GB1037367A - A process for the production of solvent-resistant textile coatings - Google Patents

A process for the production of solvent-resistant textile coatings

Info

Publication number
GB1037367A
GB1037367A GB20985/65A GB2098565A GB1037367A GB 1037367 A GB1037367 A GB 1037367A GB 20985/65 A GB20985/65 A GB 20985/65A GB 2098565 A GB2098565 A GB 2098565A GB 1037367 A GB1037367 A GB 1037367A
Authority
GB
United Kingdom
Prior art keywords
cross
linking
acid
solvent
condensation products
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
GB20985/65A
Inventor
Wulfvon Bonin
Gerhard Berndt
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 GB1037367A publication Critical patent/GB1037367A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/267Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025Crosslinking or vulcanising agents; including accelerators

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Paints Or Removers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Solvent-resistant textile coatings are prepared by applying to a textile a solution of a copolymer in an organic solvent, which copolymer contains 90 to 99% by weight of an ester of acrylic acid with a monohydric alcohol having 2 to 4 carbon atoms, 0.5 to 5% by weight of 2-hydroxy-n-propyl methacrylate and 0.5 to 5% by weight of acrylic acid and/or methacrylic acid in polymerized form and which solution contains a cross-linking agent which is able to react with the hydroxyl and/or carboxylic acid groups of the polymer to form a cross-linked product, and then reacting the polymer and cross-linking agent with each other. The copolymers used are preferably prepared by copolymerizing the appropriate monomers in solution in an organic solvent below 85 DEG C. using as initiator azodiisobutyronitrile, benzoyl peroxide, lauroyl peroxide, dichlorobenzoyl peroxide, t-butyl perisobutyrate, dicyclohexyl peroxy-dicarbonate or mixtures thereof, e.g. azodiisobutyronitrile plus benzoyl peroxide. Suitable cross-linking agents include condensation products of formaldehyde with urea, thiourea, ethylene or propylene urea, aminotriazines, e.g. melamine, guanamines and ethers thereof; di- and poly-isocyanates; masked isocyanates; polymers or copolymers containing optionally etherified N - methylol - acrylamide groupings; and phenol-formaldehyde condensation products. Cross-linking is preferably completed, during or after evaporation of the solvent, at 30 DEG to 150 DEG C. When formaldehyde condensation products are used for cross-linking, a free acid such as oxalic or maleic acid may be included in the coating compositions. The compositions may be pigmented with organic pigments or inorganic pigments, e.g. kaolin, titanium dioxide, iron oxide, chromium oxide and silica.ALSO:Solvent-resistant textile coatings are prepared by applying to a textile a solution of a copolymer in an organic solvent, which copolymer contains 90 to 99% by weight of an ester of acrylic acid with a monohydric alcohol having 2 to 4 carbon atoms, 0.5 to 5% by weight of 2-hydroxy-n-propyl methacrylate and 0.5 to 5% by weight of acrylic acid and/or methacrylic acid in polymerized form and which solution contains a cross-linking agent which is able to react with the hydroxyl and/or carboxylic acid groups of the polymer to form a cross-linked product, and then reacting the polymer and cross-linking agent with each other. Suitable cross-linking agents include condensation products of formaldehyde with urea, thiourea, ethylene or propylene urea, amino-triazines, e.g. melamine, quanamines and ethers thereof; di- and poly-isocyanates; masked isocyanates; polymers or copolymers containing optionally etherified N-methylol-acrylamide groupings; and phenol-formaldehyde condensation products. Cross-linking is preferably completed, during or after evaporation of the solvent, at 30 to 150 DEG C., for example by passing the coated fabric through an optionally heated drying panel. When formaldehyde condensation products are used for cross-linking, a free acid such as oxalic acid or maleic acid may be included in the coating compositions. The compositions may be pigmented with organic pigments or inorganic pigments, e.g. kaolin, titanium dioxide, iron oxide, chromium oxide and silica. Textiles which may be treated include cotton, polyamide, polyester and polyester-cotton fabrics, which may be coated with the polymer solutions by means of a floating knife or rubber blanket coater. More than one coating may be applied, and cotton or blended cotton fabrics may be calendered before or after the first coat is applied. The treated textiles may subsequently be coated with hydrophobic agents, e.g. silicone-based impregnating agents, and those based on paraffin or perfluorocarboxylic acid/chromium complexes, or hydrophobic agents modified by masked isocyanates.
GB20985/65A 1964-05-19 1965-05-18 A process for the production of solvent-resistant textile coatings Expired GB1037367A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF42913A DE1247259B (en) 1964-05-19 1964-05-19 Process for the production of solvent-resistant textile coatings

Publications (1)

Publication Number Publication Date
GB1037367A true GB1037367A (en) 1966-07-27

Family

ID=7099317

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20985/65A Expired GB1037367A (en) 1964-05-19 1965-05-18 A process for the production of solvent-resistant textile coatings

Country Status (9)

Country Link
AT (1) AT252865B (en)
BE (1) BE662797A (en)
DE (1) DE1247259B (en)
DK (1) DK109637C (en)
ES (1) ES313006A1 (en)
FR (1) FR1433012A (en)
GB (1) GB1037367A (en)
NL (1) NL6506308A (en)
SE (1) SE308290B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989001500A1 (en) * 1987-08-10 1989-02-23 Desoto, Inc. Thermosetting size press composition
CN114438774A (en) * 2022-03-08 2022-05-06 罗莱生活科技股份有限公司 Self-cleaning cotton fiber and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3327016C2 (en) * 1983-07-27 1986-09-25 Mechanische Leinenweberei Laichingen Dr. R. Woernle GmbH & Co, 7903 Laichingen Tarpaulin fabric and process for its manufacture

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1124465B (en) * 1957-05-18 1962-03-01 Roehm & Haas Gmbh Process for synthetic resin finishing of textile structures

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989001500A1 (en) * 1987-08-10 1989-02-23 Desoto, Inc. Thermosetting size press composition
CN114438774A (en) * 2022-03-08 2022-05-06 罗莱生活科技股份有限公司 Self-cleaning cotton fiber and preparation method thereof

Also Published As

Publication number Publication date
AT252865B (en) 1967-03-10
ES313006A1 (en) 1966-02-01
NL6506308A (en) 1965-11-22
DE1247259B (en) 1967-08-17
BE662797A (en) 1965-08-17
SE308290B (en) 1969-02-10
FR1433012A (en) 1966-03-25
DK109637C (en) 1968-05-27

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