Binder compositions and methods of preparing and using the same
Abstract
The present disclosure relates to compositions comprising a copolymer derived from a vinyl aromatic monomer, a (meth)acrylate monomer, an acid monomer, and a copolymerizable surfactant and compositions comprising the same. The (meth)acrylate monomer can be selected from a monomer having a theoretical glass transition temperature (Tg) for its corresponding homopolymer of 0° C. or less or a hydrophobic (meth)acrylate monomer. In some embodiments, the copolymer is further derived from an organosilane. The copolymers can have a theoretical glass transition temperature (Tg) from −60° C. to 80° C. and a number average particle size of 250 nm or less. The compositions can be used to prepare compositions such as coatings that have improved water resistance, blush resistance, and/or resistance to hydrostatic pressures. Methods of making the copolymers are also provided.
Claims
exact text as granted — not AI-modified1 . A composition, comprising:
a copolymer derived from monomers comprising 40% to 65% by weight styrene; 30% to 55% by weight of a (meth)acrylate monomer selected from butyl acrylate, ethyl hexyl acrylate, or a mixture thereof; 1% to 4% by weight of an acid monomer selected from itaconic acid, acrylic acid, or a mixture thereof; 0% to 4% by weight of an additional monomer selected from methyl methacrylate, (meth)acrylonitrile, (meth)acrylamide, an acetoacetoxy monomer, a hydroxyl (meth)acrylate, an organosilane, or a mixture thereof; and 0.05% to 2% by weight of the copolymerizable surfactant; wherein the copolymer has a theoretical glass transition temperature (T g ) from −60° C. to 80° C.; and wherein the copolymer has a number average particle size of 200 nm or less.
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11 . The composition according to claim 1 , wherein the copolymer further includes lauryl (meth)acrylate.
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21 . The composition according to claim 1 , wherein the copolymerizable surfactant is of formula III, or a salt thereof:
wherein R 1 represents a branched aliphatic hydrocarbon group, a secondary aliphatic hydrocarbon group or a branched aliphatic acyl group, AO and AO′ each independently represents an oxyalkylene group having 2 to 4 carbon atoms, R 2 and R 3 each independently represents a hydrogen atom or a methyl group, X represents a hydrogen atom or an ionic hydrophilic group, x is an integer from 0 to 12, y is 0 or 1, z is an integer from 1 to 10, m is an integer from 0 to 1,000, and n is an integer from 0 to 1,000.
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25 . The composition according to claim 1 , wherein the copolymer includes:
50% to 60% by weight styrene; 35% to 45% by weight of a (meth)acrylate monomer selected from butyl acrylate, ethyl hexyl acrylate, or a mixture thereof; 1% to 3% by weight of an acid monomer selected from itaconic acid, acrylic acid, or a mixture thereof; 0% to 2% by weight of an additional monomer selected from methyl methacrylate, (meth)acrylonitrile, (meth)acrylamide, an acetoacetoxy monomer, a hydroxyl (meth)acrylate, an organosilane, or a mixture thereof; and 0.05% to 2% by weight of the copolymerizable surfactant.
26 . The composition according to claim 1 , wherein
the copolymer has a theoretical glass-transition temperature of from −40° C. to 80° C.
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36 . The composition according to claim 1 , wherein the copolymer has a number average particle size of 100 nm or less.
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40 . A coating comprising the composition according to claim 1 and one or more coalescing aids.
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42 . The coating according to claim 40 , wherein the coating when applied on porous walls provides a resistance to hydrostatic pressure of at least 4 psi in accordance with ASTM D7088-08.
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44 . The coating according to claim 40 , wherein the coating has a blush resistance of at least 16 hours when exposed to water.
45 . The coating according to claim 40 , wherein the coating is a paint, membrane, or adhesive.
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51 . A method of making a composition according to claim 1 , comprising: polymerizing monomers including
40% to 65% by weight styrene: 30% to 55% by weight of a (meth)acrylate monomer selected from butyl acrylate, ethyl hexyl acrylate, or a mixture thereof; 1% to 4% by weight of an acid monomer selected from itaconic acid, acrylic acid, or a mixture thereof; 0% to 4% by weight of an additional monomer selected from methyl methacrylate, (meth)acrylonitrile, (meth)acrylamide, an acetoacetoxy monomer, a hydroxyl (meth)acrylate, an organosilane, or a mixture thereof; and 0.05% to 2% by weight of the copolymerizable surfactant to produce a copolymer having a theoretical glass transition temperature (T g ) from −60° C. to 80° C. and a number average particle size of less than 200 microns.
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61 . A method, comprising:
coating a composition comprising a copolymer derived from monomers comprising a vinyl aromatic monomer, a (meth)acrylate monomer having a theoretical glass transition temperature (T g ) for its corresponding homopolymer of 0° C. or less, an acid monomer, an organosilane monomer, and a copolymerizable surfactant to a porous wall; wherein the copolymer has a theoretical glass transition temperature (T g ) from −60° C. to 80° C. and a number average particle size of 200 nm or less; and wherein the coating when applied on the porous wall provides a resistance to hydrostatic pressure of at least 4 psi in accordance with ASTM D7088-08.
62 . A composition, comprising:
a copolymer derived from monomers comprising 40% to 65% by weight of styrene; 30% to 55% by weight of a (meth)acrylate monomer selected from butyl acrylate, ethyl hexyl acrylate, or a mixture thereof, 1% to 4% by weight of an acid monomer selected from itaconic acid, acrylic acid, or a mixture thereof; 0.5 to 4% by weight of an additional monomer selected from methyl methacrylate, (meth)acrylonitrile, (meth)acrylamide, an acetoacetoxy monomer, a hydroxyl (meth)acrylate, an organosilane, or a mixture thereof, and 0.1 to 0.75% by weight of a copolymerizable surfactant which is selected from the group consisting of formula (I), (II), (III) and a salt of formula (III)
wherein R 1 represents a branched aliphatic hydrocarbon group, a secondary aliphatic hydrocarbon group or a branched aliphatic acyl group, AO and AO′ each independently represents an oxyalkylene group having 2 to 4 carbon atoms, R 2 and R 3 each independently represents a hydrogen atom or a methyl group, X represents a hydrogen atom or an ionic hydrophilic group, x is an integer from 0 to 12, y is 0 or 1, z is an integer from 1 to 10, m is an integer from 0 to 1,000, and n is an integer from 0 to 1,000; and
wherein the copolymer has a theoretical glass transition temperature (T g ) from −60° C. to 80° C.; and
wherein the copolymer has a number average particle size of 200 nm or less.
63 . The composition as claimed in claim 62 , wherein the surfactant is according to Formula IIIa:
wherein R 1 is C 9 -C 15 alkyl or C 7 -C 11 alkyl-phenyl, X is H, SO 3 NH-4 and/or SO 3 Na, and m is 3 to 50.
64 . The composition according to claim 62 , wherein the copolymer has a theoretical glass-transition temperature of from −10° C. to 40° C.
65 . The composition according to claim 63 , wherein R 1 is C 10 -C 14 alkyl, X is H and/or SO 3 NH 4 , and m is 5 to 40.
66 . The composition according to claim 63 , wherein m is 5 to 25.
67 . The composition according to claim 63 , wherein m is 5 to 15.
68 . The composition according to claim 63 , wherein m is 10.
69 . The composition according to claim 63 , which further comprises 0.5% by weight to 2.5% by weight of a polyamine based on the dry weight of the copolymer and wherein the copolymerizable surfactant is present in an amount from 0.3 to 0.5% by weight.Join the waitlist — get patent alerts
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