Latex binders useful in zero or low VOC coating compositions

US9834698B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9834698-B2
Application numberUS-201314376702-A
CountryUS
Kind codeB2
Filing dateFeb 5, 2013
Priority dateFeb 10, 2012
Publication dateDec 5, 2017
Grant dateDec 5, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

Latex binders useful for preparing zero or low VOC coating compositions having excellent freeze-thaw stability, good tint strength and good scrub resistance when cured may be obtained using a polymerizable polyalkylene glycol monomer such as polyethylene glycol methacrylate in combination with one or both of an emulsifier or a polymerizable polyalkylene glycol monomer containing bulky hydrophobic groups substituted on an aromatic ring.

First claim

Opening claim text (preview).

What is claimed is: 1. A polymer latex binder useful in a zero or low VOC latex coating composition comprising: a) a polymer which is a polymerization product of at least: i) at least one polymerizable polyalkylene glycol monomer corresponding to structural formula (I): R 1 —(XO) x —R 2   (I) wherein R 1 is a first polymerizable moiety selected from the group consisting of (meth)acrylate, allyl, vinyl, maleate, itaconate and fumarate, X is a C 2 -C 3 ; divalent alkylene group, x is from 4 to 25, and R 2 is H or CH 3 ; ii) at least one acrylic monomer which is copolymerizable with the polymerizable polyalkylene glycol monomer; iii) optionally, at least one polymerizable polyalkylene glycol monomer corresponding to structural formula (II): Ph—(OY) n —R 6   (II) wherein Ph is a phenyl group substituted at the 2, 4 and 6 positions with groups R 3 , R 4 and R 5 respectively, with R 3 , R 4 and R 5 being independently selected from the group consisting of butyl, tert-butyl, isobutyl, —CH 2 -A, and —CH(CH 3 )-A, where A is phenyl or cyclohexyl, wherein Y is a divalent hydrocarbon radical comprising a linear or branched alkylene radical having from about 2 to 8 carbon atoms; wherein n is an integer of from 1 to 100; and wherein R 6 is a second polymerizable moiety selected from the group consisting of (meth)acrylate, allyl, vinyl, maleate, itaconate and fumarate; b) water; c) at least one emulsifier; and d) from 0 to 4 pphm of ionic monomer, subject to the proviso that if a polymerizable polyethylene glycol monomer corresponding to structural formula (II) is not employed in the polymer the latex binder comprises an emulsifier corresponding to structural formula (III): Ph—(OZ) m —R 10   (III) wherein Ph is a phenyl group substituted at the 2, 4 and 6 positions with groups R 7 , R 8 and R 9 respectively, with R 7 , R 8 and R 9 being independently selected from the group consisting of butyl, tert-butyl, isobutyl, —CH 2 -E, and —CH(CH 3 )-E, where E is phenyl or cyclohexyl; wherein Z is a divalent hydrocarbon radical comprising a linear or branched alkylene radical having from about 2 to 8 carbon atoms; wherein m is an integer of from 1 to 100; and wherein R 10 is selected from the group consisting of —OH, —OCH 3 , —OC 2 H 5 , —OC 3 H 7 , —OC 4 H 9 , —OC 5 H 11 , —OC 6 H 13 , —Cl, —Br, —CN, phosphonate (—PO 3 − M + ), phosphate (PO 4 − M + ), sulfate (SO 4 − M + ), sulfonate (SO 3 − M + ), carboxylate (CO 2 − M + ), and a quaternary ammonium ion, wherein M + is a cation, wherein the total by weight of polymerizable polyalkylene glycol monomer of structural formula (I), polymerizable polyalkylene glycol monomer of structural formula (II), and emulsifier of structural formula (III) is from about 1 to about 8 pphm. 2. The latex binder of claim 1 wherein the number average molecular weight of the polyalkylene glycol moiety in the polymerizable polyalkylene glycol monomer of structural formula (I) is from about 200 to about 1000. 3. The latex binder of claim 1 wherein X is ethylene and R 2 is H. 4. The latex binder of claim 1 , wherein the polymerizable polyalkylene glycol monomer of structural formula (I) is utilized in an amount of at least about 1 pphm. 5. The latex binder of claim 1 , wherein emulsifier in accordance with structural formula (III) is present in an amount of at least about 1 pphm. 6. The latex binder of claim 1 , wherein the acrylic monomer is selected from the group consisting of C 1 -C 10 alkyl esters of α,β-ethylenically unsaturated C 2 -C 6 monocarboxylic acids, hydroxyl C 1 -C 10 alkyl esters of α,β-ethylenically unsaturated C 2 -C 6 monocarboxylic acids, C 1 -C 10 alkyl diesters of α,β-ethylenically unsaturated C 4 -C 8 dicarboxylic acids, and mixtures thereof. 7. The latex binder of claim 1 wherein at least one polymerizable polyalkylene glycol monomer of structural formula (I) and at least one polymerizable polyalkylene glycol monomer of structural formula (II) are employed in a weight ratio of from about 1:4 to about 4:1 structural formula (I):structural formula (II). 8. The latex binder of claim 1 wherein at least one polymerizable polyalkylene glycol monomer of structural formula (I) and at least one emulsifier of structural formula (III) are employed in a weight ratio of from about 1:4 to about 4:1 structural formula (I):structural formula (III). 9. A coating composition comprising a pigment and a latex binder in accordance with claim 1 . 10. A latex binder useful in preparing a zero or low VOC latex coating composition, the latex binder comprising: a) a polymer which is a polymerization product of at least: i) at least one polymerizable polyalkylene glycol monomer corresponding to structural formula (I): R 1 —(XO) x —R 2   (I) wherein R 1 is a first polymerizable moiety selected from the group consisting of (meth)acrylate, allyl, vinyl, maleate, itaconate and fumarate, X is a C 2 -C 3 divalent alkylene group, x is from 4 to 25, and R 2 is H or CH 3 ; ii) at least one acrylic monomer which is copolymerizable with the polymerizable polyethylene glycol monomer; b) water; c) an emulsifier corresponding to structural formula (III): Ph—(OZ) m —R 10   (III) wherein Ph is a phenyl group substituted at the 2, 4 and 6 positions with groups R 7 , R 8 and R 9 respectively, with R 7 , R 8 and R 9 being independently selected from the group consisting of butyl, tert-butyl, isobutyl, —CH 2 -E, and —CH(CH 3 )-E, where E is phenyl or cyciohexyl; wherein Z is a divalent hydrocarbon radical comprising a linear or branched alkylene radical having from about 2 to 8 carbon atoms; wherein m is an integer of from 1 to 100; and wherein R 10 is selected from the group consisting of —OH, —OCH 3 , —OC 2 H 5 , —OC 3 H 7 , —OC 4 H 9 , —OC 5 H 11 , —OC 6 H 13 , —Cl, —Br, —CN, phosphonate (—PO 3 − M + ), phosphate (PO 4 − M + ), sulfate (SO 4 − M + ), sulfonate (SO 3 − M + ), carboxylate (CO 2 − M − ), and a quaternary ammonium ion, wherein M + is a cation; and d) from 0 to 4 pphm of ionic monomer, wherein the total by weight of polymerizable polyalkylene glycol monomer of structural formula (I) and emulsifer of structural formula (III) is from about 1 to about 8 pphm. 11. The latex binder of claim 10 wherein the number average molecular weight of the polyalkylene glycol moiety in the polymerizable polyalkylene glycol monomer of structural formula (I) is from about 200 to about 1000. 12. The latex binder of claim 10 wherein X is ethylene and R 2 is H. 13. The latex binder of claim 10 , wherein polymerizable polyalkylene glycol monomer of structural formula (I) is utilized in an amount of at least about 1 pphm. 14. The latex binder of claim 10 , wherein emulsifier in accordance with structural formula (III) is present in an amount of at least about 1 pphm. 15. The latex binder of claim 10 , wherein the acrylic monomer includes one or more monomers selected from the group consisting of C 1 -C 10 alkyl esters of acrylic acid and methacrylic acid. 16. The latex binder of claim 10 wherein at least one polymerizable polyaikylene glycol monomer of structural formula (I) and at least one emulsifier of structural formula (III) are employed in a weight ratio of from about 1:4 to about 4:1 structural formula (I):structural formula (III). 17. A coating composition comprising a pigment and a latex binder in accordance with claim 10 . 18. A latex binder useful in preparing a zero or low VOC latex coating composition, the latex binder comprising: a) a polymer which is a po

Assignees

Inventors

Classifications

  • C09D151/08Primary

    grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

  • on to unsaturated polyethers, polyoxymethylenes or polyacetals · CPC title

  • C09D133/08Primary

    Homopolymers or copolymers of acrylic acid esters · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9834698B2 cover?
Latex binders useful for preparing zero or low VOC coating compositions having excellent freeze-thaw stability, good tint strength and good scrub resistance when cured may be obtained using a polymerizable polyalkylene glycol monomer such as polyethylene glycol methacrylate in combination with one or both of an emulsifier or a polymerizable polyalkylene glycol monomer containing bulky hydrophob…
Who is the assignee on this patent?
Arkema Inc
What technology area does this patent fall under?
Primary CPC classification C09D151/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 05 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).