GB1168872A - Vapour-Permeable Coatings - Google Patents

Vapour-Permeable Coatings

Info

Publication number
GB1168872A
GB1168872A GB2136167A GB2136167A GB1168872A GB 1168872 A GB1168872 A GB 1168872A GB 2136167 A GB2136167 A GB 2136167A GB 2136167 A GB2136167 A GB 2136167A GB 1168872 A GB1168872 A GB 1168872A
Authority
GB
United Kingdom
Prior art keywords
polymer
substrate
solvent
urethane
dimethylol
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
GB2136167A
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.)
Sanyo Chemical Industries Ltd
Original Assignee
Sanyo Chemical Industries 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 Sanyo Chemical Industries Ltd filed Critical Sanyo Chemical Industries Ltd
Publication of GB1168872A publication Critical patent/GB1168872A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/14Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/83Chemically modified polymers
    • C08G18/84Chemically modified polymers by aldehydes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)

Abstract

1,168,872. Leather substitutes. SANYO CHEMICAL INDUSTRIES Ltd. 8 May, 1967 [7 May, 1966], No. 21361/67. Heading B2E. Leather substitutes are prepared by coating a fibrous substrate with a solution of a substantially linear urethane polymer in a solvent which is inert with respect to the substrate, removing the solvent from the polymer by treating the coated substrate with a solvent which is a solvent of the polymer solvent yet inert with respect to the urethane polymer and the substrate and cross-linking the urethane polymer with at least one aldehyde containing 1 to 4 carbon atoms for at least one derivative of formaldehyde with which there are at least two groups of the general formula N(OH 2 OR) n in which R is a hydrogen atom or a methyl group and n is 1 or 2, at any stage in the production of the leather substitute. The fibrous substrates may be woven, non-woven or knitted fabrics and felts made from polyamides, polyesters, viscose rayon, wool, cotton, glass or mixtures of these. Inert liquids used for extraction of the polymer solvent may be water, ethylene, glycol, monoethyl, ether, hydroxyethyl acetate, ethylene glycol, glycerine or mixtures of these. The aldehyde may be formaldehyde, acetaldehyde, glyoxal or mixtures thereof. Suitable formaldehyde derivatives are methylol urea, methylol melamine, dimethylol adipic acid diamide, dimethylol butane diol urethane, dimethylol ethylene urea, dimethylol hydroxy ethylene urea, tetramethylol acetylene urea, dimethylol triazone, hexamethylol melamine and the methyl ethers thereof. A catalyst may be used to accelerate the action of the cross-linking unit with the urethane groups or urea groups of the polymer. Such catalysts may be inorganic acids such as hydrochloric acid, phosphoric acid, organic acids such as acetic acid, oxalic acid, amine salts such as the hydrochloride salts of mono- and di-alkyl amines, inorganic salts such as magnesium chloride, zinc nitrate, sodium hydrogen sulphate, sodium ethyl sulphate, barium ethyl sulphate, ammonium salts such as ammonium chloride and mixtures thereof. The cross-linking agent may be added to urethane polymer at any stage, e.g. added the agent to the solution of the urethane polymer before it is applied to the substrate, applied to the substrate before it is coated with a solution of urethane polymer, added to the inert liquid used for extraction step or sprayed as a solution onto the substrate coating of the polymer. The coated substrate may be dipped into a separately prepared bath containing the cross-linking agent. The cross-linking reaction is generally carried out after the extraction step by heating a coated substrate to a temperature of from 80 to 250‹C. and the preferred amount of crosslinking agent to be added to the polymer is 0.5-5% by weight based on the weight of the urethane polymer. The coating may be applied by spraying, knife coating, roller coating, casting, pressing or dipping. The product may be buffed and top-dressed.
GB2136167A 1966-05-07 1967-05-08 Vapour-Permeable Coatings Expired GB1168872A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2905066 1966-05-07

Publications (1)

Publication Number Publication Date
GB1168872A true GB1168872A (en) 1969-10-29

Family

ID=12265542

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2136167A Expired GB1168872A (en) 1966-05-07 1967-05-08 Vapour-Permeable Coatings

Country Status (2)

Country Link
DE (1) DE1619289A1 (en)
GB (1) GB1168872A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018159359A1 (en) 2017-02-28 2018-09-07 三洋化成工業株式会社 Polyurethane resin for synthetic leather

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4019479A1 (en) 2020-12-23 2022-06-29 Prefere Resins Holding GmbH Water-dilutable binders

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018159359A1 (en) 2017-02-28 2018-09-07 三洋化成工業株式会社 Polyurethane resin for synthetic leather

Also Published As

Publication number Publication date
DE1619289A1 (en) 1971-01-21

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