GB817308A - Novel catalyst composition, preparation and use thereof - Google Patents
Novel catalyst composition, preparation and use thereofInfo
- Publication number
- GB817308A GB817308A GB20131/57A GB2013157A GB817308A GB 817308 A GB817308 A GB 817308A GB 20131/57 A GB20131/57 A GB 20131/57A GB 2013157 A GB2013157 A GB 2013157A GB 817308 A GB817308 A GB 817308A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compounds
- catalyst
- aluminium
- vinyl
- olefins
- 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
- 239000003054 catalyst Substances 0.000 title abstract 10
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 8
- -1 hexane Chemical class 0.000 abstract 6
- 150000002894 organic compounds Chemical class 0.000 abstract 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 5
- 239000005977 Ethylene Substances 0.000 abstract 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 5
- 150000001336 alkenes Chemical class 0.000 abstract 4
- 229910052751 metal Inorganic materials 0.000 abstract 4
- 239000002184 metal Substances 0.000 abstract 4
- 238000006116 polymerization reaction Methods 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- 150000002902 organometallic compounds Chemical class 0.000 abstract 3
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 abstract 3
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 abstract 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 abstract 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 2
- 150000001260 acyclic compounds Chemical class 0.000 abstract 2
- 150000001334 alicyclic compounds Chemical class 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 2
- CMWCOKOTCLFJOP-UHFFFAOYSA-N titanium(3+) Chemical compound [Ti+3] CMWCOKOTCLFJOP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 2
- JTGATPUEEONCSG-UHFFFAOYSA-N 1,1,3-trifluorobuta-1,3-diene Chemical compound FC(F)=CC(F)=C JTGATPUEEONCSG-UHFFFAOYSA-N 0.000 abstract 1
- SUTQSIHGGHVXFK-UHFFFAOYSA-N 1,2,2-trifluoroethenylbenzene Chemical group FC(F)=C(F)C1=CC=CC=C1 SUTQSIHGGHVXFK-UHFFFAOYSA-N 0.000 abstract 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 abstract 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminum fluoride Inorganic materials F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 abstract 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 abstract 1
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 229910001510 metal chloride Inorganic materials 0.000 abstract 1
- 150000002736 metal compounds Chemical class 0.000 abstract 1
- 229910001507 metal halide Inorganic materials 0.000 abstract 1
- 150000005309 metal halides Chemical class 0.000 abstract 1
- 239000000178 monomer Chemical class 0.000 abstract 1
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 abstract 1
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 abstract 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 abstract 1
- IBEFSUTVZWZJEL-UHFFFAOYSA-N trimethylindium Chemical compound C[In](C)C IBEFSUTVZWZJEL-UHFFFAOYSA-N 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 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
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/52—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides selected from boron, aluminium, gallium, indium, thallium or rare earths
-
- 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
- C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F16/12—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A catalyst for the polymerization of olefins comprises (i) an organo-metallic compound of a metal of Group IIIb, e.g. tri-ethyl aluminium, (ii) a halide of a metal of Groups IVa, Va, VIa, VIIa or VIII, e.g. titanium tetrachloride, and (iii) a chlorine-substituted organic compound, e.g. carbon tetrachloride or trichloroethylene. The catalyst is prepared by independently adding the organo-metallic compound and the inorganic metal halide to the chlorine-substituted organic compound in the absence of air and moisture, whereby a red liquid complex is formed. A stable liquid catalyst is obtained by also having a hydrocarbon, e.g. hexane, present when the starting materials are independently mixed. The presence of the hydrocarbon is unnecessary when the chlorine-substituted organic compound is carbon tetrachloride. Preferred chlorine-substituted organic compounds may be aliphatic or aromatic and include methylene dichloride, chloroform, carbon tetrachloride, trichloroethylene, tetrachloroethylene, tetrachloroethane, pentachloroethane and chlorobenzene. Some preferred metal compounds of Group IIIb are trimethyl aluminium, triethyl aluminium, tri-isobutyl aluminium, aluminium tri-n-hexyl, trimethyl indium, diethyl aluminium fluoride, ethyl aluminium dihydride. The preferred inorganic metal chlorides are titanium tetrachloride, zirconium tetrachloride and ferric chloride. The polymers produced by the catalysts may be derived from substituted or unsubstituted olefins including vinyl compounds and organic compounds having at least one ethylenic carbonto-carbon double bond, including both acyclic and alicyclic compounds.ALSO:Vinyl-type compounds, i.e. compounds having at least one ethylenic carbon-to-carbon double bond, including both acyclic and alicyclic compounds, are polymerized at a temperature of -100 DEG to 200 DEG C., preferably at -20 DEG to 100 DEG C., in the presence of a catalyst comprising (i) an organo-metallic compound of a metal of Group IIIb, e.g. tri-ethyl aluminium, (ii) a halide of a metal of Groups IVa, Va, VIa, VIIa or VIII, e.g. titanium tetrachloride, and (iii) a chlorine-substituted organic compound, e.g. carbon tetrachloride or trichlorethylene (see Group III). The catalysts are liquid and stable, although stability may be further improved by adding n-hexane. Hence polymerization may be effected in a homogeneous liquid phase and so is easier to control, can be carried out in a simplified apparatus, and the polymer does not become occluded within the catalyst and may be freed from catalyst by simple washing. Vinyl-type compounds which may be polymerized include aliphatic mono-olefins of up to 20 DEG C. atoms, e.g. ethylene, aliphatic polyolefins such as conjugated dienes, e.g. butadiene, halogen-substituted olefins, e.g. vinyl chloride, alkoxy and aryl substituted olefins, e.g. vinyl ethly ether, and monomers containing any combination of halogen, alkoxy and aryl substituents, e.g. phenyltrifluoroethylene. The polymerization is preferably carried out between -20 DEG and 65 DEG C., under pressures of 1-1000 atmospheres and ethylene may be polymerized at room temperature and atmospheric pressure by simply passing it through the catalyst in an open vessel. Examples describe the polymerization of: (Ex. 2-4) trifluorochloroethylene, (Ex. 11) ethylene, (Ex. 12) propylene, (Ex. 14) isobutylene, (Ex. 15) 2-olefins, (Ex. 16, 17) copolymerization of ethylene and propylene, (Ex. 18) butadiene-1,3, (Ex. 19) vinyl chloride, (Ex. 20) styrene, (Ex. 21) vinyl isobutyl ether, (Ex. 22, 23) ethylene, (Ex. 24) 1,1,3-trifluorobutadiene.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US817308XA | 1956-07-02 | 1956-07-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB817308A true GB817308A (en) | 1959-07-29 |
Family
ID=22166022
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB20131/57A Expired GB817308A (en) | 1956-07-02 | 1957-06-26 | Novel catalyst composition, preparation and use thereof |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB817308A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1164096B (en) * | 1962-05-02 | 1964-02-27 | Bayer Ag | Process for the production of polybutadiene |
| DE1253917B (en) * | 1965-05-24 | 1967-11-09 | Bayer Ag | Process for the solution polymerization of isoprene |
| DE1292844B (en) * | 1964-11-10 | 1969-04-17 | Bayer Ag | Process for the polymerization of isoprene |
-
1957
- 1957-06-26 GB GB20131/57A patent/GB817308A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1164096B (en) * | 1962-05-02 | 1964-02-27 | Bayer Ag | Process for the production of polybutadiene |
| DE1292844B (en) * | 1964-11-10 | 1969-04-17 | Bayer Ag | Process for the polymerization of isoprene |
| DE1253917B (en) * | 1965-05-24 | 1967-11-09 | Bayer Ag | Process for the solution polymerization of isoprene |
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