IP Library Granted Patent US 10,108,101
Granted Patent B2
US 10,108,101 · App. 15/583,070 · Granted Oct 23, 2018

Toner formulation using crystalline polyester encapsulated with a styrene acrylate latex and method of preparing the same

Inventors: Jing X Sun (Lexington, KY); Cory Nathan Hammond (Winchester, KY)
Assignee: LEXMARK INTERNATIONAL, INC.
G03G9/09371G03G9/0819G03G9/0821G03G9/08755G03G9/09328G03G9/09364G03G9/09392
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Quick Facts
Patent No.
US 10,108,101
App. No.
15/583,070
Granted
Oct 23, 2018
Kind
B2
Abstract

The present disclosure relates to a chemically prepared toner composition including a toner particle having a core including a first polymer binder, an styrene acrylate encapsulated crystalline polyester latex, a pigment, and a shell formed around the core including a second polymer binder and method to make the same. The disclosed method of preparing the toner results in a change in the distribution of the components of the toner particle wherein the lower molecular weight resins, the pigment and the wax are located away from the surface of the toner particle and the pigment is clinging to the edge of the wax domain.

Claims (8)

1. A chemically prepared toner comprising:

a core including a first polyester resin polymer binder, a crystalline polyester encapsulated by a polymer latex that is polymerized by a monomer solution including a hydrophilic monomer having one of a carboxyl (—COOH) functional group and a hydroxyl (—OH) functional group and hydrophobic styrene and acrylate monomers, a pigment, and a wax; and

a shell formed around the core including a second polyester resin polymer binder, wherein the pigment and wax are located away from the surface of the toner particle and the hydrophilic monomer having the carboxyl (—COOH) functional group is beta-carboxyethyl acrylate and the hydrophilic monomer having the hydroxy (—OH) functional group is hydroxyethyl methacrylate.

2. The chemically prepared toner of claim 1 , wherein the hydrophobic acrylate monomer is an alkyl acrylate.

3. The chemically prepared toner of claim 2 , wherein the alkyl acrylate monomer is butyl acrylate.

4. The chemically prepared toner of claim 2 , wherein the alkyl acrylate monomer is lauryl acrylate.

5. The chemically prepared toner of claim 1 , wherein a glass transition temperature (Tg) of the polymer latex is between 20° C. and 60° C.

6. The chemically prepared toner of claim 1 , further comprising a borax coupling agent between the outer surface of the core and the shell.

Assignments (6)
SECURITY INTEREST Recorded Jan 5, 2026
From: LEXMARK INTERNATIONAL, INC.
To: BANK TRUST COMPANY, NATIONAL ASSOCIATION
Reel/Frame 074202/0192 →
SECURITY INTEREST Recorded Jan 5, 2026
From: LEXMARK INTERNATIONAL, INC.
To: BANK TRUST COMPANY, NATIONAL ASSOCIATION
Reel/Frame 074202/0293 →
SECURITY INTEREST Recorded Sep 23, 2025
From: LEXMARK INTERNATIONAL, INC.
To: CITIBANK, N.A.
Reel/Frame 073007/0118 →
SECURITY INTEREST Recorded Sep 23, 2025
From: LEXMARK INTERNATIONAL, INC.
To: JEFFERIES FINANCE LLC
Reel/Frame 073007/0346 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2017
From: SUN, JING X; HAMMOND, COREY NATHAN
To: LEXMARK INTERNATIONAL, INC.
Reel/Frame 042193/0223 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2017
From: SUN, JING X; HAMMOND, COREY NATHAN
To: LEXMARK INTERNATIONAL, INC.
Reel/Frame 042193/0250 →
Continuity (2)
Continuation 14937282 · Nov 10, 2015
Related Publication 20170235244A1 · Aug 17, 2017