU1674687A3 (en)) |
| TR (1) | TR25127A (en)) |
| YU (2) | YU46229B (en)) |
| ZA (1) | ZA876968B (en)) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2628430B1 (fr) * | 1988-03-09 | 1992-04-17 | Solvay | Procede pour la polymerisation stereospecifique des alpha-olefines et systeme catalytique utilisable pour cette polymerisation |
| US5780379A (en) * | 1987-09-25 | 1998-07-14 | Solvay Polyolefins Europe-Belgium (Societe Anonyme) | Process for the stereospecific polymerization of alpha-olefins and catalyst system which can be employed for this polymerization |
| FR2647454B1 (fr) * | 1989-05-29 | 1993-01-22 | Solvay | Suspensions de particules contenant des composes de metaux de transition dans des huiles et procedes de polymerisation d'alpha-olefines effectues en presence de ces suspensions |
| BE1004563A3 (fr) * | 1990-08-30 | 1992-12-15 | Solvay | Composition cocatalytique utilisable pour la polymerisation des alpha-olefines. |
| BE1003968A3 (fr) * | 1990-11-08 | 1992-07-28 | Solvay | Solide catalytique utilisable pour la polymerisation stereospecifique des alpha-olefines, procede pour le preparer et procede pour polymeriser des alpha-olefines en sa presence |
| BE1006840A5 (fr) * | 1992-05-04 | 1995-01-03 | Solvay | Systeme catalytique pour la polymerisation d'olefines; procede pour cette polymerisation et polymeres ainsi obtenus. |
| BE1005792A3 (fr) * | 1992-05-04 | 1994-02-01 | Solvay | Systeme catalytique utilisable pour la polymerisation stereospecifique des alpha-olefines, procede pour cette polymerisation et polymeres obtenus. |
| US5449732A (en) * | 1993-06-18 | 1995-09-12 | Conoco Inc. | Solvent free oil soluble drag reducing polymer suspension |
| BE1007698A3 (fr) * | 1993-11-04 | 1995-10-03 | Solvay | Systeme catalytique utilisable pour la polymerisation des alpha-olefines et procede pour cette polymerisation. |
| BE1009962A3 (fr) * | 1995-12-21 | 1997-11-04 | Solvay | Compositions a base de polymeres du propylene et leur utilisation. |
| GB2322376B (en) * | 1997-02-25 | 2000-11-29 | Solvay | Polypropylene block copolymers and containers made therefrom |
| US6586528B1 (en) | 2000-11-15 | 2003-07-01 | Polypropylene Belgium (Naamlose Vennootshap) | Composition based on propylene polymers and process for obtaining same |
| US6642317B1 (en) | 2000-11-15 | 2003-11-04 | Polypropylene Belgium Naamlose Vennootschap | Composition based on propylene polymers and process for obtaining same |
| KR100522205B1 (ko) * | 2004-03-30 | 2005-10-18 | 삼성탈레스 주식회사 | 선박에 장착되는 조준 장치의 시차 보정 방법 |
| JP4969070B2 (ja) * | 2005-03-11 | 2012-07-04 | 株式会社Ａｄｅｋａ | 安定化されたポリマーの製造方法 |
| JP5501962B2 (ja) | 2008-06-05 | 2014-05-28 | 株式会社Ａｄｅｋａ | アルミニウムフェノキシド化合物を用いた安定化ポリマーの製造方法。 |
| CN102695728B (zh) | 2009-11-06 | 2014-05-07 | 日本聚丙烯株式会社 | 丙烯聚合用反应器和丙烯聚合物的生产方法 |
| BR122019017983B1 (pt) | 2010-11-16 | 2021-01-12 | Adeka Corporation | método de produção de um tecido falso a partir de pelo menos uma olefina |
| KR101966269B1 (ko) | 2011-03-02 | 2019-04-05 | 가부시키가이샤 아데카 | 라미네이트 필름 및 도장 부재용 수지 조성물의 제조 방법 |
| EP2578606B2 (en) | 2011-10-04 | 2019-08-28 | Borealis AG | Process for the production of polyolefins wherein an antioxidant is fed to the reaction mixture during the process |
| JP2013199551A (ja) | 2012-03-23 | 2013-10-03 | Adeka Corp | 家電材料用及び自動車内装材料用オレフィン樹脂組成物の製造方法 |
| CN105026485A (zh) | 2012-12-07 | 2015-11-04 | 日本聚丙烯株式会社 | 纤维补强的聚丙烯类树脂组合物和其成形体 |
| BR112016008951B1 (pt) | 2013-10-21 | 2021-11-03 | Adeka Corporation | Método para produção de polímero estabilizado |
| CN113571768B (zh) * | 2021-09-23 | 2022-02-18 | 浙江金羽新能源科技有限公司 | 改性铝基化聚合物及制备方法、耐高压固态聚合物电解质膜及制备方法、金属锂二次电池 |
| EP4421101A1 (en) * | 2023-02-22 | 2024-08-28 | Sumitomo Chemical Company, Limited | Method for producing heterophasic propylene polymerization material and method for producing olefin polymer |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU65954A1 (en)) * | 1972-08-25 | 1974-03-07 | ||
| CA1152056A (en) * | 1979-06-11 | 1983-08-16 | Brian L. Goodall | Process for the stereospecific polymerization of an alpha-olefin and an alpha-olefin polymerization catalyst system |
| US4529780A (en) * | 1981-11-19 | 1985-07-16 | Northern Petrochemical Company | Process for polymerizing alpha olefins with phenolic compound containing catalysts |
| US4463102A (en) * | 1981-11-19 | 1984-07-31 | Northern Petrochemical Company | Polyolefin polymerization catalyst containing sterically unhindered phenolic compounds (II) |
| EP0107871B1 (en) * | 1982-10-27 | 1986-10-15 | Shell Internationale Researchmaatschappij B.V. | Process for the preparation of polyisoprene |
-
1986
- 1986-09-26 FR FR8613649A patent/FR2604439B1/fr not_active Expired
-
1987
- 1987-09-15 ES ES87201762T patent/ES2052548T3/es not_active Expired - Lifetime
- 1987-09-15 DE DE8787201762T patent/DE3782903T2/de not_active Expired - Fee Related
- 1987-09-15 AT AT87201762T patent/ATE82986T1/de not_active IP Right Cessation
- 1987-09-15 EP EP87201762A patent/EP0261727B1/fr not_active Expired - Lifetime
- 1987-09-16 ZA ZA876968A patent/ZA876968B/xx unknown
- 1987-09-18 PT PT85751A patent/PT85751B/pt not_active IP Right Cessation
- 1987-09-18 IN IN826/DEL/87A patent/IN172196B/en unknown
- 1987-09-21 PH PH35835A patent/PH27151A/en unknown
- 1987-09-21 CA CA000547421A patent/CA1327965C/fr not_active Expired - Fee Related
- 1987-09-24 CZ CS905098A patent/CZ509890A3/cs not_active IP Right Cessation
- 1987-09-24 SK SK5098-90A patent/SK279077B6/sk unknown
- 1987-09-24 CZ CS876865A patent/CZ280899B6/cs not_active IP Right Cessation
- 1987-09-24 SK SK6865-87A patent/SK278631B6/sk unknown
- 1987-09-25 SU SU874203442A patent/SU1674687A3/ru active
- 1987-09-25 HU HU874313A patent/HU202562B/hu not_active IP Right Cessation
- 1987-09-25 KR KR1019870010661A patent/KR940010961B1/ko not_active Expired - Fee Related
- 1987-09-25 DK DK505187A patent/DK505187A/da not_active Application Discontinuation
- 1987-09-25 BR BR8704955A patent/BR8704955A/pt not_active IP Right Cessation
- 1987-09-25 JP JP62240560A patent/JP2625126B2/ja not_active Expired - Lifetime
- 1987-09-25 PL PL1987267910A patent/PL152012B1/pl unknown
- 1987-09-25 TR TR87/0660A patent/TR25127A/xx unknown
- 1987-09-25 NO NO874037A patent/NO171070C/no unknown
- 1987-09-25 AU AU78955/87A patent/AU601769B2/en not_active Ceased
- 1987-09-25 IE IE258187A patent/IE63110B1/en not_active IP Right Cessation
- 1987-09-25 PL PL1987282656A patent/PL152519B1/pl unknown
- 1987-09-25 FI FI874210A patent/FI92834C/fi not_active IP Right Cessation
- 1987-09-25 AR AR87308842A patent/AR246277A1/es active
- 1987-09-25 BG BG81279A patent/BG60622B1/bg unknown
- 1987-09-26 CN CN87104353A patent/CN1010781B/zh not_active Expired
- 1987-09-28 YU YU178987A patent/YU46229B/sh unknown
- 1987-09-28 SI SI8711789A patent/SI8711789A8/sl unknown
- 1987-11-26 RO RO139230A patent/RO103447B1/ro unknown
-
1988
- 1988-09-19 YU YU175988A patent/YU46678B/sh unknown
- 1988-09-19 SI SI8811759A patent/SI8811759A8/sl unknown
-
1992
- 1992-10-02 HR HRP920976AA patent/HRP920976A2/hr not_active Application Discontinuation
- 1992-10-02 HR HR920970A patent/HRP920970A2/hr not_active Application Discontinuation
- 1992-12-08 GR GR920402832T patent/GR3006472T3/el unknown
-
1993
- 1993-05-20 HK HK488/93A patent/HK48893A/xx not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SI8711789A8 (en) | Method of titanium three-chlorides containing catalyt's solid component production for application during alpha-olefines polymerisation. | |
| FI58928B (fi) | Foerfarande och katalysatorsystem foer laogtryckspolymerisering av eten enbart eller tillsammans med en alfa-olefin med 3-6 kolatomer | |
| FI81815C (fi) | Foerfarande foer polymerisering eller kopolymerisering av alfa-olefiner i en fluidiserad baedd under naervaro av ett ziegler-natta-katalysatorsystem. | |
| CA1335094C (en) | Titanium catalyst components, process for preparing same, catalysts containing same for preparing ethylene polymers and process for preparing said ethylene polymers | |
| US5214114A (en) | Process for producing ethylene polymers | |
| WO1999047568A1 (fr) | Systeme catalyseur a utiliser dans la polymerisation et copolymerisation d'ethylene et son procede de preparation | |
| JPH04224806A (ja) | ガス相におけるエチレンの（共）重合化に対する担持されたポリオレフィン用触媒 | |
| RU2066240C1 (ru) | Сокаталитическая композиция для полимеризации альфа-олефинов, каталитическая система на ее основе и способ полимеризации альфа-олефинов | |
| CA2058215A1 (en) | High activity vanadium-based catalyst | |
| US4027088A (en) | Process of preparing polyolefins | |
| US5332794A (en) | Process of preparing butadiene-styrene copolymer with nickel compound and alkylaluminoxane compound catalysts | |
| KR0137775B1 (ko) | 알파-올레핀의 입체특이적 중합법과 중합용 촉매 | |
| FI61500B (fi) | Foerfarande foer stereospecifik polymerisation av alfa-olefiner med 2-6 kolatomer i naervaro av ett katalytiskt system innehaollande titantrikloridpartiklar och de vid foerfarandet anvaenda titantrikloridpartiklarna | |
| US4987111A (en) | Catalyst component and catalyst for the polymerization of ethylene and the copolymerization of ethylene with alpha-olefins | |
| US4013822A (en) | Chromium-containing catalyst systems and their use for the polymerization of olefins | |
| US5286819A (en) | Polymerization process employing transition metal catalyst and polymer produced | |
| JPH0119406B2 (en)) | ||
| JPS5835601B2 (ja) | オレフインの重合および共重合法 | |
| JPS60135408A (ja) | ポリオレフインの製造方法 | |
| CA2058454A1 (en) | High activity vanadium-based catalyst | |
| CA2052513A1 (en) | High activity vanadium-based catalyst | |
| JPH055842B2 (en)) | ||
| JPS6123605A (ja) | α−オレフインの重合方法 | |
| JPS5952647B2 (ja) | ４−メチル−１−ペンテン重合体組成物の製造方法 | |
| JPH04153204A (ja) | アルファーオレフィンの重合方法 |