ES249862A1 - New copolymers and their manufacture and use - Google Patents

New copolymers and their manufacture and use

Info

Publication number
ES249862A1
ES249862A1 ES0249862A ES249862A ES249862A1 ES 249862 A1 ES249862 A1 ES 249862A1 ES 0249862 A ES0249862 A ES 0249862A ES 249862 A ES249862 A ES 249862A ES 249862 A1 ES249862 A1 ES 249862A1
Authority
ES
Spain
Prior art keywords
esters
alkyl
vinyl
alcohols
acid
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
ES0249862A
Other languages
Spanish (es)
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.)
Novartis AG
BASF Schweiz AG
Original Assignee
Ciba Geigy AG
Ciba 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 Ciba Geigy AG, Ciba AG filed Critical Ciba Geigy AG
Publication of ES249862A1 publication Critical patent/ES249862A1/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • 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
    • C08F214/00Copolymers 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
    • C08F214/02Monomers containing chlorine
    • C08F214/04Monomers containing two carbon atoms
    • C08F214/08Vinylidene chloride
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/52General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
    • D06P1/5207Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • D06P1/5214Polymers of unsaturated compounds containing no COOH groups or functional derivatives thereof
    • D06P1/5235Polyalkenyl halides, e.g. PVC
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/52General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
    • D06P1/5207Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • D06P1/525Polymers of unsaturated carboxylic acids or functional derivatives thereof
    • D06P1/5257(Meth)acrylic acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Paints Or Removers (AREA)
  • Coloring (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)

Abstract

Copolymers are prepared from 28 to 50% vinylidene chloride 4 to 10% of an acid <FORM:0908222/IV(a)/1> where R1 is H or a C1 to C4 alkyl group a least 35% of an ester <FORM:0908222/IV(a)/2> where R1 is C1-4 alkyl and R2 is derived from an aliphatic, heterocyclic or alicyclic alcohol and, optionally, up to 20% of a further monomer containing a single ethylenic double bond. Mixtures of monomers of the specified formulae may be used. Numerous alcohols R2OH from which the acrylate or alkacrylate ester may be derived are specified including alkyl, alkenyl, alicyclic, heterocyclic, hydro-aromatic, terepene and alkoxy alcohols. Optional further monomers specified are acrylonitrile, methacrylonitrile, styrene, vinyl chloride, chlorotrifluoroethylene, 1:1-difluoroethylene, acrylamide or methacrylamide which may have a C1-8 radical substituted on the N atom, vinyl C2-10 alkyl ethers, e.g. the butyl, 2-ethyl-butyl, and 2-ethyl-hexyl ethers, and vinyl esters of C2-4 carboxylic acids, e.g. vinyl acetate. Polymerization may be in bulk, solution or, preferably, emulsion. Emulsifying agents mentioned include fatty alcohol acid sulphates sulphonated castor oil alkyl, alkaryl or oxyalkyl sulphonates sulpho-dicarboxylic acid esters, e.g. the sodium salt of sulphosuccinic acid dioctyl ester polyglycol ethers of higher alcohols such as cetyl, oleyl, octadecyl and dodecyl alcohols, and of octyl phenol and the sulphuric acid esters of octyl-phenol polyglycol ether. Protective colloids which may be used with the emulsifiers are alginic acid esters, polyvinyl alcohols, partially hydrolysed polyvinyl esters, proteins, starches, and starch derivatives. Catalysts mentioned are organic and inorganic peroxides or per-salts, e.g. peracetic acid, acetyl-, benzoyl-, benzoyl acetyl-, lauryl- or hydrogen peroxide, percarbonates, persulphates and perborates. Two or more catalysts may be used and heat and/or actinic rays may be used instead of, or to augment, the catalyst. Regulators and activators may also be used, e.g. mercaptans inorganic oxidizable oxygen-containing sulphur compounds such as sulphur dioxide, sodium bisulphate, sulphite, hydrosulphite or thiosulphate, and ammonium bisulphite (which may form redox systems with oxidizing catalysts) water-soluble aliphatic tertiary amines such as triethanolamine or diethyl-ethanolamine multivalent heavy metal compounds in a lower valence state and complex cyanides of one or more of iron, cobalt, molybdenum, mercury, copper, zinc and silver. The polymerization may be effected in the absence of air or oxygen and the presence of inert gas, e.g. nitrogen or carbon dioxide. The polymerization may take place in two stages and one of the components may be partially prepolymerized. The product dispersions are generally acidic thin liquids which may be neutralized and thickened with concentrated ammonia pigments, fillers and plasticizer, e.g. dibutyl or dioctyl phthalate or sebacate esters may be incorporated therein. Applications of copolymer compositions. The compositions are used to produce elastic coatings on fabrics which may be made from cotton, linen, jute, hemp straw, polyesters, artificial or natural silk, regenerated cellulose or cellulose esters, wool, polyamides, polyacrylonitrile, glass, or mixtures thereof. They are of particular application as binding agents in pigment dyeing and printing, but may also be spread on fabrics to produce water-resistant raincoat materials, imitation wax or oil cloth, oiled silk material, and rear dressings on corduroy or carpets. They may also be used as a filling dressing for fabrics by the immersion method to produce bed ticking material, feel-modified wash-resistant cloths, water-resistant tent materials, and dry-cleaning-resistant lining materials. Other uses are as backing layers under polyvinyl chloride coatings, e.g. for artificial leather as binding agents for colouring compositions applied to leather and as a laminating adhesive for polyvinyl chloride foils or for paper/paper, paper/metal, or metal/metal laminates. In an example bleached cotton is dyed with a composition of a vinylidene chloride/isobutylacrylate/acrylic acid copolymer emulsion, sodium alginate, diammonium phosphate and a copper phthalocyanine or an azo pigment. Specification 908,223 is referred to.ALSO:Copolymers are prepared from 28 to 50% vinylidene chloride 0.2 to 10% of an acid <FORM:0908222/IV (b)/1> , where R1 is H or a C1-4 alkyl group at least 35% of an ester <FORM:0908222/IV (b)/2> , where R1 is C1-4 alkyl and R2 is derived from an aliphatic, alicyclic or heterocyclic alcohol and, optionally, up to 20% of a further monomer containing a single ethylenic double bond. Mixtures of monomers of the specified formulae may be used. Numerous alcohols R2OH from which the acrylate or alkacrylate ester may be derived are specified including alkyl, alkenyl, alicyclic, heterocyclic, hydro-aromatic, terepene and alkoxy alcohols. Optional further monomers specified are acrylonitrile, methacrylonitrile, styrene, vinyl chloride, chlorotrifluoroethylene, 1 : 1-difluoroethylene, acrylamide or methacrylamide which may have a C1-8 radical substituted on the N atom, vinyl C2-10 alkyl ethers, e.g. the butyl, 2-ethyl-butyl, and 2-ethyl-hexyl ethers, and vinyl esters of C2-4 carboxylic acids, e.g. vinyl acetate (see also Group IV(a)). The product dispersions are generally acidic thin liquids which may be neutralised and thickened with concentrated ammonia pigments, fillers and plasticizer, e.g. dibutyl or dioctyl phthalate or sebacate esters, may be incorporated therein. The compositions are of particular application as binding agents in pigment dyeing and printing or as binding agents for colouring compositions applied to leather. In an example bleached cotton is dyed with a composition of a vinylidene chloride/isobutylacrylate/acrylic acid copolymer emulsion, sodium alginate, diammonium phosphate and a copper phthalocyanine or an azo pigment. Numerous examples are given which describe the treatment of cotton, polyglycol terephthalate fibre fabric and regenerated cellulose fibre fabrics with compositions containing various of the following ingredients:-Turkey red oil triethanolamine sodium alginate ammonium sulphate copper phthalocyanine or azo pigments concentrated ammonia solution ammonium nitrate gas soot paste a silicone anti-foam agent: ammonium chloride and petroleum. Specification 908,223 is referred to.
ES0249862A 1958-06-06 1959-06-05 New copolymers and their manufacture and use Expired ES249862A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH6030158 1958-06-06
CH950660A CH381194A (en) 1958-06-06 1959-10-01 Process for finishing textile fibers

Publications (1)

Publication Number Publication Date
ES249862A1 true ES249862A1 (en) 1960-01-01

Family

ID=25704910

Family Applications (2)

Application Number Title Priority Date Filing Date
ES0249862A Expired ES249862A1 (en) 1958-06-06 1959-06-05 New copolymers and their manufacture and use
ES0249863A Expired ES249863A1 (en) 1958-06-06 1959-06-05 New copolymers and their manufacture and use

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES0249863A Expired ES249863A1 (en) 1958-06-06 1959-06-05 New copolymers and their manufacture and use

Country Status (7)

Country Link
BE (1) BE579381A (en)
CH (3) CH351108A (en)
DE (1) DE1113820B (en)
ES (2) ES249862A1 (en)
FR (2) FR1237744A (en)
GB (2) GB908223A (en)
NL (1) NL239911A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3739148A1 (en) * 1987-11-19 1989-06-01 Basf Ag METHOD FOR COATING TEXTILES
CN103342771B (en) * 2013-07-19 2015-12-23 海南必凯水性涂料有限公司 Special PVDC latex of a kind of internal lining paper and preparation method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1138278A (en) * 1954-03-31 1957-06-12 Kodak Pathe New ternary polymers, process for their preparation, and their applications in particular in photography

Also Published As

Publication number Publication date
CH381194A (en) 1962-12-15
CH950660A4 (en) 1962-12-15
FR1237745A (en) 1960-11-25
GB908222A (en) 1962-10-17
NL239911A (en)
BE579381A (en) 1959-12-07
FR1237744A (en) 1960-11-25
CH351108A (en) 1960-12-31
DE1113820B (en) 1961-09-14
ES249863A1 (en) 1960-01-01
GB908223A (en) 1962-10-17

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