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US4200705A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing blends of vinyl esters and reactive diluents

Assignee: Dow Chemical Co
•
Filing: 1979-01-02
•
Granted: 1980-04-29
•
Expires: 1999-01-02
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Abstract

Abstract A curable vinyl ester composition is prepared by the process wherein an organic hydroxy compound is reacted with a stoichiometric excess of an ethylenically unsaturated carboxylic acid and, after substantial completion of that esterification, reacting an oxirane compound with the unesterified carboxyl groups.

Inventors

  • 👤 Rhetta Q. Davis

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 21:03
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/14; C08G59/1433; C08G59/1438; C08G59/1455; C09; C09D; C09D163/00

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 138 words
In the process for preparing a curable composition of (1) a vinyl ester resin prepared from an α,β-ethylenically unsaturated carboxylic acid and a compound containing at least one oxirane group and (2) as a reactive diluent, an ester prepared from the same unsaturated carboxylic acid and an organic hydroxy compound, the improvement being a sequential process wherein said organic hydroxy compound is reacted in a first esterification with an excess of equivalents of said carboxylic acid over that required to make said reactive diluent, and after substantial completion of the esterification, introducing into the reaction mixture of reactive diluent and unreacted carboxylic acid an amount of said oxirane compound in an amount equivalent to the unreacted acid from the first esterification, and causing substantially complete reaction of said oxirane compound and said carboxylic acid in a second esterification.
Claim 2
Dependent Claim 138 words
In the process for preparing a curable composition of (1) a vinyl ester resin prepared from an α,β-ethylenically unsaturated carboxylic acid and a compound containing at least one oxirane group and (2) as a reactive diluent, an ester prepared from the same unsaturated carboxylic acid and an organic hydroxy compound, the improvement being a sequential process wherein said organic hydroxy compound is reacted in a first esterification with an excess of equivalents of said carboxylic acid over that required to make said reactive diluent, and after substantial completion of the esterification, introducing into the reaction mixture of reactive diluent and unreacted carboxylic acid an amount of said oxirane compound in an amount equivalent to the unreacted acid from the first esterification, and causing substantially complete reaction of said oxirane compound and said carboxylic acid in a second esterification.
Claim 3
Dependent Claim 15 words
The process claimed in claim 1 wherein said organic hydroxy compound is a monohydroxy compound.
Claim 4
Dependent Claim 40 words
The process claimed in claim 2 wherein said monohydroxy compound is an ether of a glycol having the formula: ##STR2## wherein R is alkyl or aryl; R' and R" are individually H or methyl and n is 0 or 1.
Claim 5
Dependent Claim 16 words
The process claimed in claim 3 wherein said ether is the phenyl ether of ethylene glycol.
Claim 6
Dependent Claim 14 words
The process claimed in claim 1 wherein said organic hydroxy compound is a polyol.
Claim 7
Dependent Claim 26 words
The process claimed in claim 5 wherein said polyol is a novolac of phenol and formaldehyde extended with about 4 moles ethylene oxide for each hydroxyl.
Claim 8
Dependent Claim 14 words
The process claimed in claim 1 wherein said unsaturated carboxylic acid is acrylic acid.
Claim 9
Dependent Claim 13 words
The process claimed in claim 1 wherein said oxirane compound is a polyepoxide.
Claim 10
Dependent Claim 16 words
The process claimed in claim 8 wherein said polyepoxide is the diglycidyl ether of bisphenol A.
Claim 11
Dependent Claim 28 words
The process claimed in claim 1 wherein from about 1.5 to about 10 equivalents of said unsaturated acid are initially reacted with each equivalent of organic hydroxy compound.

References Cited (Backward Citations)

US3179623A Cited
US3301743A Cited
US3317465A Cited
US3377406A Cited
US3367992A Cited
US3256226A Cited
US3867354A Cited
US3933935A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-04-29 1983-10-29 1984-04-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-04-29 1987-10-29 1988-04-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-04-29 1991-10-29 1992-04-29 $7700.00 Window Closed / Lapsed

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