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JPS57192433A - Water dilution type alkyd resin - Google Patents

Water dilution type alkyd resin

Info

Publication number
JPS57192433A
JPS57192433A JP56077231A JP7723181A JPS57192433A JP S57192433 A JPS57192433 A JP S57192433A JP 56077231 A JP56077231 A JP 56077231A JP 7723181 A JP7723181 A JP 7723181A JP S57192433 A JPS57192433 A JP S57192433A
Authority
JP
Japan
Prior art keywords
alkyd resin
acid
maleic anhydride
reacted
diisocyanate
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.)
Pending
Application number
JP56077231A
Other languages
Japanese (ja)
Inventor
Motohide Shimomura
Hiroichi Yokoyama
Susumu Nakamura
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.)
Nippon Synthetic Chemical Industry Co Ltd
Original Assignee
Nippon Synthetic Chemical Industry Co 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 Nippon Synthetic Chemical Industry Co Ltd filed Critical Nippon Synthetic Chemical Industry Co Ltd
Priority to JP56077231A priority Critical patent/JPS57192433A/en
Publication of JPS57192433A publication Critical patent/JPS57192433A/en
Pending legal-status Critical Current

Links

Landscapes

  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE: To provide the titled resin which is suitable as a raw material for baking type paint and has excellent hardness, water resistance, etc., by incorporating a sorbic acid/maleic anhydride Diels-Alder adduct and a diisocyanate compd. as modifying components.
CONSTITUTION: A fatty acid such as stearic acid or an oil, a polyol such as ethylene glycol and a polycarboxylic acid such as phthalic acid or its anhydride, are reacted together to produce an alkyd resin precursor. Sorbic and maleic anhydride are reacted with said alkyd resin precursor. Then the resulting product is reacted with a diisocyanate compd. such as isophorone diisocyanate to obtain the desired water dilution type alkyd resin in which a portion modified by the sorbic acid/maleic anhydride Diels-Alder adduct is 5W25wt% and a portion modified by the diisocyanate compd. is 2.5W15wt%.
COPYRIGHT: (C)1982,JPO&Japio
JP56077231A 1981-05-20 1981-05-20 Water dilution type alkyd resin Pending JPS57192433A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56077231A JPS57192433A (en) 1981-05-20 1981-05-20 Water dilution type alkyd resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56077231A JPS57192433A (en) 1981-05-20 1981-05-20 Water dilution type alkyd resin

Publications (1)

Publication Number Publication Date
JPS57192433A true JPS57192433A (en) 1982-11-26

Family

ID=13628082

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56077231A Pending JPS57192433A (en) 1981-05-20 1981-05-20 Water dilution type alkyd resin

Country Status (1)

Country Link
JP (1) JPS57192433A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8372914B2 (en) * 2005-03-02 2013-02-12 Cytec Surface Specialties Austria Gmbh Urethane modified water-reducible alkyd resins
JP2014529346A (en) * 2011-07-29 2014-11-06 エボニック デグサ ゲーエムベーハーＥｖｏｎｉｋ Ｄｅｇｕｓｓａ ＧｍｂＨ Low molecular weight products and their use as reversible or permanent low temperature crosslinkers during Diels-Alder reactions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8372914B2 (en) * 2005-03-02 2013-02-12 Cytec Surface Specialties Austria Gmbh Urethane modified water-reducible alkyd resins
JP2014529346A (en) * 2011-07-29 2014-11-06 エボニック デグサ ゲーエムベーハーＥｖｏｎｉｋ Ｄｅｇｕｓｓａ ＧｍｂＨ Low molecular weight products and their use as reversible or permanent low temperature crosslinkers during Diels-Alder reactions

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