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US4459401A Expired / Lapsed US ⏱️ 0.0 years remaining

Polyester oligomer and high solids thermosetting coatings

Assignee: DeSoto Inc
•
Filing: 1983-05-04
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Granted: 1984-07-10
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Expires: 2003-05-04
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Abstract

Abstract An essentially linear polyester oligomer having hydroxyl and carboxyl terminal groups for subsequent cure and its production are disclosed. This polyester oligomer is produced by first adducting approximately equimolar amounts of diol carrying two primary hydroxyl groups and a dicarboxylic acid anhydride to form an hydroxy acid. The carboxyl groups of this hydroxy acid are then esterified by reaction with an approximately stoichiometric proportion of diol carrying one primary hydroxyl group and one secondary hydroxyl group, the stoichiometry being based on the total hydroxyl content of the diol and the carboxyl content of the hydroxy acid, to form an hydroxyl-terminated oligomer. This hydroxyl-terminated oligomer is then adducted with a polycarboxylic acid monoanhydride having a carboxyl functionality of at least 3, this monoanhydride being used in an amount of 0.01 to 0.15 equivalents of anhydride per hydroxyl equivalent in the hydroxyl-terminated oligomer. The resulting polyester oligomer is essentially linear and possesses low solution viscosity at high resin solids content combined with high reactivity enabling low temperature cure with aminoplast resins.

Inventors

  • 👤 Kazys Sekmakas
  • 👤 Raj Shah
  • 👤 Ronald J. Lewarchiki
  • 👤 Kevin P. Murray

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 11:20
CPC Classifications
C; C08; C08G; C08G63/00; C08G63/02; C08G63/12; C08G63/16; C08G63/18; C08G63/181; C08G63/183; C09; C09D; C09D167/00; C09D167/02

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 161 words
A method of producing an essentially linear polyester oligomer having hydroxyl and carboxyl terminal groups for subsequent cure comprising, adducting approximately equimolar amounts of diol carrying two primary hydroxyl groups and a dicarboxylic acid anhydride to form an hydroxy acid, esterifying the carboxyl groups of said hydroxy acid by reaction with an approximately stoichiometric proportion of diol carrying one primary hydroxyl group and one secondary hydroxyl group, the stoichiometry being based on the total hydroxyl content of the diol and the carboxyl content of the hydroxy acid, to form an hydroxyl-terminated oligomer, and then adducting said hydroxyl-terminated oligomer with a polycarboxylic acid monoanhydride having a carboxyl functionality of at least 3, said monoanhydride being used in an amount of 0.01 to 0.15 equivalents of anhydride per hydroxyl equivalent in said hydroxyl-terminated oligomer, whereby the polyester oligomer so-produced is essentially linear and possesses low solution viscosity at high resin solids content combined with high reactivity enabling low temperature cure with hexamethoxymethyl melamine.
Claim 2
Independent Claim 161 words
A method of producing an essentially linear polyester oligomer having hydroxyl and carboxyl terminal groups for subsequent cure comprising, adducting approximately equimolar amounts of diol carrying two primary hydroxyl groups and a dicarboxylic acid anhydride to form an hydroxy acid, esterifying the carboxyl groups of said hydroxy acid by reaction with an approximately stoichiometric proportion of diol carrying one primary hydroxyl group and one secondary hydroxyl group, the stoichiometry being based on the total hydroxyl content of the diol and the carboxyl content of the hydroxy acid, to form an hydroxyl-terminated oligomer, and then adducting said hydroxyl-terminated oligomer with a polycarboxylic acid monoanhydride having a carboxyl functionality of at least 3, said monoanhydride being used in an amount of 0.01 to 0.15 equivalents of anhydride per hydroxyl equivalent in said hydroxyl-terminated oligomer, whereby the polyester oligomer so-produced is essentially linear and possesses low solution viscosity at high resin solids content combined with high reactivity enabling low temperature cure with hexamethoxymethyl melamine.
Claim 3
Dependent Claim 35 words
A method as recited in claim 1 in which said diol carrying two primary hydroxyl groups is neopentyl glycol, and the diol carrying one primary hydroxyl group and one secondary hydroxyl group is 2,2,4-trimethyl 1,3-pentanediol.
Claim 4
Dependent Claim 16 words
A method as recited in claim 2 in which said dicarboxylic acid monoanhydride is phthalic anhydride.
Claim 5
Dependent Claim 16 words
A method as recited in claim 2 in which said polycarboxylic acid monoanhydride is trimellitic anhydride.
Claim 6
Dependent Claim 35 words
A method as recited in claim 3 in which said polycarboxylic acid monoanhydride is trimellitic anhydride and a 2% to 15% excess in the molar proportion of diol containing two primary hydroxy groups is used.
Claim 7
Dependent Claim 7 words
The polyester oligomer product of claim 1.
Claim 8
Dependent Claim 7 words
The polyester oligomer product of claim 5.

References Cited (Backward Citations)

US3549577A Cited
US4088619A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-07-10 1988-01-09 1988-07-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-07-10 1992-01-09 1992-07-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-07-10 1996-01-09 1996-07-10 $7700.00 Window Closed / Lapsed

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