Wood article and process for the preparation of the wood article
US-12152130-B2 · Nov 26, 2024 · US
US9410054B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9410054-B2 |
| Application number | US-201414310688-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 20, 2014 |
| Priority date | Dec 19, 2008 |
| Publication date | Aug 9, 2016 |
| Grant date | Aug 9, 2016 |
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The present invention provides a composition for treatment, the composition comprising dispersed in water (i) a fluorinated compound, (ii) a potassium or lithium silicate and (iii) an acrylic polymer. The invention further provides a method of treating substrates with the composition.
Opening claim text (preview).
What is claimed is: 1. A method for providing stain release or stain repellence properties to natural or man-made stone, the method comprising applying a treatment composition to the natural or man-made stone, wherein the treatment composition comprises (i) a fluorinated compound, (ii) a potassium or lithium silicate and (iii) an acrylic polymer, dispersed in water; wherein stains are removable from natural or man-made stone having the composition disposed thereon; wherein the treatment composition comprises a total amount of (i), (ii), and (iii) in an amount between 0.5% and 60% by weight. 2. The method according to claim 1 wherein stains caused by oils, food dressings, wine, coffee, tea, or soft drinks are removable from natural or man-made stone having the composition disposed thereon. 3. The method according to claim 1 wherein said acrylic polymer is selected from the group consisting of homo- and copolymers of an acrylate. 4. The method according to claim 3 wherein said acrylic polymer is a copolymer of an acrylate and styrene. 5. The method according to claim 1 wherein the amount of fluorinated compound is between 10 and 70% by weight of the total weight of solids. 6. The method according to claim 1 wherein the fluorinated compound comprises one or more perfluorinated hydrocarbon residues having at least 3 carbon atoms. 7. The method according to claim 6 wherein the perfluorinated hydrocarbon residues have 4 to 6 carbon atoms each. 8. A method for providing stain release or stain repellence properties to natural or man-made stone, the method comprising applying a treatment composition to the natural or man-made stone, wherein the treatment composition comprises (i) a fluorinated compound, (ii) a potassium or lithium silicate and (iii) an acrylic polymer, dispersed in water; wherein the fluorinated compound comprises one or more units derived from a fluorinated monomer of the formula: R f -Q-E wherein: R f represents a partially or fully fluorinated aliphatic group having 3 to 12 carbon atoms; Q represents a covalent bond or a non-fluorinated organic linking group; and E represents a free radical polymerizable group; wherein the treatment composition comprises a total amount of (i), (ii), and (iii) in an amount between 0.5% and 60% by weight. 9. A method for providing stain release or stain repellence properties to natural or man-made stone, the method comprising applying a composition to the natural or man-made stone, wherein the composition comprises (i) a fluorinated compound, (ii) a potassium or lithium silicate and (iii) an acrylic polymer, dispersed in water; wherein the fluorinated compound is a reaction product of an isocyanate, a fluorinated oligomer having an isocyanate reactive group, and an aliphatic compound having an isocyanate reactive group; wherein the fluorinated oligomer having an isocyanate reactive group is a free-radical polymerization reaction product of fluorinated monomers and optionally non-fluorinated monomers in the presence of a mercapto functional chain transfer agent; wherein the fluorinated monomers are represented by the formula: R f -Q-C(R 1 )═C(R 2 ) 2 (II) wherein: Rf represents a partially or fully fluorinated aliphatic group having 3 to 12 carbon atoms; Q represents a covalent bond or a non-fluorinated organic linking group; R 1 represent H or a lower alkyl group having 1 to 4 carbon atoms; and each R 2 independently represents H or a straight chain or branched chain alkyl group having 1 to 4 carbon atoms; wherein the optional non-fluorinated monomers are represented by the formula: R h -Q′-C(R 3 )═C(R 4 ) 2 (IV) wherein: R h represents a non-fluorinated group; Q′ represents a covalent bond or a non-fluorinated organic linking group; R 3 represent H or a lower alkyl group having 1 to 4 carbon atoms; and each R 4 independently represents H or a straight chain or branched chain alkyl group having 1 to 4 carbon atoms; and wherein the mercapto functional chain transfer agent is represented by the formula: R′(SH) m wherein: R′ represents a hydrocarbon group comprising an isocyanate reactive group; and m is 1 to 4. 10. The method according to claim 9 wherein the fluorinated monomers are selected from the group consisting of: CF 3 CF 2 CF 2 CF 2 CH 2 CH 2 OCOCR 3 ═CH 2 CF 3 (CF 2 ) 3 CH 2 OCOCR 3 ═CH 2 CF 3 (CF 2 ) 3 SO 2 N(CH 3 )CH 2 CH 2 OCOCR 3 ═CH 2 CF 3 (CF 2 ) 3 SO 2 N(C 2 H 5 )CH 2 CH 2 OCOCR 3 ═CH 2 CF 3 (CF 2 ) 3 SO 2 N(CH 3 )CH 2 CH(CH 3 )OCOCR 3 ═CH 2 (CF 3 ) 2 CFCF 2 SO 2 N(CH 3 )CH 2 CH 2 OCOCR 3 ═CH 2 CF 3 CF 2 (CF 2 CF 2 ) 2 CH 2 CH 2 OCOCH═CH 2 wherein R 3 is hydrogen, methyl or n-butyl. 11. The method according to claim 9 wherein the aliphatic compound having an isocyanate reactive group is represented by the formula: R 3 —(Z) q wherein: Z is an isocyanate reactive group selected from the group consisting of an amino group, a hydroxy group, and a carboxyl group; q is 1 to 4; and R 3 is an organic aliphatic group having from 1 to 75 carbon atoms. 12. The method according to claim 11 wherein Z is a hydroxyl group, q is 1, and R 3 is a monovalent alkyl group having from 12 to 75 carbon atoms. 13. The method according to claim 9 wherein the isocyanate is selected from the group consisting of a biuret-containing triisocyanate, an isocyanurate-containing tri-isocyanate, and an azetedinedione-containing diisocyanate. 14. A method for providing stain release or stain repellence properties to natural or man-made stone, the method comprising applying a composition to the natural or man-made stone, wherein the composition comprises (i) a fluorinated compound, (ii) a potassium or lithium silicate and (iii) an acrylic polymer, dispersed in water; wherein the fluorinated compound corresponds to at least one compound of the following formulas: [(A) m L] n R wherein: m is a value of 1 to 4; n is a value of 1 to 3; L represents a linking group; R is an aliphatic group; and A is a fluorinated residue of the formula: wherein: a has a value of 1 to 100; b has a value of 0 to 100; the sum of a and b being at least 2; R 1 and R 2 each independently represent H or an alkyl group of 1 to 4 carbon atoms; Q and Q′ each independently represent a covalent bond or a non-fluorinated organic linking group; Rf represents a partially or fully fluoroaliphatic group having 3 to 12 carbon atoms; Rh represents a non-fluorinated group; and X 1 is H or the residue of a free radical initiator. 15. The method according to claim 14 wherein the composition comprises (i) the fluorinated compound in an amount of 10 to 70% by weight of the total weight of solids, (ii) the potassium or lithium silicate in an amount of 10 to 80% by weight of the total weight of solids and (iii) the acrylic polymer in an amount of 10 to 80% by weight of the total weight of solids. 16. The method according to claim 14 wherein: m is a value of 1 to 4; n is a value of 1 to 3; L is selected from the group consisting of a straight chain, branched chain, or cyclic alkylene, arylene, aralkylene, oxy, oxo, hydroxy, thio, sulfonyl, sulfoxy, amino, imino, sulfonamido, carboxamido, carbonyloxy, urethanylene, ureylene, and combinations thereof; R is a branched aliphatic group having 12 to 75 carbon atoms; and A is a fluorinated residue of the formula:
Homopolymers or copolymers of acrylic acid esters · CPC title
Macromolecular compounds · CPC title
Vinyl-type polymers · CPC title
Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers · CPC title
characterised by the material treated · CPC title
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