IP Library Granted Patent US 8,338,069
Granted Patent B2
US 8,338,069 · App. 12/838,693 · Granted Dec 25, 2012

Toner compositions

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Quick Facts
Patent No.
US 8,338,069
App. No.
12/838,693
Granted
Dec 25, 2012
Kind
B2
Abstract

The present disclosure provides processes for producing toner particles, and toner particles produced by such processes. The processes of the present disclosure combine melt-mixing and grinding of toner components to produce toner particles, followed by a coalescing treatment which provides toner particles having desirable spherical properties.

Claims (37)

1. A process comprising:

melt-mixing an amorphous resin, an optional crystalline resin, an optional wax, and an optional colorant to form a toner;

pelletizing the toner to form toner pellets; optionally annealing said toner pellets; grinding the toner pellets to form toner particles;

contacting the toner particles with deionized water and at least one surfactant to form a mixture;

coalescing the toner particles by heating the mixture to a temperature of from about 50° C. to about 100° C.; and

recovering toner particles from the mixture,

wherein the recovered toner particles possess a circularity of from about 0.92 to about 0.999.

2. The process of claim 1 , wherein the amorphous resin comprises an amorphous bio-based polyester resin derived at least in part from a material selected from the group consisting of natural triglyceride vegetable oils, phenolic plant oils, and combinations thereof present in an amount of from about 1 percent by weight of the toner particles to about 95 percent by weight of the toner particles.

3. The process of claim 1 , wherein the amorphous resin comprises an amorphous bin-based polyester resin derived from a fatty dimer acid, a fatty dimer diol, a fatty dimer diacid, D-isosorbide, L-tyrosine, glutamic acid, and combinations thereof.

4. The process of claim 1 , wherein the amorphous resin further comprises at least one amorphous polyester resin selected from the group consisting of poly(propoxylated bisphenol co-fumarate), poly(ethoxylated bisphenolco-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), polty(ethoxylated bisphenol co-itaconate), poly(butyloxylated bisphenol co-itaconate), poly(co-propoxylated bisphenol co-ethoxylated bisphenol co-itaconate), poly(1,2-propylene itaconate), and combinations thereof.

5. The process of claim 1 ,. wherein the toner particles further comprise a crystalline polyester resin selected from the group consisting of poly(ethylene-adipate), poly(propylene-adipate), poly(butylene-adipate), poly(pentylene-adipate), poly(hexylene-adipate), poly(octylene-adipate), poly(ethylene-succinate), poly(propylene-succinate), poly(butylene-succinate), poly(pentylene-succinate), poly(hexylene-succinate), poly(octylene-succinate), poly(ethylene-sebacate), poly(propylene-sebacate), poly(butylene-sebacate), poly(pentylene-sebacate), poly(hexylene-sebacate), poly(octylene-sebacate), poly(decylene-sebacate), poly(decylene-decanoate), poly-(ethylene-decanoate), poly-(ethylene-dodecanoate), poly(nonylene-sebacate), poly (nonylene-decanoate), copoly(ethylene-fumarate)-copoly (ethylene-sebacate), copoly(ethylene-fumarate)-copoly(ethylene-decanoate), copoly(ethylene-fumarate)-copoly(ethylene-dodecanoate), and combinations thereof.

6. The process of claim 1 , wherein the surfactant is selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants, and combinations thereof, present in an amount from about 0.01% to about 5% by weight of the toner particles.

7. The process of claim 1 , wherein the surfactant is selected from the group consisting of sodium lauryl sulfate, sodium dodecylbenzene sulfonate, sodium dodecylnaphthalene sulfate, dialkyl benzenealkyl sulfates, dialkyl benzenealkyl sulfonates, abitic acid, alkyldiphenyloxide disulfonate, branched sodium dodecyl benzene sulfonates, and combinations thereof.

8. The process of claim 1 , wherein coalescing the toner particles further comprises mixing the mixture at a rate of from about 50 revolutions per minute to about 500 revolutions per minute.

9. The process of claim 1 , wherein coalescing the toner particles occurs for a period of time of from about 0.1 hours to about 9 hours.

10. The process of claim 1 , wherein coalescing the toner particles occurs at a pH of from about 6 to about 10.

11. A process comprising:

melt-mixing an amorphous bio-based polyester resin, a crystalline resin, an optional wax, and an optional colorant to form a toner;

pelletizing the toner to form toner pellets; optionally annealing said toner pellets; grinding the toner pellets to form toner particles;

contacting the toner particles with deionized water and at least one surfactant selected from the group consisting of nonionic surfactants, anionic surfactants, cationic surfactants, and combinations thereof, to form a mixture;

coalescing the toner particles by heating the mixture to a temperature of from about 50° C. to about 100° C., with mixing at a rate of from about 75 revolutions per minute to about 400 revolutions per minute, for a period of time of from about 0.1 hours to about 9 hours; and

recovering toner particles from the mixture,

wherein the recovered toner particles possess a circularity of from about 0.93 to about 0.995.

12. The process of claim 11 , wherein the amorphous bio-based polyester resin is derived at least in part from a material selected from the group consisting of natural triglyceride vegetable oils, phenolic plant oils, and combinations thereof, present in an amount of from about 5 percent by weight of the toner particles to about 50 percent by weight of the toner particles.

13. The process of claim 11 , wherein the amorphous bio-based polyester resin derived from a fatty dimer acid, a fatty dimer diol, a fatty dimer diacid, D-isosorbide, L-tyrosine, glutamic acid, and combinations thereof.

14. The process of claim 11 , wherein the toner particles further comprise at least one amorphous polyester resin selected from the group consisting 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), poly(1,2-propylene itaconate), and combinations thereof.

15. The process of claim 11 , wherein the crystalline resin comprises a crystalline polyester resin selected from the group consisting of poly(ethylene-adipate), poly(propylene-adipate), poly(butylene-adipate), poly(pentylene-adipate), poly(hexylene-adipate), poly(octylene-adipate), poly(ethylene-succinate), poly(propylene-succinate), poly(butylene-succinate), poly(pentylene-succinate), poly(hexylene-succinate), poly(octylene-succinate), poly(ethylene-sebacate), poly(propylene-sebacate), poly(butylene-sebacate), poly(pentylene-sebacate), poly(hexylene-sebacate), poly(octylene-sebacate), poly(decylene-sebacate), poly(decylene-decanoate), poly-(ethylene-decanoate), poly-(ethylene-dodecanoate), poly(nonylene-sebacate), poly (nonylene-decanoate), copoly(ethylene-fumarate)-copoly (ethylene-sebacate), copoly(ethylene-fumarate)-copo(ethylene-decanoate), copoly(ethylene-fumarate)-copoly(ethylene-dodecanoate), and combinations thereof.

16. The process of claim 11 , wherein the surfactant is selected from the group consisting of sodium lauryl sulfate, sodium dodecylbenzene sulfonate, sodium dodecylnaphthalene sulfate, dialky benzenealkyl sulfates, dialkyl benzenealkyl sulfonates, abitic acid, alkyldiphenyloxide disulfonate, branched sodium dodecyl benzene sulfonates, combinations thereof, present in an amount from about 0.75% to about 4% by weight of the toner particles.

17. The process of claim 11 , wherein coalescing the toner particles occurs at a pH of from about 6.2 to about 8.

18. A process comprising:

melt-mixing an amorphous bio-based polyester resin derived at least in part from a material selected from the group consisting of a fatty dimer acid, a fatty dimer diol, a fatty dimer diacid, D-isosorbide, L-tyrosine, glutamic acid, natural triglyceride vegetable oils, phenol plant oils, and combinations thereof, a crystalline resin, an optional wax, and an optional colorant to form a toner;

pelletizing the toner to form toner pellets; optionally annealing said toner pellets; grinding the toner pellets to form toner particles;

contacting the toner particles with deionized water and at least one surfactant selected from the group consisting of sodium lauryl sulfate, sodium dodecylhenzene sultanate, sodium dodecylnaphthalene sulfate, dialkyl benzenealkyl sulfates, dialkyl benzenealkyl sulfonates, abitic acid, alkyldiphenyloxide disulfonate, branched sodium dodecyl benzene sulfonates, and combinations thereof, to form a mixture;

coalescing the toner particles in the mixture by heating the mixture to a temperature of from about 50° C. to about 100° C., with mixing at a rate of from about 50 revolutions per minute to about 500 revolutions per minute, for a period of time of from about 0.1 hours to about 9 hours, at a pH of from about 6 to about 10; and

recovering toner particles from the mixture,

wherein the amorphous bio-based polyester resin is present in an amount of from about 1 percent by weight of the toner components to about 95 percent by weight of the toner components, the surfactant is present in an amount from about 0.01% to about 5% by weight of the toner particles, and the recovered toner particles possess a circularity of from about 0.92 to about 0.999.

19. The process of claim 18 , wherein the toner particles further comprise at least one amorphous polyester resin selected from the group consisting 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), poly(1,2-propylene itaconate), and combinations thereof.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2025
From: XEROX CORPORATION
To: GENESEE VALLEY INNOVATIONS, LLC
Reel/Frame 073842/0479 →
SECOND LIEN NOTES PATENT SECURITY AGREEMENT Recorded Jul 2, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071785/0550 →
FIRST LIEN NOTES PATENT SECURITY AGREEMENT Recorded Apr 11, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 070824/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 062740/0214 Recorded May 18, 2023
From: CITIBANK, N.A., AS AGENT
To: XEROX CORPORATION
Reel/Frame 063694/0122 →
SECURITY INTEREST Recorded Nov 10, 2022
From: XEROX CORPORATION
To: CITIBANK, N.A., AS AGENT
Reel/Frame 062740/0214 →