GB871296A - Adhesives and composite materials produced therewith - Google Patents

Adhesives and composite materials produced therewith

Info

Publication number
GB871296A
GB871296A GB17383/58A GB1738358A GB871296A GB 871296 A GB871296 A GB 871296A GB 17383/58 A GB17383/58 A GB 17383/58A GB 1738358 A GB1738358 A GB 1738358A GB 871296 A GB871296 A GB 871296A
Authority
GB
United Kingdom
Prior art keywords
polyvinyl chloride
butadiene
acid dimethyl
dipped
acrylonitrile
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
GB17383/58A
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 GB871296A publication Critical patent/GB871296A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C09J133/00Adhesives based on 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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/18Homopolymers or copolymers of nitriles
    • C09J133/20Homopolymers or copolymers of acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/04Condensation polymers of aldehydes or ketones with phenols only
    • C08L61/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • 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
    • C09J121/00Adhesives based on unspecified rubbers
    • 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
    • C09J161/00Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
    • C09J161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09J161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/04Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/14Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/14Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
    • C08L2666/16Addition or condensation polymers of aldehydes or ketones according to C08L59/00 - C08L61/00; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/28Non-macromolecular organic substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/54Inorganic substances

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Laminated Bodies (AREA)

Abstract

An adhesive composition comprises a synthetic elastomer such as a butadiene/acrylonitrile copolymer with a Defs value lower than 2000 or butadiene/styrene, a thermosetting formaldehyde condensate which is soluble in organic solvents, one or more chromates, and an organic solvent for the synthetic elastomer and the formaldehyde condensate. The adhesive composition gives high bonding strengths when producing composite materials with polyvinyl chloride layers and other high molecular weight organic compounds. According to Examples, (1) a sheet, tube, or rod of iron, aluminium, copper or brass was cleaned with benzine, was sand-blasted and then dipped in to a solution having the following composition: 1000 ml. methyl ethyl ketone, 150g. copolymer of butadiene and acrylonitrile of Defs value about 500; 150g. thermosetting condensation product of phenol and formaldehyde, 20-45g. zinc chromate, 10-25g. potassium bichromate and 15-60g. zinc oxide. The coated material was dried for 10 minutes at 130 DEG -180 DEG C. and then dipped while hot or after cooling to room temperature, into a plasticized, pigmented polyvinyl chloride paste. After draining, curing was effected for 15 minutes at 180 DEG C. Bonds were also produced employing, in place of metals, polyamides, polyesters, glass, and glass fabrics. In other examples, the polyvinyl chloride paste had the following compositions: (4) 55 parts of polyvinyl chloride powder, 45 parts of a gelling or plasticizing mixture containing a relatively low volatile plasticizer, such as dioctyl phthalate or mepasin-sulphonic acid phenyl ethyl ester, a relatively highly volatile plasticizer or gelling agent, such as phthalic acid dimethyl ester, adipic acid dimethyl ester, glyceryl triacetate, diethyl adipate, benzoic acid dimethyl ester or mixtures thereof, stabilizers and pigments; (5) 100g. polyvinyl chloride, 150g. phthalic acid dimethyl ester (or the diethyl ester), 7g. kaolin, 1,5g. brown iron oxide, 0,7g. yellow iron oxide and 0,1g. carbon black.ALSO:An adhesive composition comprising a synthetic elastomer, such as butadiene/acrylonitrile or butadiene/styrene, a thermosetting formaldehyde condensate which is soluble in organic solvents, one or more chromates and an organic solvent for the elastomer and the condensate, is employed to bond polyinyl chloride, polyamide, synthetic or natural rubber, polyurethanes, polystyrene, polyacrylates and polycarbonates, including foamed polymers, to surfaces of synthetic resin, glass and metals such as iron, galvanised iron, aluminium, copper and brass. The bonding agent may be applied by spraying, dipping, brushing or with a roller. In Example (1) metal sheets, rods and tubes are cleaned with benzine, sandblasted and dipped into a methyl ethyl ketone solution containing a copolymer of butadiene and acrylonitrile, a thermosetting condensation product of phenol and formaldehyde, zinc chromate, potassium bichromate and zinc oxide, dried by heat, dipped while still hot into a plasticized polyvinyl chloride paste, drained and cured by heat. More than one coating of polyvinyl chloride may be applied. In Example 4 a metal tube is similarly coated, but the polyvinyl chloride paste contains both relatively low and relatively high volatile plasticizers. In Example 5 a diluted adhesive composition as in Example 1 is applied to metal plates by spraying, the plates are dried by heat and while still hot are sprayed with a pigmented polyvinyl chloride composition containing phthalic acid dimethyl or diethyl ester, and dried by heat. In Example 6 the inner wall of a metal vessel is coated with the diluted adhesive of Example 5 and heated, and a foam material containing urethane groups produced in the vessel, e.g. by reaction of polyisocyanates with polyesters containing hydroxyl or carboxyl groups.
GB17383/58A 1957-05-31 1958-05-30 Adhesives and composite materials produced therewith Expired GB871296A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF24475A DE1221007B (en) 1957-05-31 1957-05-31 Binder for composite bodies

Publications (1)

Publication Number Publication Date
GB871296A true GB871296A (en) 1961-06-28

Family

ID=7091244

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17383/58A Expired GB871296A (en) 1957-05-31 1958-05-30 Adhesives and composite materials produced therewith

Country Status (4)

Country Link
BE (1) BE568164A (en)
DE (1) DE1221007B (en)
FR (1) FR1207018A (en)
GB (1) GB871296A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3839271A (en) * 1972-02-25 1974-10-01 Du Pont Primer compositions comprising zinc chromate, stabilizers and acrylate polymers containing oxazolidine units

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2459739A (en) * 1944-04-01 1949-01-18 Firestone Tire & Rubber Co Elastomeric copolymer mixed with phenol-aldehyde resin

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3839271A (en) * 1972-02-25 1974-10-01 Du Pont Primer compositions comprising zinc chromate, stabilizers and acrylate polymers containing oxazolidine units

Also Published As

Publication number Publication date
FR1207018A (en) 1960-02-12
DE1221007B (en) 1966-07-14
BE568164A (en) 1958-06-14

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