GB1031406A - Low friction materials - Google Patents

Low friction materials

Info

Publication number
GB1031406A
GB1031406A GB4500564A GB4500564A GB1031406A GB 1031406 A GB1031406 A GB 1031406A GB 4500564 A GB4500564 A GB 4500564A GB 4500564 A GB4500564 A GB 4500564A GB 1031406 A GB1031406 A GB 1031406A
Authority
GB
United Kingdom
Prior art keywords
resin
per cent
toluene
weight per
butanol
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
GB4500564A
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.)
Acheson Industries Inc
Original Assignee
Acheson Industries Inc
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 Acheson Industries Inc filed Critical Acheson Industries Inc
Publication of GB1031406A publication Critical patent/GB1031406A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers 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; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers 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; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12Compositions of homopolymers or copolymers 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; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Abstract

Fluid dispersions containing more than 50 weight per cent total solids comprise 25 to 95 weight per cent of total solids of a thermosettable resin and 5 to 75 weight per cent of total solids of a wax-like, solid, fluorocarbon polymer having a molecular weight of 1300 to 15000, a crystalline melting point of 225 DEG to 320 DEG C., a chlorine content of 0.05 to 2 weight per cent and a hydrogen content of 0.05 to 2 weight per cent, and being the reaction product of 1 mol. tetrafluoroethylene, a solution of 0.01 to 0.6 mol. active telogen and 1.7 to 15 mols. trichlorotrifluoroethane in the presence of 0.05 to 3 weight per cent based on tetrafluoroethylene of a free radical generating catalyst. The compositions may also comprise high molecular weight polytetrafluoroethylenes, reinforcing agents, e.g. silica, asbestos, glass flour and fibres, metallic fibres, cellulose fibres and carbon black; and lubricants, e.g. graphite, molybdenum disulphide, tungsten disulphide, boron nitride, talc, vermiculite, silver sulphide and lead monoxide; and may be used for casting shaped articles or coating, e.g. metal, wood, glass, plastics, rubbers, leather and cloth. Many suitable thermosettable resins are specified, including phenolic and rosin, rosin ester and alkyd modified phenolic resins; ureaformaldehyde and melamine - formaldehyde resins; saturated and unsaturated polyester and phenol and drying oil modified polyester resins; epoxy and polyester, phenolic and fatty acid modified epoxy resins; reaction products of polyesters and polyethers with polyisocyanates; thermosetting methyl, ethyl and methyl phenyl silicones; furfuryl alcohol polymers and reaction products of furfural with aniline, ketones and phenols; and thermosetting acrylic resins. Polymerization and curing catalysts, e.g. peroxides, amines and acids may be present. Examples describe compositions comprising wax-like, solid, fluorocarbon polymers, and (I and II) epoxy resin and triethylene tetramine; (III) orthophthalic based polyester, styrene, methyl ethyl ketone peroxide and cobalt octoate; (IV) furfuryl alcohol resin and p-toluene sulphonic acid; (V) epoxy resin, triethylene tetramine and graphite; (VI) epoxy resin, tetraethylene pentamine and silica; (VII) epoxy resin, polyamide resin, copper bronze powder and ethoxyethyl acetate; (VIII) epoxy resin, triethylene diamine, ethoxyethyl acetate, toluene and n-butanol; (IX) epoxy resin, triethylene tetramine, ethoxyethyl acetate and trichloro-trifluoroethane; (X) phenol/formaldehyde resin and organic solvent; (XI) alkylated urea/formaldehyde resin, ethoxyethanol, toluene and n-butanol; (XII) silicone resin, ethoxyethanol, toluene and n-butanol; (XIII) soya oil modified alkyd resin, lead octoate, cobalt octoate and xylene; (XIV) an ethyl acrylate/methyl methacrylate/acrylic acid copolymer, ethoxyethanol, toluene, xylene and n-butanol; (XV) polyurethane resin and organic solvents; and (XVI) phenol/formaldehyde resin, an aqueous dispersion of polytetrafluoroethylene, ethoxyethanol, toluene and n-butanol.ALSO:Substrates may be coated with fluid dispersions containing more than 50 weight per cent total solids and comprising 25 to 95 weight per cent of total solids of a thermosettable resin and 5 to 75 weight per cent of total solids of a wax-like, solid, fluorocarbon polymer having a molecular weight of 1300 to 15000, a crystalline melting point of 225 to 320 DEG C., a chlorine content of 0. 05 to 2 weight per cent and a hydrogen content of 0. 05 to 2 weight per cent, and being the reaction product of 1 mol of tetrafluoroethylene, a solution of 0. 01 to 0. 6 mol of active telogen and 1.7 to 15 mols of trichlorotrifluoroethane in the presence of 0. 05 to 3 weight per cent based on the tetrafluoroethylene of a free radical generating catalyst. Specified substrates are metal, wood, glass, plastics, rubbers, leather and cloth. The compositions may also contain high molecular weight polytetrafluoroethylenes reinforcing agents, solid lubricants and volatile solvents. Examples describe the application of compositions comprising wax-like, solid, fluorocarbon polymers and (I and II) epoxy resin and triethylene tetramine to wood panels; (III) orthophthalic based polyester, styrene, methyl ethyl ketone peroxide and cobalt octoate to wood panels; (V) epoxy resin, triethylene tetramine and graphite to steel panels; (VII) epoxy resin, polyamide resin, copper bronze powder and ethoxyethyl acetate to birch plywood panels; (VIII) epoxy resin, triethylene diamine, ethoxyethyl acetate, toluene and n-butanol to steel panels; (IX) epoxy resin, triethylene tetramine, ethoxyethyl acetate,and trichlorotrifluoroethane to wood panels; (X) phenol/formaldehyde resin and organic solvents to glass; (XI) alkylated urea/formaldehyde resin, ethoxyethanol, toluene and n-butanol to glass; (XII) silicone resin, ethoxyethanol, toluene and n-butanol to glass and steel; (XIII) soya oil modified alkyl resin, lead octoate, cobalt octoate and xylene to wood, cloth, leather, natural rubber and butyl rubber; (XIV) an ethyl acrylate/methyl methacrylate/methacrylic acid copolymer, ethoxyethanol, toluene, xylene and n-butanol to steel; (XV) polyurethane resin and organic solvents to rubber; and (XVI) phenol/formaldehyde resin, an aqueous dispersion of polytetrafluoroethylene, ethoxyethanol, toluene and n-butanol to steel and wood.
GB4500564A 1963-11-05 1964-11-04 Low friction materials Expired GB1031406A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US32142863A 1963-11-05 1963-11-05

Publications (1)

Publication Number Publication Date
GB1031406A true GB1031406A (en) 1966-06-02

Family

ID=23250569

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4500564A Expired GB1031406A (en) 1963-11-05 1964-11-04 Low friction materials

Country Status (2)

Country Link
DE (1) DE1519010A1 (en)
GB (1) GB1031406A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5008135A (en) * 1985-09-19 1991-04-16 The Standard Oil Company Epoxy fluorocarbon coating compositions and the process to make the same
WO2001012344A1 (en) * 1999-08-12 2001-02-22 Alliedsignal Inc. Tungsten disulfide modified epoxy, high temperature/low friction/machinable
US20110085831A1 (en) * 2009-10-13 2011-04-14 David William Hullman Fuser for an Image-Forming Apparatus and Method of Using Same
EP2548902A1 (en) * 2011-07-19 2013-01-23 Milliken & Company Composition and method for improving adhesion of textile substrates to rubber and articles resulting therefrom
CN107083183A (en) * 2017-05-24 2017-08-22 中南大学 A kind of boron bakelite resin/epoxy modified silicone resin self-lubricating coat in use of resistance to ablation and preparation method thereof
CN107201171A (en) * 2017-05-24 2017-09-26 中南大学 A kind of boron bakelite resin/epoxy modified silicone resin coating of resistance to ablation protection and preparation method thereof
CN112517904A (en) * 2020-11-27 2021-03-19 无锡科宇模具有限公司 Preparation method of tough anti-friction part

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1300787C (en) * 1985-09-19 1992-05-12 Paul J. Giordano Epoxy fluorocarbon coating compositions and the process to make thesame
DE3670860D1 (en) * 1985-12-23 1990-06-07 Standard Oil Co Ohio COATING COMPOSITION CONTAINING FLUOR ON THE BASIS OF EPOXY RESIN AND FLUOROCOLOON RESIN AND METHOD FOR THE PRODUCTION THEREOF.
EP0920482A1 (en) * 1996-08-26 1999-06-09 Minnesota Mining And Manufacturing Company Fluoropolymer-epoxy resin semi-interpenetrating network composition

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5008135A (en) * 1985-09-19 1991-04-16 The Standard Oil Company Epoxy fluorocarbon coating compositions and the process to make the same
WO2001012344A1 (en) * 1999-08-12 2001-02-22 Alliedsignal Inc. Tungsten disulfide modified epoxy, high temperature/low friction/machinable
US6524646B2 (en) 1999-08-12 2003-02-25 Honeywell International, Inc. Method for restoring a surface on a metal substrate
US20110085831A1 (en) * 2009-10-13 2011-04-14 David William Hullman Fuser for an Image-Forming Apparatus and Method of Using Same
EP2548902A1 (en) * 2011-07-19 2013-01-23 Milliken & Company Composition and method for improving adhesion of textile substrates to rubber and articles resulting therefrom
CN107083183A (en) * 2017-05-24 2017-08-22 中南大学 A kind of boron bakelite resin/epoxy modified silicone resin self-lubricating coat in use of resistance to ablation and preparation method thereof
CN107201171A (en) * 2017-05-24 2017-09-26 中南大学 A kind of boron bakelite resin/epoxy modified silicone resin coating of resistance to ablation protection and preparation method thereof
CN107201171B (en) * 2017-05-24 2019-08-23 中南大学 A kind of boron bakelite resin/epoxy modified silicone resin coating of resistance to ablation protection and preparation method thereof
CN107083183B (en) * 2017-05-24 2019-09-03 中南大学 A kind of boron bakelite resin/epoxy modified silicone resin self-lubricating coat in use of resistance to ablation and preparation method thereof
CN112517904A (en) * 2020-11-27 2021-03-19 无锡科宇模具有限公司 Preparation method of tough anti-friction part

Also Published As

Publication number Publication date
DE1519010A1 (en) 1969-11-13

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