GB1459843A - Contact adhesive - Google Patents

Contact adhesive

Info

Publication number
GB1459843A
GB1459843A GB1873074A GB1873074A GB1459843A GB 1459843 A GB1459843 A GB 1459843A GB 1873074 A GB1873074 A GB 1873074A GB 1873074 A GB1873074 A GB 1873074A GB 1459843 A GB1459843 A GB 1459843A
Authority
GB
United Kingdom
Prior art keywords
dispersion
acrylate
resole
phenol
latex
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
GB1873074A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB1459843A publication Critical patent/GB1459843A/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
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/08Homopolymers or copolymers of acrylic acid esters
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Adhesive Tapes (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

1459843 Aqueous phenolic resin dispersion/ acrylate latex contact adhesives UNION CARBIDE CORP 29 April 1974 [30 April 1973] 18730/74 Headings C3R and C3P A contact adhesive composition comprises an aqueous mixed dispersion containing: (a) an alkyl acrylate polymer resin latex having a second order transition temperature not greater than 30‹ C.; and (b) an aqueous phenolic resole dispersion having a weight average M.Wt. of from 200 to 3000 and comprising either: (i) a first resole formed by the alkaline condensation of an aldehyde and a phenol and which is employed in the dispersion as solid particles suspended in water, substantially all of which have diameters of less than 60 microns; or (ii) a second resole comprising the alkaline condensed reaction product of formaldehyde and a difunctional phenol and having a labile formaldehyde content of from 0 to 12% wt., based on the weight of the second resole and wherein the second resole is employed in the dispersion as a solution in a water-immiscible organic solvent. The acrylate polymer preferably comprises at least 25% wt. of units derived from alkyl acrylates; and preferably has a mean average ultimate elongation of at least 500%. The first resole dispersion may be prepared by condensing at least one phenol selected from phenol itself, trifunctional monohydric mono- or dimeta-substituted C 1 -C 9 alkyl or alkoxy, or halo-phenols, and bisphenols with formaldehyde or furfural in the presence of an alkaline catalyst and optionally a mixture of gum arabic and at least one polysaccharide gum having mannose and galactose units or D-mannuronic and L-guluronic acid units. The second resole dispersion may be prepared by reacting a para-substituted phenol preferably a para-C 1 -C 12 alkyl-phenol with formaldehyde in the presence of an alkaline catalyst and emulsifying the resole formed with up to 50% wt. of a water-immiscible solvent e.g. an aromatic or aliphatic hydrocarbon, before adding it to water to form the dispersion optionally in the presence of an emulsifier such as an alkali metal salt of a C 12 -C 24 aliphatic fatty acid alone or together with the corresponding amine or ammonium salt or with casein, ammoniated casein and various gums. The composition preferably comprises 5-45 wt. per cent phenolic resin solids and 95-55 wt. per cent acrylate resin solids, based on the combined weight of the resins and optionally up to 50 wt. per cent of a filler or pigment determined on a solids basis of the total formulation. In the examples adhesives are prepared from (1) either (i) a latex copolymer of ethyl acrylate, acrylonitrile, acrylic acid and N-methylol acrylamide alone or in admixture with an acrylate latex copolymer (B) of vinyl acetate and isobutyl acrylate, or (ii) an acrylate latex prepared by adding an aqueous dispersion of a copolymer of ethylene and acrylic acid partially neutralized with N,N-dimethylolethanolamine to an acrylate copolymer latex of ethyl acrylate, methyl methacrylate and methacrylic acid and then heating, alone or in admixture with acrylate latex (B), and (2) either (i) a bisphenol-AHCHO resin aqueous dispersion prepared in presence of gum arabic and "Jaguar" (R.T.M.) gum, or (ii) a phenol-HCHO resin aqueous dispersion prepared in the presence of gum arabic and either guar gum or a gum comprising galactose units, or (iii) an aqueous dispersion of either p-tert-butylphenol-HCHO resin having a labile HCHO content of 6À3% wt., or an aqueous phenol-cresol-HCHO dispersion each containing oleic acid, NaOH, ammoniated casein, gum arabic and an organic solvent.
GB1873074A 1973-04-30 1974-04-29 Contact adhesive Expired GB1459843A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US35567673A 1973-04-30 1973-04-30

Publications (1)

Publication Number Publication Date
GB1459843A true GB1459843A (en) 1976-12-31

Family

ID=23398361

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1873074A Expired GB1459843A (en) 1973-04-30 1974-04-29 Contact adhesive

Country Status (6)

Country Link
JP (1) JPS5014735A (en)
AU (1) AU6836374A (en)
DE (1) DE2420683B2 (en)
FR (1) FR2227309B1 (en)
GB (1) GB1459843A (en)
IT (1) IT1010238B (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4543386A (en) * 1983-02-21 1985-09-24 Imperial Chemical Industries Plc Vinylidene chloride copolymer aqueous latex composition
US4543387A (en) * 1983-02-21 1985-09-24 Imperial Chemical Industries Plc Aqueous latex copolymer compositions
EP0262376A2 (en) * 1986-08-30 1988-04-06 BASF Aktiengesellschaft Aqueous binder dispersions for the preparation of spreading and coating compounds
US4783499A (en) * 1984-12-06 1988-11-08 Imperial Chemical Industries Plc Vinylidene chloride polymer aqueous latex compositions
US4975484A (en) * 1985-05-10 1990-12-04 E. I. Du Pont De Nemours And Company Acrylic copolymer composition and adhesive coatings therefrom
US4980410A (en) * 1985-05-10 1990-12-25 E. I. Du Pont De Nemours And Company Acrylic copolymer composition and adhesive coatings therefrom
US5418262A (en) * 1991-12-09 1995-05-23 Heraeus Kulzer Gmbh Adhesive, waterproof and hydrolysis-resistant bonding layer for metal, ceramic, glass, polymer-plastic bonds and dispersion for producing it
WO2014134442A1 (en) * 2013-03-01 2014-09-04 Valspar Corporation Aqueous coating compositions including phenolic resin(s)
TWI621675B (en) * 2016-12-21 2018-04-21 Adhesive composition, treated fabric and composite laminate
US10486865B2 (en) 2013-10-02 2019-11-26 The Sherwin-Williams Company Removable closure and coating system
US11377277B2 (en) 2013-10-02 2022-07-05 Swimc Llc Removable closure and coating system

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53121038A (en) * 1977-02-09 1978-10-23 Nitto Electric Ind Co Ltd Hot pressure-sensitive tapes or sheets
US4228055A (en) * 1978-09-06 1980-10-14 Ppg Industries, Inc. Aqueous coating compositions containing flatting agents and low molecular weight polyethers
EP0553448A1 (en) * 1991-12-09 1993-08-04 Kettenbach GmbH & CO. KG Surface conditioned impression tray

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4543387A (en) * 1983-02-21 1985-09-24 Imperial Chemical Industries Plc Aqueous latex copolymer compositions
US4543386A (en) * 1983-02-21 1985-09-24 Imperial Chemical Industries Plc Vinylidene chloride copolymer aqueous latex composition
US4783499A (en) * 1984-12-06 1988-11-08 Imperial Chemical Industries Plc Vinylidene chloride polymer aqueous latex compositions
US4980410A (en) * 1985-05-10 1990-12-25 E. I. Du Pont De Nemours And Company Acrylic copolymer composition and adhesive coatings therefrom
US4975484A (en) * 1985-05-10 1990-12-04 E. I. Du Pont De Nemours And Company Acrylic copolymer composition and adhesive coatings therefrom
EP0262376A3 (en) * 1986-08-30 1989-10-11 Basf Aktiengesellschaft Aqueous binder dispersions for the preparation of spreading and coating compounds
EP0262376A2 (en) * 1986-08-30 1988-04-06 BASF Aktiengesellschaft Aqueous binder dispersions for the preparation of spreading and coating compounds
US5418262A (en) * 1991-12-09 1995-05-23 Heraeus Kulzer Gmbh Adhesive, waterproof and hydrolysis-resistant bonding layer for metal, ceramic, glass, polymer-plastic bonds and dispersion for producing it
WO2014134442A1 (en) * 2013-03-01 2014-09-04 Valspar Corporation Aqueous coating compositions including phenolic resin(s)
US10358571B2 (en) 2013-03-01 2019-07-23 The Sherwin-Williams Company Aqueous coating compositions including phenolic resin(s)
US11225586B2 (en) 2013-03-01 2022-01-18 Swimc Llc Aqueous coating compositions including phenolic resin(s)
US10486865B2 (en) 2013-10-02 2019-11-26 The Sherwin-Williams Company Removable closure and coating system
US11377277B2 (en) 2013-10-02 2022-07-05 Swimc Llc Removable closure and coating system
TWI621675B (en) * 2016-12-21 2018-04-21 Adhesive composition, treated fabric and composite laminate

Also Published As

Publication number Publication date
DE2420683A1 (en) 1974-11-07
JPS5014735A (en) 1975-02-17
IT1010238B (en) 1977-01-10
FR2227309B1 (en) 1978-01-20
FR2227309A1 (en) 1974-11-22
DE2420683B2 (en) 1977-10-06
AU6836374A (en) 1975-10-30

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee