IP Library › Granted Patent US 9,056,986
Granted Patent B2
US 9,056,986 · App. 13/292,219 · Granted Jun 16, 2015

Ultraviolet curable type ink-jet ink composition, recording method and recording apparatus using same

Inventors: Taketoshi Kagose (Shiojiri, JP); Hiroki Nakane (Matsumoto, JP); Chigusa Sato (Shiojiri, JP); Hiroaki Kida (Shiojiri, JP); Toru Saito (Yamagaramu, JP)
Assignee: Seiko Epson Corporation
C09D4/00B41J2/2107C09D11/101C09D11/322
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Quick Facts
Patent No.
US 9,056,986
App. No.
13/292,219
Granted
Jun 16, 2015
Kind
B2
Abstract

Provided is a UV curable type ink-jet ink composition containing a monomer A which is expressed by the following general formula (I): CH 2 ═CR 1 —COOR 2 —O—CH═CH—R 3   (I) (in the formula, R 1 is a hydrogen atom or methyl radical, R 2 is a bivalent organic residue radical having a carbon number in a range of 2 to 20, and R 3 is a hydrogen atom or a univalent organic residue radical having a carbon number in a range of 1 to 11), a compound B containing five or more (meth)acryloyl radicals per molecule, and a monofunctional (meth)acrylate C having an aromatic ring skeleton, wherein the monofunctional (meth)acrylate C which is in a range of 5 to 35 wt % with respect to the total weight of the ink composition is contained, wherein the compound B is in a range of 5 to 40 wt % with respect to the total weight of the ink composition, wherein the monomer A is in a range of 10 to 70 wt % with respect to the total weight of the ink composition.

Claims (22)

1. A UV curable type ink-jet ink composition containing a monomer A which is expressed by the following general formula (I):

CH2=CR 1 —COOR 2 —O—CH═CH—R 3   (I)

(in the formula, R 1 is a hydrogen atom or methyl radical, R 2 is a bivalent organic residue radical having a carbon number in a range of 2 to 20, and R 3 is a hydrogen atom or a univalent organic residue radical having a carbon number in a range of 1 to 11),

a compound B containing five or more (meth) acryloyl radicals per molecule, and

a monofunctional (meth)acrylate C having an aromatic ring skeleton,

wherein the monofunctional (meth)acrylate C which is in a range of 5 to 35 wt % with respect to the total weight of the ink composition is contained,

wherein the compound B is in a range of 5 to 40 wt % with respect to the total of the ink composition,

wherein the monomer A is in a range of 10 to 70% with respect to the total weight of the ink composition.

2. The UV curable type ink-jet ink composition according to claim 1 , wherein the monomer A is (meth)acrylic acid 2-(vinyloxyethoxy)ethyl.

3. The UV curable type ink-jet ink composition according to claim 1 , wherein the compound B contains at least one of a hexa (meth)acrylate compound having six (meth) acryloyl radicals per molecule and a penta(meth)acrylate compound having five (meth) acryloyl radicals per molecule.

4. The UV curable type ink-jet ink composition according to claim 1 , wherein the compound B contain a (meth)acrylate having a dipentaerythritol skeleton.

5. The UV curable type ink-jet ink composition according to claim 3 , wherein the compound B contains a dipentaerythritol hexa (meth)acrylate or a dipentaerythritol penta (meth)acrylate.

6. The UV curable type ink-jet ink composition according to claim 1 , wherein the monofunctional (meth)acrylate C having an aromatic ring skeleton is at least one of a benzyl (meth)acrylate and a phenoxyethyl (meth)acrylate.

7. The UV curable type ink-jet ink composition according to claim 1 , wherein an acylphosphine oxide compound is contained as the photopolymerization initiator.

8. The UV curable type ink-jet ink composition according to claim 7 , wherein an acylphosphine oxide compound which is in a range of 7 to 15 wt % with respect to the total weight of the ink composition is contained as the photopolymerization initiator.

9. The UV curable type ink-jet ink composition according to claim 1 , wherein the curing is performed through illumination of ultraviolet rays of which the light emitting peak wavelength is in a range of 350 to 420 nm with an illumination energy of equal to or less than 300 mJ/cm 2 .

10. The UV curable type ink-jet ink composition according to claim 1 , wherein viscosity at 20° C. is in a range of 3 to 30 mPa·s.

11. The UV curable type ink-jet ink composition according to claim 1 , wherein the curing is performed in a state of a thin film having a thickness of 0.5 to 3 μm.

12. An ink jet recording method of ejecting the UV curable type ink-jet ink composition according to claim 1 on a recording medium and curing the ejected UV curable type ink-jet ink composition through illumination using a UV-LED of which the light emitting peak wavelength is in a range of 350 to 420 nm.

13. An ink jet recording apparatus for ejecting the UV curable type ink-jet ink composition according to claim 1 on a recording medium and curing the ejected UV curable type ink-jet ink composition through illumination using a UV-LED of which the light emitting peak wavelength is in a range of 350 to 420 nm.

14. The UV curable type ink-jet ink composition according to claim 1 , wherein the monomer A is present in a range of 10 to 41 wt. % with respect to the total weight of the ink composition.

15. The UV curable type ink-jet ink composition according to claim 1 , wherein the monomer B is present in a range of 5 to 30 wt. % with respect to the total weight of the ink composition.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2011
From: KAGOSE, TAKETOSHI; NAKANE, HIROKI; SATO, CHIGUSA; KIDA, HIROAKI; SAITO, TORU
To: SEIKO EPSON CORPORATION
Reel/Frame 027198/0456 →
Priority Claims (4)
JP 2010-251004 · Nov 9, 2010 · national
JP 2010-260050 · Nov 22, 2010 · national
JP 2011-025920 · Feb 9, 2011 · national
JP 2011-207187 · Sep 22, 2011 · national
Continuity (1)
Related Publication 20120113201A1 · May 10, 2012