IP Library Granted Patent US 11,608,403
Granted Patent B2
US 11,608,403 · App. 17/230,083 · Granted Mar 21, 2023

High viscosity latexes

Inventor: Sepehr M. Tehrani (North York, CA)
Assignee: Xerox Corporation
C08F283/06C08K3/36C08F2/24C08F2/32C08F2/38C08F212/36C08F220/04C08F220/06C08F220/14C08F220/20C08F220/286C08F220/58C08F222/02C08F222/102C08K2201/011
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Quick Facts
Patent No.
US 11,608,403
App. No.
17/230,083
Granted
Mar 21, 2023
Kind
B2
Abstract

Methods for forming latexes are provided. In an embodiment, such a method comprises adding a monomer emulsion comprising water, a monomer, an acidic monomer, a hydrophilic monomer, a difunctional monomer, a first reactive surfactant, and a chain transfer agent, to a reactive surfactant solution comprising water, a second reactive surfactant, and an initiator, at a feed rate over a period of time so that monomers of the monomer emulsion undergo polymerization reactions to form resin particles in a latex. The reactive surfactant solution does not comprise monomers other than the second reactive surfactant, the reactive surfactant solution does not comprise a resin seed, and the monomer emulsion does not comprise the resin seed. The latex is characterized by a viscosity in a range of from about 10 cP to about 100 cP as measured at a solid content of about 30% and at room temperature. The latexes are also provided.

Claims (16)

1. A method for forming a latex, the method comprising:

adding a monomer emulsion comprising water, a monomer, an acidic monomer, a hydrophilic monomer, a difunctional monomer, a first reactive surfactant, and a chain transfer agent, to a reactive surfactant solution comprising water, a second reactive surfactant, and an initiator, at a feed rate over a period of time so that monomers of the monomer emulsion undergo polymerization reactions to form resin particles in a latex,

wherein the reactive surfactant solution does not comprise monomers other than the second reactive surfactant, the reactive surfactant solution does not comprise a resin seed, and the monomer emulsion does not comprise the resin seed,

further wherein the latex is characterized by a viscosity in a range of from about 10 cP to about 100 cP as measured at a solid content of about 30% and at room temperature.

2. The method of claim 1 , wherein the hydrophilic monomer comprises a hydroxyl moiety, a glycol moiety, or both.

3. The method of claim 1 , wherein the hydrophilic monomer is selected from hydroxyethyl (meth)acrylate, n-hydroxyethyl (meth)acrylamide, hydroxypropyl (meth)acrylate, hydroxypropyl (meth)acrylamide, ethylene glycol (meth)acrylate, propylene glycol (meth)acrylate, a poly(ethylene glycol) (meth)acrylate, and a poly(propylene glycol) (meth)acrylate.

4. The method of claim 1 , wherein the hydrophilic monomer is a poly(ethylene glycol) methacrylate having a molecular weight in a range of from about 185 g/mol to about 1500 g/mol.

5. The method of claim 4 , wherein the molecular weight is in a range of from about 360 g/mol to about 1500 g/mol.

6. The method of claim 1 , wherein the difunctional monomer is a poly(ethylene glycol) diacrylate.

7. The method of claim 1 , wherein the monomer emulsion comprises styrene, an alkyl acrylate, methacrylic acid, styrenesulfonic acid, a poly(ethylene glycol) methacrylate, a polyethylene glycol diacrylate, an anionic ether sulfate reactive surfactant, and the chain transfer agent.

8. The method of claim 1 , wherein the acidic monomer, the hydrophilic monomer, and the difunctional monomer are present at an amount in a range of from about 10 weight % to about 30 weight %.

9. The method of claim 8 , wherein the difunctional monomer is present at an amount in a range of from about 0.01 weight % to about 0.8 weight %.

10. The method of claim 1 , wherein the resin particles of the latex are further characterized by a glass transition temperature T g in a range of from about 35° C. to about 100° C.

11. The method of claim 1 , wherein the monomer emulsion consists of one or more types of the monomer, one or more types of the acidic monomer, one or more types of the hydrophilic monomer, one or more types of the difunctional monomer, one or more types of the first reactive surfactant, and one or more types of the chain transfer agent.

12. The method of claim 1 , wherein the monomer emulsion consists of styrene, an alkyl acrylate, methacrylic acid, styrenesulfonic acid, a poly(ethylene glycol) methacrylate, a polyethylene glycol diacrylate, an anionic ether sulfate reactive surfactant, and the chain transfer agent.

13. The method of claim 1 , wherein the reactive surfactant solution further comprises silica nanoparticles.

Assignments (9)
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 →
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 Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2021
From: TEHRANI, SEPEHR
To: XEROX CORPORATION
Reel/Frame 055938/0344 →
Continuity (2)
Continuation In Part 17102725 · Nov 24, 2020
Related Publication 20220162368A1 · May 26, 2022