GB720035A - Improvements in the production of hardenable resins - Google Patents

Improvements in the production of hardenable resins

Info

Publication number
GB720035A
GB720035A GB584452A GB584452A GB720035A GB 720035 A GB720035 A GB 720035A GB 584452 A GB584452 A GB 584452A GB 584452 A GB584452 A GB 584452A GB 720035 A GB720035 A GB 720035A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
parts
phenol
aldehyde
product
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
GB584452A
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB720035A publication Critical patent/GB720035A/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
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • 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
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • C08G14/04Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Hardenable resins are prepared by condensing an aldehyde with a condensation product prepared from 40-200 parts of a phenol with 100 parts of an oxygen-containing reaction product of an aromatic hydrocarbon and an aldehyde. The aromatic hydrocarbon may be alkylated, e.g. xylene or polynuclear non-alkylated as in Specification 720,034. Preferably 50-200 parts of 30 per cent formaldehyde or an equivalent amount of a formaldehyde polymer or of a substance generating formaldehyde, e.g. hexamethylene-tetramine, are used per 100 parts of condensation product. Substances which can react with aldehydes to form resins, e.g. acid amides, phenols, amines, urethanes or ketones may be added to the condensation products prior to their further reaction with aldehyde. Fillers, dyestuffs or pigments, e.g. graphite or carbon black, may be added to the products during their working up. Small amounts of high molecular weight chlorinated aliphatic hydrocarbons may also be incorporated. The products are soluble in ethanol or toluene-alcohol mixtures. In the examples (1) a naphthalene formaldehyde resin is condensed with phenol and the product reacted with formaldehyde in presence of ammonia; (2) is similar, but the reaction with formaldehyde is performed under acid conditions; (3) a xylene-formaldehyde-phenol condensate is reacted with formaldehyde under acid conditions. In example (4) a naphthalene-formaldehyde-phenol condensate is worked up to a pressing mass with a novolac, wood meal, hexamethylene tetramine, magnesium oxide and bleached montan wax. In example (5) a product prepared as in example (2) is mixed with graphite, hexamethylene tetramine and highly chlorinated paraffin on mixing rollers and moulded at 170 DEG C. and 150 kgm/cm.2.
GB584452A 1951-03-08 1952-03-06 Improvements in the production of hardenable resins Expired GB720035A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB14089A DE884424C (en) 1951-03-08 1951-03-08 Process for the production of curable synthetic resins

Publications (1)

Publication Number Publication Date
GB720035A true GB720035A (en) 1954-12-15

Family

ID=6957835

Family Applications (1)

Application Number Title Priority Date Filing Date
GB584452A Expired GB720035A (en) 1951-03-08 1952-03-06 Improvements in the production of hardenable resins

Country Status (3)

Country Link
DE (1) DE884424C (en)
FR (1) FR1051868A (en)
GB (1) GB720035A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4395498A (en) 1981-09-18 1983-07-26 Minnesota Mining And Manufacturing Company High temperature phenolic resins and friction elements prepared therefrom

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4395498A (en) 1981-09-18 1983-07-26 Minnesota Mining And Manufacturing Company High temperature phenolic resins and friction elements prepared therefrom

Also Published As

Publication number Publication date
FR1051868A (en) 1954-01-19
DE884424C (en) 1953-07-27

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