GB909842A - - Google Patents

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Publication number
GB909842A
GB909842A GB909842DA GB909842A GB 909842 A GB909842 A GB 909842A GB 909842D A GB909842D A GB 909842DA GB 909842 A GB909842 A GB 909842A
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United Kingdom
Prior art keywords
derived
prepared
polyols
oct
alkali metal
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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.)
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Publication of GB909842A publication Critical patent/GB909842A/en
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    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule

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  • 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

909,842. Alkylene oxide modified novolaks, and esters prepared therefrom. DISTILLERS CO. Ltd. Oct. 21, 1959 [Oct. 22, 1958], No. 33787/58. Class 2(5) Polyols are prepared by reacting, at an elevated temperature, a phenol-formaldehyde novolak resin, derived from phenol itself and which has at least three phenolic units per molecule, with ethylene oxide and/or 1:2-propylene oxide under atmospheric pressure and under anhydrous conditions, part of said novolak resin being in the form of its alkali metal salt. The examples describe the preparation of the novolaks and their subsequent convertion in part to their alkali metal salts. The polyol prepared in Example 1 is soluble in ethanol and acetone. The polyols may be esterified with fatty acids derived from drying and semi-drying oils to give esters which are compatible with white spirit and xylene; cobalt, calcium and lead naphthenate driers may be added to the ester solutions. Fatty acids utilized in the examples are those derived from linseed oil and dehydrated castor oil. Specifications 757,392, 760,698, 760,699, 775,459 and 775,460 are referred to.
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ID=1753365

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3423356A (en) * 1965-07-23 1969-01-21 Dunlop Co Ltd Polymer compositions comprising the reaction products of polyepisulphides and phenolic resins

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3423356A (en) * 1965-07-23 1969-01-21 Dunlop Co Ltd Polymer compositions comprising the reaction products of polyepisulphides and phenolic resins

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