GB646080A - A process for the preparation and application of reactive phenol-aldehyde resins - Google Patents

A process for the preparation and application of reactive phenol-aldehyde resins

Info

Publication number
GB646080A
GB646080A GB4189/48A GB418948A GB646080A GB 646080 A GB646080 A GB 646080A GB 4189/48 A GB4189/48 A GB 4189/48A GB 418948 A GB418948 A GB 418948A GB 646080 A GB646080 A GB 646080A
Authority
GB
United Kingdom
Prior art keywords
phenol
aldehyde
novolak
reacted
mixture
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
GB4189/48A
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.)
Beck Koller and Company England Ltd
Original Assignee
Beck Koller and Company England 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 Beck Koller and Company England Ltd filed Critical Beck Koller and Company England Ltd
Publication of GB646080A publication Critical patent/GB646080A/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
    • C08G8/34Chemically modified polycondensates by natural resins or resin acids, e.g. rosin
    • 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

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)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Phenol-aldehyde resins, which are suitable for modifying rosin or ester gum in making drying oil varnishes, are prepared by reacting phenol and an aldehyde in two steps: (1) forming a Novolak in acid medium by condensing all the phenol with less than an equi-molecular ambient of aldehyde; and (2) condensing the Novolak with aqueous formaldehyde in a medium of strong alkali without addition of further phenol at a temperature not above 40 DEG C. to convert it into a Novolak polyalcohol, i.e. a Novolak in which the reactive positions have been wholly or partly substituted by methylol groups. The second amount of aldehyde is added in sufficient quantity to bring the ratio of total combined aldehyde to phenol up to at least 1 : 1. At the end of the first (acid) reaction the mixture contains about 20 per cent free phenol which may be distilled off or reacted with the aldehyde in the second stage. In examples: (1a) phenol, 470 g., and 37 per cent aqueous formaldehyde, 243 g., are reacted at 100 DEG C. in acid solution for 1 to 2 hours, 70 g. of 50 per cent NaOH is added, and the mixture reacted 4 to 5 days at 30 DEG C. with 485 g. aqueous formaldehyde. The mixture is neutralized with HCl and the resin filtered off; (1b) the product of (1a) is reacted with a mixture of gum rosin and glycerol; (2) similar procedure to that of (1) is followed, using, however, paraformaldehyde in forming the Novolak; (3a and 3b) similar procedure to that in (2) is followed. The product is then (3c) cooked with linseed oil and diluted with mineral spirits to form a varnish. Specification 261,472, [Class 81 (ii)], and U.S.A. Specification 1,699,727 are referred to.
GB4189/48A 1941-11-04 1948-02-12 A process for the preparation and application of reactive phenol-aldehyde resins Expired GB646080A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US646080XA 1941-11-04 1941-11-04

Publications (1)

Publication Number Publication Date
GB646080A true GB646080A (en) 1950-11-15

Family

ID=22057100

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4189/48A Expired GB646080A (en) 1941-11-04 1948-02-12 A process for the preparation and application of reactive phenol-aldehyde resins

Country Status (1)

Country Link
GB (1) GB646080A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226365A (en) * 1960-12-10 1965-12-28 Toyo Kogyo Company Ltd Process for producing liquid novolak type phenol-formaldehyde resin compositions
FR2350365A1 (en) * 1976-05-07 1977-12-02 Basf Ag Rapid hardening phenol-formaldehyde glues mfr. - giving a stability which is less alkali dependent

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226365A (en) * 1960-12-10 1965-12-28 Toyo Kogyo Company Ltd Process for producing liquid novolak type phenol-formaldehyde resin compositions
FR2350365A1 (en) * 1976-05-07 1977-12-02 Basf Ag Rapid hardening phenol-formaldehyde glues mfr. - giving a stability which is less alkali dependent

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