FI57601C - Saett att homopolymerisera eller sampolymerisera etylen propylen en blandning av etylen eller en annan alfa-olefin en blandning av etylen eller propylen och en diolefin eller en blandning av etylen en annan alfa-olefin och diolefin samt en katalysatorkomplex foer anvaendning daeri - Google Patents
Saett att homopolymerisera eller sampolymerisera etylen propylen en blandning av etylen eller en annan alfa-olefin en blandning av etylen eller propylen och en diolefin eller en blandning av etylen en annan alfa-olefin och diolefin samt en katalysatorkomplex foer anvaendning daeri Download PDFInfo
- Publication number
- FI57601C FI57601C FI345373A FI345373A FI57601C FI 57601 C FI57601 C FI 57601C FI 345373 A FI345373 A FI 345373A FI 345373 A FI345373 A FI 345373A FI 57601 C FI57601 C FI 57601C
- Authority
- FI
- Finland
- Prior art keywords
- carbon atoms
- compound
- carboxylic acid
- saturated
- unsaturated aliphatic
- Prior art date
Links
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title claims description 12
- 239000003054 catalyst Substances 0.000 claims description 92
- 125000004432 carbon atom Chemical group C* 0.000 claims description 52
- 150000001875 compounds Chemical class 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 35
- 239000010936 titanium Substances 0.000 claims description 34
- 239000011777 magnesium Substances 0.000 claims description 31
- -1 ethylene, propylene Chemical group 0.000 claims description 30
- 229910052719 titanium Inorganic materials 0.000 claims description 30
- 229910052749 magnesium Inorganic materials 0.000 claims description 29
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 27
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 25
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 21
- 239000005977 Ethylene Substances 0.000 claims description 21
- 229910052710 silicon Inorganic materials 0.000 claims description 21
- 150000003624 transition metals Chemical class 0.000 claims description 21
- 238000006243 chemical reaction Methods 0.000 claims description 20
- 239000007787 solid Substances 0.000 claims description 20
- 229910052718 tin Inorganic materials 0.000 claims description 20
- 229910052723 transition metal Inorganic materials 0.000 claims description 19
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical class C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 17
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 15
- 150000002148 esters Chemical class 0.000 claims description 15
- 229920006395 saturated elastomer Polymers 0.000 claims description 15
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 11
- 150000001993 dienes Chemical class 0.000 claims description 9
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 150000003682 vanadium compounds Chemical class 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 150000002902 organometallic compounds Chemical class 0.000 claims description 7
- 235000011147 magnesium chloride Nutrition 0.000 claims description 6
- 230000000737 periodic effect Effects 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 5
- 238000007334 copolymerization reaction Methods 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 3
- OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 claims description 3
- 150000002681 magnesium compounds Chemical class 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 description 38
- 229920000642 polymer Polymers 0.000 description 36
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 24
- 239000002245 particle Substances 0.000 description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- 239000007795 chemical reaction product Substances 0.000 description 18
- 239000003208 petroleum Substances 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 14
- 150000001336 alkenes Chemical class 0.000 description 13
- 150000003623 transition metal compounds Chemical class 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 10
- 238000009826 distribution Methods 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 9
- 150000002367 halogens Chemical class 0.000 description 9
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 9
- 229910052720 vanadium Inorganic materials 0.000 description 8
- JLNTWVDSQRNWFU-UHFFFAOYSA-N OOOOOOO Chemical compound OOOOOOO JLNTWVDSQRNWFU-UHFFFAOYSA-N 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 150000002896 organic halogen compounds Chemical class 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical group [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 5
- OZBZONOEYUBXTD-UHFFFAOYSA-N OOOOOOOOO Chemical compound OOOOOOOOO OZBZONOEYUBXTD-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 150000002366 halogen compounds Chemical class 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 4
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000011362 coarse particle Substances 0.000 description 3
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 239000005049 silicon tetrachloride Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 150000003609 titanium compounds Chemical class 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 101000713575 Homo sapiens Tubulin beta-3 chain Proteins 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 2
- 241000209094 Oryza Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 102100036790 Tubulin beta-3 chain Human genes 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000037048 polymerization activity Effects 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-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
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000958593 Cuon Species 0.000 description 1
- 101000788853 Homo sapiens Zinc finger CCHC domain-containing protein 7 Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 102100025395 Zinc finger CCHC domain-containing protein 7 Human genes 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005234 alkyl aluminium group Chemical group 0.000 description 1
- 150000004791 alkyl magnesium halides Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- AZWXAPCAJCYGIA-UHFFFAOYSA-N bis(2-methylpropyl)alumane Chemical compound CC(C)C[AlH]CC(C)C AZWXAPCAJCYGIA-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- SLLGVCUQYRMELA-UHFFFAOYSA-N chlorosilicon Chemical compound Cl[Si] SLLGVCUQYRMELA-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- 150000004796 dialkyl magnesium compounds Chemical class 0.000 description 1
- JJSGABFIILQOEY-UHFFFAOYSA-M diethylalumanylium;bromide Chemical compound CC[Al](Br)CC JJSGABFIILQOEY-UHFFFAOYSA-M 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 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
- 150000002431 hydrogen Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 125000001905 inorganic group Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910001623 magnesium bromide Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000002901 organomagnesium compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 239000011591 potassium Chemical group 0.000 description 1
- 229910052700 potassium Chemical group 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000011734 sodium Chemical group 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000008096 xylene Substances 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
- C08F4/02—Carriers therefor
- C08F4/022—Magnesium halide as support anhydrous or hydrated or complexed by means of a Lewis base for Ziegler-type 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)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11215172A JPS531796B2 (en:Method) | 1972-11-10 | 1972-11-10 | |
JP11215172 | 1972-11-10 | ||
JP13005272A JPS5425517B2 (en:Method) | 1972-12-27 | 1972-12-27 | |
JP13005272 | 1972-12-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
FI57601B FI57601B (fi) | 1980-05-30 |
FI57601C true FI57601C (fi) | 1980-09-10 |
Family
ID=26451378
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI345373A FI57601C (fi) | 1972-11-10 | 1973-11-08 | Saett att homopolymerisera eller sampolymerisera etylen propylen en blandning av etylen eller en annan alfa-olefin en blandning av etylen eller propylen och en diolefin eller en blandning av etylen en annan alfa-olefin och diolefin samt en katalysatorkomplex foer anvaendning daeri |
Country Status (13)
Country | Link |
---|---|
BG (1) | BG27241A3 (en:Method) |
BR (1) | BR7308816D0 (en:Method) |
CA (1) | CA1007393A (en:Method) |
DE (1) | DE2355886A1 (en:Method) |
FI (1) | FI57601C (en:Method) |
FR (1) | FR2206339B1 (en:Method) |
GB (1) | GB1452314A (en:Method) |
IT (1) | IT1001685B (en:Method) |
NL (1) | NL153557B (en:Method) |
NO (1) | NO145660C (en:Method) |
PH (1) | PH12460A (en:Method) |
RO (1) | RO67844A (en:Method) |
SE (1) | SE412242B (en:Method) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5120297A (en) * | 1974-08-10 | 1976-02-18 | Mitsui Petrochemical Ind | Arufua orefuinno koritsutaikisokuseijugohoho |
GB1492618A (en) * | 1974-02-01 | 1977-11-23 | Mitsui Petrochemical Ind | Process for preparing highly stereoregular polyolefins and catalyst used therefor |
JPS565404B2 (en:Method) * | 1975-02-14 | 1981-02-04 | ||
DE2553104A1 (de) * | 1975-11-26 | 1977-06-08 | Mitsui Petrochemical Ind | Verfahren zur herstellung einer auf einen traeger mit hoher leistungsfaehigkeit aufgebrachten katalysatorkomponente |
SE7613662L (sv) * | 1975-12-10 | 1977-06-11 | Mitsui Petrochemical Ind | Polymerisation av alfa-olefiner |
US4175171A (en) * | 1976-08-02 | 1979-11-20 | Mitsui Toatsu Chemicals, Inc. | Catalyst for polymerizing α-olefins |
IT1068112B (it) * | 1976-08-09 | 1985-03-21 | Montedison Spa | Componenti di catalizzatori per la polimerizzazione delle alfa olefine e catalizzatori da essi ottenuti |
JPS5952643B2 (ja) * | 1977-01-27 | 1984-12-20 | 三井化学株式会社 | エチレン共重合体 |
IT1078995B (it) * | 1977-05-24 | 1985-05-08 | Montedison Spa | Catalizzatori per la polimeriazzazione di olefine |
US4220745A (en) * | 1978-03-01 | 1980-09-02 | Mitsui Toatsu Chemicals, Inc. | Process for polymerization of α-olefins |
DE2839136A1 (de) * | 1978-09-08 | 1980-03-20 | Bayer Ag | Katalysator auf einem festen traeger zur polymerisation von alpha -olefinen |
JPS6037804B2 (ja) | 1979-04-11 | 1985-08-28 | 三井化学株式会社 | オレフイン重合触媒用担体の製法 |
DE3068239D1 (en) * | 1979-11-20 | 1984-07-19 | Shell Int Research | Preparation of catalyst components and polymerization of olefins employing such catalyst components |
IT1209255B (it) * | 1980-08-13 | 1989-07-16 | Montedison Spa | Catalizzatori per la polimerizzazione di olefine. |
US6777508B1 (en) | 1980-08-13 | 2004-08-17 | Basell Poliolefine Italia S.P.A. | Catalysts for the polymerization of olefins |
FR2495162B1 (fr) * | 1980-12-02 | 1985-09-27 | Charbonnages Ste Chimique | Catalyseur de polymerisation de l'ethylene comprenant un compose aromatique du silicium |
JPS5834810A (ja) * | 1981-08-25 | 1983-03-01 | Nippon Oil Co Ltd | ポリオレフインの製造方法 |
DE69600154T2 (de) * | 1995-05-22 | 1998-06-10 | Mitsui Petrochemical Ind | Festes Titan enthaltender Katalysatorbestandteil, diesen enthaltender Katalysator für die Ethylenpolymerisation und Ethylenpolymerisationverfahren |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3676418A (en) * | 1968-07-20 | 1972-07-11 | Mitsubishi Petrochemical Co | Catalytic production of olefin polymers |
CA920299A (en) * | 1968-08-01 | 1973-01-30 | Mitsui Petrochemical Industries | Process for the polymerization and/or copolymerization of olefins with use of ziegler-type catalytsts supported on carrier |
NL163523C (nl) * | 1970-07-31 | 1983-11-16 | Montedison Spa | Werkwijze om een polymerisatiekatalysator te bereiden. |
DE2043508A1 (de) * | 1970-09-02 | 1972-03-16 | Farbwerke Hoechst AG, vorm. Meister Lucius & Brüning, 6000 Frankfurt | Verfahren zur Herstellung von Polyolefinen |
NL7114641A (en:Method) * | 1970-10-29 | 1972-05-03 | ||
DE2111455A1 (de) * | 1971-03-10 | 1972-09-28 | Hoechst Ag | Verfahren zur Herstellung von Polyolefinen |
NL170962C (nl) * | 1971-04-06 | 1983-01-17 | Montedison Spa | Werkwijze om katalysatoren te bereiden om alkenen te polymeriseren. |
-
1973
- 1973-11-06 GB GB5152373A patent/GB1452314A/en not_active Expired
- 1973-11-08 FI FI345373A patent/FI57601C/fi active
- 1973-11-08 SE SE7315161A patent/SE412242B/sv unknown
- 1973-11-08 DE DE19732355886 patent/DE2355886A1/de active Granted
- 1973-11-09 BR BR881673A patent/BR7308816D0/pt unknown
- 1973-11-09 PH PH15207A patent/PH12460A/en unknown
- 1973-11-09 NO NO432273A patent/NO145660C/no unknown
- 1973-11-09 CA CA185,440A patent/CA1007393A/en not_active Expired
- 1973-11-09 RO RO7376588A patent/RO67844A/ro unknown
- 1973-11-09 IT IT3114873A patent/IT1001685B/it active
- 1973-11-09 NL NL7315375A patent/NL153557B/xx not_active IP Right Cessation
- 1973-11-10 BG BG024963A patent/BG27241A3/xx unknown
- 1973-11-12 FR FR7340137A patent/FR2206339B1/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BG27241A3 (en) | 1979-09-14 |
FR2206339B1 (en:Method) | 1977-03-11 |
DE2355886C2 (en:Method) | 1987-06-19 |
SE412242B (sv) | 1980-02-25 |
NO145660B (no) | 1982-01-25 |
DE2355886A1 (de) | 1974-05-16 |
FI57601B (fi) | 1980-05-30 |
FR2206339A1 (en:Method) | 1974-06-07 |
GB1452314A (en) | 1976-10-13 |
CA1007393A (en) | 1977-03-22 |
PH12460A (en) | 1979-03-08 |
IT1001685B (it) | 1976-04-30 |
RO67844A (ro) | 1983-08-03 |
NL7315375A (en:Method) | 1974-05-14 |
NL153557B (nl) | 1977-06-15 |
BR7308816D0 (pt) | 1974-09-05 |
NO145660C (no) | 1982-05-05 |
AU6228473A (en) | 1975-05-08 |
RO67844B (ro) | 1983-07-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FI57601C (fi) | Saett att homopolymerisera eller sampolymerisera etylen propylen en blandning av etylen eller en annan alfa-olefin en blandning av etylen eller propylen och en diolefin eller en blandning av etylen en annan alfa-olefin och diolefin samt en katalysatorkomplex foer anvaendning daeri | |
JP4394280B2 (ja) | エチレン重合又は共重合での使用に適した触媒系、及び該触媒系を調整するための工程 | |
EP3257871B1 (en) | Method for reducing olefin oligomerization byproduct using a deactivating agent | |
DE69328955T2 (de) | Katalysatorzusammensetzungen und Verfahren zur Herstellung von Polyolefinen | |
FI61494B (fi) | Foerfarande foer polymerisation av eten allena eller tillsammans med en annan alfa-olefin vid foerfarandet anvaendbart katalysatorkomplex och dess framstaellning | |
DE60005185T2 (de) | Übergangsmetallkomplexe und olefin-polymerisationsverfahren | |
DE69216654T2 (de) | Olefinpolymerisationskatalysator | |
DK152738B (da) | Fremgangsmaade til polymerisation af alfa-olefiner samt fast katalytisk komplex til brug ved fremgangsmaaden | |
DE3784173T2 (de) | Olefinpolymerisationskatalysator. | |
DE102006001959A1 (de) | Verfahren zur Herstellung von unsymmetrischen Bis(imino)verbindungen | |
US20070093623A1 (en) | Catalyst components, process for their preparation and their use as catalyst components in polymerization of olefins | |
JPH10502951A (ja) | エチレン重合体製造のためのプロ触媒、その製造方法及び用途 | |
CA2255522C (en) | Novel electron donor containing compositions | |
DE68919940T2 (de) | Olefinpolymerisationskatalysator. | |
JP2018188636A (ja) | プロピレン・エチレン・1−ブテンターポリマー及びその製造方法 | |
JP2002523571A (ja) | オレフィン重合 | |
FI91264B (fi) | Menetelmä alfa-mono-olefiinien polymeroimiseksi | |
JPS59138206A (ja) | オレフィン重合用触媒成分の製造方法 | |
GB2085016A (en) | Catalytic composition and its use for producing highly stereoregular a-olefin polymers | |
DE3003327C2 (en:Method) | ||
CA1139738A (en) | Catalysts for the polymerization of olefins | |
ITMI980104A1 (it) | Procedimento migliorato per la polimerizzazione e la copolimerizzazione di olefine | |
DE102011011237A1 (de) | Katalysatorkomponente zur Olefinpolymerisation und Verfahren zu Ihrer Herstellung und Verfahren zur Herstellung eines Katalysators zur Olefinpolymerisation und Olefinpolymer | |
DE4102300A1 (de) | Vanadium und magnesium enthaltende komponente fuer ein ziegler-katalysatorsystem | |
EP1830954A2 (en) | Soluble magnesium complexes useful for the production of polyolefin catalysts and catalysts prepared therewith |