ES250334A1 - Un procedimiento para producir copolimeros de etileno y 1-olefina normalmente sëlidos - Google Patents
Un procedimiento para producir copolimeros de etileno y 1-olefina normalmente sëlidosInfo
- Publication number
- ES250334A1 ES250334A1 ES0250334A ES250334A ES250334A1 ES 250334 A1 ES250334 A1 ES 250334A1 ES 0250334 A ES0250334 A ES 0250334A ES 250334 A ES250334 A ES 250334A ES 250334 A1 ES250334 A1 ES 250334A1
- Authority
- ES
- Spain
- Prior art keywords
- tin
- triphenyl
- tetra
- lead
- catalyst
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920000089 Cyclic olefin copolymer Polymers 0.000 title 1
- -1 dibutyl Chemical compound 0.000 abstract 6
- 229910052718 tin Inorganic materials 0.000 abstract 5
- KEVMYFLMMDUPJE-UHFFFAOYSA-N 2,7-dimethyloctane Chemical group CC(C)CCCCC(C)C KEVMYFLMMDUPJE-UHFFFAOYSA-N 0.000 abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 4
- 229910052782 aluminium Inorganic materials 0.000 abstract 4
- 239000004411 aluminium Substances 0.000 abstract 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- 229930195733 hydrocarbon Natural products 0.000 abstract 4
- 150000002430 hydrocarbons Chemical class 0.000 abstract 4
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 3
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 abstract 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 2
- GAQKSIBCPKUKPL-UHFFFAOYSA-N CC(C)CC[Cd]CCC(C)C Chemical compound CC(C)CC[Cd]CCC(C)C GAQKSIBCPKUKPL-UHFFFAOYSA-N 0.000 abstract 2
- KPIWMDFVPRFCJG-UHFFFAOYSA-N CC1=CC=CC=C1[Zn]C1=CC=CC=C1C Chemical compound CC1=CC=CC=C1[Zn]C1=CC=CC=C1C KPIWMDFVPRFCJG-UHFFFAOYSA-N 0.000 abstract 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 abstract 2
- 229910021549 Vanadium(II) chloride Inorganic materials 0.000 abstract 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052787 antimony Inorganic materials 0.000 abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 235000010290 biphenyl Nutrition 0.000 abstract 2
- 239000004305 biphenyl Substances 0.000 abstract 2
- 125000006267 biphenyl group Chemical group 0.000 abstract 2
- 229910052797 bismuth Inorganic materials 0.000 abstract 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 abstract 2
- FAMUPMBATZGWOV-UHFFFAOYSA-M bromo(triphenyl)stannane Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Br)C1=CC=CC=C1 FAMUPMBATZGWOV-UHFFFAOYSA-M 0.000 abstract 2
- ZSDPTSLWBDOFEA-UHFFFAOYSA-N butyl(triphenyl)germane Chemical compound C=1C=CC=CC=1[Ge](C=1C=CC=CC=1)(CCCC)C1=CC=CC=C1 ZSDPTSLWBDOFEA-UHFFFAOYSA-N 0.000 abstract 2
- 229910052793 cadmium Inorganic materials 0.000 abstract 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 2
- MDWJZZZKWHLMQP-UHFFFAOYSA-L cyclopentane;dichlorovanadium Chemical compound Cl[V]Cl.[CH]1[CH][CH][CH][CH]1.[CH]1[CH][CH][CH][CH]1 MDWJZZZKWHLMQP-UHFFFAOYSA-L 0.000 abstract 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 abstract 2
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 abstract 2
- KQEIOCQUCGCMHX-UHFFFAOYSA-N diethyl(dimethyl)stannane Chemical compound CC[Sn](C)(C)CC KQEIOCQUCGCMHX-UHFFFAOYSA-N 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 abstract 2
- 229910052732 germanium Inorganic materials 0.000 abstract 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 abstract 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 2
- 239000004615 ingredient Substances 0.000 abstract 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 2
- 229910052753 mercury Inorganic materials 0.000 abstract 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 abstract 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- 150000002902 organometallic compounds Chemical class 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- 235000021286 stilbenes Nutrition 0.000 abstract 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 abstract 2
- CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 abstract 2
- PZBSVWLAICUFBC-UHFFFAOYSA-N tribenzyl(phenyl)stannane Chemical compound C=1C=CC=CC=1C[Sn](C=1C=CC=CC=1)(CC=1C=CC=CC=1)CC1=CC=CC=C1 PZBSVWLAICUFBC-UHFFFAOYSA-N 0.000 abstract 2
- FPYOWXFLVWSKPS-UHFFFAOYSA-N triethylbismuthane Chemical compound CC[Bi](CC)CC FPYOWXFLVWSKPS-UHFFFAOYSA-N 0.000 abstract 2
- LOAWHQCNQSFKDK-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC.CC[Sn](CC)CC LOAWHQCNQSFKDK-UHFFFAOYSA-N 0.000 abstract 2
- ZHXAZZQXWJJBHA-UHFFFAOYSA-N triphenylbismuthane Chemical compound C1=CC=CC=C1[Bi](C=1C=CC=CC=1)C1=CC=CC=C1 ZHXAZZQXWJJBHA-UHFFFAOYSA-N 0.000 abstract 2
- JQHWEIUKAAZLFP-UHFFFAOYSA-N triphenylgermanium Chemical compound C1=CC=CC=C1[Ge](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[Ge](C=1C=CC=CC=1)C1=CC=CC=C1 JQHWEIUKAAZLFP-UHFFFAOYSA-N 0.000 abstract 2
- UAPQJVJCJITJET-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 UAPQJVJCJITJET-UHFFFAOYSA-N 0.000 abstract 2
- 150000003682 vanadium compounds Chemical class 0.000 abstract 2
- WSJLOGNSKRVGAD-UHFFFAOYSA-L vanadium(ii) bromide Chemical compound [V+2].[Br-].[Br-] WSJLOGNSKRVGAD-UHFFFAOYSA-L 0.000 abstract 2
- ITAKKORXEUJTBC-UHFFFAOYSA-L vanadium(ii) chloride Chemical compound Cl[V]Cl ITAKKORXEUJTBC-UHFFFAOYSA-L 0.000 abstract 2
- 229910052725 zinc Inorganic materials 0.000 abstract 2
- 239000011701 zinc Substances 0.000 abstract 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 abstract 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 abstract 1
- NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 abstract 1
- 229920006158 high molecular weight polymer Polymers 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 abstract 1
- JUISPCSEIXBMNI-UHFFFAOYSA-N tetracyclohexylstannane Chemical compound C1CCCCC1[Sn](C1CCCCC1)(C1CCCCC1)C1CCCCC1 JUISPCSEIXBMNI-UHFFFAOYSA-N 0.000 abstract 1
- KKOFCVMVBJXDFP-UHFFFAOYSA-N triethylstibane Chemical compound CC[Sb](CC)CC KKOFCVMVBJXDFP-UHFFFAOYSA-N 0.000 abstract 1
- HVYVMSPIJIWUNA-UHFFFAOYSA-N triphenylstibine Chemical compound C1=CC=CC=C1[Sb](C=1C=CC=CC=1)C1=CC=CC=C1 HVYVMSPIJIWUNA-UHFFFAOYSA-N 0.000 abstract 1
- HEPBQSXQJMTVFI-UHFFFAOYSA-N zinc;butane Chemical group [Zn+2].CCC[CH2-].CCC[CH2-] HEPBQSXQJMTVFI-UHFFFAOYSA-N 0.000 abstract 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
- C08F210/00—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)
Abstract
Procedimiento para producir copolímeros de etileno y una l-olefina, normalmente sólidos, que comprende la operación de poner en contacto etileno y una olefina que contiene hasta 8 átomos de carbono, con una mezcla catalítica que comprende, como uno de los componentes, un trihaluro de aluminio soluble en hidrocarburo, como segundo componente, un compuesto órgano metálico de cinc, cadmio, mercurio, germanio, estaño, plomo antimonio o bismuto; y como tercer componente, por lo menos, una cantidad traza de un compuesto de vanadio.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US752176A US3073809A (en) | 1958-07-31 | 1958-07-31 | Process for producing ethylene-1-olefin copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES250334A1 true ES250334A1 (es) | 1960-01-16 |
Family
ID=25025219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0250334A Expired ES250334A1 (es) | 1958-07-31 | 1959-06-25 | Un procedimiento para producir copolimeros de etileno y 1-olefina normalmente sëlidos |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3073809A (es) |
| BE (1) | BE581026A (es) |
| DE (1) | DE1158714B (es) |
| ES (1) | ES250334A1 (es) |
| FR (1) | FR1237352A (es) |
| GB (1) | GB856859A (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4133944A (en) * | 1973-03-29 | 1979-01-09 | Imperial Chemical Industries Limited | Ethylene polymerization |
| GB1419012A (en) * | 1973-03-29 | 1975-12-24 | Ici Ltd | Production of polyethylene |
| US4302566A (en) * | 1978-03-31 | 1981-11-24 | Union Carbide Corporation | Preparation of ethylene copolymers in fluid bed reactor |
| US4390677A (en) * | 1978-03-31 | 1983-06-28 | Karol Frederick J | Article molded from ethylene hydrocarbon copolymer |
| US5175326A (en) * | 1985-10-15 | 1992-12-29 | E. I. Du Pont De Nemours And Company | Nickel containing organo-metallic compound as catalyst |
| US4698403A (en) * | 1985-10-15 | 1987-10-06 | E. I. Du Pont De Nemours And Company | Nickel-catalyzed copolymerization of ethylene |
| US4906754A (en) * | 1985-10-15 | 1990-03-06 | E. I. Du Pont De Nemours And Company | Nickel catalysts for copolymerization of ethylene |
| US5030606A (en) * | 1985-10-15 | 1991-07-09 | E. I. Du Pont De Nemours And Company | Nickel-catalyzed copolymerization of ethylene |
| CA2037025C (en) * | 1990-02-27 | 1996-12-03 | Mitsui Chemicals, Incorporated | Ethylene/pentene-1 copolymer, process for the preparation of the same, and ethylene/pentene-1 copolymer composition |
| ES2138352T3 (es) * | 1995-05-31 | 2000-01-01 | Sasol Tech Pty Ltd | Copolimero de etileno-penteno-hexeno, procedimiento para su preparacion y utilizacion para la produccion de peliculas. |
| KR101430845B1 (ko) * | 2009-12-18 | 2014-08-18 | 토탈 리서치 앤드 테크놀로지 펠루이 | 중합 촉매를 중화하는 방법 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT513721A (es) * | 1953-01-27 | 1900-01-01 | ||
| NL229912A (es) * | 1954-12-24 | |||
| US2900374A (en) * | 1956-11-15 | 1959-08-18 | Robert S Aries | Aluminum halide catalysis of ethylene polymerization |
| US2846427A (en) * | 1957-03-14 | 1958-08-05 | Phillips Petroleum Co | Treatment of polymers |
-
0
- BE BE581026D patent/BE581026A/xx unknown
-
1958
- 1958-07-31 US US752176A patent/US3073809A/en not_active Expired - Lifetime
-
1959
- 1959-06-25 ES ES0250334A patent/ES250334A1/es not_active Expired
- 1959-07-25 DE DEU6381A patent/DE1158714B/de active Pending
- 1959-07-27 GB GB25613/59A patent/GB856859A/en not_active Expired
- 1959-07-28 FR FR801395A patent/FR1237352A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE1158714B (de) | 1963-12-05 |
| GB856859A (en) | 1960-12-21 |
| BE581026A (es) | |
| US3073809A (en) | 1963-01-15 |
| FR1237352A (fr) | 1960-07-29 |
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