GB377587A - Improvements in or relating to resinous condensation products and coating compositions - Google Patents

Improvements in or relating to resinous condensation products and coating compositions

Info

Publication number
GB377587A
GB377587A GB411932A GB411932A GB377587A GB 377587 A GB377587 A GB 377587A GB 411932 A GB411932 A GB 411932A GB 411932 A GB411932 A GB 411932A GB 377587 A GB377587 A GB 377587A
Authority
GB
United Kingdom
Prior art keywords
phenol
oil
oxidized
aldehyde
formaldehyde
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
GB411932A
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.)
Cook Paint and Varnish Co
Original Assignee
Cook Paint and Varnish Co
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 Cook Paint and Varnish Co filed Critical Cook Paint and Varnish Co
Priority to GB411932A priority Critical patent/GB377587A/en
Publication of GB377587A publication Critical patent/GB377587A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/28Chemically modified polycondensates
    • C08G8/32Chemically modified polycondensates by organic acids or derivatives thereof, e.g. fatty oils
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/28Chemically modified polycondensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/28Chemically modified polycondensates
    • C08G8/34Chemically modified polycondensates by natural resins or resin acids, e.g. rosin

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Resinous products are obtained by reacting together, in the presence of an alkaline catalyst, an oxidized drying oil, about an equal amount of a phenol or hydrogenated phenol, a natural resin, and an aldehyde, the molecular ratio of aldehyde to phenol or hydrogenated phenol lying between about 1 and 0.25. As the phenolic component there may be used ordinary phenol, a cresol, cresylic acid, a naphthol, or cyclohexanol; the oxidized drying oil may be oxidized or blown tung oil, linseed oil, perilla oil, soya bean oil, or fish oil; the natural resin may be colophony or Manila copal; the aldehyde may be formaldehyde, acetaldehyde, or benzaldehyde; the catalyst may be ammonia or a caustic alkali or alkali metal carbonate. In an example, oxidized linseed oil is dissolved in the warm in an equal amount of commercial phenol, and the solution is treated with commercial resin and formaldehyde solution (about 0.7 mol. calculated on the phenol), with addition of a little ammonia; the mixture is heated under reflux and the water then distilled off. The products are soluble in hydrocarbon oils and drying oils, and are useful as varnish bases, preferably in association with plasticizers such as tricresyl phosphate or castor oil, and driers such as manganese dioxide or resinates. The Specification refers to prior methods, for making resins of similar properties, comprising (1) condensing phenol and formaldehyde in about equimolecular amounts in the presence of oxidized drying oils and an alkaline catalyst; (2) condensing a phenol with 0.5-1 mol. of an aldehyde in the presence of oxidized drying oils (other than tung oil) and an alkaline catalyst.
GB411932A 1932-02-11 1932-02-11 Improvements in or relating to resinous condensation products and coating compositions Expired GB377587A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB411932A GB377587A (en) 1932-02-11 1932-02-11 Improvements in or relating to resinous condensation products and coating compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB411932A GB377587A (en) 1932-02-11 1932-02-11 Improvements in or relating to resinous condensation products and coating compositions

Publications (1)

Publication Number Publication Date
GB377587A true GB377587A (en) 1932-07-28

Family

ID=9771109

Family Applications (1)

Application Number Title Priority Date Filing Date
GB411932A Expired GB377587A (en) 1932-02-11 1932-02-11 Improvements in or relating to resinous condensation products and coating compositions

Country Status (1)

Country Link
GB (1) GB377587A (en)

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