GB488557A - Improvements in or relating to adhesive compositions - Google Patents

Improvements in or relating to adhesive compositions

Info

Publication number
GB488557A
GB488557A GB380/37A GB38037A GB488557A GB 488557 A GB488557 A GB 488557A GB 380/37 A GB380/37 A GB 380/37A GB 38037 A GB38037 A GB 38037A GB 488557 A GB488557 A GB 488557A
Authority
GB
United Kingdom
Prior art keywords
resin
mixture
oil
ammonia
rubber
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
GB380/37A
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.)
Dunlop Rubber Co Ltd
Original Assignee
Dunlop Rubber Co 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 Dunlop Rubber Co Ltd filed Critical Dunlop Rubber Co Ltd
Priority to GB380/37A priority Critical patent/GB488557A/en
Publication of GB488557A publication Critical patent/GB488557A/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
    • C09J193/00Adhesives based on natural resins; Adhesives based on derivatives thereof
    • 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
    • C09J193/00Adhesives based on natural resins; Adhesives based on derivatives thereof
    • C09J193/04Rosin
    • 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
    • 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
    • C08L2666/08Homopolymers or copolymers according to C08L7/00 - C08L21/00; Derivatives thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

A permanently tacky adhesive composition, in the form of an emulsion containing water as the discontinuous phase, is obtained by mixing, with heat, or fusible resin with a non-drying oil or fatty acid derived therefrom and then incorporating into the mixture a small proportion, not exceeding 10 per cent by weight of the total composition, of rubber in the form of an aqueous dispersion. Prior to incorporating the rubber a small proportion of water containing an alkaline substance such as ammonia may be emulsified into the resin mixture. In an example (1) a mixture of colophony and castor oil is heated at 120 DEG C. until homogeneous, cooled to 90-95 DEG C. and an aqueous solution of ammonia added gradually with constant stirring, then further cooled to 50 to 60 DEG C. and rubber latex added while keeping the mixture agitated. In further examples, ammonia and rubber latex are similarly incorporated into mixtures of (2) oleic acid and wood resin, (3) wood resin and resin oil, (4) colophony and mineral oil and (5) castor oil and a phenol-formaldehyde resin formed by heating, by weight, 50 parts each of phenol and 40 per cent formaldehyde and 5 parts concentrated hydrochloric acid until an exothermic reaction develops, cooling to moderate the reaction and continuing until a viscous syrup-like layer separates and pouring this into cold water, washing the solid plastic by kneading in warm water and drying; the resin is dissolved in warm alcohol and the solution stirred into castor oil at 60 DEG C. the alcohol being then removed by heating to 80-90 DEG C.ALSO:A permanently tacky adhesive composition, in the form of an emulsion containing water as the discontinuous phase, is obtained by mixing, with heat, a fusible resin with a non-drying oil or fatty acid derived therefrom and then incorporating into the mixture a small proportion, not exceeding 10 per cent by weight of the total composition, of rubber in the form of an aqueous dispersion. Prior to incorporating the rubber a small proportion of water containing an alkaline substance such as ammonia may be emulsified into the resin mixture. In an example (1) a mixture of colophony and castor oil is heated at 120 DEG C. until homogeneous, cooled to 90-95 DEG C. and an aqueous solution of ammonia added gradually with constant stirring, then further cooled to 50-60 DEG C. and rubber latex added while keeping the mixture agitated. In further examples, ammonia and rubber latex are similarly incorporated into mixtures of (2) oleic acid and wood resin; (3) wood resin and resin oil; (4) colophony and mineral oil; and (5) castor oil and a phenol-formaldehyde resin formed by heating, by weight; 50 part each of phenol and 40 per cent formaldehyde and 5 parts concentrated hydrochloric acid until an exothermic reaction develops, cooling to moderate the reaction and continuing until a viscous syrup-like layer separates and pouring this into cold water, washing the solid plastic by kneading in warm water and drying; the resin is dissolved in warm alcohol and the solution stirred into castor oil at 60 DEG C., the alcohol being then removed by heating to 80-90 DEG C.ALSO:A permanently tacky adhesive composition in the form of an emulsion containing water as the discontinuous phase, is obtained by mixing, with heat, a fusible resin with a non-drying oil or fatty acid derived therefrom and then incorporating into the mixture a small proportion, not exceeding 10 per cent by weight of the total composition, of rubber in the form of an aqueous dispersion. Prior to incorporating the rubber a small proportion of water containing an alkaline substance such as ammonia may be emulsified into the resin mixture. In an example, (1) a mixture of colophony and castor oil is heated as 120 DEG C. until homogeneous, cooled to 90-95 DEG C. and an aqueous solution of ammonia added gradually with constant stirring, then further cooled to 50-60 DEG C. and rubber latex added while keeping the mixture agitated. In further examples, ammonia and rubber latex are similarly incorporated into mixtures of (2) oleic acid and wood resin, (3) wood resin and resin oil, (4) colophony and mineral oil, and (5) castor oil and a phenolformaldehyde resin formed by heating, by weight, 50 part each of phenol and 40 per cent formaldehyde and 5 parts concentrated hydrochloric acid until an exothermic reaction develops, cooling to moderate the reaction and continuing until a viscous syrup-like layer separates and pouring this into cold water, washing the solid plastic by kneading in warm water and drying; the resin is dissolved in warm alcohol and the solution stirred into castor oil at 60 DEG C. the alcohol being then removed by heating to 80-90 DEG C.
GB380/37A 1937-01-06 1937-01-06 Improvements in or relating to adhesive compositions Expired GB488557A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB380/37A GB488557A (en) 1937-01-06 1937-01-06 Improvements in or relating to adhesive compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB380/37A GB488557A (en) 1937-01-06 1937-01-06 Improvements in or relating to adhesive compositions

Publications (1)

Publication Number Publication Date
GB488557A true GB488557A (en) 1938-07-06

Family

ID=9703397

Family Applications (1)

Application Number Title Priority Date Filing Date
GB380/37A Expired GB488557A (en) 1937-01-06 1937-01-06 Improvements in or relating to adhesive compositions

Country Status (1)

Country Link
GB (1) GB488557A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2007836A2 (en) * 2006-02-06 2008-12-31 Brewer Science, Inc. Thermal-and chemical-resistant acid protection coating material and spin-on thermoplastic adhesive

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2007836A2 (en) * 2006-02-06 2008-12-31 Brewer Science, Inc. Thermal-and chemical-resistant acid protection coating material and spin-on thermoplastic adhesive
EP2007836A4 (en) * 2006-02-06 2013-01-23 Brewer Science Inc Thermal-and chemical-resistant acid protection coating material and spin-on thermoplastic adhesive

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