Phosphorus acid functionalized opaque polymer

US9988547B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9988547-B2
Application numberUS-201514949159-A
CountryUS
Kind codeB2
Filing dateNov 23, 2015
Priority dateDec 1, 2014
Publication dateJun 5, 2018
Grant dateJun 5, 2018

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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The present invention relates to opaque polymers functionalized with phosphorus acid groups, composites of TiO 2 particles and the opaque polymers, and methods for their preparation. The composites are useful in coatings formulations and have been shown to exhibit improved hiding benefits in coated substrates over compositions containing non-functionalized opaque polymer and TiO 2 .

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for preparing an aqueous dispersion of phosphorus acid functionalized core-shell polymer particles comprising the steps of a) contacting under emulsion polymerization conditions i) a first monomer emulsion with ii) an aqueous dispersion of carboxylic acid functionalized polymer particles having an average particle size of from 80 to 180 nm to form an aqueous dispersion of core-shell polymer particles; then b) plasticizing the shell portion of the core-shell polymer particles with a polymerizable plasticizing agent; then c) contacting the core-shell polymer particles with an aqueous base to swell the core without substantially polymerizing the plasticizing agent; and then d) polymerizing the plasticizing agent; wherein the first monomer emulsion comprises, based on the weight of the monomers in the first monomer emulsion a) from 0.1 to 5 weight percent of a phosphorus acid monomer; and b) from 50 to 99.8 weight percent of at least one first nonionic ethylenically unsaturated monomer selected from the group consisting of styrene, methyl methacrylate, acrylonitrile, and t-butyl acrylate; and c) from 0.1 to 15 weight percent of a carboxylic acid functionalized monomer; wherein the carboxylic acid functionalized polymer particles comprise from 20 to 50 weight percent structural units of a carboxylic acid monomer, based on the weight of the carboxylic acid functionalized polymer particles; and 50 to 80 weight percent of structural units of a second nonionic ethylenically unsaturated monomer, based on the weight of the carboxylic acid functionalized polymer particles; wherein the plasticizing agent comprises from 7 to 30 percent of a third nonionic ethylenically unsaturated monomer based on the weight of the phosphorus acid functionalized core-shell polymer particles; wherein the phosphorus acid functionalized core-shell polymer particles have an average particle size after step d) in the range of 250 nm to 1.6 μm. 2. The method of claim 1 , wherein the concentration of the phosphorus acid monomer in the first monomer emulsion is from 0.2 to 3 weight percent based on the weight of the monomers in the first monomer emulsion; wherein the concentration of the first nonionic ethylenically unsaturated monomer in the first monomer emulsion is from 70 to 95 weight percent, and wherein the concentration of the carboxylic acid functionalized monomer in the first monomer emulsion is from 0.2 to 0.5 weight percent, all based on the weight of the monomers in the first monomer emulsion; and wherein the plasticizing agent comprises from 10 to 25 weight percent, based on the weight of the core-shell polymer particles. 3. The method of claim 2 , wherein the concentration of the structural units of the carboxylic acid monomer in the acid functionalized polymer particles is from 25 to 40 weight percent and wherein the concentration of the structural units of the second nonionic ethylenically unsaturated monomer is from 60 to 75 weight percent, based on the weight of the acid functionalized polymer particles; and wherein acid functionalized polymer particles have an average particle size of from 125 nm to 150 nm. 4. The method of claim 3 , wherein the first monomer emulsion further comprises from 0.1 to 10 weight percent of a diethylenically or triethylenically unsaturated monomer selected from the group consisting of allyl methacrylate, divinyl benzene, ethylene glycol diacrylate, ethylene glycol dimethacrylate, trimethylolpropane triacrylate, and trimethylolpropane trimethacrylate. 5. The method of claim 3 , wherein the phosphorus acid monomer is phosphoethyl methacrylate, wherein the concentration of structural units of the carboxylic acid monomer acid in the acid functionalized polymer particles is from 32 to 36 weight percent, and the concentration of structural units of the second nonionic ethylenically unsaturated monomer is 64 to 68 weight, wherein the carboxylic acid monomer is acrylic acid or methacrylic acid, and wherein the second nonionic ethylenically unsaturated monomer is methyl methacrylate. 6. The method of claim 5 , wherein the first monomer emulsion comprises from 0.5 to 2 weight percent phosphoethyl methacrylate, based on the weight of the monomers in the first monomer emulsion; and from 0.5 to 5 weight percent the acrylic acid or methacrylic acid. 7. The method of claim 1 , wherein in step a), the first monomer emulsion is added to the aqueous dispersion of the acid functionalized polymer particles under emulsion polymerization conditions over a first period of time, and the phosphorus acid monomer portion of the first monomer emulsion is added to the aqueous dispersion of the acid functionalized polymer particles over a second period of time that is less than 60% of the first period of time. 8. The method of claim 7 , wherein the phosphorus acid monomer addition is delayed until 40% to 75% of the first monomer emulsion, absent the phosphorus acid monomer, is added to the aqueous dispersion of the carboxylic acid functionalized polymer particles. 9. The method of claim 8 , wherein the polymerization of the first monomer emulsion with the aqueous dispersion of acid functionalized polymer particles is allowed to proceed to at least 98% conversion of monomers to the core-shell polymer particles, after which time an inhibitor is contacted with the aqueous dispersion of the core-shell polymer particles to stop or substantially stop polymerization. 10. The method of claim 9 , wherein the polymerizable plasticizing agent is added at a concentration of from 12 to 20 weight percent, based on weight of the phosphorus acid functionalized core-shell polymer particles, wherein the plasticizing agent is styrene or methyl methacrylate, or a combination of a) butyl acrylate and b) divinyl benzene or allyl methacrylate, wherein the aqueous base is NaOH, KOH, or NH 4 OH. 11. The method of claim 10 , wherein less than 0.01 percent of the polymerizable plasticizing agent remains after it is polymerized. 12. A method for preparing an aqueous dispersion of composite particles comprising the method of claim 1 , wherein after step d), the aqueous dispersion of phosphorus acid functionalized core-shell polymer particles are admixed with TiO 2 particles to form an aqueous dispersion of composite particles.

Assignees

Inventors

Classifications

  • characterised by shape, e.g. fibres, flakes or microspheres · CPC title

  • as weight or mass percentages · CPC title

  • Homopolymers or copolymers of acrylic acid esters · CPC title

  • Particle size larger than 1000 nm · CPC title

  • Treatment with macromolecular organic compounds {(C09C3/006 takes precedence)} · CPC title

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What does patent US9988547B2 cover?
The present invention relates to opaque polymers functionalized with phosphorus acid groups, composites of TiO 2 particles and the opaque polymers, and methods for their preparation. The composites are useful in coatings formulations and have been shown to exhibit improved hiding benefits in coated substrates over compositions containing non-functionalized opaque polymer and TiO 2 .
Who is the assignee on this patent?
Dow Global Technologies Llc, Rohm & Haas
What technology area does this patent fall under?
Primary CPC classification C09D125/12. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 05 2018 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).