GB634503A - Improvements in or relating to emulsion polymerization - Google Patents
Improvements in or relating to emulsion polymerizationInfo
- Publication number
- GB634503A GB634503A GB5966/47A GB596647A GB634503A GB 634503 A GB634503 A GB 634503A GB 5966/47 A GB5966/47 A GB 5966/47A GB 596647 A GB596647 A GB 596647A GB 634503 A GB634503 A GB 634503A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- sodium
- acids
- potassium
- 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
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
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
In the emulsion polymerization of a mixture of 40 to 100 per cent of a diolefin and 0 to 60 per cent of a mono-olefinic monomer, the monomers are dispersed in water with a catalyst and 0.1 to 1.5 per cent of a "soap," the dispersion is heated with agitation until a latex containing more than 5 per cent solids is obtained, more soap is added in one or more increments or continuously and polymerization continued to produce a concentrated latex of large particle size. The "soaps" are emulsion stabilizers having a hydrophilic alkali metal or ammonium radical and a hydrophilic organic radical. They may be formed in situ. Specified are salts of rosin acids, e.g. pimeric, sapinic, colophonic, abietic and abietinic acids such as sodium abietate and potassium rosinate; of fatty acids, e.g. stearic, beheric, margaric, arachidic, palmitic, myristic, oleic and lauric acids such as sodium, potassium and ammonium oleates; of sulphonic acids, e.g. sodium naphthalene sulphonate; sulphates, e.g. sodium lauryl sulphate; sulphonated ethers R-O-RySO2-OX, esters R-COORySO2-OX, and amides RC-NH-RySO2-OX, where R and Ry are aliphatic monovalent and divalent hydrocarbon radicals respectively and X is alkali metal or ammonium. Also included are neutralized alkylamines, e.g. dodecylamine hydrochloride and substituted alkylamine esters of fatty acids such as diethyl-ethanolamine oleate. Diolefins specified are butadiene-1,3, isoprene and other alkyl-substituted butadienes and the co-monomers may be styrene, acrylonitrile, methacrylonitrile, methyl acrylate, methacrylate and a -chloracrylate, 2,3-dichloro-styrene and vinyl pyridine. Suitable catalysts are potassium persulphate and potassium ferricyanide. The emulsions may contain also n-or tert.-dodecyl mercaptan, trisodium phosphate, and inert hydrocarbons, and the sodium salts of polymerized alkyl naphthalene sulphonic acids. In an example: (2) a butadiene emulsion is heated at 125 DEG F. for 12.5 hours to obtain 20 per cent solids content, when an aqueous solution of sodium hydroxide and a solution of stearic acid in warm styrene are added. After 43.5 hours an aqueous solution of potassium oleate is added and polymerization continued to 59 per cent solids content.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US634503XA | 1946-09-25 | 1946-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB634503A true GB634503A (en) | 1950-03-22 |
Family
ID=22049262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5966/47A Expired GB634503A (en) | 1946-09-25 | 1947-03-03 | Improvements in or relating to emulsion polymerization |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB634503A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1138917B (en) * | 1955-12-30 | 1962-10-31 | Phillips Petroleum Co | Rubber-like copolymer mixtures containing reinforcing filler |
EP0050226A1 (en) * | 1980-10-18 | 1982-04-28 | BASF Aktiengesellschaft | Process for preparing aqueous dispersions of butadiene copolymers by emulsion polymerisation with the addition of resins |
-
1947
- 1947-03-03 GB GB5966/47A patent/GB634503A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1138917B (en) * | 1955-12-30 | 1962-10-31 | Phillips Petroleum Co | Rubber-like copolymer mixtures containing reinforcing filler |
EP0050226A1 (en) * | 1980-10-18 | 1982-04-28 | BASF Aktiengesellschaft | Process for preparing aqueous dispersions of butadiene copolymers by emulsion polymerisation with the addition of resins |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB969115A (en) | Improved process for preparing inter-polymer latexes | |
GB1157068A (en) | Improvements in or relating to Latices | |
GB634503A (en) | Improvements in or relating to emulsion polymerization | |
GB625647A (en) | Production of polymers and copolymers of diolefins | |
GB835674A (en) | Improvements in catalysts for aqueous emulsion polymerizations | |
US3288741A (en) | Glycol and acid salt treatment for increasing the particle size of synthetic rubber latex | |
GB702879A (en) | Improvements in reinforcing synthetic rubber | |
ES482364A1 (en) | Process for the production of rubber latices free from specks and having a high surface tension. | |
GB1179428A (en) | Process for preparing High Solids Concentrated Latex | |
GB961551A (en) | Method of improving the colloidal properties of a high solids synthetic rubber latex | |
GB865863A (en) | Stable emulsifier-free latices and method of preparation thereof | |
US2562191A (en) | Process for coagulating synthetic latices | |
GB572475A (en) | An improved manufacture of vulcanisable polymers from diolefins | |
US3014040A (en) | Method of increasing the particle size of synthetic rubber latex comprising the incorporation of a polyvinylpyridine resin latex therein | |
GB719174A (en) | Improvements in or relating to an aqueous emulsion polymerization process | |
GB745383A (en) | Improvements in or relating to emulsion polymerisation | |
GB1337615A (en) | Latex preparation | |
GB913590A (en) | Production of copolymers of conjugated diolefines and acrylonitrile | |
GB1072694A (en) | Latex compositions | |
US3095398A (en) | Process of increasing the particle size of synthetic rubber latex | |
GB1128114A (en) | Process for preparing agglomerated polystyrene latices | |
GB598322A (en) | Improvements in or relating to the stabilization of synthetic rubber latices | |
US2491433A (en) | Interpolymers of butadiene, acrylonitrile, and a hexadiene | |
US3184424A (en) | Method of making a synthetic rubber latex employing an alkali polyacrylate | |
US3056758A (en) | Butadiene polymer latex treated with a cross-linked polyvinyl methyl ether |