Alkali swellable acrylic emulsions without surfactants, use thereof in aqueous formulations, and formulations containing them

US9487597B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9487597-B2
Application numberUS-201113160558-A
CountryUS
Kind codeB2
Filing dateJun 15, 2011
Priority dateJun 25, 2010
Publication dateNov 8, 2016
Grant dateNov 8, 2016

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.

The present invention pertains to new alkali swellable thickening emulsions, free of surfactants and solvents other than water: as a result, all drawbacks related to the use of solvents, or to the formation of foam in the case of surfactants, are avoided. These new emulsions contain a certain quantity of 2-acrylamido-2-methylpropane sulfonic acid (or AMPS, CAS #: 40623-75-4). They have proven effective at thickening aqueous mediums, particularly water-based paints, paper coatings, aqueous suspensions of mineral materials, detergents, cosmetic formulations, or formulations containing a hydraulic binder.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for manufacturing a direct emulsion of a polymer in water, comprising polymerizing monomer group B in a polymerization medium consisting of water and catalyst: wherein monomer group B consists of: a) 20% to 60% by weight of at least one of methacrylic acid and acrylic acid, b) 40% to 80% by weight of at least one ester of (meth)acrylic acid, c) 0.5% to 25% by weight of a monomer comprising at least one hydrophobic group, d) 0.05% to 22% by weight of 2-acrylamido-2-methylpropane sulfonic acid, and e) 0 to 1% by weight of at least one cross-linking monomer, provided that the total of a)+b)+c)+d)+e) is equal to 100%, and wherein the monomer comprising at least one hydrophobic group has the formula (I): where: m, n, p and q are integers and m, n, and p are less than 150, q is greater than 0, and at least one integer among m, n and p is nonzero; R has a polymerizable vinyl function, R 1 and R 2 are identical or different, and represent hydrogen atoms or alkyl groups, R′ is a hydrophobic group comprising at least 6 and at most 36 carbon atoms. 2. The method according to claim 1 , wherein the ester of (meth)acrylic acid is selected from the group consisting of ethyl acrylate, butyl acrylate, methyl methacrylate, and mixtures thereof. 3. The method according to claim 1 , wherein the cross-linking monomer is present and is selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, diallyl phthalate, allyl acrylate, allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allylic ethers obtained from polyols, and mixtures thereof. 4. The method according to claim 1 , wherein the emulsion has a solids content of 10%-50% by weight in relation to the total weight of the emulsion. 5. The method according to claim 1 , wherein polymer particles in the emulsion have a particle size between 50 nm and 500 nm. 6. The method according to claim 1 , wherein the polymer has a M w of 20,000 g/mol-1,000,000 g/mol. 7. The method according to claim 1 , wherein the ester of (meth)acrylic acid is selected from the group consisting of ethyl acrylate, butyl acrylate, methyl methacrylate, and mixtures thereof; the cross-linking monomer is present and is selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, diallyl phthalate, allyl acrylate, allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allylic ethers obtained from polyols, and mixtures thereof; the emulsion has a solids content of 10%-50% by weight in relation to the total weight of the emulsion; polymer particles in the emulsion have a particle size between 50 nm and 500 nm; and the polymer has a M w of 20,000 g/mol-1,000,000 g/mol. 8. The method according to claim 1 , wherein the cross-linking monomer is present in monomer group B. 9. A direct emulsion of a polymer in water, consisting of water, catalyst and polymer, wherein said polymer consists of polymerized monomers of monomer group B: wherein monomer group B consists of: a) 20% to 60% by weight of at least one of methacrylic acid and acrylic acid, b) 40% to 80% by weight of at least one ester of (meth)acrylic acid, c) 0.5% to 25% by weight of the monomer comprising at least one hydrophobic group, d) 0.05% to 22% by weight of 2-acrylamido-2-methylpropane sulfonic acid, and e) 0 to 1% by weight of at least one cross-linking monomer, provided that the total of a)+b)+c)+d)+e) is equal to 100%, and wherein the monomer comprising at least one hydrophobic group has the formula (I): where: m, n, p and q are integers and m, n, and p are less than 150, q is greater than 0, and at least one integer among m, n and p is nonzero; R has a polymerizable vinyl function, R 1 and R 2 are identical or different, and represent hydrogen atoms or alkyl groups, R′ is a hydrophobic group comprising at least 6 and at most 36 carbon atoms. 10. The direct emulsion as claimed in claim 9 , wherein the cross-linking monomer is present and is selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, diallyl phthalate, allyl acrylate, allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allylic ethers obtained from polyols, and mixtures thereof. 11. The direct emulsion as claimed in claim 9 , having a solids content of 10%-50% by weight in relation to the total weight of the emulsion. 12. The direct emulsion as claimed in claim 9 , wherein polymer particles in the emulsion have a particle size of 50 nm-500 nm. 13. The direct emulsion as claimed in claim 9 , wherein the polymer has a M w of 20,000 g/mol-1,000,000 g/mol. 14. A method, comprising adding the direct emulsion as claimed in claim 9 to an aqueous formulation. 15. The method according to claim 14 , wherein said formulation is selected from the group consisting of an aqueous paint, a paper coating, an aqueous suspension of mineral materials, a detergent, a cosmetic formulation, and a formulation containing a hydraulic binder. 16. An aqueous formulation comprising the direct emulsion as claimed in claim 9 . 17. The formulation according to claim 16 , wherein the aqueous formulation is selected form the group consisting of a water-based paint, a paper coating, an aqueous suspension of mineral materials, a detergent, a cosmetic formulation, and a formulation containing a hydraulic binder. 18. The direct emulsion as claimed in claim 9 , wherein: the direct emulsion has a solids content of 10%-50% by weight in relation to the total weight of the emulsion, the polymer particles in the emulsion have a particle size of 50 nm-500 nm, and the polymer has a M w of 20,000 g/mol-1,000,000 g/mol. 19. The direct emulstion according to claim 9 , wherein the cross-linking monomer is present in monomer group B. 20. The direct emulsion as claimed in claim 9 , wherein: the cross-linking monomer is present and is selected from the group consisting of ethylene glycol dimethacrylate, trimethylolpropanetriacrylate, diallyl phthalate, allyl acrylate, allyl maleates, methylene-bis-acrylamide, methylene-bis-methacrylamide, tetrallyloxyethane, triallylcyanurates, allylic ethers obtained from polyols, and mixtures thereof; the direct emulsion has a solids content of 10%-50% by weight in relation to the total weight of the emulsion; polymer particles in the emulsion have a particle size of 50 nm-500 nm; and the polymer has a M w of 20,000 g/mol-1,000,000 g/mol.

Assignees

Inventors

Classifications

  • C08F2/22Primary

    Emulsion polymerisation · CPC title

  • obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

  • Thickener, Thickening system · CPC title

  • of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen · CPC title

  • Preparations for care of the skin · 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 US9487597B2 cover?
The present invention pertains to new alkali swellable thickening emulsions, free of surfactants and solvents other than water: as a result, all drawbacks related to the use of solvents, or to the formation of foam in the case of surfactants, are avoided. These new emulsions contain a certain quantity of 2-acrylamido-2-methylpropane sulfonic acid (or AMPS, CAS #: 40623-75-4). They have proven e…
Who is the assignee on this patent?
Suau Jean-Marc, Coatex Sas
What technology area does this patent fall under?
Primary CPC classification C08F2/22. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 08 2016 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).