Electrically debondable uv activated adhesives
US-2024263044-A1 · Aug 8, 2024 · US
US12545813B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12545813-B2 |
| Application number | US-202418631645-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 10, 2024 |
| Priority date | Oct 10, 2022 |
| Publication date | Feb 10, 2026 |
| Grant date | Feb 10, 2026 |
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Curable and cured compositions as well as articles containing the curable or cured compositions are provided. The cured compositions are typically a semi-structural or structural adhesive. Advantageously, the cured compositions can be removed (e.g., de-bonded) from the various surfaces of the articles after the useful lifetime of the articles, to correct misplacement of a part during manufacturing, or to repair the electronic device. The separation step occurs using a direct current electric potential across the cured composition.
Opening claim text (preview).
What is claimed is: 1 . A curable composition comprising: a film forming polymeric material; an epoxy resin; a photoacid generator; and an ionic liquid that has a melting point less than 100 degrees Celsius and that has an anion selected from SbF 6 − , PF 6 − , or a mixture thereof. 2 . The curable composition of claim 1 wherein the film forming polymeric material comprises a (meth)acrylic-based block copolymer, a statistical (meth)acrylic-based copolymer, or a combination thereof. 3 . The curable composition of claim 1 wherein the curable composition comprises (meth)acrylic-based block copolymer, wherein the (meth)acrylic-based block copolymer is a triblock copolymer of formula A-B-A with the A blocks microphase separating from the B block, wherein the A block has a glass transition temperature equal to at least 50 degrees Celsius and the B block has a glass transition temperature equal to no greater than 20 degrees Celsius as measured using Dynamic Mechanical Analysis. 4 . The curable composition of claim 2 wherein the curable composition comprises 10 to 40 weight percent of the (meth)acrylic-based block copolymer based on a total weight of resin components in the curable composition. 5 . The curable composition of claim 2 wherein the curable composition comprises greater than 40 wt. % of the (meth)acrylic-based block copolymer based on a total weight of resin components in the curable composition. 6 . The curable composition of claim 2 wherein the curable composition comprises statistical (meth)acrylic-based copolymer having a glass transition temperature no greater than 20 degrees Celsius when measured using Dynamic Mechanical Analysis. 7 . The curable composition of claim 2 wherein the statistical (meth)acylate-based copolymer is crosslinked. 8 . The curable composition of claim 2 wherein the curable composition contains 20 to 60 weight percent of the statistical (meth)acrylic-based copolymer based on a total weight of resin components in the curable composition. 9 . The curable composition of claim 2 wherein the curable composition comprises greater than 60 weight percent up to 90% of the statistical (meth)acrylic-based copolymer based on a total weight of resin components in the curable composition. 10 . The curable composition of claim 2 wherein the statistical (meth)acrylic-based copolymer comprises monomeric units derived from a (meth)acrylate macromer having a number average molecular weight of at least 300 Daltons, a polyol, or a combination thereof. 11 . The curable composition of claim 1 wherein the statistical (meth)acrylic-based comprises at least 10 wt. % of polymerized units of a (meth)acrylate monomer having a Tg of at least 30° C. 12 . The curable composition of claim 1 wherein the film forming polymeric material comprises polyurethane, polyester, polyvinyl acetal, a block copolymer of styrene and isoprene or butadiene, or a combination thereof. 13 . The curable composition of claim 1 wherein the film forming polymeric material has a molecular weight greater than 50,000 Daltons. 14 . The curable composition of claim 1 wherein the photoacid generator is an aryl-containing iodonium salt or a triaryl sulfonium salt. 15 . The curable composition of claim 1 wherein the ionic liquid is an ammonium salt of Formula (VI), a sulfonium salt of Formula (VII), an imidazolium salt of Formula (VIII), a pyridinium salt of Formula (IX), or a pyrrolidinium salt of Formula (X) wherein each R 20 , R 21 , R 22 , R 23 , and R 24 is independently an alkyl, a hydroxy-substituted alkyl, or an ether-containing group of formula —(R 30 —O) y —R 31 wherein R 30 is an alkylene, R 31 is an alkyl, and y is an integer in a range of 1 to 10; and X − is SbF 6 − or PF 6 − . 16 . A first article comprising: a layer of a curable composition according to claim 1 wherein the curable composition has a first surface and a second surface opposite the first surface; and a first substrate or a first release liner positioned adjacent to a first surface of the first curable composition. 17 . The first article of claim 16 wherein the layer of curable composition comprises an electrically conductive layer. 18 . A second article comprising: a first substrate; a second substrate; and a layer of cured composition of claim 1 positioned between the first substrate and the second substrate, wherein the first substate is bonded to the second substrate with the first cured composition. 19 . The second article of claim 18 wherein the first substrate, the second substrate, or both are electrically conductive or the layer of cured composition comprises an electrically conductive layer. 20 . A method for separating the second article of claim 18 the comprising applying a direct current electric potential across the cured composition to separate the first substrate from the second substrate.
Presence of block copolymer · CPC title
in the substrate · CPC title
use in electrical or conductive gadgets · CPC title
grafted on to block copolymers containing at least one sequence of polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
Conductive additives · CPC title
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