GB745927A - Improvements in or relating to emulsion polymerisation - Google Patents

Improvements in or relating to emulsion polymerisation

Info

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
Application number
GB1194053A
Inventor
Peter George Edgerley
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1194053A priority Critical patent/GB745927A/en
Publication of GB745927A publication Critical patent/GB745927A/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)
  • 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.
GB1194053A 1953-04-30 1953-04-30 Improvements in or relating to emulsion polymerisation Expired GB745927A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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