GB1057723A - Polymeric thickening agents - Google Patents

Polymeric thickening agents

Info

Publication number
GB1057723A
GB1057723A GB772663A GB772663A GB1057723A GB 1057723 A GB1057723 A GB 1057723A GB 772663 A GB772663 A GB 772663A GB 772663 A GB772663 A GB 772663A GB 1057723 A GB1057723 A GB 1057723A
Authority
GB
United Kingdom
Prior art keywords
acid
butyl
ammonium
copolymer
compositions
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
GB772663A
Inventor
Kenneth Elliott Piggott
Wilfred Bernard Smith
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.)
Styrene Co Polymers Ltd
Original Assignee
Styrene Co Polymers 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 Styrene Co Polymers Ltd filed Critical Styrene Co Polymers Ltd
Priority to GB772663A priority Critical patent/GB1057723A/en
Publication of GB1057723A publication Critical patent/GB1057723A/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
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/52Amides or imides
    • C08F20/54Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
    • C08F20/58Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-acryloylmorpholine

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Novel water-soluble copolymer salts are prepared by polymerizing in aqueous emulsion an N-alkoxyalkyl or N-cycloalkoxyalkyl derivative of an ethylenically unsaturated amide and an a ,b -ethylenically unsaturated carboxylic acid, and reacting the product with a basic substance, e.g. an alkali metal or ammonium hydroxide, or an organic base, e.g. diethylamine, morpholine, hydrazine or dimethylaminoethanol. The amide monomer is suitably a compound of the formula <FORM:1057723/C3/1> in which R is an alkyl or cycloalkyl radical having up to twelve carbon atoms and R1 is hydrogen, chlorine or a cyano or alkyl radical. Acid comonomers specified are acrylic acid, methacrylic acid, itaconic acid, maleic acid and fumaric acid; derivatives of suitable polycarboxylic acids, e.g. partial esters, having at least one free carboxylic acid group may also be used. Other monomers may additionally be used, e.g. styrene, vinyl toluene, methyl methacrylate, ethyl acrylate, di-n-butyl itaconate, di-n-butyl maleate, di-n-octyl maleate, acrylonitrile, 2-hydroxyethyl methacrylate, 2-hydroxy propyl methacrylate, divinylbenzene, glycol dimethacrylate and methylene-bis-acrylamide. In examples, N-n-butoxy methylacrylamide, ethyl acrylate, methyl methacrylate and methacrylic acid are emulsion polymerized using ammonium persulphate catalyst, sodium N-methyl-N-oleoyl-taurate emulsifier and lauryl mercaptan modifier, part of the components being added during the course of polymerization, and the product is neutralized with ammonia or dimethylamino-ethanol. The water-soluble copolymer salts can be rendered insoluble by curing and are suitable as thickening agents in coating compositions and textile-treating compositions. In the examples, such compositions include the following ingredients: red iron oxide, barytes, talc, tri-n-butyl phosphate, ethylene glycol mono-n-butyl ether, titanium dioxide, isophorone, calcium carbonate, methyl cellulose, polyacrylic acid (Trade Mark Primal ), polyvinyl acetate, ammonium chloride and a styrene-n-butyl acrylate - N - cyclohexyloxymethyl - acrylamide copolymer. Reference has been directed by the Comptroller to Specification 792,874.ALSO:Compositions suitable for coating steel, aluminium and asbestos (e.g. priming and lacquer compositions) and for application to textiles, e.g. cotton fabric, comprise as thickener a water-soluble inorganic (e.g. alkali metal or ammonium) or organic base salt of a copolymer comprising as essential components units of an N-alkoxy alkyl or N-cyclo-alkoxy alkyl deravative of an ethylenically unsaturated amide and units of an a , b -ethylenically unsaturated carboxylic acid. The thickener can be cured to a water-insoluble form. Exemplified thickeners are the ammonium and dimethyl-aminoethanol salts of a copolymer of N-n-butoxymethylacrylamide, ethyl acrylate, methyl methacrylate and methacrylic acid. Other ingredients included in the coating compositions illustrated are red iron oxide, barytes, talc, tri-n-butyl phosphate, ethylene glycol mono-n-butyl ether, titanium dioxide, isophorone, calcium carbonate, methylcellulose, polyacrylic acid (Trade Mark "Primal"), polyvinyl acetate, ammonium chloride and a styrene-n-butyl acrylate-N-cyclohexyloxymethyl-acrylamide copolymer. Reference has been directed by the Comptroller to Specification 792,874.
GB772663A 1963-02-26 1963-02-26 Polymeric thickening agents Expired GB1057723A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB772663A GB1057723A (en) 1963-02-26 1963-02-26 Polymeric thickening agents

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB772663A GB1057723A (en) 1963-02-26 1963-02-26 Polymeric thickening agents

Publications (1)

Publication Number Publication Date
GB1057723A true GB1057723A (en) 1967-02-08

Family

ID=9838575

Family Applications (1)

Application Number Title Priority Date Filing Date
GB772663A Expired GB1057723A (en) 1963-02-26 1963-02-26 Polymeric thickening agents

Country Status (1)

Country Link
GB (1) GB1057723A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004045755A2 (en) * 2002-11-20 2004-06-03 Efka Additives B.V. Aqueous emulsion polymer as dispersant

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004045755A2 (en) * 2002-11-20 2004-06-03 Efka Additives B.V. Aqueous emulsion polymer as dispersant
WO2004045755A3 (en) * 2002-11-20 2004-07-29 Efka Additives B V Aqueous emulsion polymer as dispersant
CN100364649C (en) * 2002-11-20 2008-01-30 埃弗卡添加剂股份有限公司 Aqueous emulsion polymer as dispersant
US8822592B2 (en) 2002-11-20 2014-09-02 Basf Se Aqueous emulsion polymer as dispersant

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