GB814837A - Improvements in the production of polymers from olefinically unsaturated hydrocarbons - Google Patents
Improvements in the production of polymers from olefinically unsaturated hydrocarbonsInfo
- Publication number
- GB814837A GB814837A GB3024656A GB3024656A GB814837A GB 814837 A GB814837 A GB 814837A GB 3024656 A GB3024656 A GB 3024656A GB 3024656 A GB3024656 A GB 3024656A GB 814837 A GB814837 A GB 814837A
- Authority
- GB
- United Kingdom
- Prior art keywords
- halogen
- chloride
- titanium
- catalyst
- aluminium
- 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
- 229930195735 unsaturated hydrocarbon Natural products 0.000 title abstract 3
- 229920000642 polymer Polymers 0.000 title abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- -1 titanium halide Chemical class 0.000 abstract 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 6
- 239000003054 catalyst Substances 0.000 abstract 6
- 239000010936 titanium Substances 0.000 abstract 5
- 229910052719 titanium Inorganic materials 0.000 abstract 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 4
- 150000007824 aliphatic compounds Chemical class 0.000 abstract 3
- 239000004411 aluminium Substances 0.000 abstract 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 3
- 229910052782 aluminium Inorganic materials 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 238000002360 preparation method Methods 0.000 abstract 3
- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 abstract 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 abstract 2
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 abstract 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229960003750 ethyl chloride Drugs 0.000 abstract 2
- 150000002366 halogen compounds Chemical class 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000011888 foil Substances 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 1
- UBZYKBZMAMTNKW-UHFFFAOYSA-J titanium tetrabromide Chemical compound Br[Ti](Br)(Br)Br UBZYKBZMAMTNKW-UHFFFAOYSA-J 0.000 abstract 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 abstract 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- 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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A crystalline catalyst suitable for use in the polymerization of olefinically unsaturated hydrocarbons is made by reacting aluminium with a titanium halide in the presence of a halogen-containing aliphatic compound and optionally aluminium chloride and/or a halogen such as chlorine, bromine, or iodine, or a halogen hydracid e.g. hydrochloric acid. The reaction may be carried out at temperatures between room and 100 DEG C. After the reaction any excess halogen compound is distilled off and the catalyst separated with the aid of an organic precipitant such as dimethylcyclohexane. Specified titanium halides are the tetrachloride, tetrabromide, and trichloride. The halogen-containing compound may be ethyl chloride or bromide, propyl or butyl chloride, methylene chloride, ethylene chloride, ethylene bromide, chloroform, trichlorethane, or carbon tetrachloride. In the preparation of the catalyst generally 1 mol. of titanium halide is reacted with 2 to 8 mols. of aluminium and the aluminium chloride when present is used in an amount up to 5 times the amount of the halide. Specification 781,837 is referred to.ALSO:Olefinically unsaturated hydrocarbons are polymerized, e.g continuously in the absence of any halogen-containing aliphatic compound in the presence of a catalyst obtained by the reaction of aluminium with a titanium halide in the presence of a halogen-containing aliphatic compound and optionally aluminium chloride, and/or a halogen or halogen hydracid. In the preparation of the catalyst any excess halogen compound is removed. Hydrocarbons mentioned are ethylene, propylene, butylene, isobutylene, and mixtures, and butadiene, isoprene, and styrene. The polymerization may be effected in the presence of diluents such as pentane, octane, cyclohexane, gasoline, or aromatic hydrocarbons, and at temperatures between - 120 DEG and 200 DEG C. The titanium halide used in the preparation of the catalyst may be titanium tetrachloride, titanium tetra-bromide, or titanium trichloride. The halogen-containing compound may be ethyl chloride or bromide, propyl or butyl chloride, methylene chloride, ethylene chloride, ethylene bromide, chloroform, trichlorethane, or carbon tetrachloride. The polymer may be purified by washing with methanolic hydrochloric acid, water, or tetrahydrofurane, and made into films, foils, fibres, or threads. Specification 781,837 is referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB37510A DE1026524B (en) | 1955-10-13 | 1955-10-13 | Process for the production of polymers from olefins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB814837A true GB814837A (en) | 1959-06-10 |
Family
ID=6965218
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3024656A Expired GB814837A (en) | 1955-10-13 | 1956-10-04 | Improvements in the production of polymers from olefinically unsaturated hydrocarbons |
Country Status (5)
| Country | Link |
|---|---|
| DE (1) | DE1026524B (en) |
| FR (1) | FR1161506A (en) |
| GB (1) | GB814837A (en) |
| IT (1) | IT560850A (en) |
| NL (1) | NL102400C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3365434A (en) * | 1963-09-05 | 1968-01-23 | Eastman Kodak Co | Metal-reduced transition metal halide catalyst |
| US3432513A (en) * | 1964-02-12 | 1969-03-11 | Continental Oil Co | Olefin polymerization process for producing highly isotactic polymers |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL266379A (en) * | 1960-06-27 | |||
| DE1268598B (en) * | 1964-03-04 | 1968-05-22 | Rexall Drug Chemical | Process for the preparation of a catalyst for the polymerization of alpha-olefins |
| DE1229050B (en) * | 1965-01-13 | 1966-11-24 | Basf Ag | Process for the preparation of a catalyst component which is particularly active in the polymerization of propylene using Ziegler catalysts |
-
0
- NL NL102400D patent/NL102400C/xx active
- IT IT560850D patent/IT560850A/it unknown
-
1955
- 1955-10-13 DE DEB37510A patent/DE1026524B/en active Pending
-
1956
- 1956-10-03 FR FR1161506D patent/FR1161506A/en not_active Expired
- 1956-10-04 GB GB3024656A patent/GB814837A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3365434A (en) * | 1963-09-05 | 1968-01-23 | Eastman Kodak Co | Metal-reduced transition metal halide catalyst |
| US3432513A (en) * | 1964-02-12 | 1969-03-11 | Continental Oil Co | Olefin polymerization process for producing highly isotactic polymers |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1161506A (en) | 1958-09-01 |
| DE1026524B (en) | 1958-03-20 |
| NL102400C (en) | |
| IT560850A (en) |
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