GB753322A - Styrene copolymer emulsions - Google Patents
Styrene copolymer emulsionsInfo
- Publication number
- GB753322A GB753322A GB1816253A GB1816253A GB753322A GB 753322 A GB753322 A GB 753322A GB 1816253 A GB1816253 A GB 1816253A GB 1816253 A GB1816253 A GB 1816253A GB 753322 A GB753322 A GB 753322A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acrylic
- acids
- butyl
- esters
- methacrylic
- 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
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Styrene is copolymerized with at least two polymerizable esters of ethylenic carboxylic acids of 3 to 5 carbon atoms and having at least two hydrogen atoms attached to the ethylenically linked carbon atoms, the copolymerization being in emulsion in an aqueous solution of one or more hydrophilic colloids and in the presence of one or more plasticizers, one or more free radical catalysts and one or more surface-active agents. Esters specified are the alkyl and substituted alkyl esters of acrylic, methacrylic, crotonic, 2-chloroacrylic and maleic acids, as exemplified by methyl and butyl methacrylates and di-(ethyl hexyl) maleate. The colloids may be the alkali metal and ammonium salts of polyacrylic and polymethacrylic acids, of styrene copolymers with acrylic and/or methacrylic acids, of copolymers of acrylic and/or methacrylic acid esters with acrylic and/or methacrylic acids, and of styrene-maleic acid copolymers; the water soluble ethers of cellulose and starch; degraded starch; dextrin; pectin; salts of carboxy methyl cellulose; and gums such as arabic and tragacanth. Plasticizers listed are chlorinated diphenyls; tricresyl and tributyl phosphates; di-butyl, dioctyl, di-butoxy-ethyl and butyl benzyl phthalates and tri-ethyleneglycol hexoate. Catalysts disclosed are hydrogen, benzoyl and di-t.-butyl peroxides, cumene hydroperoxide and potassium persulphate. A number of conventional surface-active agents are listed. Molecular weight regulators such as carbon tetrachloride, chloroform, bromoform and hexachloroethane may be used and the rate of radical formation of the catalyst may be adjusted with compounds such as ferrous compounds, hydrazine hydrate, sulphoxylates, sulphites, cane sugar, glucose, dodecyl mercaptan, diisopropyl xanthogen disulphide, mercaptobenzthiazyl disulphide, mercaptobenzthiazol, zinc isopropyl zanthate, cyclohexyl amine, ammonium diethyl dithiocarbamate and formic acid or its salts. Other materials included in the examples are hydroquinone and ammonia. The reaction mixture may be replenished by continuous or intermittent addition of any or all of the components as is illustrated in the examples. The products are of particle size less than 2 microns and are useful in emulsion paints, coating compositions, adhesives and in impregnants for porous materials.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1816253A GB753322A (en) | 1953-06-30 | 1953-06-30 | Styrene copolymer emulsions |
FR1107760D FR1107760A (en) | 1953-06-30 | 1954-06-29 | Process for preparing emulsions of styrene copolymers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1816253A GB753322A (en) | 1953-06-30 | 1953-06-30 | Styrene copolymer emulsions |
Publications (1)
Publication Number | Publication Date |
---|---|
GB753322A true GB753322A (en) | 1956-07-25 |
Family
ID=10107709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1816253A Expired GB753322A (en) | 1953-06-30 | 1953-06-30 | Styrene copolymer emulsions |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1107760A (en) |
GB (1) | GB753322A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3037952A (en) * | 1957-12-12 | 1962-06-05 | Rohm & Haas | Aqueous compositions comprising water insoluble linear polymer and an ammonium salt of a copolymer of methyl methacrylate and acrylic acid monomer and article coated therewith |
-
1953
- 1953-06-30 GB GB1816253A patent/GB753322A/en not_active Expired
-
1954
- 1954-06-29 FR FR1107760D patent/FR1107760A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3037952A (en) * | 1957-12-12 | 1962-06-05 | Rohm & Haas | Aqueous compositions comprising water insoluble linear polymer and an ammonium salt of a copolymer of methyl methacrylate and acrylic acid monomer and article coated therewith |
Also Published As
Publication number | Publication date |
---|---|
FR1107760A (en) | 1956-01-05 |
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