Ink-jet ink set
US-9676951-B2 · Jun 13, 2017 · US
US9914844B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9914844-B2 |
| Application number | US-201514928745-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 30, 2015 |
| Priority date | Nov 5, 2014 |
| Publication date | Mar 13, 2018 |
| Grant date | Mar 13, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
There is provided an ink composition, including: a combination of specific dyes, in which the dynamic contact angle of the ink to a silicon wafer is 24° or lower at 100 msec after dropping, and is 9° or lower at 5,100 msec after dropping.
Opening claim text (preview).
What is claimed is: 1. An ink composition, comprising: a dye (Y-1) represented by a formula below; a dye (Y-2) selected from the group consisting of C.I. Direct Yellows 86, 132, and 142; and a polyoxyakylene alkyl ether, wherein a content ratio A of the dye (Y-1) and the dye (Y-2) (the dye (Y-1):the dye (Y-2)) is 7:3 to 9.5:0.5 , a content of the dye (Y-1) is 2.0 mass % to 5.0 mass %, and a dynamic contact angle of the composition to a silicon wafer is 24° or lower at 100 msec after dropping, and is 9° or lower at 5,100 msec after dropping, wherein in Formula (Y-1), R 4 represents a substituent, R 5 represents —OR 6 or —NHR 7 , each of R 6 and R 7 represents a hydrogen atom or a substituent, X 3 represents a divalent linking group, n0 is 0 or 1, Ar 3 represents a divalent heterocyclic group, and Ar 4 represents an alkyl group, an aryl group, or a triazine group. 2. The ink composition according to claim 1 , wherein a content of the dye (Y-2) is 0.10 mass % to 1.0 mass %. 3. The ink composition according to claim 1 , comprising a dye (Y-3) represented by a formula below, wherein a content of the dye (Y-3) is 0.50 mass % to 1.5 mass %, wherein in Formula (Y-3), R 13 's each independently represent a hydrogen atom or a substituent, R 14 's each independently represent —OR 16 , —NHR 17 , or a cyano group, each of R 16 and R 17 represents a hydrogen atom or a substituent, X 1 represents a substituted or unsubstituted aryl group or a substituted or unsubstituted triazine group, n6 is 0 or 1, Ar 1 's each independently represent a divalent heterocyclic group, and Ar 2 's each independently represent a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted triazine group. 4. The ink composition according to claim 1 , comprising triethylene glycol alkyl ether. 5. The ink composition according to claim 4 , wherein a mass ratio of the triethylene glycol alkyl ether to the polyoxyalkylene alkyl ether is 2 or more. 6. The ink composition according to claim 1 , wherein a content of the polyoxyalkylene alkyl ether is 1.0 mass % to 5.0 mass %. 7. The ink composition according to claim 4 , wherein a content of the triethylene glycol alkyl ether is 3.0 mass % to 15 mass %. 8. The ink composition according to claim 4 , wherein the triethylene glycol alkyl ether includes triethylene glycol monobutyl ether. 9. An ink composition, comprising: a dye (Y-1) represented by a formula below; a dye (Y-2) selected from the group consisting of C.I. Direct Yellows 86, 132, and 142; an alkylene oxide adduct of an acetylene glycol having a main chain of 12 or more carbon atoms; and an acetylene glycol having a main chain of 10 or more carbon atoms, wherein a content ratio A of the dye (Y-1) and the dye (Y-2)(Y-1):the dye (y-2)is 7:3to 9.5:0.5, acontent of the dye (Y-1) is 2.0 mass %, and a dynamic contact angle of the composition to a silcon wafer is 24° or lower at 100 msec after dropping, and is 9° or lower at 5,100 msec dropping, wherein in Formula (Y-1), R 4 represents a substituent, R 5 represents —OR 6 or —NHR 7 , each of R 6 and R 7 represents a hydrgen atom or a substituent, X 3 represents a divalent linking group, n0 is 0 or 1, Ar 3 represents a divalent heterocyclic group, and Ar 4 represents an alkyl group, an aryl group, or a triazine group.
characterised by dyes · CPC title
characterised by non-macromolecular additives other than solvents, pigments or dyes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.