GB804448A - Polymerisation of vinyl halides - Google Patents

Polymerisation of vinyl halides

Info

Publication number
GB804448A
GB804448A GB25933/56A GB2593356A GB804448A GB 804448 A GB804448 A GB 804448A GB 25933/56 A GB25933/56 A GB 25933/56A GB 2593356 A GB2593356 A GB 2593356A GB 804448 A GB804448 A GB 804448A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
maleic
polymerization
ethylene
interpolymer
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
GB25933/56A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
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 Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB804448A publication Critical patent/GB804448A/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
    • C08F263/00Macromolecular compounds obtained by polymerising monomers on to polymers of esters of unsaturated alcohols with saturated acids as defined in group C08F18/00
    • C08F263/02Macromolecular compounds obtained by polymerising monomers on to polymers of esters of unsaturated alcohols with saturated acids as defined in group C08F18/00 on to polymers of vinyl esters with monocarboxylic acids
    • C08F263/04Macromolecular compounds obtained by polymerising monomers on to polymers of esters of unsaturated alcohols with saturated acids as defined in group C08F18/00 on to polymers of vinyl esters with monocarboxylic acids on to polymers of vinyl acetate
    • 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
    • C08F14/00Homopolymers and 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 a halogen
    • C08F14/02Monomers containing chlorine
    • C08F14/04Monomers containing two carbon atoms
    • C08F14/06Vinyl chloride
    • 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
    • C08F267/00Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated polycarboxylic acids or derivatives thereof as defined in group C08F22/00
    • C08F267/04Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated polycarboxylic acids or derivatives thereof as defined in group C08F22/00 on to polymers of anhydrides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Polymers and copolymers of vinyl halides containing a halogen having an atomic number not exceeding 35, are made by polymerization in aqueous dispersion in the presence of (1) an interpolymer of ethylene and maleic anhydride of specific viscosity at least 1.1, determined in 1 per cent dimethylformamide solution at 25 DEG C.; or (2) an interpolymer of ethylene and maleic acid obtainable by hydrolysis of an interpolymer under (1); or (3) a partial ester of an interpolymer under (1) or (2) having up to 15 mol. per cent of the carboxyl and/or anhydride groups esterified with a monohydric acyclic, carbocyclic or heterocyclic alcohol or a monohydric phenol containing up to 10 carbon atoms which is free from groups, other than hydroxyl groups, which will react with a carboxyl or carboxylic anhydride group and does not constitute more than 20 per cent by weight of the molecule of the partial ester, all of said interpolymers being free from salt groups. The vinyl halide may be vinyl fluoride, chloride or bromide and copolymers may be made with vinyl acetate, propionate, butyrate or benzoate or methyl, ethyl, butyl or allyl acrylates or methacrylates or acrylamide, acrylanilide, acrylonitrile, vinylidene chloride, trichloroethylene or the methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, allyl or methallyl esters of maleic, citraconic, itaconic or fumaric acids. The ethylenemaleic interpolymers may be made by heating maleic acid or anhydride in an aromatic solvent, e.g. benzene, with ethylene under pressure and in the presence of a catalyst. The maleic interpolymer may be partially esterified after polymerization or partially esterified maleic acid or anhydride may be used in the polymerization or the esterification may take place simultaneously with the polymerization. The interpolymers usually contain substantially equimolar proportions of ethylene and the maleic constituent. The monohydric alcohol may be methanol, ethanol, isopropanol, n-propanol, methoxyethanol, n-butanol, n-hexanol, octanol, n-decanol, cyclopentanol, cyclohexanol, phenol, cresol, xylenol or tetrahydrofurfuryl alcohol. In the vinyl halide polymerization there may be present in addition to the maleic-ethylene interpolymers particle size reducing agents such as unsaturated aliphatic carboxylic acids having 10 to 20 carbon atoms or their halogen-substituted derivatives, hydroxyl-substituted aliphatic carboxylic acids having 10 to 20 carbon atoms or partial esters of polyhydric alcohols having 2 to 8 carbon atoms with aliphatic carboxylic acids having 10 to 20 carbon atoms, e.g. glyceryl mono-octadecanoate. There may also be present during the polymerization plasticizers such as dialkyl phthalates in which the alkyl groups contain 2 to 10 carbon atoms, e.g. dibutyl phthalate, esters of glycols containing not more than 10 carbon atoms with fatty acids containing 2 to 9 carbon atoms or phosphoric acid esters of phenol, the cresols and the xylenols and there may be used as catalysts benzoyl, lauroyl, ditertiary butyl, oleyl or toluyl peroxides.
GB25933/56A 1955-08-25 1956-08-24 Polymerisation of vinyl halides Expired GB804448A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US804448XA 1955-08-25 1955-08-25

Publications (1)

Publication Number Publication Date
GB804448A true GB804448A (en) 1958-11-19

Family

ID=22157426

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25933/56A Expired GB804448A (en) 1955-08-25 1956-08-24 Polymerisation of vinyl halides

Country Status (1)

Country Link
GB (1) GB804448A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0492712A1 (en) * 1990-12-24 1992-07-01 Akzo Nobel N.V. Peroxide compositions with ethoxylated water-soluble polymers
US5508365A (en) * 1992-03-30 1996-04-16 Sumitomo Chemical Company, Limited Method of producing vinyl chloride resins having improved moldability and processability using mixtures of fatty acid esters

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0492712A1 (en) * 1990-12-24 1992-07-01 Akzo Nobel N.V. Peroxide compositions with ethoxylated water-soluble polymers
US5508365A (en) * 1992-03-30 1996-04-16 Sumitomo Chemical Company, Limited Method of producing vinyl chloride resins having improved moldability and processability using mixtures of fatty acid esters

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