GB1329859A - Polymerisation process - Google Patents
Polymerisation processInfo
- Publication number
- GB1329859A GB1329859A GB1329859DA GB1329859A GB 1329859 A GB1329859 A GB 1329859A GB 1329859D A GB1329859D A GB 1329859DA GB 1329859 A GB1329859 A GB 1329859A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymerization
- styrene
- acrylonitrile
- compound
- monomer
- 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
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
- C08F4/28—Oxygen or compounds releasing free oxygen
- C08F4/32—Organic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
Abstract
1329859 Initiators in addition polymerization processes MONSANTO CHEMICALS Ltd 6 Oct 1971 [6 Nov 1970] 52863/70 Heading C3P An initiating system for the polymerization of olefinically unsaturated monomers comprises a main initiator and, as a coinitiator which encourages the polymerization of substantially all the monomer, a compound of the formula in which each R is a C 1-4 alkyl group. The preferred compound is 1,1,4,4,7,7-hexamethylcyclo-4, 7-diperoxynonane. The main initiator is preferably of the free radical type such as a dialkyl or diacyl peroxide, cumene hydroperoxide, an alkyl perester, or an azodiisobutyronitrile or similar compound. Any monomer or monomer mixture may be polymerized, and the polymerization may be by any well known method. Bulk polymerization is preferred, at 85-220‹ C., especially where a prepolymer is formed in one vessel, and then subsequently transferred to further vessels until polymerization is complete. In the example styrene is bulk polymerized using ditertiary butyl peroxide and the above preferred compound. Other monomers specified are α-methylstyrene, vinyl toluene, methyl acrylate or methacrylate, vinyl chloride, acrylonitrile, methacrylonitrile, styrene/acrylonitrile, styrene/butadiene, or styrene/divinyl benzene. A graft polymer e.g. of styrene and acrylonitrile or polybutadiene, may also be produced.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5286370 | 1970-11-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1329859A true GB1329859A (en) | 1973-09-12 |
Family
ID=10465608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1329859D Expired GB1329859A (en) | 1970-11-06 | 1970-11-06 | Polymerisation process |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1329859A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2600656A1 (en) | 1975-06-30 | 1977-01-27 | Argus Chem | CYCLIC PERKETALS AND THEIR USE FOR CROSS-LINKING HIGH DENSITY POLYAETHYLENE |
DE2756035A1 (en) * | 1977-01-06 | 1978-07-13 | Pennwalt Corp | METHOD FOR RADICAL CHAIN POLYMERIZATION OF VINYL MONOMERS |
US4197244A (en) * | 1975-06-30 | 1980-04-08 | Argus Chemical Corporation | Cyclic perketals and their use for cross-linking high density polyethylene |
US4267109A (en) | 1975-06-30 | 1981-05-12 | Argus Chemical Corporation | Cyclic perketals and their use for cross-linking high density polyethylene |
WO1996027620A1 (en) * | 1995-03-06 | 1996-09-12 | Akzo Nobel N.V. | Cyclic ketone peroxides as polymer initiators |
WO1997026283A1 (en) * | 1996-01-16 | 1997-07-24 | The Dow Chemical Company | Free radical polymerization |
-
1970
- 1970-11-06 GB GB1329859D patent/GB1329859A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2600656A1 (en) | 1975-06-30 | 1977-01-27 | Argus Chem | CYCLIC PERKETALS AND THEIR USE FOR CROSS-LINKING HIGH DENSITY POLYAETHYLENE |
US4197244A (en) * | 1975-06-30 | 1980-04-08 | Argus Chemical Corporation | Cyclic perketals and their use for cross-linking high density polyethylene |
US4267109A (en) | 1975-06-30 | 1981-05-12 | Argus Chemical Corporation | Cyclic perketals and their use for cross-linking high density polyethylene |
DE2660923C2 (en) * | 1975-06-30 | 1987-03-19 | Argus Chemical Corp., New York, N.Y. | Mass for producing cross-linked high density polyethylene and process for its production |
DE2756035A1 (en) * | 1977-01-06 | 1978-07-13 | Pennwalt Corp | METHOD FOR RADICAL CHAIN POLYMERIZATION OF VINYL MONOMERS |
WO1996027620A1 (en) * | 1995-03-06 | 1996-09-12 | Akzo Nobel N.V. | Cyclic ketone peroxides as polymer initiators |
WO1997026283A1 (en) * | 1996-01-16 | 1997-07-24 | The Dow Chemical Company | Free radical polymerization |
AU709727B2 (en) * | 1996-01-16 | 1999-09-02 | Dow Chemical Company, The | Free radical polymerization |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |