GB590595A - Improved process and apparatus for the polymerisation of iso-olefins - Google Patents
Improved process and apparatus for the polymerisation of iso-olefinsInfo
- Publication number
- GB590595A GB590595A GB477144A GB477144A GB590595A GB 590595 A GB590595 A GB 590595A GB 477144 A GB477144 A GB 477144A GB 477144 A GB477144 A GB 477144A GB 590595 A GB590595 A GB 590595A
- Authority
- GB
- United Kingdom
- Prior art keywords
- liquid
- slurry
- polymer
- cold
- reaction
- 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
- 238000000034 method Methods 0.000 title abstract 2
- 229920000642 polymer Polymers 0.000 abstract 7
- 239000007788 liquid Substances 0.000 abstract 6
- 239000002002 slurry Substances 0.000 abstract 6
- 238000006243 chemical reaction Methods 0.000 abstract 5
- 239000002245 particle Substances 0.000 abstract 4
- 239000005977 Ethylene Substances 0.000 abstract 2
- 150000001350 alkyl halides Chemical class 0.000 abstract 2
- 125000004432 carbon atoms Chemical group C* 0.000 abstract 2
- 239000012295 chemical reaction liquid Substances 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- 229920000098 polyolefin Polymers 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 abstract 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K Aluminium chloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 1
- 229920002456 HOTAIR Polymers 0.000 abstract 1
- UAHWPYUMFXYFJY-UHFFFAOYSA-N Myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 abstract 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N Piperylene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 abstract 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N Sulfuryl chloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 abstract 1
- 229930006719 beta-myrcene Natural products 0.000 abstract 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N carbon bisulphide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 238000007710 freezing Methods 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000003507 refrigerant Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000002904 solvent Substances 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
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/08—Butenes
- C08F210/10—Isobutene
- C08F210/12—Isobutene with conjugated diolefins, e.g. butyl rubber
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
<PICT:0590595/IV/1> <PICT:0590595/IV/2> An iso-olefine having up to 8 carbon atoms with or without a minor proportion of a polyolefine having from 4 to 14 carbon atoms is continuously polymerized at a temperature below -60 DEG F. in the presence of a Friedel-Crafts catalyst, to form a slurry of cold polymer particles in cold reaction liquid, the slurry is withdrawn from the reaction zone and the polymer particles separated from the liquid at substantially the same temperature, the liquid being returned to the reaction zone and the solid particles led into warm water to flush off residual reaction liquid and form an aqueous slurry of polymer. The specified proportions of polymerizable materials comprise from 50-95 per cent of iso-olefine and from 50-5 per cent of a C4 diolefine, or (when used) less than 10 per cent of a C5 or higher diolefine. The preferred iso-olefine is isobutylene and listed polyolefines include butadiene, isoprene, piperylene, dimethyl butadiene, myrcene and dimethylallene. Preferably, the process p is carried out in solution, liquid ethylene and alkyl halides being specified solvents and the Friedal-Crafts catalyst is dissolved in a low-freezing inert solvent, e.g. alkyl halides, carbon disulphide or sulphuryl chloride. In Fig. 1, an internal refrigerant, e.g. liquid ethylene, is used in the continuous polymerization vessel 1 and the cold slurry of polymer is continuously withdrawn through line 9 and pumped to the sump 10 of an enclosed rotary filter 11 operated at the same temperature as the reaction vessel. As the filter drum is rotated a doctor blade 17 removes the polymer which drops on to a vibrating feeder 18 which conducts it into the flash chamber 19. Steam and water are sprayed on to the polymer on an endless screen as it moves past the jets 21. The copolymer is dried, e.g. in a hot air tunnel drier. In Fig. 2, cold slurry from the reaction vessel is pumped through line 61 to an enclosed jacketed or refrigerated chamber 62 provided with a vibrating screen 63. The slurry is distributed from weir box 64 across the screen, cold liquid passing through and is collected and discharged through line 66 back to the reaction system, and polymer particles falling through hopper 72 into heated liquid in the flash chamber 71. Specifications 432,196, 580,407, [Group III], and Australian Specification 112,875 are referred to.
Publications (1)
Publication Number | Publication Date |
---|---|
GB590595A true GB590595A (en) | 1947-07-23 |
Family
ID=1628109
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB477144A Expired GB590595A (en) | 1944-03-14 | Improved process and apparatus for the polymerisation of iso-olefins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB590595A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6743869B2 (en) | 1997-07-15 | 2004-06-01 | Phillips Petroleum Company | High polymer solids slurry polymerization employing 1-olefin comonomer |
WO2013120984A1 (en) * | 2012-02-17 | 2013-08-22 | Basf Se | Method for producing high-molecular-weight polyisobutylene |
US10029230B1 (en) | 2017-01-24 | 2018-07-24 | Chevron Phillips Chemical Company Lp | Flow in a slurry loop reactor |
-
1944
- 1944-03-14 GB GB477144A patent/GB590595A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6743869B2 (en) | 1997-07-15 | 2004-06-01 | Phillips Petroleum Company | High polymer solids slurry polymerization employing 1-olefin comonomer |
US6806324B2 (en) | 1997-07-15 | 2004-10-19 | Phillips Petroleum Company | High solids slurry polymerization using heat exchange to condense the flashed diluent |
WO2013120984A1 (en) * | 2012-02-17 | 2013-08-22 | Basf Se | Method for producing high-molecular-weight polyisobutylene |
US10029230B1 (en) | 2017-01-24 | 2018-07-24 | Chevron Phillips Chemical Company Lp | Flow in a slurry loop reactor |
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