IP Library Granted Patent US 8,124,666
Granted Patent B2
US 8,124,666 · App. 12/365,710 · Granted Feb 28, 2012

Energy ray-curable ink composition

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Quick Facts
Patent No.
US 8,124,666
App. No.
12/365,710
Granted
Feb 28, 2012
Kind
B2
Abstract

An object of the present invention is to provide an energy ray-curable ink composition which is excellent in curability and adhesion, and is also excellent in storage stability. The present invention relates to an energy ray-curable ink composition comprising a coloring material; a polyfunctional monomer having three or more ethylenical double bonds in one molecule as a polymerizable compound; an α-aminoalkylphenone-based compound and a thioxanthone-based compound as photopolymerization initiators; and a hindered amine-based compound having a 2,2,6,6-tetramethylpiperidinyl group as an antigelling agent.

Claims (8)

1. An energy ray-curable ink composition comprising a coloring material; a polyfunctional monomer having three or more ethylenical double bonds in one molecule and a polymerizable monomer having one or two ethylenical double bonds in one molecule as polymerizable compounds, said polymerizable compounds consisting of (meth)acrylate monomers; an α-aminoalkylphenone-based compound and a thioxanthone-based compound as photopolymerization initiators; and a hindered amine-based compound having a 2,2,6,6-tetramethylpiperidinyl group as an antigelling agent, wherein said energy ray-curable ink composition contains the polyfunctional monomer in an amount of 10 to 65% by mass, the polymerizable monomer having one or two ethylenical double bonds in one molecule in an amount of 10 to 70% by mass, the α-aminoalkylphenone-based compound in an amount of 2 to 20% by mass, the thioxanthone-based compound in an amount of 0.1 to 10% by mass and the hindered amine-based compound in an amount of 0.01 to 2% by mass, based on the entire amount of the ink composition, and wherein said energy ray-curable ink composition contains the α-aminoalkylphenone-based compound in an amount of 40 to 99% by mass and the thioxanthone-based compound in an amount of 1 to 60% by mass, based on the entire amount of the photopolymerization initiator;

wherein the thioxanthone-based compound is selected from the group consisting of thioxanthone, 2-methylthioxanthone, 2-ethylthioxanthone, 2-isopropylthioxanthone, 4-isopropylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone, 2,4-dichlorothioxanthone, and 1-chloro-4-propoxythioxanthone.

2. The energy ray-curable ink composition according to claim 1 , wherein the hindered amine-based compound has a 1-hydroxy-2,2,6,6-tetramethylpiperidinyl group.

3. The energy ray-curable ink composition according to claim 1 , which contains, as the hindered amine-based compound, bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)sebacate.

4. An energy ray-curable ink composition comprising a coloring material; at least one of a polyfunctional monomer selected from the group consisting of trimethylolpropane tri(meth)acrylate and pentaerythritol tri(meth)acrylate as a polymerizable compound; at least one of an α-aminoalkylphenone-based compound selected from the group consisting of 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one and 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone, and a thioxanthone-based compound as photopolymerization initiators; and bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)sebacate as an antigelling agent; wherein

the energy ray-curable ink composition contains the polyfunctional monomer in an amount of 10 to 65% by mass, the α-aminoalkylphenone-based compound in an amount of 2 to 20% by mass, the thioxanthone-based compound in an amount of 0.1 to 10% by mass and the bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)sebacate in an amount of 0.01 to 2% by mass, based on the entire amount of the ink composition; and

also contains the α-aminoalkylphenone-based compound in an amount of 40 to 99% by mass and the thioxanthone-based compound in an amount of 1 to 60% by mass, based on the entire amount of the photopolymerization initiator;

wherein the thioxanthone-based compound is selected from the group consisting of thioxanthone, 2-methylthioxanthone, 2-ethylthioxanthone, 2-isopropylthioxanthone, 4-isopropylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone, 2,4-dichlorothioxanthone, and 1-chloro-4-propoxythioxanthone.

Assignments (4)
CHANGE OF NAME Recorded Dec 3, 2021
From: MAXELL HOLDINGS, LTD.
To: MAXELL, LTD.
Reel/Frame 058301/0318 →
CHANGE OF NAME AND ADDRESS Recorded Feb 5, 2018
From: HITACHI MAXELL, LTD.
To: MAXELL HOLDINGS, LTD.
Reel/Frame 045243/0893 →
CORRECTIVE ASSIGNMENT TO CORRECT THE EXECUTION DATE FOR INVENTORS 2 AND 3 PREVIOUSLY RECORDED ON REEL 022229 FRAME 0659. ASSIGNOR(S) HEREBY CONFIRMS THE EXECUTION DATES FOR MASAYUKI OYA IS 01/28/2009 AND FOR SATOSHI KOBAYASHI IS 01/27/2009. Recorded Mar 11, 2009
From: KITO, KATSUYUKI; OYA, MASAYUKI; KOBAYASHI, SATOSHI
To: HITACHI MAXELL, LTD.
Reel/Frame 022379/0822 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2009
From: KITO, KATSUYUKI; OYA, MASAYUKI; KOBAYASHI, SATOSHI
To: HITACHI MAXELL, LTD.
Reel/Frame 022229/0659 →