GB434783A - Manufacture of products of polymerisation - Google Patents

Manufacture of products of polymerisation

Info

Publication number
GB434783A
GB434783A GB3380233A GB3380233A GB434783A GB 434783 A GB434783 A GB 434783A GB 3380233 A GB3380233 A GB 3380233A GB 3380233 A GB3380233 A GB 3380233A GB 434783 A GB434783 A GB 434783A
Authority
GB
United Kingdom
Prior art keywords
heated
benzoyl peroxide
benzine
vinyl
vinyl chloride
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
GB3380233A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB434783A publication Critical patent/GB434783A/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
    • C08F2/00Processes of polymerisation
    • C08F2/04Polymerisation in solution
    • C08F2/06Organic solvent
    • C08F2/08Organic solvent with the aid of dispersing agents for the polymer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Polymerisation Methods In General (AREA)

Abstract

Polymerization products are manufactured by effecting polymerization in the presence of an indifferent organic liquid diluent which does not dissolve the polymerization product, e.g. aliphatic hydrocarbons, alcohols or ethers, and in the presence of an emulsifying agent, e.g. compounds of high molecular weight such as synthetic or natural resins, wax, or derivatives of cellulose or other hydroxy-compounds of high molecular weight, e.g. hydroxyalkylated cellulose. The product remains in the form of an emulsion, which may be used directly, e.g. for impregnating purposes, or separates in a finely divided form. The process is applicable to the polymerization of individual monomeric compounds, e.g. butadiene, vinyl chloride or chloracetate, or of mixtures of monomeric compounds, e.g. of maleic anhydride with styrene or vinyl butyl ether. In examples: (1) maleic anhydride and styrene are heated in the presence of benzine and the reaction product of dodecylic alcohol with ethylene oxide; (2) maleic anhydride and vinyl butyl ether are heated with benzoyl peroxide in the presence of benzine and hydroxyethylated oleic acid; (3) vinyl chloride is heated in a bomb with benzoyl peroxide in the presence of benzine and the reaction product of ethylene oxide on a mixture of alcohols prepared by hydrogenation of coconut oil fatty acids; the resulting emulsion may be employed in the manufacture of coatings resistant to water, acid and alkalies; (4) vinyl chloracetate is heated with benzoyl peroxide in the presence of benzine and a solution of masticated rubber in benzene; the resulting suspension is suitable as a basis for a waterproof lacquer; (5) vinyl chloride is heated in a bomb with benzoyl peroxide in the presence of a mixture of benzine and alcohol and a solution of masticated rubber in benzene; the resulting emulsion may be used in the paint and varnish industry; (6) vinyl chloride and vinyl acetate are heated in a bomb with benzoyl peroxide in the presence of alcohol and the reaction product of castor oil with ethylene oxide; the resulting emulsion, with or without the addition of solvents, may be employed in the paint and varnish industry.ALSO:As coating-compositions may be employed emulsions of polymerization products obtained by effecting polymerization in the presence of an indifferent organic liquid diluent which does not dissolve the polymerization product, e.g. aliphatic hydrocarbons, alcohols or ethers, and in the presence of an emulsifying agent, e.g. compounds of high molecular weight such as synthetic or natural resins, wax, or derivatives of cellulose or other hydroxy compounds of high molecular weight, e.g. hydroxyalkylated cellulose. The process is applicable to the polymerization of individual monomeric compounds, e.g. butadiene, vinyl chloride or chloracetate, or of mixtures of monomeric compounds, e.g. of maleic anhydride with styrene or vinyl butyl ether. In examples: (1) vinyl chloride is heated with benzoyl peroxide in the presence of benzine and the reaction product of ethylene oxide on a mixture of alcohols prepared by hydrogenation of coconut oil fatty acids; the resulting emulsion may be employed in the manufacture of coatings resistant to water, acid and alkalies; (2) vinyl chloracetate is heated with benzoyl peroxide in the presence of benzine and a solution of masticated rubber in benzene; the resulting suspension is suitable as a basis for a waterproof lacquer; (3) vinyl chloride is heated with benzoyl peroxide in the presence of a mixture of benzine and alcohol and a solution of masticated rubber in benzene; the resulting emulsion may be used in the paint and varnish industry; (4) vinyl chloride and vinyl acetate are heated with benzoyl peroxide in the presence of alcohol and the reaction product of castor oil with ethylene oxide; the resulting emulsion, with or without the addition of solvents, may be employed in the paint and varnish industry.
GB3380233A 1932-12-11 1933-12-01 Manufacture of products of polymerisation Expired GB434783A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI46006D DE675146C (en) 1932-12-11 1932-12-11 Method of polymerizing substances containing the vinyl group

Publications (1)

Publication Number Publication Date
GB434783A true GB434783A (en) 1935-09-09

Family

ID=10357624

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3380233A Expired GB434783A (en) 1932-12-11 1933-12-01 Manufacture of products of polymerisation

Country Status (3)

Country Link
DE (1) DE675146C (en)
FR (1) FR765363A (en)
GB (1) GB434783A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE972982C (en) * 1947-01-30 1959-11-12 Heresite & Chemical Company Process for the copolymerization of butadiene with a polymerizable substance from the styrene and acrylonitrile group
USRE28715E (en) 1964-08-12 1976-02-17 Polyurethanes, reactive solutions and methods and their production
USRE29118E (en) 1963-02-06 1977-01-18 Method of preparing polyurethanes from liquid, stable, reactive, film-forming polymer/polyol mixtures formed by polymerizing an ethylenically unsaturated monomer in a polyol
EP0510580A1 (en) * 1991-04-23 1992-10-28 National Starch and Chemical Investment Holding Corporation Polymers and their preparation

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE932456C (en) * 1951-05-05 1955-09-01 Hoechst Ag Process for the production of copolymers with carboxyl groups
NL300246A (en) * 1958-09-04
DE1224504B (en) * 1958-11-05 1966-09-08 Ici Ltd Process for the production of polymer dispersions in hydrocarbons

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE972982C (en) * 1947-01-30 1959-11-12 Heresite & Chemical Company Process for the copolymerization of butadiene with a polymerizable substance from the styrene and acrylonitrile group
USRE29118E (en) 1963-02-06 1977-01-18 Method of preparing polyurethanes from liquid, stable, reactive, film-forming polymer/polyol mixtures formed by polymerizing an ethylenically unsaturated monomer in a polyol
USRE28715E (en) 1964-08-12 1976-02-17 Polyurethanes, reactive solutions and methods and their production
EP0510580A1 (en) * 1991-04-23 1992-10-28 National Starch and Chemical Investment Holding Corporation Polymers and their preparation
AU661683B2 (en) * 1991-04-23 1995-08-03 National Starch And Chemical Investment Holding Corporation Polymers & their preparation

Also Published As

Publication number Publication date
DE675146C (en) 1939-05-02
FR765363A (en) 1934-06-07

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