IP Library Granted Patent US 8,802,339
Granted Patent B2
US 8,802,339 · App. 13/731,582 · Granted Aug 12, 2014

Crosslinkable urethane acrylate charge transport molecules for overcoat

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Quick Facts
Patent No.
US 8,802,339
App. No.
13/731,582
Granted
Aug 12, 2014
Kind
B2
Abstract

An overcoat layer for an organic photoconductor drum of an electrophotographic image forming device is provided. The overcoat layer is prepared from a curable composition including a urethane methacrylate functional charge transport molecule, and a photoinitiator. The urethane acrylate functional charge transport molecule is a reaction product of hydroxyl functional charge transport molecule and a monomer having an isocyanate group and an acrylate group. This overcoat layer improves wear resistance of the organic photoconductor drum without negatively altering the electrophotographic properties, thus protecting the organic photoconductor drum from damage and extending its useful life.

Claims (22)

1. An overcoat layer for an organic photoconductor drum, the overcoat layer prepared from a curable composition comprising:

a urethane acrylate functional charge transport molecule that is a reaction product of hydroxyl functional charge transport molecule and a monomer having an isocyanate group and an acrylate group; and

a photoinitiator.

2. The overcoat layer of claim 1 , wherein the hydroxyl functional charge transport molecule is selected from the group consisting of a di-hydroxy functional charge transport molecule, a tri-hydroxy functional charge transport molecule, and a tetra-hydroxy functional charge transport molecule.

3. The overcoat layer of claim 1 , wherein the urethane acrylate functional charge transport molecule comprises tri-arylamine of formulae (I)-(IV):

wherein x has a value of a whole number; n has a value of a counting number; R′ is H or CH 3 ; and R is H or CH 3 .

4. The overcoat layer of claim 1 , wherein the urethane acrylate functional charge transport molecule comprises tetra-aryl benzidine of formulae (V)-(XII):

wherein x has a value of a whole number; n has a value of a counting number; R is H or CH 3 ; R1 is H or CH 3 ; and R2 is H or CH 3 .

5. The overcoat layer of claim 1 , wherein the urethane acrylate functional charge transport molecule comprises tetra-aryl phenylene diamine of formulae (XIII)-(XVI):

wherein x has a value of a whole number; n has a value of a counting number; R is H or CH 3 ; R1 is H or CH 3 ; and R2 is H or CH 3 .

6. The overcoat layer of claim 1 , wherein the curable composition further comprises crosslinkable additives comprising acrylates, diacrylates or urethane acrylates.

7. The overcoat layer of claim 1 , wherein the curable composition further comprises a hexa-functional aromatic urethane acrylate resin.

8. The overcoat layer of claim 1 , wherein the curable composition further comprises a hexa-functional aliphatic urethane acrylate resin.

9. The overcoat layer of claim 1 , wherein the overcoat layer has a thickness of about 0.1 μm to about 10 μm.

10. An organic photoconductor drum comprising:

a support element;

a charge generation layer disposed over the support element;

a charge transport layer disposed over the charge generation layer; and

a protective overcoat layer formed as an outermost layer of the organic photoconductor drum, the protective overcoat layer being formed from a curable composition including:

a urethane methacrylate functional charge transport molecule or urethane acrylate functional charge transport molecule that is a reaction product of hydroxyl functional charge transport molecule and a monomer having an isocyanate group and an acrylate group; and

a photoinitiator.

11. The overcoat layer of claim 10 , wherein the hydroxyl functional charge transport molecule is selected from the group consisting of a di-hydroxy functional charge transport molecule, a tri-hydroxy functional charge transport molecule, and a tetra-hydroxy functional charge transport molecule.

Assignments (8)
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 →
RELEASE OF SECURITY INTEREST Recorded Jan 18, 2024
From: CHINA CITIC BANK CORPORATION LIMITED, GUANGZHOU BRANCH, AS COLLATERAL AGENT
To: LEXMARK INTERNATIONAL, INC.
Reel/Frame 066345/0026 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT U.S. PATENT NUMBER PREVIOUSLY RECORDED AT REEL: 046989 FRAME: 0396. ASSIGNOR(S) HEREBY CONFIRMS THE PATENT SECURITY AGREEMENT. Recorded Oct 24, 2018
From: LEXMARK INTERNATIONAL, INC.
To: CHINA CITIC BANK CORPORATION LIMITED, GUANGZHOU BRANCH, AS COLLATERAL AGENT
Reel/Frame 047760/0795 →
PATENT SECURITY AGREEMENT Recorded Aug 30, 2018
From: LEXMARK INTERNATIONAL, INC.
To: CHINA CITIC BANK CORPORATION LIMITED, GUANGZHOU BRANCH, AS COLLATERAL AGENT
Reel/Frame 046989/0396 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 21, 2013
From: REEVES, SCOTT DANIEL
To: LEXMARK INTERNATIONAL, INC.
Reel/Frame 029662/0666 →