Kit and laminate
US-2018012751-A1 · Jan 11, 2018 · US
US12545863B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12545863-B2 |
| Application number | US-202117913314-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 22, 2021 |
| Priority date | Mar 23, 2020 |
| Publication date | Feb 10, 2026 |
| Grant date | Feb 10, 2026 |
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A semiconductor substrate cleaning method including removing an adhesive layer provided on a semiconductor substrate by use of a remover composition, wherein the remover composition contains a solvent but no salt; and the solvent includes an organic solvent represented by any of formulae (L0) to (L4).
Opening claim text (preview).
The invention claimed is: 1 . A semiconductor substrate cleaning method comprising removing an adhesive layer provided on a semiconductor substrate by use of a remover composition, wherein the adhesive layer is a film formed from an adhesive composition comprising an adhesive component(S) containing a siloxane adhesive which comprises a polyorganosiloxane component (A) being curable through hydrosilylation; the polyorganosiloxane component (A) comprises a polysiloxane (A1) having one or more units selected from the group consisting of a siloxane unit represented by SiO 2 (unit Q), a siloxane unit represented by R 1 R 2 R 3 SiO 1/2 (unit M), a siloxane unit represented by R 4 R 5 SiO 2/2 (unit D), and a siloxane unit represented by R 6 SiO 3/2 (unit T), and a platinum group metal catalyst (A2); wherein the polysiloxane (A1) comprises a polyorganosiloxane (a1) having one or more units selected from the group consisting of a siloxane unit represented by SiO 2 (unit Q′), a siloxane unit represented by R 1′ R 2′ R 3′ SiO 1/2 (unit M′), a siloxane unit represented by R 4′ R 5′ SiO 2/2 (unit D′), and a siloxane unit represented by R 6′ SiO 3/2 (unit T′), and at least one unit selected from the group consisting of unit M′, unit D′, and unit T′, and a polyorganosiloxane (a2) having one or more units selected from the group consisting of a siloxane unit represented by SiO 2 (unit Q″), a siloxane unit represented by R 1″ R 2″ R 3″ SiO 1/2 (unit M″), a siloxane unit represented by R 4″ R 5″ SiO 2/2 (unit D″), and a siloxane unit represented by R 6″ SiO 3/2 (unit T″) and at least one unit selected from the group consisting of unit M″, unit D″, and unit T″; each of R 1 to R 6 is a group or an atom bonded to a silicon atom and represents an alkyl group, an alkenyl group, or a hydrogen atom, each of R 1′ to R 6′ is a group bonded to a silicon atom and represents an alkyl group or an alkenyl group, and at least one of R 1′ to R 6′ is an alkenyl group, each of R 1″ to R 6″ is a group or an atom bonded to a silicon atom and represents an alkyl group or a hydrogen atom, and at least one of R 1″ to R 6″ is a hydrogen atom; the remover composition contains a solvent but no salt; and the solvent includes an organic solvent represented by any of formulae (L0) to (L4): (wherein each of L 101 to L 112 independently represents a hydrogen atom, a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and at least one of L 101 to L 112 represents a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group; each of L 201 to L 210 independently represents a hydrogen atom, a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and at least one of L 201 to L 210 represents a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group; each of L 301 to L 308 independently represents a hydrogen atom, a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and at least one of L 301 to L 308 represents a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group; and each of L 401 to L 408 independently represents a hydrogen atom, a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and at least one of L 401 to L 408 represents a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group) in an amount of 80 mass % or more. 2 . The semiconductor substrate cleaning method according to claim 1 , wherein the solvent includes an organic solvent represented by any of formulae (L0) to (L4) in an amount of 85 mass % or more. 3 . The semiconductor substrate cleaning method according to claim 2 , wherein the solvent is formed of an organic solvent represented by any of formulae (L0) to (L4). 4 . The semiconductor substrate cleaning method according to claim 1 , wherein the C1 to C5 alkyl group is a methyl group, an ethyl group, an n-propyl group, or an isopropyl group; the C2 to C5 alkenyl group is an ethenyl group, a 1-methylethenyl group, or a 2-methylethenyl group; and the C2 to C5 alkynyl group is an ethynyl group or a 2-methylethynyl group. 5 . The semiconductor substrate cleaning method according to claim 4 , wherein one or two of the groups L 101 to L 112 are a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and each of the remaining groups is a hydrogen atom; one or two of the groups L 201 to L 210 are a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and each of the remaining groups is a hydrogen atom; one or two of the groups L 301 to L 308 are a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and each of the remaining groups is a hydrogen atom; and one or two of the groups L 401 to L 408 are a C1 to C5 alkyl group, a C2 to C5 alkenyl group, or a C2 to C5 alkynyl group, and each of the remaining groups is a hydrogen atom. 6 . The semiconductor substrate cleaning method according to claim 1 , wherein the adhesive component(S) containing at least one species selected from among an acrylic resin adhesive, an epoxy resin adhesive, a polyamide adhesive, a polystyrene adhesive, a polyimide adhesive, and a phenolic resin adhesive.
Cleaning of wafers, substrates or parts of devices · CPC title
Cleaning for reclaiming · CPC title
Delaminating · CPC title
Electronic devices, e.g. PCBs or semiconductors · CPC title
containing nitrogen · CPC title
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