Poly(vinyl acetal) resin compositions, layers, and interlayers having enhanced optical properties
US-10124563-B2 · Nov 13, 2018 · US
US2016347974A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016347974-A1 |
| Application number | US-201514657299-A |
| Country | US |
| Kind code | A1 |
| Filing date | Mar 13, 2015 |
| Priority date | Sep 14, 2012 |
| Publication date | Dec 1, 2016 |
| Grant date | — |
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There is provided a curable composition comprising one or more reactive components that cure upon exposure to suitable conditions, the curable composition comprising: (i) at least one aromatic nitroso or at least one aromatic nitroso precursor compound or combinations thereof; and (ii) a film former component comprising at least one non-halogenated hydroxy group-containing resin together with at least one crosslinking agent.
Opening claim text (preview).
1 . A curable composition comprising one or more reactive components that cure upon exposure to suitable conditions, the curable composition comprising: (i) at least one aromatic nitroso or at least one aromatic nitroso precursor compound or combinations thereof; and (ii) a film former component comprising at least one non-halogenated hydroxy group-containing resin together with at least one crosslinking agent. 2 . The curable composition of claim 1 wherein the at least one non-halogenated hydroxyl group-containing resin includes a co-polymer which is a co-polymer of at least one of polyvinyl alcohol, polyvinyl butyral and polycellulose acetate butyrate, wherein said co-polymer is a block co-polymer and the non-halogenated hydroxyl group-containing resin has the general structure: wherein each of n, o and p is at least 5, and the combined % wt of the m, o and p components in the non-halogenated hydroxyl group-containing resin is 100%. 3 . (canceled) 4 . (canceled) 5 . (canceled) 6 . The curable composition of claim 1 , wherein the non-halogenated hydroxy group-containing resin is present in the composition in a range of from about 0.5 to 10% wt/wt of the total weight of the curable composition. 7 . (canceled) 8 . The curable composition of claim 1 , wherein the at least one crosslinking agent is a compound having at least two reactive moieties, each of which can undergo a crosslinking reaction with a hydroxy group of the at least one non-halogenated hydroxy group-containing resin. 9 . The curable composition of claim 1 , wherein the crosslinking agent is selected from the group consisting of: epoxy resins, phenolic resins, melamine resins, isocyanates, anhydrides, aldehydes, each having at least two reactive moieties, and mixtures thereof. 10 . The curable composition of claim 1 , wherein the crosslinking agent is a phenolic resin. 11 . The curable composition of claim 1 , wherein the crosslinking agent is an epoxy resin having at least two at least two oxirane ring systems 12 . The curable composition of claim 1 , wherein the at least one aromatic nitroso compound or at least one aromatic nitroso precursor compound comprises at least one alkoxy silane moiety and at least one moiety selected from an aromatic nitroso or an aromatic nitroso precursor or combinations thereof. 13 . The curable composition of claim 1 , further comprising a sulfur impregnated particulate solid which acts as a release agent for sulfur during the cure process. 14 . The curable composition of claim 13 wherein the sulfur impregnated particulate solid is selected from the group consisting of: sulfur-impregnated clays, sulfur impregnated silicates, sulfur impregnated aluminates, sulfur impregnated charcoals and sulfur impregnated carbons such as sulfur impregnated carbon blacks, sulfur impregnated charcoals and combinations thereof. 15 . (canceled) 16 . (canceled) 17 . (canceled) 18 . (canceled) 19 . (canceled) 20 . (canceled) 21 . (canceled) 22 . The curable composition of claim 1 , further comprising a compound comprising: (a) at least one phosphonate moiety; or (b) at least one phosphinate moiety, or combinations thereof. 23 . The curable composition of claim 22 wherein the compound is of the general formula: wherein u is from 0 to 20; A is a direct bond, O, or S; R 4 is selected from the group consisting of H, C 1 -C 24 alkyl, and C 3 -C 24 acyl, preferably from C 1 -C 4 alkyl; R 5 is selected from the group consisting of C 1 -C 24 alkyl, C 1 -C 24 alkoxyl and C 3 -C 24 acyl; and R 6 is a moiety comprising nitrosobenzene, quinone oxime or quinone dioxime. 24 . (canceled) 25 . The curable composition of claim 1 , wherein the aromatic nitroso precursor is a nitrosobenzene precursor or comprises an aromatic oxime or an aromatic dioxime or combinations thereof. 26 . (canceled) 27 . (canceled) 28 . (canceled) 29 . (canceled) 30 . (canceled) 31 . A curable composition comprising: a. at least one a film former component comprising at least one non-halogenated hydroxy group-containing resin together with at least one crosslinking agent; b. at least one epoxysilane having at least one terminal alkoxy silane group; c. at least one bis-silane, and d. optionally at least one organic solvent. 32 . (canceled) 33 . (canceled) 34 . A process for bonding a material to a substrate, comprising the steps of: a) providing a curable composition as defined in claim 1 ; b) providing the material to be bonded in a non-cured form, and c) simultaneously curing the composition and the material to be bonded so that the material is bonded to the substrate. 35 . (canceled) 36 . A process for bonding a first substrate to a second substrate, comprising the steps of: a) providing a curable composition as defined in claim 1 ; b) applying the curable composition to at least one part of the surface of the first substrate; and c) contacting said surface of the first substrate with a surface of a second substrate, to which the curable composition is optionally applied, under conditions of heat and pressure sufficient to create a cured bond between the two substrates. 37 . (canceled) 38 . (canceled) 39 . (canceled) 40 . A process for crosslinking an elastomeric material, comprising the steps of: a) providing a composition in a non-cured form comprising (i) at least one aromatic nitroso compound or at least one aromatic nitroso precursor compound or combinations thereof; and (ii) a film former component comprising at least one non-halogenated hydroxy group-containing resin together with at least one crosslinking agent; b) mixing the composition with at least one elastomeric material to form a curable mixture; and c) exposing said curable mixture to conditions of heat and pressure sufficient to crosslink the elastomeric material. 41 . (canceled) 42 . (canceled) 43 . (canceled) 44 . (canceled) 45 . (canceled) 46 . (canceled) 47 . (canceled) 48 . A film forming component for use in a curable composition comprising at least one aromatic nitroso compound or at least one aromatic nitroso precursor compound or combinations thereof; together with a film former component comprising at least one non-halogenated hydroxy group-containing resin together with at least one crosslinking agent. 49 . A film forming component according to claim 48 wherein the at least one aromatic nitroso or the at least one aromatic nitroso precursor compound comprises a compound comprising: at least one alkoxy silane moiety; and at least one moiety selected from an aromatic nitroso or an aromatic nitroso precursor or combinations thereof. 50 . The cured product of a curable composition according to
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