Polyorganosiloxane having heteroatom-containing silyl group
US-2024368350-A1 · Nov 7, 2024 · US
US2019119539A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2019119539-A1 |
| Application number | US-201716094698-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 13, 2017 |
| Priority date | Apr 19, 2016 |
| Publication date | Apr 25, 2019 |
| Grant date | — |
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Disclosed is a composition comprising: a) an condensate of one or more aminohydrocarbyl alkoxy silanes and one or more alkenyl alkoxy silanes; b) one or more mercaptohydrocarbyl alkoxy silanes; and c) water; wherein the composition is useful as a primer useful with adhesives or coatings containing polymers having isocyanate functional groups, alkoxysilane functional groups or both. The composition may include one or more epoxyhydrocarbyl silanes. The composition may include one or more alkanols in sufficient amount to improve the volatilization of the liquid components away from substrate surface.
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What is claimed is: 1 : A composition comprising: a) one or more aminohydrocarbyl alkoxy silanes; b) one or more alkenyl alkoxy silanes; c) one or more mercaptohydrocarbyl alkoxy silanes; and d) water: wherein at least the aminohydrocarbyl alkoxy silanes and the alkenyl alkoxy silanes are in a condensate; wherein the composition is useful as a water-based primer for use with adhesives or coatings, wherein the adhesives and coatings contain polymers having isocyanate functional groups and/or alkoxy silane functional groups. 2 : A composition according to claim 1 comprising a) from about 1.5 to about 10 percent by weight of a condensate of one or more aminohydrocarbyl alkoxy silanes and one or more alkenyl alkoxy silanes; b) from 0.1 to about 10 percent by weight one or more mercaptohydrocarbyl alkoxy silanes; and c) from about 20 to about 89.9 percent by weight of water; wherein the percent by weight is based on the weight of the composition. 3 : The composition according to claim 2 , including e) one more epoxyhydrocarbyl silanes. 4 : The composition of claim 3 , wherein the e) one or more epoxyhydrocarbyl silanes are present in an amount of about 0.1 to about 10 percent by weight. 5 : The composition of claim 2 , wherein the aminohydrocarbyl alkoxy silanes correspond to formula 1 or 2; the alkenyl alkoxy silanes correspond to the formula; the mercaptohydrocarbyl alkoxy silanes correspond to the formula the epoxyhydrocarbyl silanes correspond to the formula wherein R 1 is separately in each occurrence a C 1-20 hydrocarbylene group; R 2 is separately in each occurrence hydrogen or a C 1-20 hydrocarbyl group; R 3 is separately in each occurrence a C 1-4 alkyl group; R 4 is separately in each occurrence a C 1-4 alkyl group; R 5 is separately in each occurrence a C 1-20 alkenyl group; a is separately in each occurrence 1 or 2; b is separately in each occurrence 1 or 2; w is separately in each occurrence 0 or 1; x is separately in each occurrence an integer of from 1 to 4; y is separately in each occurrence an integer of from 1 to 3; and z is separately and integer of from 0 to 2 provided that z=3−y; with the proviso that a+b=3. 6 . The composition of claim 2 , wherein the condensate is prepared from about 30 to 70 mole percent of the aminohydrocarbyl alkoxy silanes and from about 30 to 70 mole percent of the alkenyl alkoxy silanes. 7 . The composition according to claim 2 , wherein the composition includes one or more alkanols. 8 . The composition of claim 7 , wherein the one or more alkanols is included in an amount of about 10 to about 45 percent by weight of the composition. 9 . The composition of claim 2 , wherein the composition includes one or more non-ionic surfactants. 10 . The composition of claim 9 , wherein the one or more non-ionic surfactants are included in an amount of about 0.01 to about 3.0 percent by weight of the composition. 11 . A kit comprising a composition according to claim 1 , and an adhesive comprising a prepolymer containing isocyanate functional groups, silane groups or a mixture thereof. 12 . A process comprising steps of: a) applying a composition according to claim 1 to a surface of a first substrate; and b) wiping the applied composition off of the surface of the first substrate or allowing a major portion of the water in the composition to evaporate off of the surface of the first substrate. 13 . A process according to claim 12 wherein the applied composition is wiped off of the surface of the first substrate. 14 . A process according to claim 12 wherein the water, and optionally alkanol, in the applied composition is allowed to evaporate off of the surface of the substrate. 15 . A process according to claim 12 wherein the water, and optionally alkanol, is allowed to evaporate off for at least about 10 seconds. 16 . A process according to claim 12 , wherein the composition is applied by spraying it onto the first surface, by brushing it on the first surface, or by wiping it on the first surface using an absorbent structure. 17 . A process according to claim 12 , which further comprising a step of contacting the first substrate with an adhesive containing a prepolymer having isocyanate, silane or both functional groups and a second substrate wherein the adhesive is applied to the portion of the surface of the first substrate to which the composition was applied and the adhesive is disposed between the first and the second substrates. 18 . A process according to claim 17 wherein a time period between applying the composition to the first surface and contacting the first surface with the adhesive is from about 20 seconds to 90 days. 19 . A process according to claim 12 , wherein the first substrate is glass or glass having a ceramic or organic frit on the portion of the surface which is bonded to a second substrate. 20 . A process according to claim 19 where in the glass substrate is a window and the second substrate is a flange in a vehicle adapted to hold the window in place in the vehicle or the second substrate is a window frame in a building.
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