GB634503A - Improvements in or relating to emulsion polymerization - Google Patents

Improvements in or relating to emulsion polymerization

Info

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
Application number
GB5966/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wingfoot Corp
Original Assignee
Wingfoot Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Wingfoot Corp filed Critical Wingfoot Corp
Publication of GB634503A publication Critical patent/GB634503A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers 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
    • C08F36/04Homopolymers 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.
GB5966/47A 1946-09-25 1947-03-03 Improvements in or relating to emulsion polymerization Expired GB634503A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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