GB625385A - Reaction products of acrolein and anacardic materials - Google Patents

Reaction products of acrolein and anacardic materials

Info

Publication number
GB625385A
GB625385A GB20215/47A GB2021547A GB625385A GB 625385 A GB625385 A GB 625385A GB 20215/47 A GB20215/47 A GB 20215/47A GB 2021547 A GB2021547 A GB 2021547A GB 625385 A GB625385 A GB 625385A
Authority
GB
United Kingdom
Prior art keywords
cashew nut
nut shell
shell liquid
acrolein
anacardic
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
GB20215/47A
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.)
Harvel Corp
Original Assignee
Harvel 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 Harvel Corp filed Critical Harvel Corp
Publication of GB625385A publication Critical patent/GB625385A/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
    • C09FNATURAL RESINS; FRENCH POLISH; DRYING-OILS; DRIERS (SICCATIVES); TURPENTINE
    • C09F5/00Obtaining drying-oils
    • C09F5/06Obtaining drying-oils by dehydration of hydroxylated fatty acids or 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
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • C08G16/0212Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds
    • C08G16/0218Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen
    • C08G16/0225Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen containing oxygen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Emergency Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Thermosetting resinous compositions are produced by heating acrolein with anacardic materials which may be cashew nut shell liquid, distillate or residue obtained by distilling cashew nut shell liquid or polymers of the liquids. The cashew nut shell liquid may be raw, as obtained by the process of U.S.A. Specification 2,058,456, or treated, e.g. according to the process of U.S.A. Specification 2,128,247 or 2,067,919. Polymerized cashew nut shell liquid may be prepared according to U.S.A. Specification 2,128,247 or 2,240,038. A distillate or distillation residue may be polymerized according to U.S.A. Specifications 2,292,611 and 2,317,585. The acrolein is slowly added with stirring and cooling to the anacardic material. If desired an acid or basic condensing agent may then be added, e.g. a mineral acid to a pH of 2-5, and the mixture heated at 80-125 DEG C. The products may be used as plasticisers for rubber or synthetic rubber, or for ethyl cellulose, as impregnating or coating agents, e.g. after thinning with mineral spirits or alcohol, especially for asbestos brake and clutch linings and for electrical coils, magnets and conductors, as laminating material for paper, wood or cloth, or for addition to phenol-formaldehyde, furfuryl alcohol-formaldehyde, or furfuryl alcohol-glyoxal resins to improve their impact strength. The reaction may be performed in presence of toluene which aids separation of water formed, or with the ingredients in aqueous emulsion. Phenol may be included in the reaction mixture if desired. Specification 283,803, [Class 2 (iii)], also is referred to.ALSO:Condensation products of acrolein with cashew nut shell liquid or similar anacardic materials, or mixtures of these with ethyl cellulose are used as plasticizers for natural or reclaimed rubber or for the copolymers of butadiene 1, 3 and acrylonitrile or of butadiene 1, 3 and styrene. Specification 283,803, [Class 2 (iii)], is referred to.
GB20215/47A 1944-08-30 1947-07-28 Reaction products of acrolein and anacardic materials Expired GB625385A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US625385XA 1944-08-30 1944-08-30

Publications (1)

Publication Number Publication Date
GB625385A true GB625385A (en) 1949-06-27

Family

ID=22043151

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20215/47A Expired GB625385A (en) 1944-08-30 1947-07-28 Reaction products of acrolein and anacardic materials

Country Status (1)

Country Link
GB (1) GB625385A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0015761A2 (en) * 1979-03-09 1980-09-17 Anthony Jack Hawkes Polymer, preparation and formulations for preparation thereof and use for production of bonded materials

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0015761A2 (en) * 1979-03-09 1980-09-17 Anthony Jack Hawkes Polymer, preparation and formulations for preparation thereof and use for production of bonded materials
WO1980001918A1 (en) * 1979-03-09 1980-09-18 A Hawkes Polymer,preparation and formulations for preparation thereof use for production of bonded materials,intermediates and preparation thereof
EP0015761A3 (en) * 1979-03-09 1980-11-26 Anthony Jack Hawkes Polymer, preparation and formulations for preparation thereof, use for production of bonded materials, intermediates and preparation thereof

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