GB521799A - Improvements in and relating to the production of phenol-aldehyde synthetic resins - Google Patents

Improvements in and relating to the production of phenol-aldehyde synthetic resins

Info

Publication number
GB521799A
GB521799A GB34099/38A GB3409938A GB521799A GB 521799 A GB521799 A GB 521799A GB 34099/38 A GB34099/38 A GB 34099/38A GB 3409938 A GB3409938 A GB 3409938A GB 521799 A GB521799 A GB 521799A
Authority
GB
United Kingdom
Prior art keywords
hydroxide
ammonium hydroxide
phenol
ammonium
tetramethyl
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
GB34099/38A
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.)
Bakelite Ltd
Original Assignee
Bakelite 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 Bakelite Ltd filed Critical Bakelite Ltd
Publication of GB521799A publication Critical patent/GB521799A/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
    • 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
    • C08G8/04Condensation polymers of aldehydes or ketones with phenols only of aldehydes
    • C08G8/08Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Fireproofing Substances (AREA)
  • Paper (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)

Abstract

521,799. Phenol-aldehyde condensation products; quarternary compounds. BAKELITE, Ltd. Nov. 23, 1938, No. 34099. Convention date, Nov. 27, 1937. [Class 2 (iii)] Phenols are condensed with formaldehyde or a solid polymer thereof in the presence of quarternary bases or phenolic salts thereof. Suitable bases include ammonium, pyridinium, sulphonium, phosphonium, arsonium and stibonium bases such as tetramethyl ammonium hydroxide, tetraethyl ammonium hydroxide, trimethylbenzyl ammonium hydroxide, dicyclohexyldimethyl ammonium hydroxide, dimethylcyclohexylbenzyl ammonium hydroxide, trimethylcyclohexyl ammonium hydroxide, dimethylphenylbenzyl ammonium hydroxide, methyl pyridinium hydroxide, diethylmethyl sulphonium hydroxide, tetramethylphosphonium hydroxide and tetramethyl arsonium hydroxide. The resinous products may be cast and heat-hardened, may be moulded with or without fillers such as wood flour, asbestos or cotton flock, or may be used as ingredients for varnishes, paper sizes. Liquid compositions may be used for impregnation of bases such as paper, textiles or wood veneer and as binders in the manufacture of abrasive articles. In examples : (1) phenol or a mixture of m-cresol and p-cresol is condensed with aqueous formaldehyde in the presence of aqueous tetramethyl ammonium hydroxide, trimethylbenzyl ammonium hydroxide; dicyclohexyldimethyl ammonium hydroxide, diethylmethyl sulphonium hydroxide, tetramethylphosphonium hydroxide, methyl pyridinium hydroxide, tetramethyl arsonium hydroxide or trimethylbenzylammonium phenate and the partially dehydrated product acidified with an aqueous solution of tartaric, citric, or lactic acid and fully dehydrated and, if desired, after blending with glycerine, cast ; (2) a solution of an aqueous solution of trimethylbenzyl ammonium hydroxide in phenol is warmed with paraformaldehyde, blended with phenol, mixed with abrasive grains and with a heat-hardenable phenol-formaldehyde resin and moulded. Trimethylbenzyl ammonium phenate is prepared by reacting benzyl chloride with aqueous trimethylamine and reacting the product with phenol in the presence of sodium hydroxide.
GB34099/38A 1937-11-27 1938-11-23 Improvements in and relating to the production of phenol-aldehyde synthetic resins Expired GB521799A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US521799XA 1937-11-27 1937-11-27

Publications (1)

Publication Number Publication Date
GB521799A true GB521799A (en) 1940-05-31

Family

ID=21975963

Family Applications (1)

Application Number Title Priority Date Filing Date
GB34099/38A Expired GB521799A (en) 1937-11-27 1938-11-23 Improvements in and relating to the production of phenol-aldehyde synthetic resins

Country Status (1)

Country Link
GB (1) GB521799A (en)

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