Photocurable resin composition
US-2018362696-A1 · Dec 20, 2018 · US
US10844255B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10844255-B2 |
| Application number | US-201716329068-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 25, 2017 |
| Priority date | Aug 30, 2016 |
| Publication date | Nov 24, 2020 |
| Grant date | Nov 24, 2020 |
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A novel photosensitive adhesive composition including the following components (A), (B), (C), and (D): Component (A): a polymer having a structural unit of the following formula (1) and a structure of the following formula (2) at a terminal, Component (B): a polymer having the structural unit of formula (1), and a carboxy group or hydroxy group at a terminal, Component (C): a radical photopolymerization initiator, and Component (D): a solvent, wherein the content by mass of the component (B) is larger than that of the component (A), (wherein X is a C 1-6 alkyl group, a vinyl group, an allyl group, or a glycidyl group, m and n are each independently 0 or 1, Q is a divalent C 1-16 hydrocarbon group, Z is a divalent C 1-4 linking group, the divalent linking group being bonded to an —O— group in formula (1), and R 1 is a hydrogen atom or a methyl group.)
Opening claim text (preview).
The invention claimed is: 1. A photosensitive adhesive composition comprising the following components (A), (B), (C), and (D): Component (A): a polymer having a structural unit of the following formula (1) and a structure of the following formula (2) at a terminal, Component (B): a polymer having the structural unit of formula (1), and a carboxy group or hydroxy group at a terminal, Component (C): a radical photopolymerization initiator, and Component (D): a solvent, wherein the content by mass of the component (B) is larger than that of the component (A), wherein X is methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, i-butyl group, s-butyl group, t-butyl group, n-pentyl group, 1-methyl-n-butyl group, 2-methyl-n-butyl group, 3-methyl-n-butyl group, 1,1-dimethyl-n-propyl group, 1,2-dimethyl-n-propyl group, 2,2-dimethyl-n-propyl group, 1-ethyl-n-propyl group, n-hexyl group, 1-methyl-n-pentyl group, 2-methyl-n-pentyl group, 3-methyl-n-pentyl group, 4-methyl-n-pentyl group, 1,1-dimethyl-n-butyl group, 1,2-dimethyl-n-butyl group, 1,3-dimethyl-n-butyl group, 2,2-dimethyl-n-butyl group, 2,3-dimethyl-n-butyl group, 3,3-dimethyl-n-butyl group, 1-ethyl-n-butyl group, 2-ethyl-n-butyl group, 1,1,2-trimethyl-n-propyl group, 1,2,2-trimethyl-n-propyl group, 1-ethyl-1-methyl-n-propyl group, 1-ethyl-2-methyl-n-propyl group, —CH═CH 2 , —CH 2 —CH═CH 2 , or m and n are each independently 0 or 1, Q is a divalent C 1-16 hydrocarbon group, Z is a divalent C 1-4 linking group, the divalent linking group being bonded to an —O— group in formula (1), and R 1 is a hydrogen atom or a methyl group. 2. The photosensitive adhesive composition according to claim 1 , wherein the divalent hydrocarbon group of Q in formula (1) is a linear or branched alkylene group, a group containing two carbon atoms bonded through a double bond, or a group containing in a main chain an alicyclic hydrocarbon group or aromatic hydrocarbon group optionally having at least one substituent. 3. The photosensitive adhesive composition according to claim 1 , wherein the divalent linking group of Z in formula (2) is a linear or branched alkylene group optionally having at least one hydroxy group as a substituent. 4. The photosensitive adhesive composition according to claim 1 , wherein the mass ratio of the component (A) to the component (B) is 1:2 to 1:20. 5. The photosensitive adhesive composition according to claim 1 , further comprising a bifunctional (meth)acrylate and/or a multifunctional thiol. 6. An adhesion method comprising steps of: applying the photosensitive adhesive composition according to claim 1 to a first substrate; pre-baking the photosensitive adhesive composition applied to the first substrate at 50° C. to 160° C.; exposing the coating film on the first substrate after the pre-baking; developing the coating film after the exposure; and bonding a second substrate to the first substrate after the development and thermally curing the coating film by heating.
Treatment after imagewise removal, e.g. baking · CPC title
Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title
Polyethers derived from hydroxy compounds or from their metallic derivatives (C09J171/02 takes precedence) · CPC title
having terminal carbon-to-carbon unsaturated bonds · CPC title
involving heating of the applied adhesive · CPC title
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