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US4530947A Expired / Lapsed US ⏱️ 0.0 years remaining

Anticorrosive coating composition

Assignee: Adeka Corp
•
Filing: 1984-04-24
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Granted: 1985-07-23
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Expires: 2004-04-24
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Abstract

Abstract A coating composition which comprises (A) a polyol resin obtained by the reaction of a prepolymer of epoxy resin and polyhydroxy penolic compound such as (i) poly-nuclear polyhydroxy phenols having adjacent hydroxy groups (ii) polyol esters of polyhydroxy phenolic carboxylic acids having adjacent hydroxy groups, and (iii) a mixture thereof, and one or more compound having one or more amino groups reactive with epoxy group; (B) a compound having more than one isocyanate group or groups which change to isocyanate groups under hardening condition, and (C) a bituminous material and/or its substitute. This coating composition can be coated on rusty metal surfaces.

Inventors

  • 👤 Hidehiko Kojo
  • 👤 Koji Akimoto

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 14:19
CPC Classifications
C; C09; C09D; C09D195/00; C09D175/00; C09D175/04

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 217 words
A coating composition which comprises a mixture of (A) a polyol resin obtained by the reaction of an amino compound having at least one primary or secondary amino group with a prepolymer containing epoxy groups which prepolymer has been prepared by reacting an epoxy resin, with a polyhydroxy phenolic compound selected from the group consisting of polynuclear polyhydroxy phenols having adjacent hydroxy groups, polyol esters of polyhydroxy phenolic carboxylic acids having adjacent hydroxy groups, and mixtures thereof, said prepolymer containing at least 0.05 mole of said polyhydroxy phenolic compound, per molecule, and having an average epoxide equivalent of less than 3000; (B) a compound having more than one isocyanate group or groups which change to isocyanate groups under conditions effective for hardening the coating composition; and (C) a material selected from the group consisting of coal tar, coal tar pitch, cut-back tar, bojuntan and asphalt, wherein the reaction ratio of said amino compound to said prepolymer, by equivalents of groups of said amino compound that are reactive with the epoxy groups of said prepolymer, is from 1.1 to 0.7; the ratio of (A) to (B), by equivalents of the hydroxy groups of (A) to the isocyanate groups of (B), is from 0.4 to 1.2; and the weight ratio of (C) to (A) is from 0.5 to 2.
Claim 2
Dependent Claim 217 words
A coating composition which comprises a mixture of (A) a polyol resin obtained by the reaction of an amino compound having at least one primary or secondary amino group with a prepolymer containing epoxy groups which prepolymer has been prepared by reacting an epoxy resin, with a polyhydroxy phenolic compound selected from the group consisting of polynuclear polyhydroxy phenols having adjacent hydroxy groups, polyol esters of polyhydroxy phenolic carboxylic acids having adjacent hydroxy groups, and mixtures thereof, said prepolymer containing at least 0.05 mole of said polyhydroxy phenolic compound, per molecule, and having an average epoxide equivalent of less than 3000; (B) a compound having more than one isocyanate group or groups which change to isocyanate groups under conditions effective for hardening the coating composition; and (C) a material selected from the group consisting of coal tar, coal tar pitch, cut-back tar, bojuntan and asphalt, wherein the reaction ratio of said amino compound to said prepolymer, by equivalents of groups of said amino compound that are reactive with the epoxy groups of said prepolymer, is from 1.1 to 0.7; the ratio of (A) to (B), by equivalents of the hydroxy groups of (A) to the isocyanate groups of (B), is from 0.4 to 1.2; and the weight ratio of (C) to (A) is from 0.5 to 2.
Claim 3
Dependent Claim 42 words
A coating composition as claimed in claim 1, in which the reaction ratio of said amino compound to said prepolymer having epoxy groups is from 1.0 to 0.9 in terms of an quivalent ratio of the amino groups to the epoxy groups.
Claim 4
Dependent Claim 41 words
A coating composition as claimed in claim 1 in which the ratio of (A) to (B), in terms of the equivalent ratio of the isocyanate groups contained in (B) to the hydroxy groups contained in (A), is from 0.7 to 1.0.
Claim 5
Dependent Claim 70 words
A coating composition as claimed in claim 1 in which said polynuclear polyhydroxy phenol having adjacent hydroxy groups is a product of the condensation of formaldehyde with a polyhydroxy phenol selected from the group consisting of catechol, catechol-3-carboxylic acid and esters thereof, catechol-4-carboxylic acid and esters thereof, pyrogallol, pyrogallol-4-carboxylic acid and esters thereof, pyrogallol-4,6-dicarboxylic acid and esters thereof, gallic acid and esters thereof, tanninc acid and esters thereof, and urushiol.
Claim 6
Dependent Claim 55 words
A coating composition as claimed in claim 1 in which said polyol esters of polyhydroxy phenolic carboxylic acids having adjacent hydroxy groups are esters of aliphatic polyols with a polyhydroxy phenolic carboxylic acid selected from the group consisting of catechol-3-carboxylic acid, catechol-4-carboxylic acid, gallic acid, m-galloyl gallic acid, pyrogallol-4-carboxylic acid, pyrogallol-4,6-dicarboxylic acid and tannic acid.
Claim 7
Dependent Claim 19 words
A coating composition as claimed in claim 1 in which said amino compound is a primary or secondary amine.
Claim 8
Dependent Claim 29 words
A coating composition as claimed in claim 1 in which said amino compound is selected from the group consisting of methylamine, ethylamine, propylamine, dibutylamine, ethanolamine, propanolamine, diethanolamine and diisopropanolamine.
Claim 9
Dependent Claim 50 words
A coating composition as claimed in claim 1 in which (B) is selected from the group consisting of tolyene diisocyanate, xylylene diisocyanate, diphenyl methane diisocyanate, hexamethylene diisocyanate, an adduct of 3 moles of tolylene diisocyanate and trimethylol propane and a prepolymer obtained from the foregoing compounds and containing isocyanate group.

References Cited (Backward Citations)

CA666905A Cited
US3615801A Cited
US3846442A Cited
JPS4992125A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-07-22 1989-01-21 1989-07-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-07-22 1993-01-21 1993-07-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-07-22 1997-01-21 1997-07-23 $7700.00 Window Closed / Lapsed

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