US2010107412A1PendingUtilityA1
Ink-jet head and its manufacture method
Est. expiryJul 22, 2023(expired)· nominal 20-yr term from priority
B41J 2/1645B41J 2/1433Y10T29/49401B41J 2/1639B41J 2/1631B41J 2/162B41J 2/1603B41J 2/1606
48
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Claims
Abstract
An ink jet head is formed of a nozzle material composed of a condensation product comprising a hydrolysable silane compound having a fluorine-containing group and a photo-polymerizable resin composition.
Claims
exact text as granted — not AI-modified1 - 21 . (canceled)
22 . A method of manufacturing an ink jet head including a member provided with an ejection opening for ejecting ink, the method comprising:
applying a material comprising a condensation product comprising a hydrolysable silane compound having a fluorine-containing group and a photo-polymerizable resin composition for forming the member on a substrate; and forming the ejection opening by exposing the material and removing an unexposed portion of the material.
23 . A method of manufacturing an ink jet head including a member provided with an ejection opening for ejecting ink and an ink passage communicating with the ejection opening, the method comprising:
providing a pattern of the ink passage on a substrate provided with an ejection pressure generating element for ejecting ink; providing a coating layer comprising a condensation product comprising a hydrolysable silane compound having a fluorine-containing group and a photo-polymerizable resin composition for forming the member on the pattern; forming an opening by exposing the coating layer and removing an unexposed portion of the coating layer; and removing the pattern to form the passage.
24 . A method of manufacturing an ink jet head according to claim 22 ,
wherein after the ejection opening formation, a curing reaction is promoted with light or thermal energy.
25 . A method of manufacturing an ink jet head according to claim 24 , wherein the nozzle material is applied two or more times on the substrate.
26 . A method of manufacturing an ink jet head according to claim 22 , wherein the photo-polymerizable resin composition is a cationically photo-polymerizable resin composition.
27 . A method of manufacturing an ink jet head according to claim 26 , wherein the cationically photo-polymerizable resin composition contains an epoxy compound.
28 . A method of manufacturing an ink jet head according to claim 27 , wherein the cationically photo-polymerizable resin composition comprises an epoxy compound that is solid state at room temperature.
29 . A method of manufacturing an ink jet head according to claim 22 , wherein the condensation product further comprises a hydrolysable silane compound having no fluorine-containing group.
30 . A method of manufacturing an ink jet head according to claim 29 , wherein the hydrolysable silane compound having no fluorine-containing group is a hydrolysable silane compound having a photo-polymerizable group.
31 . A method of manufacturing an ink jet head according to claim 30 , wherein the hydrolysable silane compound having a photo-polymerizable group is a hydrolysable silane compound having a cationic polymerization group.
32 . A method of manufacturing an ink jet head according to claim 30 , wherein the hydrolysable silane compound having a photo-polymerizable group is a hydrolysable silane compound having an epoxy group.
33 . A method of manufacturing an ink jet head according to claim 29 , wherein the hydrolysable silane compound having no fluorine-containing group is selected from a silane having at least one alkyl substituent, a silane having at least one aryl substituent or a silane having no non-hydrolysable substituent.
34 . A method of manufacturing an ink jet head according to claim 22 , wherein the condensation product comprises a hydrolysable silane compound having a fluorine-containing group, a hydrolysable silane compound having a photo-polymerizable group, and a hydrolysable silane compound selected from a silane having at least one alkyl substituent, a silane having at least one aryl substituent or a silane having no non-hydrolysable substituent.
35 . A method of manufacturing an ink jet head according to claim 22 , wherein the hydrolysable silane compound having a fluorine-containing group is represented by general formula (1):
R f Si(R) b X( 3-b ) (1) wherein R f is a non-hydrolysable substituent having 1 to 30 fluorine atoms bonded to a carbon atom, R is a non-hydrolysable substituent, X is a hydrolysable substituent, and b is an integer from 0 to 2.
36 . A method of manufacturing an ink jet head according to claim 35 , wherein the non-hydrolysable substituent R f has at least 5 fluorine atoms bonded to a carbon atom.
37 . A method of manufacturing an ink jet head according to claim 35 , wherein the condensation product comprises at least two hydrolysable silane compounds having a fluorine-containing group, the silane compounds having a different number of fluorine atoms contained therein.
38 . A method of manufacturing an ink jet head according to claim 31 , wherein the hydrolysable silane compound having a cationic polymerizable group is represented by general formula (2):
R c Si(R) b X( 3-b ) (2) wherein R c is a non-hydrolysable substituent having a cationic polymerizable group, R is a non-hydrolysable substituent, X is a hydrolysable substituent, and b is an integer from 0 to 2.
39 . A method of manufacturing an ink jet head according to claim 33 , wherein the hydrolysable silane compound selected from a silane having at least one alkyl substituent, a silane having at least one aryl substituent or a silane having no non-hydrolysable substituent is represented by general formula (3):
R a SiX( 4-a ) (3) wherein R is a non-hydrolysable substituent selected from substituted or unsubstituted alkyl groups and substituted or unsubstituted aryl groups, X is a hydrolysable substituent, and a is an integer from 0 to 3.
40 . A method of manufacturing an ink jet head according to claim 22 , wherein the hydrolysable silane compound having a fluorine-containing group is represented by formula (4):
CF 3 (CF 2 ) n —Z—SiX 3 (4) wherein X is a hydrolysable substituent and preferably is methoxy or ethoxy, Z is a divalent organic group, and n is an integer from 0 to 20.Join the waitlist — get patent alerts
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