US2009163618A1PendingUtilityA1
Binders containing nanoparticles
Est. expiryDec 19, 2027(~1.4 yrs left)· nominal 20-yr term from priority
C09D 5/028C09D 133/06C08F 220/20C08G 18/6295C09D 7/62C08K 3/013C08G 18/706C08K 9/04C08G 18/6254C08K 3/36C09D 175/04C08F 220/1811B82Y 40/00C09D 183/02B82B 1/00
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Claims
Abstract
The present invention relates to aqueous binder dispersions based on silane-modified polymeric binders and inorganic nanoparticles, a process for the preparation thereof and the use thereof for the production of high quality coatings, in particular clear lacquers.
Claims
exact text as granted — not AI-modified1 . An aqueous formulation comprising
B) a silane-modified copolymer; B) optionally surface-modified inorganic particles having an average particle size (z-mean), as determined by means of dynamic light scattering in dispersion, of less than 200 nm; and C) water.
2 . The aqueous formulation of claim 1 , wherein said silane-modified copolymer A) comprises groups of general formula (1)
—Si(R 1 O) 2 R 2 (1) wherein R 1 is a C 2 - to C 8 -alkyl radical; and R 2 is (R 1 O) or a C 1 - to C 5 -alkyl radical.
3 . The aqueous formulation of claim 1 , wherein said silane-modified copolymer A) is a copolymer which is built up from
I) a hydroxy-functional hydrophobic polymer containing as builder monomers
Ia) (meth)acrylic acid esters having C 1 - to C 18 -hydrocarbon radicals in the alcohol part and/or vinylaromatics and/or vinyl esters;
Ib) hydroxy-functional monomers; and
IS1) silane-functional monomers capable of polymerization; and
II) a hydroxy-functional hydrophilic polymer containing as builder components
IIa) (meth)acrylic acid esters having C 1 - to C 18 -hydrocarbon radicals in the alcohol part and/or vinylaromatics and/or vinyl esters;
IIb) hydroxy-functional monomers; and
IIc) acid-functional monomers.
4 . The aqueous formulation of claim 1 , wherein said silane-modified copolymer A) is a copolymer which is built up from
I) a hydroxy-functional hydrophobic polymer containing as builder monomers
Ia) (meth)acrylic acid esters having C 1 - to C 18 -hydrocarbon radicals in the alcohol part and/or vinylaromatics and/or vinyl esters; and
Ib) hydroxy-functional monomers; and
II) a hydroxy-functional hydrophilic polymer containing as builder components
IIa) (meth)acrylic acid esters having C 1 - to C 18 -hydrocarbon radicals in the alcohol part and/or vinylaromatics and/or vinyl esters;
IIb) hydroxy-functional monomers;
IIe) acid-functional monomers; and
IIS1) silane-functional monomers capable of polymerization.
5 . The aqueous formulation of claim 3 , wherein said silane-functional monomer IS1), which is capable of polymerization, is a compound of the general formula (2)
(R 1 O) 2 R 2 Si—(CH═CH 2 ) (2)
wherein
R 1 is a C 2 - to C 8 -alkyl radical; and
R 2 is (R 1 O) or a C 1 - to C 5 -alkyl radical;
and/or a compound of the general formula (3)
(R 1 O) 2 R 2 Si(CH 2 ) m —O(CO)—(CR 3 ═CH 2 ) (3)
wherein
R 1 is a C 2 - to C 8 -alkyl radical;
R 2 is (R 1 O) or a C 1 - to C 5 -alkyl radical;
R 3 is H or CH 3 ; and
m is 1 to 4.
6 . The aqueous formulation of claim 4 , wherein said silane-functional monomer IIS1), which is capable of polymerization, is a compound of the general formula (2)
(R 1 O) 2 R 2 Si—(CH═CH 2 ) (2)
wherein
R 1 is a C 2 - to C 8 -alkyl radical; and
R 2 is (R 1 O)) or a C 3 - to C 5 -alkyl radical;
and/or a compound of the general formula (3)
(R 1 O) 2 R 2 Si(CH 2 ) m —O(CO)—(CR 3 ═CH 2 ) (3)
wherein
R 1 is a C 2 - to C 8 -alkyl radical;
R 2 is (R 1 O) or a C 1 - to C 5 -alkyl radical;
R 3 is H or CH 3 ; and
m is 1 to 4.
7 . The aqueous formulation of claim 3 , wherein said silane-functional monomer IS1), which are capable of polymerization, is selected from the group consisting of vinyltriethoxysilane, vinyltrisisopropoxysilane, vinyl-tris-(2-methoxyethoxy)silane, vinylmethyldiethoxysilane, vinylmethyldiisopropoxysilane, vinylethyldiethoxysilane, 3-(triethoxysilyl)-propyl methacrylate or 3-(tris-isopropoxysilyl)-propyl methacrylate, vinylphenyldiethoxysilane, vinylphenylmethylethoxysilane, and vinyltri-t-butoxysilane.
8 . The aqueous formulation of claim 4 , wherein said silane-functional monomers IIS1), which are capable of polymerization, is selected from the group consisting of vinyltriethoxysilane, vinyltrisisopropoxysilane, vinyl-tris-(2-methoxyethoxy)silane, vinylmethyldiethoxysilane, vinylmethyldiisopropoxysilane, vinylethyldiethoxysilane, 3-(triethoxysilyl)-propyl methacrylate or 3-(tris-isopropoxysilyl)-propyl methacrylate, vinylphenyldiethoxysilane, vinylphenylmethylethoxysilane, and vinyltri-t-butoxysilane.
9 . The aqueous formulation of claim 1 , wherein said silane functional copolymer A) is a copolymer which is built up from
I) a hydroxy-functional hydrophobic polymer containing as builder monomers
Ia) (meth)acrylic acid esters having C 1 - to C 18 -hydrocarbon radicals in the alcohol part and/or vinylaromatics and/or vinyl esters;
Ib) hydroxy-functional monomers; and
II) a hydroxy-functional hydrophilic polymer containing as builder components
IIa) (meth)acrylic acid esters having C 1 - to C 18 -hydrocarbon radicals in the alcohol part and/or vinylaromatics and/or vinyl esters;
IIb) hydroxy-functional monomers;
IIc) acid-functional monomers; and
IIS2) monomers which contain at least one epoxide function in addition to silane groups.
10 . The aqueous formulation of claim 9 , wherein said monomers IIS2) are selected from the group consisting of γ-glycidoxypropyltriethoxysilane, γ-glycidoxypropyl-tris-isopropoxysilane, γ-glycidoxypropyl-diethoxy-methylsilane, β-(3,4-epoxycyclohexyl)-triethoxysilane, and β-(3,4-epoxycyclohexyl)-tris-isopropoxysilane.
11 . The aqueous formulation of claim 1 , wherein said inorganic particles B) are selected from the group consisting of inorganic oxides, mixed oxides, carbides, borides, and nitrides of elements of main group II to IV and/or elements of subgroup I to VIII of the periodic table, including the lanthanides.
12 . The aqueous formulation of claim 1 , wherein said inorganic particles B) are inorganic nanoparticles in a colloidally disperse form in organic solvents or in water.
13 . The aqueous formulation of claim 1 , wherein said inorganic particles B) are inorganic particles in the form of aqueous formulations.
14 . The aqueous formulation of claim 1 , wherein said inorganic particles B) are surface-modified inorganic nanoparticles.
15 . An aqueous coating composition comprising the aqueous formulation of claim 1 and at least one crosslinking agent D).
16 . An aqueous two-component coating composition comprising the aqueous formulation of claim 1 and a polyisocyanate.
17 . A clear lacquer comprising the aqueous formulation of claim 1 .Join the waitlist — get patent alerts
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