GB1049027A - Spontaneously cross-linking polymers - Google Patents

Spontaneously cross-linking polymers

Info

Publication number
GB1049027A
GB1049027A GB22136/64A GB2213664A GB1049027A GB 1049027 A GB1049027 A GB 1049027A GB 22136/64 A GB22136/64 A GB 22136/64A GB 2213664 A GB2213664 A GB 2213664A GB 1049027 A GB1049027 A GB 1049027A
Authority
GB
United Kingdom
Prior art keywords
alkyl
acid
ester
compound
group
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
GB22136/64A
Inventor
Erwin Muller
Karl Dinges
Oskar Glenz
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Publication of GB1049027A publication Critical patent/GB1049027A/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
    • C08F20/60Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen

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

Spontaneously cross-linking copolymers are prepared by copolymerizing, in an aqueous medium containing from 0.01 to 5% by weight of a polymerization catalyst and from 0.5 to 20% by weight of an emulsifier, (a) 0.5 to 40% (based on the total monomer weight) of a monomer of the formula <FORM:1049027/C3/1> in which R is hydrogen or a methyl group and X is an organic radical which is bonded to the -CH2- group by way of nitrogen and which contains at least one grouping of the formula <FORM:1049027/C3/2> in which R1 represents an alkyl group; (b) 0 to 20% of a polymerizable, monoolefinically unsaturated compound containing either an amido group or at least one hydroxyl group; (c) 0 to 20% of a compound of the formula <FORM:1049027/C3/3> in which R is hydrogen or a methyl group and R11 is a C1-C8 alkyl radical or a carboxylic acyl radical; (d) 99.5 to 40% of at least one polymerizable vinyl compound, which is a (C1-C12 alkyl) ester of acrylic acid, a (C8-C12 alkyl) ester of methacrylic acid, a C4-C6 conjugated aliphatic diene or a vinyl (C1-C4 alkyl) ether; (e) 0 to 50% of at least one polymerizable vinyl compound which is an aromatic monovinyl compound of the benzene series, an a ,b -olefinically unsaturated aliphatic nitrile, a vinyl or vinylidene halide, a (C1-C4 alkyl) ester of methacrylic acid, an a ,b -olefinically unsaturated aliphatic monocarboxylic acid, a vinyl ester of a C2-C3 carboxylic acid, or itaconic acid. Monomers (a) exemplified are the acyclic and heterocyclic compounds obtained by reacting acrylamide or methacrylamide with various melamine or urea derivatives containing at least two <FORM:1049027/C3/4> groups (1 mole of alcohol R1OH being evolved in the reaction). Monomers (b) specified are acrylamide, methacrylamide, and the esterification products of 1 mole of an a ,b -olefinically unsaturated monocarboxylic acid such as acrylic or methacrylic acid with 1 mole of a polyhydric alcohol such as ethylene, propylene or butylene glycol, glycerol trimethylolpropane or pentaerythritol, e.g. b -hydroxy ethyl acrylate or methacrylate and b -hydroxy-n-propyl acrylate or methacrylate. Up to 5% by weight of a compound containing a plurality of non-conjugated polymerizable groups, e.g. divinyl benzene, may be included in the monomer reactants. The emulsifier used may be of the cationic, anionic or nonionic type or a combination thereof (several examples of each type are disclosed). Polymerization is generally effected at 10-80 DEG C. and at a pH of from 4 to 9. A dispersed organic solvent may be included in the aqueous polymerization medium. Catalysts specified are potassium and ammonium persulphate, hydrogen peroxide, percarbonates, benzoyl peroxide, t.-butyl hydroperoxide, cumene hydroperoxide, p-menthane hydroperoxide and di-t.-butyl peroxide; and combinations thereof with reducing agents such as sodium pyrosulphite or bisulphite, sodium formaldehyde sulphoxylate and triethanolamine. Molecular weight regulators may be used, e.g. alkyl mercaptans and diisopropyl xanthate. Some or all of the monomers may be added in portions or continuously during polymerization, and the process can be conducted in two or more stages with different monomer compositions, if desired, at each stage. In one example (16) polymerization is terminated at 80% monomer conversion by the addition of sodium dithionite. The process may also be applied to the production of graft polymers, the specified monomers being copolymerized in the presence of 3 to 50% by weight (based on the total weight of monomers and polymer) of polymers or copolymers of conjugated diolefines, e.g. butadiene, or other preformed polymers which contain free olefinic double bonds. The copolymer dispersions are useful for coating paper and leather.ALSO:Aqueous dispersions suitable for coating paper and leather comprise together with an emulsifier (cationic, anionic or non-ionic) a spontaneously cross-linking copolymer of (a) 0.5 to 40% (based on the total monomer weight) of a monomer of the formula <FORM:1049027/B1-B2/1> in which R is hydrogen or a methyl group and X is an organic radical which is bonded to the -CH2-group by way of nitrogen and which contains at least one grouping of the formula <FORM:1049027/B1-B2/2> in which R1 represents an alkyl group; (b) 0 to 20% of a polymerisable, monodefinically unsaturated compound containing either an amido group or at least one hydroxyl group; (c) 0 to 20% of a compound of the formula <FORM:1049027/B1-B2/3> in which R is hydrogen or a methyl group and R11 is a C1 - C8 alkyl radical or a carboxylic acyl radical; (d) 99.5 to 40% of at least one polymerizable vinyl compound, which is a (C1 - C12 alkyl) ester of aerylic acid, a (C8 - C12 alkyl) ester of methacrylic acid, a C4 - C6 conjugated aliphatic diene or a vinyl (C1 - C4 alkyl) ether; (e) 0 to 50% of at least one polymerizable vinyl compound which is an aromatic monovinyl compound of the benzene series, an a , b -definically unsaturated nitrile, a vinyl or vinylidene halide, a (C1 - C4 alkyl) ester of methaerylic acid, an a , b -definically unsaturated aliphatic monocarboxylic acid, a vinyl ester of a C2 - C3 carboxylic acid, or itaconic acid. The copolymer can be one wherein the monomers specified above are graft polymerized on to an unsaturated polymer such as a conjugated diene polymer, e.g. polybutadiene.
GB22136/64A 1963-05-29 1964-05-28 Spontaneously cross-linking polymers Expired GB1049027A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF39868A DE1207629B (en) 1963-05-29 1963-05-29 Process for the production of self-crosslinking polymers

Publications (1)

Publication Number Publication Date
GB1049027A true GB1049027A (en) 1966-11-23

Family

ID=7097982

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22136/64A Expired GB1049027A (en) 1963-05-29 1964-05-28 Spontaneously cross-linking polymers

Country Status (6)

Country Link
BE (1) BE648511A (en)
CH (1) CH465234A (en)
DE (1) DE1207629B (en)
FR (1) FR1396854A (en)
GB (1) GB1049027A (en)
NL (1) NL6406091A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992007011A1 (en) * 1990-10-18 1992-04-30 Isp Investments Inc. Swellable, crosslinked polyvinylpyrrolidone and cosmetic compositions therewith

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1330053A (en) * 1961-08-03 1963-06-14 Bayer Ag New stable aqueous emulsions of self-crosslinking copolymers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992007011A1 (en) * 1990-10-18 1992-04-30 Isp Investments Inc. Swellable, crosslinked polyvinylpyrrolidone and cosmetic compositions therewith

Also Published As

Publication number Publication date
DE1207629B (en) 1965-12-23
CH465234A (en) 1968-11-15
FR1396854A (en) 1965-04-23
BE648511A (en) 1964-11-30
NL6406091A (en) 1964-11-30

Similar Documents

Publication Publication Date Title
US3498942A (en) Emulsion polymerization of unsaturated monomers utilizing alkyl sulfide terminated oligomers as emulsifiers and resulting product
US3265654A (en) Stable, aqueous dispersions of ethylene copolymers
US5385971A (en) Method of producing aqueous polymer dispersions
NO880391L (en) PAPER PAPER ON THE BASIS OF Aqueous DISPERSIONS.
DK422187D0 (en) PAPER FOR PAPER BASED ON FINISHED, WALL-DISPERSE
US3562229A (en) Process for the preparation of copolymers from ethylene and vinyl esters
US3832317A (en) Process for reducing acrylic ester monomer residues in acrylate latices
GB928621A (en) Improvements in or relating to the production of plastics
GB690937A (en) A process for copolymerising unsaturated monomers and the copolymers produced thereby
US3865772A (en) Polymerization process
US2434536A (en) Emulsion polymerization process
US3249595A (en) Aqueous emulsion polymerization process employing water-soluble peroxides
US3925327A (en) Method for producing vinyl acetate-ethylene-dicarboxylic acid diallyl ester copolymer
GB1049027A (en) Spontaneously cross-linking polymers
GB1182149A (en) Polymer Composition.
GB762159A (en) Production of terpolymers
US4039513A (en) Polymers containing formamide groups
US3236798A (en) Film-forming acrylonitrile polyer latex and method for preparing same
US2537015A (en) Process for polymerizing unsaturated compounds
US3501445A (en) Polyacrylate thickeners and copolymers used to produce same
US3243399A (en) Stable aqueous emulsions of copolymers having self-cross-linking properties
US4138542A (en) Polymers which contain 2-(4-methyl-cyclohex-3-en-1-yl)-propyl-N-acrylamide or -N-methacrylamide groups
ES489503A1 (en) Process for preparing aqueous dispersions of butadiene copolymers having a polymer content of at least 58% by weight by emulsion copolymerization.
US3325458A (en) Acrylonitrile interpolymers
US2922781A (en) Process for polymerizing a conjugated diolefin in the presence of an unsaturated dimer of alphamethylstyrene