IP Library › Granted Patent US 9,090,787
Granted Patent B2
US 9,090,787 · App. 13/611,095 · Granted Jul 28, 2015

Photocurable ink jet recording ink composition and ink jet recording method

Inventors: Toshiyuki Yoda (Matsumoto, JP); Hiroshi Fukumoto (Shiojiri, JP)
Assignee: Seiko Epson Corporation
C09D11/101B41J2/2107C09D11/30
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 9,090,787
App. No.
13/611,095
Granted
Jul 28, 2015
Kind
B2
Abstract

Provided is a photocurable ink jet recording ink composition having a low viscosity and excellent curing property and photopolymerization initiator solubility. The photocurable ink jet recording ink composition includes a polymerizable compound and a photopolymerization initiator. The polymerizable compound includes vinyl ether group-containing (meth)acrylic esters represented by Formula (I) in an amount of 20% by mass or more based on the total mass of the ink composition. The photopolymerization initiator includes a bisacylphosphine oxide photopolymerization initiator in an amount of 5% by mass or more based on the total mass of the ink composition and a thioxanthone photopolymerization initiator. The content ratio of the bisacylphosphine oxide photopolymerization initiator to the thioxanthone photopolymerization initiator is from 3:1 to 5:4.

Claims (30)

1. A photocurable ink jet recording ink composition comprising a polymerizable compound and a photopolymerization initiator, wherein

the polymerizable compound includes:

vinyl ether group-containing (meth)acrylic esters represented by the following Formula (I):

CH 2 ═CR 1 —COOR 2 —CH═CH—R 3   (I)

(wherein, R 1 represents a hydrogen atom or a methyl group; R 2 represents a divalent organic residue having 2 to 20 carbon atoms; and R 3 represents a hydrogen atom or a monovalent organic residue having 1 to 11 carbon atoms) in an amount of 20% by mass or more based on the total mass of the ink composition;

the polymerizable compound further includes at least one monymer wich is monofunctional, difunctional, or tri- or more-functional monomer other than the vinyl ether group-containing (meth)acrylate esters represented by the formula (I), in an amount of 40% by mass or less of the ink composition; and

the photopolymerization initiator includes a bisacylphosphine oxide photopolymerization initiator in an amount of 5% by mass or more based on the total mass of the ink composition and a thioxanthone photopolymerization initiator, wherein the content ratio of the bisacylphosphine oxide photopolymerization initiator to the thioxanthone photopolymerization initiator is from 3:1 to 5:4 by mass standard.

2. The photocurable ink jet recording ink composition according to claim 1 , wherein the thioxanthone photopolymerization initiator is at least one of 2,4-diethylthioxanthone and 2-isopropylthioxanthone.

3. The photocurable ink jet recording ink composition according to claim 1 , wherein the content of the thioxanthone photopolymerization initiator is 4% by mass or less based on the total mass of the ink composition.

4. The photocurable ink jet recording ink composition according to claim 1 , wherein the bisacylphosphine oxide photopolymerization initiator is bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide.

5. The photocurable ink jet recording ink composition according to claim 1 , wherein the polymerizable compound further includes phenoxyethyl (meth)acrylate in an amount of less than 30% by mass based on the total mass of the ink composition.

6. The photocurable ink jet recording ink composition according to claim 1 , wherein the vinyl ether group-containing (meth)acrylic esters are 2-(vinyloxyethoxy)ethyl acrylate.

7. An ink jet recording method comprising:

discharging a photocurable ink jet recording ink composition according to claim 1 onto a recording medium; and

curing the discharged ink composition by irradiating the ink composition with ultraviolet light having an emission peak wavelength in a range of 350 to 420 nm using an LED.

8. An ink jet recording method comprising:

discharging a photocurable ink jet recording ink composition according to claim 2 onto a recording medium; and

curing the discharged ink composition by irradiating the ink composition with ultraviolet light having an emission peak wavelength in a range of 350 to 420 nm using an LED.

9. An ink jet recording method comprising:

discharging a photocurable ink jet recording ink composition according to claim 3 onto a recording medium; and

curing the discharged ink composition by irradiating the ink composition with ultraviolet light having an emission peak wavelength in a range of 350 to 420 nm using an LED.

10. An ink jet recording method comprising:

discharging a photocurable ink jet recording ink composition according to claim 4 onto a recording medium; and

curing the discharged ink composition by irradiating the ink composition with ultraviolet light having an emission peak wavelength in a range of 350 to 420 nm using an LED.

11. An ink jet recording method comprising:

discharging a photocurable ink jet recording ink composition according to claim 5 onto a recording medium; and

curing the discharged ink composition by irradiating the ink composition with ultraviolet light having an emission peak wavelength in a range of 350 to 420 nm using an LED.

12. An ink jet recording method comprising:

discharging a photocurable ink jet recording ink composition according to claim 6 onto a recording medium; and

curing the discharged ink composition by irradiating the ink composition with ultraviolet light having an emission peak wavelength in a range of 350 to 420 nm using an LED.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2012
From: YODA, TOSHIYUKI; FUKUMOTO, HIROSHI
To: SEIKO EPSON CORPORATION
Reel/Frame 029145/0548 →
Priority Claims (1)
JP 2011-198184 · Sep 12, 2011 · national
Continuity (1)
Related Publication 20130063535A1 · Mar 14, 2013