Wood coating composition

US2016122575A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016122575-A1
Application numberUS-201314891044-A
CountryUS
Kind codeA1
Filing dateMay 30, 2013
Priority dateMay 30, 2013
Publication dateMay 5, 2016
Grant date

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

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A wood coating formulation with improved water repellency while maintaining coating performance such as clarity and hardness, the process of making thereof.

First claim

Opening claim text (preview).

1 . A polymer dispersion comprising, based on the total weight of the polymer dispersion, from 40 wt. % to 70 wt. % of water and from 30 wt. % to 60 wt. % of polymer particles comprising, as polymerized units, based on the total weight of the polymer particles, i) from 28 wt. % to 46 wt. % of at least one (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer; ii) from 0.1 wt. % to 10 wt. % of at least one self-crosslinking monomer; iii) from 2 wt. % to 4 wt. % of at least one reactive silicone with at least one carbon-carbon double bond; iv) from 0.5 wt. % to 5 wt. % of a reactive surfactant; wherein the reactive silicone with at least one double bond and the (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer are polymerized through the carbon-carbon double bond; the polymer particles have a Tg of from 20° C. to 50° C.; and a particle size of from 50 to 150 nm; wherein the reactive silicone has one of the following formulas (I) to (III): wherein R 1 or R 4 is the same or different, and represents a hydrogen atom or a methyl group; R 2 or R 3 is the same or different, and represents a C 1 -C 6 bivalent hydrocarbon group; and n represents an integer of from 1 to 100; wherein R 1 represents a hydrogen atom or a methyl group; R 2 represents a C 1 -C 6 bivalent hydrocarbon group; R 3 represents a C 1 -C 10 alkyl group or a C 1 -C 10 alkoxyl group; and n represents an integer of from 1 to 100; or wherein R 1 represents a hydrogen atom or a methyl group, and R 2 represents a C 1 -C 6 bivalent hydrocarbon group; and wherein the reactive surfactant has a structure of R 1 -R 2 ; wherein R 1 is an alkenyl group selected from CH 3 —CH═CH—, CH 2 ═CH—HC—, CH 2 ═C(CH 3 )—CH 2 —CH 2 —; R 2 is a radical comprising at least two carbon atoms and at least one oxylene, oxypropylene or oxybutylene unit. 2 . The polymer dispersion according to claim 1 wherein the (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer is selected from 2-ethylhexyl (meth)acrylate, decyl (meth)acrylate, lauryl (meth)acrylate, isodecyl (meth)acrylate, and the combination thereof. 3 . The polymer dispersion according to claim 2 wherein the (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer is selected from 2-ethylhexyl (meth)acrylate, lauryl (meth)acrylate, and the combination thereof. 4 . The polymer dispersion according to claim 1 wherein the self-crosslinking monomer is selected from diacetone acrylamide, acetoacetoxyethyl (meth)acrylate, acetoacetoxypropyl (meth)acrylate, allyl acetoacetate, acetoacetoxybutyl (meth)acrylate, 2,3-di(acetoacetoxy)propyl (meth) acrylate, and the composition thereof. 5 . The polymer dispersion according to claim 1 wherein the reactive surfactant has a structure of R 1 -R 2 ; wherein R 2 is —C 6 H 3 (R 3 )—O—(CH 2 —CH 2 —O) n —R 4 , —O—CH 2 —CH(CH 2 —O—C 6 H 4 —R 3 )—O—(CH 2 —CH 2 —O) n —R 4 , —O—(CH 2 —CH 2 —O) n —R 4 , —O—(CH 2 —CH(CH 3 )—O) n —R 4 , —O—(CH 2 —CH(CH 2 CH 3 )—O) n —R 4 , —O—(CH 2 —CH 2 —O) m —(CH 2 —CH(CH 3 )—O) n —R 4 , —O—(CH 2 —CH(CH 3 )—O) m —(CH 2 —CH 2 —O) n —R 4 , —O—(CH 2 —CH(CH 2 CH 3 )—O) m —(CH 2 —CH 2 —O) n —R 4 , or —O—(CH 2 —CH 2 —O) m —(CH 2 —CH(CH 2 CH 3 )—O) n —R 4 ; wherein R 3 is an alkyl group; R 4 is hydrogen or a polar group; n is from 5 to 100; and m is from 0 to 100. 6 . A wood coating composition comprising from 50 wt. % to 85 wt. %, based on the total weight of the wood coating composition, a polymer dispersion comprising, based on the total weight of the polymer dispersion, from 40 wt. % to 70 wt. % of water and from 30 wt. % to 60 wt. % of polymer particles comprising, as polymerized units, based on the total weight of the polymer particles, i) from 28 wt. % to 46 wt. % of at least one (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer; ii) from 0.1 wt. % to 10 wt. % of at least one self-crosslinking monomer; iii) from 2 wt. % to 4 wt. % of at least one reactive silicone with at least one carbon-carbon double bond; iv) from 0.5 wt. % to 5 wt. % of a reactive surfactant; wherein the reactive silicone with at least one double bond and the (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer are polymerized through the carbon-carbon double bond; the polymer particles have a Tg of from 20° C. to 50° C.; and a particle size of from 50 to 150 nm; wherein the reactive silicone has one of the following formulas (I) to (III): wherein R 1 or R 4 is the same or different, and represents a hydrogen atom or a methyl group; R 2 or R 3 is the same or different, and represents a C 1 -C 6 bivalent hydrocarbon group; and n represents an integer of from 1 to 100; wherein R 1 represents a hydrogen atom or a methyl group; R 2 represents a C 1 -C 6 bivalent hydrocarbon group; R 3 represents a C 1 -C 10 alkyl group or a C 1 -C 10 alkoxyl group; and n represents an integer of from 1 to 100; or wherein R 1 represents a hydrogen atom or a methyl group, and R 2 represents a C 1 -C 6 bivalent hydrocarbon group; and wherein the reactive surfactant has a structure of R 1 -R 2 ; wherein R 1 is an alkenyl group selected from CH 3 —CH═CH—, CH 2 ═CH—HC—, CH 2 ═C(CH 3 )—CH 2 —CH 2 —; R 2 is a radical comprising at least two carbon atoms and at least one oxylene, oxypropylene or oxybutylene unit. 7 . The wood coating composition according to claim 6 wherein the (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer is selected from 2-ethylhexyl (meth)acrylate, decyl (meth)acrylate, lauryl (meth)acrylate, isodecyl (meth)acrylate, and the combination thereof. 8 . The wood coating composition according to claim 7 wherein the (meth)acrylate C 6 -C 22 alkyl ester nonionic monomer is selected from 2-ethylhexyl (meth)acrylate, lauryl (meth)acrylate, and the combination thereof. 9 . The wood coating composition according to claim 6 wherein the self-crosslinking monomer is selected from diacetone acrylamide, acetoacetoxyethyl (meth)acrylate, acetoacetoxypropyl (meth)acrylate, allyl acetoacetate, acetoacetoxybutyl (meth)acrylate, 2,3-di(acetoacetoxy)propyl (meth) acrylate, and the composition thereof. 10 . The wood coating composition according to claim 6 wherein the reactive surfactant has a structure of R 1 -R 2 ; wherein R 2 is —C 6 H 3 (R 3 )—O—(CH 2 —CH 2 —O) n —R 4 , —O—CH 2 —CH(CH 2 —O—C 6 H 4 —R 3 )—O—(CH 2 —CH 2 —O) n —R 4 , —O—(CH 2 —CH 2 —O) n —R 4 , —O—(CH 2 —CH(CH 3 )—O) n —R 4 , —O—(CH 2 —CH(CH 2 CH 3 )—O) n —R 4 , —O—(CH 2 —CH 2 —O) m —(CH 2 —CH(CH 3 )—O) n —R 4 , —O—(CH 2 —CH(CH 3 )—O) m —(CH 2 —CH 2 —O) n —R 4 , —O—(CH 2 —CH(CH 2 CH 3 )—O) m —(CH 2 —CH 2 —O) n —R 4 , or —O—(CH 2 —CH 2 —O) m —(CH 2 —CH(CH 2 CH 3 )—O) n —R 4 ; wherein R 3 is an alkyl group; R 4 is hydrogen or a polar group; n is from 5 to 100; and m is from 0 to 100.

Assignees

Inventors

Classifications

  • containing silicon · CPC title

  • {Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond} in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00 · CPC title

  • containing silicon bound to unsaturated aliphatic groups · CPC title

  • Homopolymers or copolymers of methyl methacrylate · CPC title

  • Methyl esters {, e.g. methyl (meth)acrylate} · CPC title

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What does patent US2016122575A1 cover?
A wood coating formulation with improved water repellency while maintaining coating performance such as clarity and hardness, the process of making thereof.
Who is the assignee on this patent?
Dow Global Technologies Llc, Rohm & Haas
What technology area does this patent fall under?
Primary CPC classification C09D133/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu May 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).