GB1042376A - Polyurethane lacquers - Google Patents

Polyurethane lacquers

Info

Publication number
GB1042376A
GB1042376A GB3093463A GB3093463A GB1042376A GB 1042376 A GB1042376 A GB 1042376A GB 3093463 A GB3093463 A GB 3093463A GB 3093463 A GB3093463 A GB 3093463A GB 1042376 A GB1042376 A GB 1042376A
Authority
GB
United Kingdom
Prior art keywords
oil
alkyd resin
resin
weight
acids
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
GB3093463A
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 & Co Dr GmbH
Original Assignee
Beck & Co Dr GmbH
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 & Co Dr GmbH filed Critical Beck & Co Dr GmbH
Publication of GB1042376A publication Critical patent/GB1042376A/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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4288Polycondensates having carboxylic or carbonic ester groups in the main chain modified by higher fatty oils or their acids or by resin acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)

Abstract

A heat hardenable polyurethane lacquer which contains no free -NCO groups and which is stable on storage at room temperature, is prepared by reacting (1) an alkyd resin having more than 2 free -OH groups and containing inert, saturated or unsaturated, straight or branched chain aliphatic residues having at least 8 C atoms in an amount of at least 40% of the weight of the resin, said resin having a viscosity when dissolved in 50% by weight of xylene of less than 200 seconds, measured in accordance with German Standard Specification DIN 53211 in a 4 mm. cup at 20 DEG C., with (2) a diisocyanate in an amount of more than 1 mol. per mol. of alkyd resin, but not more than the stoichiometric amount, in an inert solvent, the solvent forming more than 40% by weight of the reaction mixture, until no free isocyanate groups can be detected in the reaction product. The alkyd resin may contain natural or synthetic higher fatty acid residues, e.g. alkyd resins modified with linseed oil, soya bean oil, coconut oil or the corresponding fatty acids or the fatty acids of cotton seed oil, corn oil, sunflower oil or tall oil. The fatty acids may be replaced by fatty alcohols. Polycarboxylic acids which may be used to prepare the alkyd resin are: succinic, adipic, maleic and phthalic acids or their anhydrides. In Example (1) an alkyd resin prepared from soya bean oil fatty acid, pentaerythritol (containing 12% dipentaerythritol), glycerine and isophthalic acid, having a viscosity of 60 seconds (M.W. about 1600) was dissolved in white spirit and reacted with tolylene diisocyanate. A lacquer was obtained after heating for several hours at 80-100 DEG C.
GB3093463A 1962-08-14 1963-08-06 Polyurethane lacquers Expired GB1042376A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB0068422 1962-08-14

Publications (1)

Publication Number Publication Date
GB1042376A true GB1042376A (en) 1966-09-14

Family

ID=6975880

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3093463A Expired GB1042376A (en) 1962-08-14 1963-08-06 Polyurethane lacquers

Country Status (1)

Country Link
GB (1) GB1042376A (en)

Also Published As

Publication number Publication date
DE1494409A1 (en) 1969-01-02

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