GB947585A - Artificial leathers and foils provided with an adhesive layer - Google Patents

Artificial leathers and foils provided with an adhesive layer

Info

Publication number
GB947585A
GB947585A GB8359/60A GB835960A GB947585A GB 947585 A GB947585 A GB 947585A GB 8359/60 A GB8359/60 A GB 8359/60A GB 835960 A GB835960 A GB 835960A GB 947585 A GB947585 A GB 947585A
Authority
GB
United Kingdom
Prior art keywords
compound
halogenous
synthetic rubber
weight
dithiocarbamate
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
GB8359/60A
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.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Deutsche Gold und Silber Scheideanstalt
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 Degussa GmbH, Deutsche Gold und Silber Scheideanstalt filed Critical Degussa GmbH
Publication of GB947585A publication Critical patent/GB947585A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/17Amines; Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/25Plastics; Metallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/29Compounds containing one or more carbon-to-nitrogen double bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J111/00Adhesives based on homopolymers or copolymers of chloroprene
    • 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
    • D06N3/04Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N3/10Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with styrene-butadiene copolymerisation products or other synthetic rubbers or elastomers except polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2315/00Characterised by the use of rubber derivatives
    • C08J2315/02Rubber derivatives containing halogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Laminated Bodies (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A sheet structure, e.g. artificial leather or foil, consists essentially of a halogenous synthetic rubber carrier layer provided wholly or in part with at least one adhesive layer, wherein the halogenous synthetic rubber has been vulcanized by means of a compound (A) which contains at least two -N=C< groups which are not part of a ring and/or a N,N1-dimethylol compound (B), general formulae of which are given, at a temperature below 150 DEG C. and which contains only few or no crystalline fractions but contains those fractions of the compounds (A) and/or (B) which are not used up by the vulcanization and wherein the adhesive layer consists essentially of poly-2-chlorobutadiene and contains relatively large quantities of crystalline fractions. The halogenous synthetic rubber may have been vulcanized in the presence of compound (A) and/or compound (B), to the extent of 0,1 - 12% by weight, preferably 1,0-7% by weight, based on the weight of halogenous synthetic rubber, and of 0,1-6%, advantageously 0,3-4% by weight of a diisocyanate and/or polyisocyanate (C). The poly-2-chlorobutadiene of the adhesive coating may contain 35-100% by weight of crystalline fractions. The halogenous synthetic rubber may have been vulcanized at a temperature which is at least 10 degrees below the decomposition temperature of the substances (A), (B) and (C). The compound (A) may be a reaction product of a diamine or polyamine with an aldehyde or a ketone, e.g. cyclohexanone, acetophenone, methyl ethyl ketone, ethyl amyl ketone, acetylacetone, acetone - dicarboxylic acid - dimethyl ester, acetoacetic ester and aldehyde, benzaldehyde, acrolein, glyoxal, crotonaldehyde, and furfural. The amine may contain two terminal primary amino groups and may have a carbon chain containing fewer than 19 carbon atoms, e.g. ethylene, propylene, butylene, and hexamethylene diamine, diethylene and dipropylene triamine, and tetramethylene pentamine, or mixtures thereof. The compound (A) may be a reaction product of a dinitroso and/or polynitroso compound with a compound which contains at least one methylene group with active hydrogen, e.g. acetyl acetone, acetoacetic and malonic ester. The halogenous synthetic rubber may contain up to 200% by weight of fillers and/or dyestuffs, e.g. carbon black, metal or metalloid oxides or silicates, textile, asbestos or glass fibres. Sulphur and/or organic sulphur compounds may be additionally used as well as the compounds (A), (B) and (C) in the vulcanization of the halogenous synthetic rubber, examples of such compounds being thiuram sulphide, disulphide and tetrasulphide; dithiocarbamates generally, e.g. ethyl phenyl dithiocarbamate, zinc dimethyl dithiocarbamate, N-cyclohexyl ethyl ammonium cyclohexyl ethyl dithiocarbamate, N-pentamethylene ammonium pentamethylene dithiocarbamate, and xanthates. The sheet structures may be laminated to each other and to textile fabric by the application of heat. Examples of isocyanates are hexamethylene and toluidine diisocyanate, triphenyl methane triisocyanate and methylene bis (4-phenyl isocyanate).
GB8359/60A 1959-03-11 1960-03-09 Artificial leathers and foils provided with an adhesive layer Expired GB947585A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DED30168A DE1258596B (en) 1959-03-11 1959-03-11 Process for the production of laminated bodies from vulcanized polychlorobutadiene layers

Publications (1)

Publication Number Publication Date
GB947585A true GB947585A (en) 1964-01-22

Family

ID=7040386

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8359/60A Expired GB947585A (en) 1959-03-11 1960-03-09 Artificial leathers and foils provided with an adhesive layer

Country Status (5)

Country Link
BE (1) BE588469A (en)
CH (1) CH398968A (en)
DE (1) DE1258596B (en)
GB (1) GB947585A (en)
NL (1) NL249334A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1013934A (en) * 1942-09-25 1952-08-06 Ig Farbenindustrie Ag Agglutinants
NL170472B (en) * 1951-09-06 Ibm SLIDE REGISTER MEMORY.

Also Published As

Publication number Publication date
CH398968A (en) 1966-03-15
NL249334A (en)
DE1258596B (en) 1968-01-11
BE588469A (en)

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