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Acid-capped polyester resins

Assignee: Goodyear Tire and Rubber Co
•
Filing: 1982-01-28
•
Granted: 1983-04-12
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Expires: 2002-01-28
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Abstract

Abstract A polyester resin having a low intrinsic viscosity and suitable for use as a powdered resin is modified by being capped with organic acids. The resins are made from the reaction of diesters with diols with up to 30 mole percent of the diester being replaced with various diacids. The polyester is capped following the condensation reaction stage, but before any finishing stage. The polyester resins have an acid number of from 1 to 100 and allow greater flexibility in the type of acid functionality than previously available.

Inventors

  • 👤 Harlan W. Frerking, Jr.
  • 👤 Mellis M. Kelley

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 22:05
CPC Classifications
C; C08; C08G; C08G63/00; C08G63/02; C08G63/12; C08G63/123; C08G63/127; C08G63/16; C08G63/20

Claims Analysis

Total Claims: 20
Claim 1
Independent Claim 378 words
A process for preparing an acid capped polyester resin, suitable for use in powdered polyester resins, comprising the steps of: reacting a diester with a diol, said diester selected from the group consisting of an alkyl diester having from 4 to 50 carbon atoms, an alkyl substituted aryl diester having from 10 to 24 carbon atoms, and combinations thereof, said diester optionally containing from about 0.01 percent to about 30 mole percent of a diacid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 16 carbon atoms, an aryl dicarboxylic acid having from 8 to 16 carbon atoms, an alkyl substituted aryl dicarboxylic acid having from 9 to 16 carbon atoms, a dimer acid having from 34 to 40 carbon atoms, and combinations thereof; said diol having from 2 to 50 carbon atoms; the mole ratio of said diol to said diester and diacid ranging from about 1.20 to about 2.5, and forming the polyester resin having hydroxyl groups thereon; adding from about 0.01 to 1 mole of an acid for each hydroxyl equivalent in said polyester resin, said acid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 20 carbon atoms; a dimer acid having from 34 to 40 carbon atoms, an acid of Formula No. 1; an acid of Formula No. 2; and combinations thereof; ##STR4## where A is an aromatic compound having from 6 to 18 carbon atoms, where R is an alkyl having from 1 to 18 carbon atoms, or a carboxylic acid group, or hydrogen, where R 1 and R 2 are an alkyl having from 1 to 18 carbon atoms, and where R 3 is an alkyl having from 1 to 18 carbon atoms, or an alkyl carboxylic acid group having from 1 to 18 carbon atoms, or hydrogen, and wherein R 1 and R 2 can be the same or different; heating and reacting said acid with said polyester resin at a temperature of from about 180° C. to about 280° C. to acid cap said polyester; and carrying out said reaction until said polyester resin acid number is from about 1 to about 100 and the amount of remaining free acid is less than 20 percent of the added amount.
Claim 2
Dependent Claim 378 words
A process for preparing an acid capped polyester resin, suitable for use in powdered polyester resins, comprising the steps of: reacting a diester with a diol, said diester selected from the group consisting of an alkyl diester having from 4 to 50 carbon atoms, an alkyl substituted aryl diester having from 10 to 24 carbon atoms, and combinations thereof, said diester optionally containing from about 0.01 percent to about 30 mole percent of a diacid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 16 carbon atoms, an aryl dicarboxylic acid having from 8 to 16 carbon atoms, an alkyl substituted aryl dicarboxylic acid having from 9 to 16 carbon atoms, a dimer acid having from 34 to 40 carbon atoms, and combinations thereof; said diol having from 2 to 50 carbon atoms; the mole ratio of said diol to said diester and diacid ranging from about 1.20 to about 2.5, and forming the polyester resin having hydroxyl groups thereon; adding from about 0.01 to 1 mole of an acid for each hydroxyl equivalent in said polyester resin, said acid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 20 carbon atoms; a dimer acid having from 34 to 40 carbon atoms, an acid of Formula No. 1; an acid of Formula No. 2; and combinations thereof; ##STR4## where A is an aromatic compound having from 6 to 18 carbon atoms, where R is an alkyl having from 1 to 18 carbon atoms, or a carboxylic acid group, or hydrogen, where R 1 and R 2 are an alkyl having from 1 to 18 carbon atoms, and where R 3 is an alkyl having from 1 to 18 carbon atoms, or an alkyl carboxylic acid group having from 1 to 18 carbon atoms, or hydrogen, and wherein R 1 and R 2 can be the same or different; heating and reacting said acid with said polyester resin at a temperature of from about 180° C. to about 280° C. to acid cap said polyester; and carrying out said reaction until said polyester resin acid number is from about 1 to about 100 and the amount of remaining free acid is less than 20 percent of the added amount.
Claim 3
Dependent Claim 22 words
A process according to claim 1, including carrying out said acid capping reaction after the condensation stage and before any finishing stage.
Claim 4
Dependent Claim 20 words
A process according to claim 2, wherein said resin has an intrinsic viscosity of from about 0.05 to about 0.35.
Claim 5
Dependent Claim 122 words
A process according to claim 3, wherein said alkyl diester has from about 6 to about 22 carbon atoms and said aryl diester has from about 10 to about 16 carbon atoms, and wherein said diol has from about 2 to about 15 carbon atoms; wherein said alkyl dicarboxylic capping acid has from 1 to 12 carbon atoms; wherein said dimer acid has 36 carbon atoms; wherein R is from 1 to 10 carbon atoms or is a carboxylic acid group, or a hydrogen, wherein R 1 and R 2 have from 1 to 12 carbon atoms, and where R 3 has from 1 to 12 carbon atoms or is an alkyl carboxylic acid group containing from 1 to 12 carbon atoms.
Claim 6
Dependent Claim 51 words
A process according to claim 4, wherein said reaction temperature ranges from about 240° to about 260° C., wherein the acid number is from about 1 to about 60, and wherein the amount of acid utilized ranges from about 0.05 to about 1.0 moles for each hydroxyl equivalent in said polymer.
Claim 7
Dependent Claim 27 words
A process according to claim 5, wherein the mole ratio of said diol to said diester and said optional acid ranges from about 1.35 to about 1.80.
Claim 8
Dependent Claim 57 words
A process according to claim 6, wherein said diester is selected from the group consisting of dimethylterephthalate, dimethylisophthalate, and combinations thereof, wherein said optional acid utilized is selected from the group consisting of terephthalic acid, and isophthalic acid, wherein said diol is selected from the group consisting of neopentyl glycol, ethylene glycol, hexamethylene glycol, and combinations thereof.
Claim 9
Dependent Claim 36 words
A process according to claim 7, wherein the intrinsic viscosity ranges from about 0.15 to about 0.25, and wherein the amount of said optional dicarboxylic acid utilized is from about 0.05 to about 20 mole percent.
Claim 10
Dependent Claim 32 words
A process according to claims 1, 3, 5, 6, 7, or 8, wherein said capping acid is selected from the group consisting of terephthalic acid, isophthalic acid, adipic acid, and combinations thereof.
Claim 11
Dependent Claim 407 words
An acid capped polyester resin suitable for use as a powdered polyester resin, comprising: an acid capped polyester resin, said acid capped polyester resin having an acid number of from about 1 to about 100; said acid capped polyester resin made by reacting an acid with a polyester having hydroxyl groups thereon; said acid capped polyester made by adding from about 0.01 to 1 mole of an acid for each hydroxyl equivalent in said polyester resin, said acid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 20 carbon atoms, a dimer acid having from 34 to 40 carbon atoms, an acid of Formula No. 1, or an acid of Formula No. 2 ##STR5## where A is an aromatic compound having from 6 to 18 carbon atoms, where R is an alkyl having from 1 to 18 carbon atoms, or a carboxylic acid group, or hydrogen, wherein R 1 and R 2 are an alkyl having from 1 to 18 carbon atoms, and where R 3 is an alkyl having from 1 to 18 carbon atoms, or an alkyl carboxylic acid group having from 1 to 18 carbon atoms, or hydrogen, wherein R 1 and R 2 can be the same or different; said reaction of said capping acid with said polyester having hydroxyl groups being carried out at a temperature of from about 180° C. to about 280° C. and to an extent such that the amount of remaining free acid is less than 20 percent of the added amount; said polyester resin made by reacting a diester with a diol, said diester selected from the group consisting of an alkyl diester having from 4 to 50 carbon atoms, an alkyl substituted aryl diester having from 10 to 24 carbon atoms, and combinations thereof, said diester optionally containing from about 0.01 percent to about 30 mole percent of a diacid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 16 carbon atoms, an aryl dicarboxylic acid having from 8 to 16 carbon atoms, an alkyl substituted aryl dicarboxylic acid having from 9 to 16 carbon atoms, a dimer acid having from about 34 to about 40 carbon atoms, and combinations thereof, said diol having from 2 to 50 carbon atoms; the mole ratio of said diol to said diester and diacid ranging from about 1.20 to about 2.5, and forming a polyester having hydroxyl groups thereon.
Claim 12
Dependent Claim 407 words
An acid capped polyester resin suitable for use as a powdered polyester resin, comprising: an acid capped polyester resin, said acid capped polyester resin having an acid number of from about 1 to about 100; said acid capped polyester resin made by reacting an acid with a polyester having hydroxyl groups thereon; said acid capped polyester made by adding from about 0.01 to 1 mole of an acid for each hydroxyl equivalent in said polyester resin, said acid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 20 carbon atoms, a dimer acid having from 34 to 40 carbon atoms, an acid of Formula No. 1, or an acid of Formula No. 2 ##STR5## where A is an aromatic compound having from 6 to 18 carbon atoms, where R is an alkyl having from 1 to 18 carbon atoms, or a carboxylic acid group, or hydrogen, wherein R 1 and R 2 are an alkyl having from 1 to 18 carbon atoms, and where R 3 is an alkyl having from 1 to 18 carbon atoms, or an alkyl carboxylic acid group having from 1 to 18 carbon atoms, or hydrogen, wherein R 1 and R 2 can be the same or different; said reaction of said capping acid with said polyester having hydroxyl groups being carried out at a temperature of from about 180° C. to about 280° C. and to an extent such that the amount of remaining free acid is less than 20 percent of the added amount; said polyester resin made by reacting a diester with a diol, said diester selected from the group consisting of an alkyl diester having from 4 to 50 carbon atoms, an alkyl substituted aryl diester having from 10 to 24 carbon atoms, and combinations thereof, said diester optionally containing from about 0.01 percent to about 30 mole percent of a diacid selected from the group consisting of an alkyl dicarboxylic acid having from 2 to 16 carbon atoms, an aryl dicarboxylic acid having from 8 to 16 carbon atoms, an alkyl substituted aryl dicarboxylic acid having from 9 to 16 carbon atoms, a dimer acid having from about 34 to about 40 carbon atoms, and combinations thereof, said diol having from 2 to 50 carbon atoms; the mole ratio of said diol to said diester and diacid ranging from about 1.20 to about 2.5, and forming a polyester having hydroxyl groups thereon.
Claim 13
Dependent Claim 35 words
An acid capped polyester resin according to claim 10, wherein said acid number is from about 1 to about 60, and the intrinsic viscosity of said polyester resin is from about 0.05 to about 0.35.
Claim 14
Dependent Claim 65 words
An acid capped polyester resin according to claim 11, wherein R has from 1 to 10 carbon atoms or is a carboxylic acid group, or a hydrogen, wherein R 1 and R 2 have from 1 to 12 carbon atoms, and where R 3 has from 1 to 12 carbon atoms or is an alkyl carboxylic acid group containing from 1 to 12 carbon atoms.
Claim 15
Dependent Claim 22 words
An acid capped polyester resin according to claim 12, wherein said reaction temperature is from about 240° C. to about 260° C.
Claim 16
Dependent Claim 20 words
An acid capped polyester resin according to claim 13, wherein the intrinsic viscosity is from about 0.15 to about 0.25.
Claim 17
Dependent Claim 34 words
An acid capped polyester resin according to claim 10, 11, 12, 13, or 14, wherein said optional acid is selected from the group consisting of isophthalic acid, terephthalic acid, adipic acid, and combinations thereof.
Claim 18
Dependent Claim 48 words
An acid capped polyester resin according to claim 15, wherein said alkyl diester has from about 6 to about 22 carbon atoms and said aryl diester has from about 10 to about 16 carbon atoms, and wherein said diol has from about 2 to about 15 carbon atoms.
Claim 19
Dependent Claim 40 words
An acid capped polyester resin according to claim 16, wherein the amount of acid utilized ranges from about 0.05 mole to about 1 mole, and wherein the mole ratio of diol to diester is from about 1.35 to about 1.80.
Claim 20
Dependent Claim 27 words
An acid capped polyester resin according to claim 17, wherein said optional acid is selected from the group consisting of terephthalic acid, isophthalic acid, and combinations thereof.

References Cited (Backward Citations)

US4155889A Cited
US4275189A Cited
US3383343A Cited
US3530082A Cited
US3953403A Cited
US4065439A Cited
US4151220A Cited
US4124570A Cited
US4195000A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-04-11 1986-10-11 1987-04-12 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-04-11 1990-10-11 1991-04-12 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-04-11 1994-10-11 1995-04-12 $7700.00 Window Closed / Lapsed

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