GB745927A - Improvements in or relating to emulsion polymerisation - Google Patents
Improvements in or relating to emulsion polymerisationInfo
- Publication number
- GB745927A GB745927A GB1194053A GB1194053A GB745927A GB 745927 A GB745927 A GB 745927A GB 1194053 A GB1194053 A GB 1194053A GB 1194053 A GB1194053 A GB 1194053A GB 745927 A GB745927 A GB 745927A
- Authority
- GB
- United Kingdom
- Prior art keywords
- potassium
- added
- emulsifier
- sodium
- per cent
- 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)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
Abstract
A mixture of butadiene and a compound containing a single olefinic double bond, containing less than 40 per cent butadiene, is copolymerized in the presence of an aqueous phase containing 0.05 to 0.5 per cent of an emulsifier which is an alkali metal salt of a long chain fatty acid (such as sodium or potassium stearate) or of a sulphated or sulphonated fatty acid, or sodium or potassium lauryl or cetyl sulphate, further emulsifier being added only when at least 5 per cent of the monomers have been copolymerized. The additional emulsifier may be added intermittently or continuously and, further, at the end of the reaction additional emulsifier, which may be different, e.g. condensates of ethylene oxide with oleyl alcohol or dioctyl cresol, or sodium b -naphthalene sulphonate/formaldehyde condensate, may also be added. Olefinic monomers specified are styrene, a -methyl styrene; vinyl carbazole, acetate and pyridine; acrylonitrile, methacrylonitrile; methyl acrylate, methacrylate and a -chloroacrylate; methacrylamide and methacrylic acid. Additional monomeric material and water may also be added as the polymerization proceeds. The mixture preferably contains a polymerization modifier such as mercaptans of six to eighteen carbon atoms, e.g. t-dodecyl and lauryl mercaptans, and organic polysulphides such as di(s-butyl)-, di-(2-methyl butyl)-, dialkyl xanthogen and di-o-dinitrophenyl disulphides. Catalysts, which are preferably used, include hydrogen peroxide, potassium persulphate and redox systems such as cumene hydroperoxide or benzoyl peroxide together with ferrous sulphate/potassium pyrophosphate complex and sorbose or fructose. Methanol may be included in low temperature systems and t-butyl catechol may be used as an inhibitor. Example III includes potassium hydroxide and chloride as buffer. Particles of large size may be obtained by using a portion of latex, produced as above, as seed in a second polymerization. The dispersions obtained are of high solid content and low viscosity and may be used in paints, lacquers, paper coating, leather finishing and strengthening foamed latex of natural or synthetic rubber. Specification 724,139 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1194053A GB745927A (en) | 1953-04-30 | 1953-04-30 | Improvements in or relating to emulsion polymerisation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1194053A GB745927A (en) | 1953-04-30 | 1953-04-30 | Improvements in or relating to emulsion polymerisation |
Publications (1)
Publication Number | Publication Date |
---|---|
GB745927A true GB745927A (en) | 1956-03-07 |
Family
ID=9995441
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1194053A Expired GB745927A (en) | 1953-04-30 | 1953-04-30 | Improvements in or relating to emulsion polymerisation |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB745927A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3052645A (en) * | 1957-12-31 | 1962-09-04 | Copolymer Rubber & Chem Corp | Process for separating unreacted polymerizable material from diene polymer latex in the presence of a long chain aliphatic alcohol |
US4623695A (en) | 1984-01-25 | 1986-11-18 | Henkel Kommanditgesellschaft Auf Aktien | Acrylate hydrosols |
US4661557A (en) * | 1984-06-28 | 1987-04-28 | Basf Aktiengesellschaft | Preparation of stable aqueous polymer dispersions which contain an alkenyl-aromatic compound as copolymerized units |
-
1953
- 1953-04-30 GB GB1194053A patent/GB745927A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3052645A (en) * | 1957-12-31 | 1962-09-04 | Copolymer Rubber & Chem Corp | Process for separating unreacted polymerizable material from diene polymer latex in the presence of a long chain aliphatic alcohol |
US4623695A (en) | 1984-01-25 | 1986-11-18 | Henkel Kommanditgesellschaft Auf Aktien | Acrylate hydrosols |
US4661557A (en) * | 1984-06-28 | 1987-04-28 | Basf Aktiengesellschaft | Preparation of stable aqueous polymer dispersions which contain an alkenyl-aromatic compound as copolymerized units |
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