Ultraviolet ray curable ink composition for use in ink jet method and printed object

US9725611B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9725611-B2
Application numberUS-201314085329-A
CountryUS
Kind codeB2
Filing dateNov 20, 2013
Priority dateDec 3, 2012
Publication dateAug 8, 2017
Grant dateAug 8, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

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An ultraviolet ray curable ink composition adapted to be ejected by using an ink jet method is provided. The ultraviolet ray curable ink composition includes a polymerizable compound, metal powder, and a liquid component having an alicyclic structure including a hetero atom. The metal powder is constituted from metal particles subjected to a surface treatment with a fluorine type silane compound and/or a fluorine type phosphoric acid ester as a surface treatment agent. An amount of the liquid component contained in the ultraviolet ray curable ink composition is in the range of 0.05 mass % or more but 7.0 mass % or less. A printed object is also provided. Such a printed object is produced by using the ultraviolet ray curable ink composition.

First claim

Opening claim text (preview).

What is claimed is: 1. An ultraviolet ray curable ink composition adapted to be ejected by using an ink jet method, comprising: a polymerizable compound; metal powder; and a liquid component other than the polymerizable compound, the liquid component having an alicyclic structure including a hetero atom; wherein the metal powder is constituted from metal particles subjected to a surface treatment with a fluorine-containing surface treatment agent, wherein the amount of the liquid component contained in the ultraviolet ray curable ink composition is in the range of 0.05 mass % or more but 7.0 mass % or less, and wherein the fluorine-containing surface treatment agent is at least one selected from the following formulas (1) to (4); P(O)R n (OH) 3-n   (1) where in the above formula (1), “R” is CF 3 (CF 2 ) m (CH 2 ) l — or CF 3 (CF 2 ) m O—, “n” is an integral number in the range of 1 or more but 3 or less, “m” is an integral number in the range of 5 or more but 17 or less, and “1” is an integral number in the range of 1 or more but 12 or less; CF 3 (CF 2 ) 5 (CH 2 ) 2 P(O)(OH)(OCH 2 CH 3 )  (2); CF 3 (CF 2 ) 4 (CH 2 ) 2 O—P(O)(OH) 2   (3); or CF 3 (CF 2 ) 5 (CH 2 ) 2 O—P(O)(OH)(OC 2 H 5 )  (4). 2. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the alicyclic structure including the hetero atom of the liquid component includes a lactone structure and/or a lactam structure. 3. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the alicyclic structure including the hetero atom of the liquid component includes a cyclic structure of a five-membered ring. 4. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the number of the hetero atom included in the alicyclic structure is 1. 5. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein each of the metal particles of the metal powder is constituted from a base particle and Al constitutes at least a surface of the base particle, and the metal particle is subjected to the surface treatment with the fluorine-containing surface treatment agent. 6. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the polymerizable compound includes a monomer having an alicyclic structure. 7. The ultraviolet ray curable ink composition as claimed in claim 6 , wherein the amount of the monomer having the alicyclic structure contained in the ultraviolet ray curable ink composition is in the range of 40 mass % or more but 90 mass % or less. 8. The ultraviolet ray curable ink composition as claimed in claim 6 , wherein the monomer having the alicyclic structure includes a monofunctional monomer having a hetero atom in the alicyclic structure. 9. The ultraviolet ray curable ink composition as claimed in claim 8 , wherein the amount of the monofunctional monomer contained in the ultraviolet ray curable ink composition is in the range of 10 mass % or more but 80 mass % or less. 10. The ultraviolet ray curable ink composition as claimed in claim 6 , wherein the monomer having the alicyclic structure includes one or more selected from the group consisting of tris(2-acryloyloxy ethyl) isocyanurate, dicyclopentenyl oxyethyl acrylate, adamantyl acrylate, γ-butyrolactone acrylate, N-vinyl caprolactam, N-vinyl pyrrolidone, pentamethyl piperidyl acrylate, tetramethyl piperidyl acrylate, 2-methyl-2-adamantyl acrylate, 2-ethyl-2-adamantyl acrylate, mevalonic acid lactone acrylate, dimethylol tricyclodecane diacrylate, dimethylol dicyclopentane diacrylate, dicyclopentenyl acrylate, dicyclopentanyl acrylate, isobornyl acrylate, cyclohexyl acrylate, acryloyl morpholine and tetrahydrofurfuryl acrylate. 11. The ultraviolet ray curable ink composition as claimed in claim 6 , wherein the polymerizable compound includes one or more selected from the group consisting of phenoxy ethyl acrylate, 2-(2-vinyloxy ethoxy) ethyl acrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, 2-hydroxy-3-phenoxy propyl acrylate and 4-hydroxy butyl acrylate in other than the monomer having the alicyclic structure. 12. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the amount of the liquid component contained in the ultraviolet ray curable ink composition is in the range of 0.06 mass % or more but 1.5 mass % or less. 13. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the liquid component includes one or more selected from the group consisting of N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, 1,3-dioxane-2-on, 2-oxazolidinone, propylene carbonate, γ-valerolactone, γ-nonalactone, N-ethylpyrrolidone, tetrahydrofurane and piperidine. 14. The ultraviolet ray curable ink composition as claimed in claim 1 , wherein the liquid component includes γ-butyrolactone and/or N-methyl-2-pyrrolidone, wherein the polymerizable compound includes one or more selected from the group consisting of γ-butyrolactone acrylate, γ-butyrolactone methacrylate, tetrahydrofurfuryl acrylate, tetrahydrofurfuryl methacrylate, N-vinyl caprolactam, N-vinyl pyrrolidone, acryloyl morpholine, tris(2-acryloyloxy ethyl) isocyanurate, dicyclopentenyl oxyethyl acrylate, dicyclopentenyl oxyethyl methacrylate, adamantyl acrylate, adamantyl methacrylate, pentamethyl piperidyl methacrylate, tetramethyl piperidyl methacrylate, 2-methyl-2-adamantyl methacrylate, 2-ethyl-2-adamantyl methacrylate, dicyclopentenyl acrylate, dicyclopentenyl methacrylate, mevalonic acid lactone methacrylate, dimethylol tricyclodecane diacrylate, dicyclopentanyl acrylate, dicyclopentanyl methacrylate, isobornyl acrylate, isobornyl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate, dimethylol dicyclopentane diacrylate, phenoxy ethyl acrylate, 2-(2-hydroxy ethoxy) ethyl acrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, 2-hydroxy-3-phenoxy propyl acrylate and 4-hydroxy butyl acrylate, wherein each of the metal particles of the metal powder is constituted from a base particle and Al constitutes at least a surface of the base particle, and wherein the fluorine-containing surface treatment agent includes one or more selected from CF 3 (CF 2 ) 5 (CH 2 ) 2 P(O)(OH) 2 , CF 3 (CF 2 ) 5 (CH 2 ) 2 P(O)(OH)(OCH 2 CH 3 ), CF 3 (CF 2 ) 4 (CH 2 ) 2 O—P(O)(OH) 2 or CF 3 (CF 2 ) 5 (CH 2 ) 2 O—P(O)(OH)(OC 2 H 5 ). 15. An ultraviolet ray curable ink composition adapted to be ejected by using an ink jet method, comprising: a polymerizable compound; metal powder; and a liquid component other than the polymerizable compound, the liquid component having an alicyclic structure including a hetero atom; wherein the metal powder is constituted from metal particles subjected to a surface treatment with a fluorine-containing surface treatment agent represented by CF 3 (CF 2 ) 5 (CH 2 ) 2 P(O)(OH) 2 and/or CF 3 (CF 2 ) 5 (CH 2 ) 2 P(O)(OH)(OCH 2 CH 3 ), and wherein the amount of the liquid component contained in the ultraviolet ray curable ink composition is in the range of 0.05 mass % or more but 7.0 mass % or less. 16. An ultraviolet ray curable ink composition adapted to be ejected by using an ink jet method, comprising: a polymerizable compound; metal powder; and a liquid component other than the polymerizable compound, the liquid component having an alicyclic structure including a hetero atom; wherein the metal powder is constituted from metal particles subjected to a surface treatment with a fluorine-containing surface treatment agent, wherein the amount of the liquid component contained in the ultraviolet ray curable ink composition is in the ran

Assignees

Inventors

Classifications

  • Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] · CPC title

  • Pigment inks · CPC title

  • Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing · CPC title

  • C09D11/38Primary

    characterised by non-macromolecular additives other than solvents, pigments or dyes · CPC title

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What does patent US9725611B2 cover?
An ultraviolet ray curable ink composition adapted to be ejected by using an ink jet method is provided. The ultraviolet ray curable ink composition includes a polymerizable compound, metal powder, and a liquid component having an alicyclic structure including a hetero atom. The metal powder is constituted from metal particles subjected to a surface treatment with a fluorine type silane compoun…
Who is the assignee on this patent?
Seiko Epson Corp
What technology area does this patent fall under?
Primary CPC classification C09D11/38. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Aug 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).