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US4094836A Expired / Lapsed US ⏱️ 0.0 years remaining

Aqueous alkyd resins

Assignee: Sumitomo Chemical Co Ltd
•
Filing: 1977-04-07
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Granted: 1978-06-13
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Expires: 1997-04-07
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Abstract

Abstract An aqueous alkyd resin obtained by the neutralization of a polycondensation resin with a base, the polycondensation resin being prepared by reacting a reaction mixture obtained by the transesterification or esterification of (a) a natural fat and oil or a fatty acid with a polyhydric alcohol with an adduct of (b) a liquid polybutadiene having a number average molecular weight of 150 to 900, a viscosity of 2 to 80 cps. at 30 DEG C and at least 50% of the cis-1,4 structure with an alpha , beta -unsaturated dicarboxylic acid or the anhydride thereof, and/or the half-ester of said adduct, and with (c) an aromatic polycarboxylic acid or the anhydride thereof, and the polycondensation resin having free carboxyl groups in the amount corresponding to an acid value of 30 to 70 and containing 5 to 50% by weight of the component (b). This alkyd shows excellent coating film properties when used for water-base paints, printing inks and the like.

Inventors

  • 👤 Seimei Yasui
  • 👤 Minoru Hino
  • 👤 Kazuya Hayashi

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 08:31
CPC Classifications
C; C09; C09D; C09D11/00; C09D11/02; C09D11/10; C09D11/102; C09D11/104; C09D11/105; C08; C08G; C08G63/00; C08G63/02; C08G63/12; C08G63/52; C08G63/54; C08G63/553; C09D167/00; C09D167/08

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 190 words
An aqueous alkyd resin obtained by the neutralization of a polycondensation resin with a base, the polycondensation resin being prepared by reacting a reaction mixture obtained by the transesterification or esterification of (a) a natural fat and oil or a fatty acid with a polyhydric alcohol with an adduct of (b) a liquid polybutadiene having a number average molecular weight of 150 to 900, a viscosity of 2 to 80 cps;. at 30° C and at least 50% of the cis-1,4 structure with an α,β-unsaturated dicarboxylic acid or the anhydride thereof, and/or the half-ester of said adduct, and (c) an aromatic polycarboxylic acid or the anhydride thereof, the proportion of the component (b) to the component (a) being in the range of 0.1 to 0.7 by weight, as calculated by (b)/(a) + (b), the polycondensation resin having free carboxyl groups in the amount corresponding to an acid value of 30 to 70 and containing 5 to 50% by weight of the component (b), wherein the total amount of the components (a) and (b) is in the range of 30 to 85% by weight on the basis of the whole resin.
Claim 2
Dependent Claim 190 words
An aqueous alkyd resin obtained by the neutralization of a polycondensation resin with a base, the polycondensation resin being prepared by reacting a reaction mixture obtained by the transesterification or esterification of (a) a natural fat and oil or a fatty acid with a polyhydric alcohol with an adduct of (b) a liquid polybutadiene having a number average molecular weight of 150 to 900, a viscosity of 2 to 80 cps;. at 30° C and at least 50% of the cis-1,4 structure with an α,β-unsaturated dicarboxylic acid or the anhydride thereof, and/or the half-ester of said adduct, and (c) an aromatic polycarboxylic acid or the anhydride thereof, the proportion of the component (b) to the component (a) being in the range of 0.1 to 0.7 by weight, as calculated by (b)/(a) + (b), the polycondensation resin having free carboxyl groups in the amount corresponding to an acid value of 30 to 70 and containing 5 to 50% by weight of the component (b), wherein the total amount of the components (a) and (b) is in the range of 30 to 85% by weight on the basis of the whole resin.
Claim 3
Dependent Claim 37 words
The aqueous alkyd resin according to claim 1, wherein the α,β-unsaturated dicarboxylic acid or the anhydride thereof is a member selected from the group consisting of maleic anhydride, maleic acid, fumaric acid, itaconic acid and citraconic acid.
Claim 4
Dependent Claim 39 words
The aqueous akyd resin according to claim 1, wherein the aromatic polycarboyxlic acid or the anhydride thereof is a member selected from the group consisting of phthalic anhydride, phthalic acid, isophthalic acid, trimellitic acid, trimellitic anhydride and pyromellitic anhydride.
Claim 5
Dependent Claim 32 words
The aqueous alkyd resin according to claim 1, wherein the polyhydric alcohol is a member selected from the group consisting of glycerin, pentaerythritol, trimethylol propane, trimethylol ethane, ethylene glycol and diethylene glycol.
Claim 6
Dependent Claim 45 words
The aqueous akyd resin according to claim 1, wherein the natural fat and oil or fatty acid is a member selected from the group consisting of linseed oil, soybean oil, tung oil, dehydrated castor oil, safflower oil, coconut oil, and a fatty acid derived therefrom.
Claim 7
Dependent Claim 28 words
The aqueous alkyd resin according to claim 1, wherein the polycondensation resin has free carboxyl groups in the amount corresponding to an acid value of 30 to 60.
Claim 8
Dependent Claim 39 words
The aqueous alkyd resin according to claim 1, wherein the neutralizing agent is a member selected from the group consisting of methylamine, ethylamine, monoethanolamine, cyclohexylamine, dimethylamine, diethylamine, morpholine, diethanolamine, trimethylamine, triethylamine, N-alkylmorpholine, triethanolamine, sodium hydroxide, potassium hydroxide and ammonia.
Claim 9
Dependent Claim 32 words
The aqueous alkyd resin according to claim 1, wherein the amount of the component (b) is in the range of 5 to 50% by weight on the basis of the whole resin.
Claim 10
Independent Claim 137 words
A method for preparing an aqueous alkyd resin, which comprises polycondensing a reaction mixture obtained by the transesterification or esterification of (a) a natural fat and oil or a fatty acid with a polyhydric alcohol with an adduct of (b) a liquid polybutadiene having a number average molecular weight of 150 to 900, a viscosity of 2 to 80 cps. at 30° C and at least 50% of the cis-1,4 structure with an α,β-unsaturated dicarboxylic acid or the anhydride thereof, and/or the half-ester of said adduct, and (c) an aromatic polycarboxylic acid or the anhydride thereof, to give a polycondensation resin having free carboxyl groups in the amount corresponding to an acid value of 30 to 70 and containing 5 to 50% by weight of the component (b), and neutralizing the polycondensation resin with a neutralizing agent.
Claim 11
Independent Claim 137 words
A method for preparing an aqueous alkyd resin, which comprises polycondensing a reaction mixture obtained by the transesterification or esterification of (a) a natural fat and oil or a fatty acid with a polyhydric alcohol with an adduct of (b) a liquid polybutadiene having a number average molecular weight of 150 to 900, a viscosity of 2 to 80 cps. at 30° C and at least 50% of the cis-1,4 structure with an α,β-unsaturated dicarboxylic acid or the anhydride thereof, and/or the half-ester of said adduct, and (c) an aromatic polycarboxylic acid or the anhydride thereof, to give a polycondensation resin having free carboxyl groups in the amount corresponding to an acid value of 30 to 70 and containing 5 to 50% by weight of the component (b), and neutralizing the polycondensation resin with a neutralizing agent.
Claim 12
Dependent Claim 27 words
The method according to claim 9, wherein the proportion of the component (b) to the component (a) is in the range of 0.1 to 0.7 by weight.
Claim 13
Dependent Claim 29 words
The method according to claim 9, wherein the neutralizing agent is used in an amount of 0.3 to 1.2 equivalent to the carboxyl groups contained in the polycondensation resin.
Claim 14
Dependent Claim 13 words
A water-base paint containing the aqueous resin as set forth in claim 1.
Claim 15
Dependent Claim 18 words
A baking paint comprising the aqueous alkyd resin as set forth in claim 1 and a melamine resin.
Claim 16
Dependent Claim 22 words
The baking paint according to claim 13, wherein the melamine resin is present in the range of 10 to 50% by weight.

References Cited (Backward Citations)

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US3457207A Cited
US3689446A Cited
US3705866A Cited
US3876721A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-06-12 1981-12-12 1982-06-13 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-06-12 1985-12-12 1986-06-13 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-06-12 1989-12-12 1990-06-13 $7700.00 Window Closed / Lapsed

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