IP Library Granted Patent US 8,268,521
Granted Patent B2
US 8,268,521 · App. 12/466,701 · Granted Sep 18, 2012

Electrophotographic photoreceptor, process cartridge, and image forming apparatus

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,268,521
App. No.
12/466,701
Granted
Sep 18, 2012
Kind
B2
Abstract

According to an aspect of the invention, an electrophotographic photoreceptor including a conductive substrate and a photosensitive layer provided on a surface of the conductive substrate is provided. In the electrophotographic photoreceptor, an outermost layer of the photosensitive layer containing a crosslinked product formed from at least one charge transporting material having at least one substituent selected from the group consisting of —OH, —OCH 3 , —NH 2 , —SH, and —COOH, an acidic substance, and at least one compound selected from the group consisting of compounds represented by the following formula (A) and compounds represented by the following formula (B).

Claims (19)

1. An electrophotographic photoreceptor comprising:

a conductive substrate; and

a photosensitive layer provided on a surface of the conductive substrate, an outermost layer of the photosensitive layer containing a crosslinked product formed from at least one charge transporting material having at least one substituent selected from the group consisting of —OH, —OCH 3 , —NH 2 , —SH, and —COOH, an acidic substance, and at least one compound selected from the group consisting of compounds represented by the following formula (A) and compounds represented by the following formula (B):

wherein, in formula (A), L 1 and L 2 each independently represent a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms; L 3 and L 4 each independently represent a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 5 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms; and f and g each independently represent 1 or 2; and

wherein, in formula (B), L 5 to L 8 each independently represent hydrogen, a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 5 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 15 carbon atoms; at least one of L 5 to L 8 has a structure represented by the following formula (C); h to k each independently represent 1 or 2; and L 9 and L 10 each independently represent hydrogen, a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 15 carbon atoms:

wherein, in formula (C), L 1 and L 2 each independently represent a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms.

2. The electrophotographic photoreceptor of claim 1 , wherein the acidic substance comprises a sulfur element.

3. The electrophotographic photoreceptor of claim 1 , wherein the acidic substance comprises a sulfonic acid group.

4. The electrophotographic photoreceptor of claim 1 , wherein the crosslinked product contains at least one compound derived from the at least one charge transporting material having at least one substituent selected from the group consisting of —OH, —OCH 3 , —NH 2 , —SH, and —COOH in an amount of at least about 50% by weight relative to the crosslinked product.

5. The electrophotographic photoreceptor of claim 1 , wherein the crosslinked product contains at least one compound derived from the at least one charge transporting material having at least one substituent selected from the group consisting of —OH, —OCH 3 , —NH 2 , —SH, and —COOH in an amount of at least about 70% by weight relative to the crosslinked product.

6. The electrophotographic photoreceptor of claim 1 , wherein the crosslinked product contains at least one compound derived from the at least one charge transporting material having at least one substituent selected from the group consisting of —OH, —OCH 3 , —NH 2 , —SH, and —COOH in an amount of at least about 80% by weight relative to the crosslinked product.

7. The electrophotographic photoreceptor of claim 1 , wherein the content of the acidic substance is from 0.01% by weight to 5% by weight with respect to the solid content of the total components for forming the outermost layer except for the acidic substance.

8. The electrophotographic photoreceptor of claim 1 , wherein the acidic substance is at least one selected from the group consisting of p-toluenesulfonic acid, dinonylnaphthalenesulfonic acid (DNNSA), dinonylnaphthalenedisulfonic acid (DNNDSA), dodecylbenzenesulfonic acid, and phenolsulfonic acid.

9. An electrophotographic photoreceptor comprising:

a conductive substrate; and

a photosensitive layer provided on a surface of the conductive substrate, an outermost layer of the photosensitive layer containing a crosslinked product formed from at least one charge transporting material, an acidic substance, and at least one compound selected from the group consisting of compounds represented by the following formula (A) and compounds represented by the following formula (B): F—((—R 1 —X) n1 R 2 Y) n2 (I), wherein, in the formula (I), F represents an organic group derived from a hole transporting compound, R 1 and R 2 each independently represent a linear or branched alkylene group having 1 to 5 carbon atoms, n 1 represents 0 or 1, n 2 represents an integer of 1 to 4, X represent an oxygen atom, NH, or a sulfur atom, and Y represents —OH or —OCH3;

wherein, in formula (A), L 1 and L 2 each independently represent a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms; L 3 and L 4 each independently represent a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 5 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 20 carbon atoms; and f and g each independently represent 1 or 2;

wherein, in formula (B), L 5 to L 8 each independently represent hydrogen, a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 5 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 15 carbon atoms; at least one of L 5 to L 8 has a structure represented by the following formula (C); h to k each independently represent 1 or 2; and L 9 and L 10 each independently represent hydrogen, a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 15 carbon atoms:

wherein, in formula (C), L 1 and L 2 each independently represent a substituted or unsubstituted alkyl group having 1 to 5 carbon atoms, or a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms.

Assignments (3)
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 →
CHANGE OF NAME Recorded Aug 12, 2021
From: FUJI XEROX CO., LTD.
To: FUJIFILM BUSINESS INNOVATION CORP.
Reel/Frame 058287/0056 →