IP Library Granted Patent US 8,871,892
Granted Patent B2
US 8,871,892 · App. 13/498,709 · Granted Oct 28, 2014

Polyoxazolidone resins

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Quick Facts
Patent No.
US 8,871,892
App. No.
13/498,709
Granted
Oct 28, 2014
Kind
B2
Abstract

An epoxy oxazolidone including the reaction product of (a) a divinylarene dioxide, and (b) an excess of a polyisocyanate to provide an epoxy oxazolidone composition; wherein the composition has an oxazolidone selectivity of greater than 40% relative to the total of the carbonyl compounds; a process for making the epoxy oxazolidone; and a curable epoxy resin composition including (i) the epoxy oxazolidone derived from a divinylarene dioxide such as divinylbenzene dioxide (DVBDO) and a polyisocyanate, (ii) at least one curing agent; and/or (iii) a catalyst. The cured product made from the above epoxy resin composition is thermally stable and offers improved properties such as a lower viscosity and a high heat resistance compared to known cured products prepared from known epoxy resins.

Claims (32)

1. An epoxy-functional oxazolidone resin composition comprising the reaction product of:

(a) a divinylarene dioxide,

(b) a polyisocyanate, and

(c) a reaction catalyst;

such that the reaction product formed is an epoxy-functional oxazolidone resin composition;

wherein the reaction catalyst is selected from the group consisting of Lewis acids, imidazoles, quaternary salts, or mixtures thereof;

wherein the epoxy-functional oxazolidone resin composition has an oxazolidone selectivity of greater than or equal to 70 percent relative to the total content of the carbonyl groups in the epoxy-functional oxazolidone resin composition;

wherein the epoxy-functional oxazolidone resin composition has a viscosity of from about 0.1 Pa-s to about 10,000 Pa-s at 150° C.;

wherein the epoxy-functional oxazolidone resin composition has a melt viscosity based on a ratio of T 500 :Tg of less than 1.5;

wherein T 500 is the temperature at which the melt viscosity of the epoxy-functional oxazolidone resin composition is about 500 Pa-s; and

wherein Tg is the glass transition temperature of the epoxy-functional oxazolidone resin composition.

2. The composition of claim 1 , wherein the divinylarene dioxide is selected from the group comprising one or more substituted divinylbenzene dioxide, divinylnaphthalene dioxide, divinylbiphenyl dioxide, divinyldiphenylether dioxide, and mixtures thereof.

3. The composition of claim 1 , wherein the divinylarene dioxide is divinylbenzene dioxide.

4. The composition of claim 1 , wherein the concentration of said divinylarene dioxide ranges from a ratio r of isocyanate to epoxide equivalents of less than 1.0; and/or wherein the concentration of said polyisocyanate ranges from a ratio r of isocyanate to epoxide equivalents of less than 1.0.

5. The composition of claim 1 , wherein the polyisocyanate is selected from the group comprising toluenediisocyanate, methylenediphenyldiisocyanate, hexanediisocyanate, isophoronediisocyanate, xylylenediisocyanate; and mixtures thereof.

6. The composition of claim 1 , wherein the Lewis acids include magnesium chloride or zirconium chloride; wherein the imidazoles include 2-phenylimidazole; and wherein the quaternary salts include tetrabutylphosphonium bromide or tetraethylammonium bromide.

7. A curable epoxy resin composition comprising (i) the epoxy-functional oxazolidone resin composition of claim 1 ; and (ii) at least one curing agent.

8. The curable composition of claim 7 , wherein the concentration of the epoxy oxazolidone ranges from about 1 weight percent to about 100 weight percent; and wherein the concentration of the curing agent ranges from about 0.01 weight percent to about 90 weight percent.

9. The curable composition of claim 7 , wherein the curing agent is selected from the group comprising anhydrides, carboxylic acids, amine compounds, phenolic compounds, polyols; and mixtures thereof.

10. A cured thermoset product prepared by curing the curable epoxy resin composition of claim 7 .

11. A process for preparing a curable epoxy resin composition comprising admixing (i) the epoxy functional oxazolidone resin composition of claim 1 ; and (ii) at least one curing agent.

12. A process for preparing an epoxy functional oxazolidone resin composition comprising reacting (a) a divinylarene dioxide,

(b) a polyisocyanate; and

(c) a reaction catalyst,

such that the reaction product formed is an epoxy-functional oxazolidone resin composition;

wherein the reaction catalyst is selected from the group consisting of Lewis acids, imidazoles, quaternary salts, or mixtures thereof;

wherein the epoxy-functional oxazolidone resin composition has an oxazolidone selectivity of greater than or equal to 70 percent relative to the total content of the carbonyl groups in the epoxy-functional oxazolidone resin composition;

wherein the epoxy-functional oxazolidone resin composition has a viscosity of from about 0.1 Pa-s to about 10,000 Pa-s at 150° C.;

wherein the epoxy-functional oxazolidone resin composition has a viscosity measured as a ratio of the following temperatures: T 500 /Tg of less than 1.5;

wherein T 500 is the temperature at which the melt viscosity of the epoxy-functional oxazolidone resin composition is about 500 Pa-s; and

wherein Tg is the glass transition temperature of the epoxy-functional oxazolidone resin composition.

13. The process of claim 12 , wherein the Lewis acids include magnesium chloride or zirconium chloride; wherein the imidazoles include 2-phenylimidazole; and wherein the quaternary salts include tetrabutylphosphonium bromide or tetraethylammonium bromide; or mixtures thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2015
From: DOW GLOBAL TECHNOLOGIES LLC
To: BLUE CUBE IP LLC
Reel/Frame 035887/0193 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2014
From: MARKS, MAURICE J
To: DOW GLOBAL TECHNOLOGIES LLC.
Reel/Frame 034066/0403 →