Methylene beta-ketoester monomers, methods for making methylene beta-ketoester monomers, polymerizable compositions and products formed therefrom
US-9527795-B2 · Dec 27, 2016 · US
US9822286B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9822286-B2 |
| Application number | US-201414787021-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 10, 2014 |
| Priority date | Jun 24, 2013 |
| Publication date | Nov 21, 2017 |
| Grant date | Nov 21, 2017 |
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.
A self-wetting adhesive composition is described comprising the reaction product of a low T g (meth)acrylate solute copolymer component; a low T g solvent monomer solvent monomer component comprising low T g monomers, a multifunctional acrylate; and a polymerizable siloxane copolymer having at least one polydiorganosiloxane segment and at least on oxyalkylene segment.
Opening claim text (preview).
What is claimed is: 1. A syrup polymer composition comprising: a) 5 to 40 parts by weight of a low T g (meth)acrylate solute copolymer component having a T g ≦0° C.; b) 60 to 95 parts by weight of a low T g solvent monomer component comprising low T g monomers having a T g ≦0° C., and a multifunctional acrylate; the sum of a) and b) being 100 parts by weight; c) 5 to 50 parts by weight, relative to 100 parts a) and b) of a segmented siloxane copolymer having at least one polydiorganosiloxane segment and at least one oxyalkylene segment. 2. The syrup polymer composition of claim 1 wherein the composition comprises 5 to 20 parts of the siloxane copolymer, relative to 100 parts of a) and b). 3. The syrup polymer composition of claim 1 wherein the solute copolymer comprises: a) 95-100 parts by weight of low T g monomer units; b) 0 to 5 parts of acid-functional monomer units; c) 0 to 5 parts of a non-acid functional polar monomer the sum being 100 parts by weight. 4. The syrup polymer composition of claim 1 wherein the solvent monomer component comprises: a) 60 to 90 parts by weight of low T g monomers; b) 0 to 5 parts of acid functional monomers; c) 10 to 40 parts of a multiacrylate; the sum being 100 parts by weight. 5. The syrup polymer composition of claim 1 comprising 20 to 50 parts of a siloxane copolymer, relative to 100 parts a) and b). 6. The syrup polymer composition of claim 1 wherein the solute low T g copolymer comprises 1 to 5 parts by weight of acid-functional monomer units and 5 to 95 parts by weight of low T g monomer units. 7. The syrup polymer composition of claim 1 wherein the solute low T g copolymer comprises 1 to 5 parts by weight of non-acid-functional monomer units. 8. The syrup polymer composition of claim 1 wherein the solvent monomer component comprises 1 to 5 parts by weight of acid-functional monomer units. 9. The syrup polymer composition of claim 1 wherein the solute low T g copolymer comprises 100 parts by weight of low T g monomer units. 10. The syrup polymer composition of claim 1 wherein the segmented siloxane copolymer comprises at least two (meth)acrylate groups. 11. The syrup polymer composition of claim 1 wherein the segmented siloxane copolymer is of the formula: X—(R 2 —O) a -Q-(SiR 1 2O) b -Q-(O—R 2 ) a —X where X is H or a free radically polymerizable group; R 2 is an alkylene group; Q is difunctional linking group; R 1 is alkyl or aryl group; and a and b are independently integers greater than 1, with the proviso that at least one X is a free radically polymerizable group. 12. The syrup polymer composition of claim 1 wherein the segmented siloxane copolymer is of the formula: R 1 3SiO—(SiR 1 2 O) b —(SiR 1 (-Q(—O—R 2 ) a —X)O) a SiR 1 3 where R 1 is alkyl or aryl group; X is a free radically polymerizable group; R 2 is an alkylene group; Q is a difunctional linking group; and a and b are independently integers greater than 1. 13. An adhesive comprising the cured syrup polymer composition of claim 1 . 14. A method of making an adhesive comprising the steps of: partially polymerizing a low T g monomer and optional acid functional monomer to a viscosity produce a syrup polymer composition, adding a multifunctional acrylate crosslinker agent, optional additional monomers, and a segmented siloxane copolymer having at least one polydiorganosiloxane segment and at least on oxyalkylene segment, and further photopolymerizing. 15. The method of claim 14 , wherein the syrup copolymer comprises up to 30 parts by weight of the solute copolymer in solvent monomers. 16. The method of claim 14 comprising the steps of partially polymerizing a low T g monomer and other optional monomers to produce a syrup polymer composition of claim 1 , adding a multifunctional acrylate crosslinker agent, additional monomers, and plasticizer, and further photopolymerizing. 17. The method of claim 14 wherein up to 20 parts of additional monomers are added relative to 100 parts total monomers. 18. An adhesive article comprising a substrate and a coating of the cured composition of claim 1 on a surface thereof. 19. An adhesive comprising a) 10 to 40 parts by weight of a low T g (meth)acrylate solute copolymer component; b) 60 to 90 parts by weight of a crosslinked low T g solvent copolymer component; and c) 5 to 50 parts by weight of a segmented siloxane copolymer having at least one polydiorganosiloxane segment and at least one oxyalkylene segment, relative to a) and b).
Homopolymers or copolymers of acrylic acid esters · CPC title
C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate · CPC title
of dialcohols, e.g. ethylene glycol di(meth)acrylate or 1,4-butanediol dimethacrylate · CPC title
containing silicon · CPC title
Crosslinking or vulcanising agents; including accelerators · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.