DE1106076B - Verfahren zur Herstellung von Olefinpolymerisaten - Google Patents
Verfahren zur Herstellung von OlefinpolymerisatenInfo
- Publication number
- DE1106076B DE1106076B DEP16851A DEP0016851A DE1106076B DE 1106076 B DE1106076 B DE 1106076B DE P16851 A DEP16851 A DE P16851A DE P0016851 A DEP0016851 A DE P0016851A DE 1106076 B DE1106076 B DE 1106076B
- Authority
- DE
- Germany
- Prior art keywords
- catalyst
- titanium
- polymer
- ethylene
- aluminum
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 31
- 229920000098 polyolefin Polymers 0.000 title claims description 5
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000003054 catalyst Substances 0.000 claims description 36
- -1 aliphatic monoolefins Chemical class 0.000 claims description 24
- 239000010936 titanium Substances 0.000 claims description 20
- 229920000642 polymer Polymers 0.000 claims description 19
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 18
- 239000003085 diluting agent Substances 0.000 claims description 16
- 229910052782 aluminium Inorganic materials 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 15
- 150000001336 alkenes Chemical class 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000005977 Ethylene Substances 0.000 claims description 13
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 13
- 238000006116 polymerization reaction Methods 0.000 claims description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 229910052719 titanium Inorganic materials 0.000 claims description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 10
- 150000004678 hydrides Chemical class 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000012280 lithium aluminium hydride Substances 0.000 claims description 6
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 6
- 150000007524 organic acids Chemical class 0.000 claims description 6
- 235000005985 organic acids Nutrition 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 claims description 5
- 229910052733 gallium Inorganic materials 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- IHEDBVUTTQXGSJ-UHFFFAOYSA-M 2-[bis(2-oxidoethyl)amino]ethanolate;titanium(4+);hydroxide Chemical compound [OH-].[Ti+4].[O-]CCN(CC[O-])CC[O-] IHEDBVUTTQXGSJ-UHFFFAOYSA-M 0.000 claims description 4
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 150000004820 halides Chemical class 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 229910052744 lithium Inorganic materials 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 150000003609 titanium compounds Chemical class 0.000 claims 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 3
- 125000002015 acyclic group Chemical group 0.000 claims 2
- 230000009849 deactivation Effects 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims 2
- 239000002002 slurry Substances 0.000 claims 2
- 238000005406 washing Methods 0.000 claims 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims 1
- 229910000831 Steel Inorganic materials 0.000 claims 1
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 claims 1
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 239000003245 coal Substances 0.000 claims 1
- 230000006835 compression Effects 0.000 claims 1
- 238000007906 compression Methods 0.000 claims 1
- 239000000356 contaminant Substances 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000002274 desiccant Substances 0.000 claims 1
- 238000005485 electric heating Methods 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- 238000004508 fractional distillation Methods 0.000 claims 1
- 238000000227 grinding Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 238000005470 impregnation Methods 0.000 claims 1
- 239000012535 impurity Substances 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 230000000704 physical effect Effects 0.000 claims 1
- 239000002574 poison Substances 0.000 claims 1
- 231100000614 poison Toxicity 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- HHDOORYZQSEMGM-UHFFFAOYSA-L potassium;oxalate;titanium(4+) Chemical compound [K+].[Ti+4].[O-]C(=O)C([O-])=O HHDOORYZQSEMGM-UHFFFAOYSA-L 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- 229940079877 pyrogallol Drugs 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 230000035484 reaction time Effects 0.000 claims 1
- 239000010959 steel Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 5
- 150000003608 titanium Chemical class 0.000 description 5
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- UHWHMHPXHWHWPX-UHFFFAOYSA-J dipotassium;oxalate;oxotitanium(2+) Chemical compound [K+].[K+].[Ti+2]=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O UHWHMHPXHWHWPX-UHFFFAOYSA-J 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229960005235 piperonyl butoxide Drugs 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 229910052716 thallium Inorganic materials 0.000 description 2
- JMXKSZRRTHPKDL-UHFFFAOYSA-N titanium ethoxide Chemical compound [Ti+4].CC[O-].CC[O-].CC[O-].CC[O-] JMXKSZRRTHPKDL-UHFFFAOYSA-N 0.000 description 2
- BUAQSUJYSBQTHA-BQYQJAHWSA-N (4e)-octa-1,4,7-triene Chemical compound C=CC\C=C\CC=C BUAQSUJYSBQTHA-BQYQJAHWSA-N 0.000 description 1
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- SDXMMMIGDDCIJV-UHFFFAOYSA-L C(CC(=O)[O-])(=O)[O-].[Ti+4].[Na+] Chemical compound C(CC(=O)[O-])(=O)[O-].[Ti+4].[Na+] SDXMMMIGDDCIJV-UHFFFAOYSA-L 0.000 description 1
- NOUKXNZPVRBJJH-UHFFFAOYSA-N CC1C[Ca]1 Chemical group CC1C[Ca]1 NOUKXNZPVRBJJH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001676573 Minium Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- JHJVIFZWGMGIQF-UHFFFAOYSA-N [InH3].[Li] Chemical compound [InH3].[Li] JHJVIFZWGMGIQF-UHFFFAOYSA-N 0.000 description 1
- UIGQEZZSKOINIE-UHFFFAOYSA-N [Li].CC=C Chemical group [Li].CC=C UIGQEZZSKOINIE-UHFFFAOYSA-N 0.000 description 1
- GPWHDDKQSYOYBF-UHFFFAOYSA-N ac1l2u0q Chemical compound Br[Br-]Br GPWHDDKQSYOYBF-UHFFFAOYSA-N 0.000 description 1
- INNSZZHSFSFSGS-UHFFFAOYSA-N acetic acid;titanium Chemical compound [Ti].CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O INNSZZHSFSFSGS-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- VRAIHTAYLFXSJJ-UHFFFAOYSA-N alumane Chemical compound [AlH3].[AlH3] VRAIHTAYLFXSJJ-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- ZRHOFLXFAAEXEE-UHFFFAOYSA-J butanoate;titanium(4+) Chemical compound [Ti+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O ZRHOFLXFAAEXEE-UHFFFAOYSA-J 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- KQJBQMSCFSJABN-UHFFFAOYSA-N octadecan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCCCCCCCCCCCCCCCC[O-].CCCCCCCCCCCCCCCCCC[O-].CCCCCCCCCCCCCCCCCC[O-].CCCCCCCCCCCCCCCCCC[O-] KQJBQMSCFSJABN-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- WRTMQOHKMFDUKX-UHFFFAOYSA-N triiodide Chemical compound I[I-]I WRTMQOHKMFDUKX-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- 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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US529918A US2962490A (en) | 1955-08-22 | 1955-08-22 | Process and catalyst for production of olefin polymers |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1106076B true DE1106076B (de) | 1961-05-04 |
Family
ID=24111743
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEP16851A Pending DE1106076B (de) | 1955-08-22 | 1956-08-16 | Verfahren zur Herstellung von Olefinpolymerisaten |
Country Status (7)
Country | Link |
---|---|
US (1) | US2962490A (en, 2012) |
BE (1) | BE550491A (en, 2012) |
CH (1) | CH375145A (en, 2012) |
DE (1) | DE1106076B (en, 2012) |
FR (1) | FR1156061A (en, 2012) |
GB (1) | GB807628A (en, 2012) |
NL (1) | NL98479C (en, 2012) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3177194A (en) * | 1960-10-12 | 1965-04-06 | Union Carbide Corp | Ethylene polymerization utilizing an insoluble titanium gel as a catalytic component |
DE1302747B (en, 2012) * | 1961-08-30 | 1971-09-23 | Philips Petroleum Co | |
US3285889A (en) * | 1963-09-16 | 1966-11-15 | Phillips Petroleum Co | Polymers of 1-monoolefins and dodecatertraenes |
DE1570525B1 (de) * | 1964-11-02 | 1970-01-22 | Exxon Research Engineering Co | Verfahren zur Herstellung von Polymerisaten konjugierter Diolefine |
LU64420A1 (en, 2012) * | 1971-12-08 | 1973-07-16 | ||
US6677013B1 (en) | 1998-04-17 | 2004-01-13 | Pechiney Emballage Flexible Europe | Transparent multilayer polypropylene container with barrier protection |
ES2428096T3 (es) | 2001-10-24 | 2013-11-05 | Amcor Rigid Plastics Usa, Inc. | Preforma para un recipiente de polipropileno |
US20050187374A1 (en) * | 2004-02-20 | 2005-08-25 | Bin Chen | Polyester synthesis with enhanced titanium catalyst composition |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE874215C (de) * | 1943-12-18 | 1953-04-20 | Basf Ag | Verfahren zur Herstellung von festen Polymerisaten aus AEthylen oder aethylenreichenGasen |
DE878560C (de) * | 1950-06-22 | 1953-06-05 | Karl Dr Ziegler | Verfahren zur Polymerisation und Mischpolymerisation von Olefinen |
BE534792A (en, 2012) * | 1954-01-19 | 1955-01-31 | ||
BE534888A (en, 2012) * | 1954-01-19 | 1955-01-31 | ||
BE533362A (en, 2012) * | 1953-11-17 | 1955-05-16 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2440498A (en) * | 1943-05-15 | 1948-04-27 | Standard Oil Dev Co | Polymerization catalysts |
US2491116A (en) * | 1943-11-16 | 1949-12-13 | Standard Oil Dev Co | Friedel-crafts type catalyst complexes and their preparation |
US2474670A (en) * | 1946-03-06 | 1949-06-28 | Atlantic Reflning Company | Production of propylene polymers |
US2634260A (en) * | 1949-11-18 | 1953-04-07 | Du Pont | Metal molybdite catalyzed polymerization |
US2721189A (en) * | 1954-08-30 | 1955-10-18 | Du Pont | Polymeric bicyclo-(2, 2, 1)-2-heptene |
NL107439C (en, 2012) * | 1954-12-24 | |||
NL203326A (en, 2012) * | 1955-01-05 | |||
US2824090A (en) * | 1955-12-27 | 1958-02-18 | Eastman Kodak Co | Polymerization of alpha-olefins with a catalyst mixture of an orthotitanate and an alkyl aluminum halide |
-
0
- BE BE550491D patent/BE550491A/xx unknown
- NL NL98479D patent/NL98479C/xx active
-
1955
- 1955-08-22 US US529918A patent/US2962490A/en not_active Expired - Lifetime
-
1956
- 1956-08-09 GB GB24398/56A patent/GB807628A/en not_active Expired
- 1956-08-16 DE DEP16851A patent/DE1106076B/de active Pending
- 1956-08-21 FR FR1156061D patent/FR1156061A/fr not_active Expired
- 1956-08-21 CH CH3671056A patent/CH375145A/fr unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE874215C (de) * | 1943-12-18 | 1953-04-20 | Basf Ag | Verfahren zur Herstellung von festen Polymerisaten aus AEthylen oder aethylenreichenGasen |
DE878560C (de) * | 1950-06-22 | 1953-06-05 | Karl Dr Ziegler | Verfahren zur Polymerisation und Mischpolymerisation von Olefinen |
BE533362A (en, 2012) * | 1953-11-17 | 1955-05-16 | ||
BE534792A (en, 2012) * | 1954-01-19 | 1955-01-31 | ||
BE534888A (en, 2012) * | 1954-01-19 | 1955-01-31 |
Also Published As
Publication number | Publication date |
---|---|
GB807628A (en) | 1959-01-21 |
NL98479C (en, 2012) | |
CH375145A (fr) | 1964-02-15 |
FR1156061A (fr) | 1958-05-12 |
BE550491A (en, 2012) | |
US2962490A (en) | 1960-11-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2318953C2 (de) | Verfahren zur Herstellung linearer α-Olefine durch Polymerisation eines Ethylen enthaltenden Gases | |
DE2626097C2 (en, 2012) | ||
DE1420648B2 (de) | Verfahren zur Polymerisation oder Mischpolymerisation wenigstens eines Olefins | |
DE1266504B (de) | Verfahren zur Polymerisation von Mono-1-Olefinen | |
DE2522331A1 (de) | Katalysator zum polymerisieren oder copolymerisieren von olefinen sowie dessen herstellung und verwendung | |
DE1520721B2 (de) | Verfahren zur polymerisation von propylen in der wirbelschicht | |
DE1106076B (de) | Verfahren zur Herstellung von Olefinpolymerisaten | |
DE3133101A1 (de) | Verfahren zur entfernung von katalysatorresten aus polyolefinen | |
DE2146688B2 (de) | Verfahren zur Polymerisation von Äthylen und Katalysator zur Durchführung dieses Verfahrens | |
DE2262156C2 (de) | Verfahren zur Herstellung von Katalysatoren zur Homopolymerisation von Äthylen oder zur Copolymerisation von Äthylen mit α-Olefinen | |
DE1219226B (de) | Verfahren zur Polymerisation oder Mischpolymerisation von AEthylen | |
DE1016018B (de) | Verfahren zur Herstellung von Polymerisaten aus Olefinen | |
DE1208077B (de) | Verfahren zur Polymerisation oder Misch-polymerisation von Olefinen | |
DE1302896C2 (de) | Verfahren zur selektiven polymerisation von alpha-olefinen | |
CH441759A (de) | Verfahren zur Polymerisation und Mischpolymerisation ungesättigter organischer Verbindungen | |
DE3030055A1 (de) | Verfahren zum herstellen von ethylen-homopolymerisaten sowie ethylen-copolymerisaten mit (alpha) -monoolefinen | |
DE1495834B1 (de) | Verfahren zur Herstellung von Homo- oder Mischpolymerisaten des AEthylens | |
DE2047140A1 (de) | Verfahren zur Herstellung von Polypropylen und/oder Polybutylen Ölen | |
DE1133890B (de) | Verfahren zur Polymerisation von Olefinen | |
EP0558981B1 (de) | Verfahren zur Herstellung von Propylen-Ethylen-Copolymerisaten | |
DE1803124A1 (de) | Verfahren zur Herstellung linearer alpha-Olefine | |
DE1924648C3 (de) | Verfahren zur Herstellung eines Katalysators für die Polymerisation von Olefinen und seine Verwendung | |
DE1026524B (de) | Verfahren zur Herstellung von Polymerisaten aus Olefinen | |
DE2350795A1 (de) | Verfahren zur polymerisation von aethylen unter verwendung eines neuen katalysators | |
AT239523B (de) | Verfahren zum Polymerisieren von Olefinen |