GB821093A - Polymerisation of unsaturated organic compounds - Google Patents
Polymerisation of unsaturated organic compoundsInfo
- Publication number
- GB821093A GB821093A GB458155A GB458155A GB821093A GB 821093 A GB821093 A GB 821093A GB 458155 A GB458155 A GB 458155A GB 458155 A GB458155 A GB 458155A GB 821093 A GB821093 A GB 821093A
- Authority
- GB
- United Kingdom
- Prior art keywords
- allyl
- alkali metal
- salts
- esters
- styrene
- 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
- C08F2/00—Processes of polymerisation
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
Aqueous dispersions of polymers, of average molecular weight of at least 3000, of allyl esters of carboxylic acids of formula XCOOH where X represents an aryl or substituted aryl radical, HOOC(CH2)n or R(CH2)n where n is 1 to 16 and R is a hydrogen atom or an alkyl, alkenyl, alkoxy, epoxy or hydroxyl radical or any combination thereof, are prepared by polymerizing the ester in the presence of water, a dispersion stabilizer and a polymerization catalyst, the feed ratio of monomer to water being from 10/90 to 70/30 parts by weight. The dispersion may be an emulsion or a granular or bead suspension. The allyl ester may be diallyl sebacate, diallyl phthalate or allyl caproate. Comonomers, when employed, may be vinyl or allyl esters of carboxylic acids, e.g. vinyl acetate, allyl acetate and diallyl phthalate, styrene, a -methyl styrene, acrylonitrile, methacrylic acid esters, e.g. methyl methacrylate, vinyl chloride or vinylidene chloride. Specified dispersion stabilizers are polyvinyl alcohol, partially hydrolysed polyvinyl acetate, acrylic and methacrylic acid polymers and salts thereof, alkali metal salts of styrene-maleic acid resins, potassium palmitate, sodium oleate, triethanolamine soaps, rosin soaps, sulphonated oils, alcohols and esters, sulphated compounds, salts of sulphosuccinic acid esters, cetyl trimethyl ammonium chloride, cetyl pyridinium bromide, alkali metal phosphonium halides, alkali metal sulphonium halides, ethylene oxide condensates with fatty alcohols, fatty acids, alkylphenols and castor oil, gum arabic, gum tragacanth, casein, lecithin, gelatin, alginates, calcium, barium and magnesium carbonates, silicates, sulphates and phosphates, alumina, fuller's earth, milk of magnesia, talc and bentonite. The catalyst may be diazaminobenzene, hydrogen peroxide, sodium peroxide, ammonium persulphate, sodium perborate, tertiary butyl hydroperoxide, cumene hydroperoxide and benzoyl peroxide, optionally together with activators, e.g. alkali metal thiosulphates, sulphites, bisulphites, metabisulphites, hydrosulphites and sulphoxylates, hydroxylamine and its salts, hydrazine, dextrose, ferrous ammonium sulphate and copper sulphate. Electrolytes and thickeners may be added and the density of the medium adjusted by adding ethylene glycol or glycerol. Polymerization may be effected by heat or ultra-violet light, preferably under an inert atmosphere, e.g. of nitrogen, by batch or continuous processes. The reactants may be added, mixed or separately, portionwise as the reaction proceeds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB458155A GB821093A (en) | 1955-02-16 | 1955-02-16 | Polymerisation of unsaturated organic compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB458155A GB821093A (en) | 1955-02-16 | 1955-02-16 | Polymerisation of unsaturated organic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB821093A true GB821093A (en) | 1959-09-30 |
Family
ID=9779861
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB458155A Expired GB821093A (en) | 1955-02-16 | 1955-02-16 | Polymerisation of unsaturated organic compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB821093A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1183685B (en) * | 1963-01-17 | 1964-12-17 | Goldschmidt Ag Th | Process for the production of stable and finely divided dispersions of prepolymers from allyl esters of polybasic carboxylic acids |
US3975349A (en) | 1974-09-06 | 1976-08-17 | Osaka Soda Co., Ltd. | Process for preparing diallyl phthalate latex |
-
1955
- 1955-02-16 GB GB458155A patent/GB821093A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1183685B (en) * | 1963-01-17 | 1964-12-17 | Goldschmidt Ag Th | Process for the production of stable and finely divided dispersions of prepolymers from allyl esters of polybasic carboxylic acids |
US3975349A (en) | 1974-09-06 | 1976-08-17 | Osaka Soda Co., Ltd. | Process for preparing diallyl phthalate latex |
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