GB629093A - Curing polymerizable materials - Google Patents
Curing polymerizable materialsInfo
- Publication number
- GB629093A GB629093A GB1593546A GB1593546A GB629093A GB 629093 A GB629093 A GB 629093A GB 1593546 A GB1593546 A GB 1593546A GB 1593546 A GB1593546 A GB 1593546A GB 629093 A GB629093 A GB 629093A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- stands
- allyl
- polymerized
- crotyl
- 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)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
<FORM:0629093/IV (a)/1> Substances having a plurality of unconjugated double bonds are polymerized in thick sections by heating at below 180 DEG F. in the presence of an organic peroxide or ozonide, and a cobalt, iron, copper or manganese drier, the inhibitory effect of oxygen present at the surface being counteracted by the metallic drier. The thick section may comprise plies of inert materials. The polymerizable substances specified are diallyl, -crotyl, -methallyl, -alpha methyl allyl, -beta chloroallyl, -beta methyl crotyl esters of maleic, chloromaleic, bromomaleic, fumaric, chlorofumaric, bromofumaric, mesaconic, citraconic, itaconic, carbonic, oxalic, malonic, succinic, glutaric, adipic, pimelic, suberic, az<\>gelaic, sebacic, benzene-, diphenyl-, cyclohexane- or naphthalenedicarboxylic acids, or pyrotartaric acid. Other compounds which can be so polymerized are of the formul in Figs. 2, 3, 4, 5 and 6, in which F stands for an acrylic, methacrylic or a -chloracrylic acid group, B stands for a methylene, methyl methylene or phenylene group. Ru stands for an allyl, crotyl, a -methyl allyl, b -methyl allyl, b -chloro-allyl or b -methyl crotyl group, Du stands for a maleic, chloromaleic, bromomaleic, fumaric, chloro- and bromofumaric, mesaconic, citraconic or itaconic acid group, Rs stands for a methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec. butyl or tert. butyl alcohol group, D stands for all the di-basic acids listed above, E stands for ethylene glycol, propylene glycol, 1,2-butylene glycol, 2,3-butylene glycol, trimethylene glycol, tetramethylene-, pentamethylene-, hexamethylene-, heptamethylene-, octamethylene-glycols, and diethylene-, triethylene- and tetraethylene-glycols, and o-, m- or p-dihydroxybenzene. Driers specified are cobalt, iron, copper and manganese naphthenates, resinates, linoleates or salts of other unsaturated acids. Peroxides and ozonides specified are benzoyl, succinyl, acetyl, toluyl, p-bromobenzoyl, anisoyl, chloroacetyl and furoyl peroxides, peracetic and perbenzoic acids, di-isopropylene ozonide, and diisobutylene ozonide. Inhibitors such as hydroquinone, pyrogallol, tannic acid, aniline or phenylene diamine may be employed. When polyesters are to be polymerized excess polyhydric alcohol may be used and the excess hydroxy groups in the ester may be reacted with phosgene, acetyl chloride, chloroacetyl chloride, succinyl or benzoyl chlorides or silicon tetrachloride, or tetramethylene-, or octamethylene-di-isocyanate or phenyl isocyanate. An excess of polybasic acid may also be used when excess acidic groups may be reacted with a metallic base or with a monohydric alcohol or with an amine such as butylamine, aniline or phenylene diamine. If both free hydroxy and carboxy groups are present in the polyester successive reagents, as set out above, may be used. Styrene, vinyl acetate, methyl methacrylate or methyl acrylate may be used in conjunction with an unsaturated polyester. The substance to be polymerized may be used as a binder for laminated canvas or the like, or may be whipped into a foam to give, on polymerizing, a porous product. Specification 540,168 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1593546A GB629093A (en) | 1946-05-25 | 1946-05-25 | Curing polymerizable materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1593546A GB629093A (en) | 1946-05-25 | 1946-05-25 | Curing polymerizable materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB629093A true GB629093A (en) | 1949-09-12 |
Family
ID=10068189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1593546A Expired GB629093A (en) | 1946-05-25 | 1946-05-25 | Curing polymerizable materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB629093A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3437715A (en) * | 1955-04-15 | 1969-04-08 | Pittsburgh Plate Glass Co | Resin composition |
EP0242791A2 (en) * | 1986-04-25 | 1987-10-28 | Ethyl Corporation | Process for producing polymers of monoallylamine |
WO2008107146A1 (en) * | 2007-03-06 | 2008-09-12 | Dsm Ip Assets B.V. | Pre-accelerated resin composition |
-
1946
- 1946-05-25 GB GB1593546A patent/GB629093A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3437715A (en) * | 1955-04-15 | 1969-04-08 | Pittsburgh Plate Glass Co | Resin composition |
EP0242791A2 (en) * | 1986-04-25 | 1987-10-28 | Ethyl Corporation | Process for producing polymers of monoallylamine |
EP0242791A3 (en) * | 1986-04-25 | 1988-01-07 | Ethyl Corporation | Process for producing polymers of monoallylamine |
WO2008107146A1 (en) * | 2007-03-06 | 2008-09-12 | Dsm Ip Assets B.V. | Pre-accelerated resin composition |
US20100087601A1 (en) * | 2007-03-06 | 2010-04-08 | Dsm Ip Assets B.V. | Pre-accelerated resin composition |
CN101627080B (en) * | 2007-03-06 | 2012-09-26 | 帝斯曼知识产权资产管理有限公司 | Pre-accelerated resin composition |
US8501851B2 (en) | 2007-03-06 | 2013-08-06 | Dsm Ip Assets B.V. | Pre-accelerated resin composition |
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