Toner resins and processes for making the same

Patent metadata

Field	Value
Publication number	US-9229344-B2
Application number	US-201414255874-A
Country	US
Kind code	B2
Filing date	Apr 17, 2014
Priority date	Apr 17, 2014
Publication date	Jan 5, 2016
Grant date	Jan 5, 2016

Abstract

Unsaturated polyester resins and processes for making the same are disclosed herein. In particular, the process for making the resin provides resins with improved properties. The unsaturated polyester resins have substantially reduced free fumaric acid as compared to that made from conventional processes. The toner resins are used to prepare toner compositions that have improved performance.

First claim

What is claimed is:

1. A process for making a toner resin comprising:
reacting an organic diol with a cyclic alkylene carbonate in the presence of a first catalyst to thereby form a polyalkoxy diol;
reacting the polyalkoxy diol with one or more diacid reagents in the presence of a second catalyst in an esterification reaction;
monitoring an acid value of a resulting mixture from the esterification reaction; and
subsequently polycondensing the resulting mixture with an unsaturated diacid to form an unsaturated polyester resin.

2. The process of claim 1 , wherein the diol is selected from the group consisting of 1,2-propanediol, 1,3-propanediol, 1,3-butane diol, pentylene glycol, hexylene glycol, diphenol, neopentyl glycol, diethylene glycol, dipropylene glycol, 2,2-bis-(4-hydroxy phenyl) propane, 2,2-bis-(3-hydroxy phenyl) propane, 2,2-bis-(2-hydroxy phenyl) propane, 2,2-bis-(3-hydroxy phenyl) propane, 2,2-bis-(5-hydroxy phenyl) propane, bisphenol A, ethoxylated bisphenol A, propoxylated bisphenol A, bis-(4-hydroxy phenyl) methane, 1,1-bis-(4-hydroxy phenyl) ethane, cis-1,4-dihydroxy-cyclohexane, trans-1,4-dihydroxy-cyclohexane, cis-1,2-dihydroxy-cyclohexane, trans-1,2-dihydroxy-cyclohexane, trans-1,3-dihydroxy-cyclohexane, cis-1,3-dihydroxy-cyclohexane, and mixtures thereof and which diol is optionally selected in an amount of from about 0.90 mole equivalents to about 1.1 mole equivalents, based on about 1 mole equivalent of unsaturated diacid utilized.

3. The process of claim 1 , wherein the first catalyst is present in an amount of from about 0.001 mole percent to about 0.5 mole percent based on of the starting organic diol utilized.

4. The process of claim 3 , wherein the first catalyst is present in an amount of from about 0.002 mole percent to about 0.3 mole percent based on of the starting organic diol utilized.

5. The process of claim 1 , wherein the first catalyst is selected from the group consisting of sodium carbonate, lithium carbonate, potassium carbonate, sodium carbonate, rubidium carbonate, cesium carbonate, beryllium carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, beryllium carbonate, manganese carbonate, barium carbonate and mixtures thereof.

6. The process of claim 1 , wherein the second catalyst is selected from the group consisting of tetraalkyl titanates, dialkyltin oxides such as dibutyltin oxide, tetraalkyltins such as dibutyltin dilaurate, and dialkyltin oxide hydroxides such as butyltin oxide hydroxide, aluminum alkoxides, alkyl zinc, dialkyl zinc, zinc oxide, stannous oxide, and mixtures thereof.

7. The process of claim 1 , wherein the second catalyst is present in an amount of from about 0.001 mole percent to about 5 mole percent based on the starting diacid or diester utilized.

8. The process of claim 1 , wherein the unsaturated diacid is added when the acid value of the resulting mixture is from about 1.5 mg KOH/g resin to about 0.5 mg KOH/g resin.

9. The process of claim 8 , wherein the unsaturated diacid is added when the acid value of the resulting mixture is from about 1.0 mg KOH/g resin to about 0.1 mg KOH/g resin.

10. The process of claim 1 , wherein the reacting step is performed at a first polymerization temperature of from about 120 to about 250° C.

11. The process of claim 1 , wherein the polycondensing step is performed at a second polymerization temperature of from about 150 to about 300° C.

12. The process of claim 1 , wherein the reacting step is perfomed at a mixing rate of from about 5 to about 600 RPM.

13. The process of claim 1 , wherein the polycondensing step is performed at a mixing rate of from about 5 to about 600 RPM.

14. The process of claim 1 further including cooling the resulting mixture before the addition of the unsaturated diacid.

15. The process of claim 1 , wherein the unsaturated polyester resin has low levels of unreacted starting material.

16. The process of claim 15 , wherein the unsaturated polyester resin has low levels of unsaturated diacid.

17. The process of claim 16 , wherein unsaturated diacid is present in an amount of less than 1.0 as analyzed by 31P NMR.

18. The toner resin of claim 1 , wherein the unsaturated polyester resin is selected from the group consisting of unsaturated polyester resin of poly(propoxylated bisphenol co-fumarate), poly(ethoxylated bisphenol co-fumarate), poly(butyloxylated bisphenol co-fumarate), poly(co-propoxylated bisphenol co ethoxylated bisphenol co-fumarate), poly(1,2-propylene fumarate), poly(propoxylated bisphenol co-maleate), poly(ethoxylated bisphenol co-maleate), poly(butyloxylated bisphenol co-maleate), poly(co-propoxylated bisphenol co ethoxylated bisphenol co-maleate), poly(1,2-propylene maleate), poly(propoxylated bisphenol co-itaconate), poly(ethoxylated bisphenol co-itaconate), poly(butyloxylated bisphenol co-itaconate), poly(co-propoxylated bisphenol co ethoxylated bisphenol co-itaconate), or poly(1,2-propylene itaconate).

19. A process for making toner resin comprising:
reacting an organic diol with a cyclic alkylene carbonate in the presence of a first catalyst to thereby form a polyalkoxy diol, wherein the first catalyst is present in an amount of greater than about 0.01 percent of the total weight of the first catalyst, organic diol and cyclic alkylene carbonate;
reacting the polyalkoxy diol with one or more diacid reagents in the presence of a second catalyst in an esterification reaction;
monitoring an acid value of a resulting mixture from the esterification reaction; and
subsequently polycondensing the resulting mixture with an unsaturated diacid to form an unsaturated polyester resin having an acid value of greater than 10.0 mg KOH/g resin.

20. A process for making toner resin comprising:
reacting an organic diol with a cyclic alkylene carbonate in the presence of a first catalyst to thereby form a polyalkoxy diol, wherein the first catalyst is present in an amount of from about 0.001 mole percent to about 0.5 mole percent based on of the starting organic diol utilized;
reacting the polyalkoxy diol with one or more organic diacid reagents in the presence of a second catalyst in an esterification reaction;
monitoring an acid value of a resulting mixture from the esterification reaction; and
subsequently polycondensing the resulting mixture with fumaric acid to form poly(propoxylated bisphenol co-fumarate) having an acid value of from about 10.0 mg KOH/g resin to about 14.0 mg KOH/g resin and a viscosity range of from about 32 to about 40 poise measured at 200° C. using a Brookfield viscometer.

Assignees

• Xerox Corp

Inventors

• Moffat Karen A
• Wang Yulin
• Qiu Shigang Steven
• Pawlak John Lawrence
• Klymachyov Alexander N
• Marcell Kevin F
• Vandewinckel Judith M
• Bashir Wafa F
• Veregin Richard P N
• Wolfe Christopher M

Classifications

• G03G9/0806

  whereby chemical synthesis of at least one of the toner components takes place · CPC title

• G03G9/0804

  whereby the components are brought together in a liquid dispersing medium · CPC title

• G03G9/08755 Primary

  Polyesters · CPC title

• C08F283/02

  on to polycarbonates or saturated polyesters {(C08F283/004 takes precedence)} · CPC title

• G03G9/08795

  characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants · CPC title