GB663079A - Acetone resin modified phenol resins - Google Patents

Acetone resin modified phenol resins

Info

Publication number
GB663079A
GB663079A GB18555/48A GB1855548A GB663079A GB 663079 A GB663079 A GB 663079A GB 18555/48 A GB18555/48 A GB 18555/48A GB 1855548 A GB1855548 A GB 1855548A GB 663079 A GB663079 A GB 663079A
Authority
GB
United Kingdom
Prior art keywords
reaction
resins
acetone
formalin
mat
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
GB18555/48A
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 Corp
Original Assignee
Bakelite 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
Priority claimed from US763739A external-priority patent/US2545559A/en
Application filed by Bakelite Corp filed Critical Bakelite Corp
Publication of GB663079A publication Critical patent/GB663079A/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
    • C08G8/04Condensation 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
    • C08G8/10Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/02Condensation polymers of aldehydes or ketones only
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/04Condensation polymers of aldehydes or ketones with phenols only
    • C08L61/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/18Condensation polymers of aldehydes or ketones with aromatic hydrocarbons or their halogen derivatives only

Landscapes

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

Abstract

Resinous compositions are made by forming water-soluble resins by partially dehydrating the mixtures resulting from (a) the reaction of phenol and formaldehyde using a caustic alkali catalyst, and (b) the reaction of acetone (1 mol.) and formaldehyde (1 to 6 mols.) using an organic amine catalyst, and mixing the resins to form a composition containing 25 to 75 per cent by weight of either resin. In the example, phenol and formalin are condensed in the presence of caustic soda and under reduced pressure, the reaction mixture being neutralized with phosphoric acid after cooling and dehydrated by distillation, while a mixture of acetone, formalin and the low molecular weight reaction product of a previous batch is condensed in the presence of aqueous dimethylamine, the reaction mixture being partially dehydrated by distillation. In the bonding of glass wool, equal parts of the constituent resins are added to a mineral oil in water emulsion and sprayed on to a mat of glass wool, the mat being subsequently baked at 200 DEG C. Hardening of the mixtures may be accelerated by conventional heat-hardening agents.
GB18555/48A 1947-07-25 1948-07-09 Acetone resin modified phenol resins Expired GB663079A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US663079XA 1947-07-25 1947-07-25
US968739XA 1947-07-25 1947-07-25
US763739A US2545559A (en) 1947-07-25 1947-07-25 Acetone resin modified phenol resins

Publications (1)

Publication Number Publication Date
GB663079A true GB663079A (en) 1951-12-19

Family

ID=31982212

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18555/48A Expired GB663079A (en) 1947-07-25 1948-07-09 Acetone resin modified phenol resins

Country Status (2)

Country Link
FR (1) FR968739A (en)
GB (1) GB663079A (en)

Also Published As

Publication number Publication date
FR968739A (en) 1950-12-04

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