IP Library Granted Patent US 7,671,115
Granted Patent B2
US 7,671,115 · App. 10/538,681 · Granted Mar 2, 2010

Method for enhancing water-repellency treatment of mineral hydraulic binder compositions and compositions obtainable by said method and their uses

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Quick Facts
Patent No.
US 7,671,115
App. No.
10/538,681
Granted
Mar 2, 2010
Kind
B2
Abstract

The invention concerns a method for enhancing water-repellency repellency treatment of mineral hydraulic binder compositions and compositions obtainable by said method and their uses in the building sector, said method comprising the step of adding a sufficient amount of at least one monovalent cation salt of a carboxylic acid to said composition.

Claims (32)

1. A method for enhancing the water repellency of an inorganic hydraulic binder composition, comprising the step of adding a sufficient amount of at least one monovalent cation salt of a carboxylic acid to said composition, said acid having an hydrocarbon chain optionally having halogens, hydroxyl groups, ether groups, thioether groups, ester groups, amide groups, carboxyl groups, sulfonic acid groups, carboxylic anhydride groups or carbonyl groups

wherein the monovalent cation salt of a carboxylic acid has the formula C n H (2n-1) OO − X + wherein n=4 to 18 and X is an alkali metal.

2. The method as claimed in claim 1 , wherein the monovalent cation salt of a carboxylic acid is in the form of a powder in the inorganic hydraulic binder composition.

3. The method as claimed in claim 1 , wherein the amount is between 0.001% and 3% by dry weight of the monovalent cation salt of a carboxylic acid, with respect to the total weight of the composition.

4. The method as claimed in claim 3 , wherein the amount is between 0.01% and 0.5%.

5. The method as claimed in claim 4 , wherein the amount is between 0.03% and 0.15%.

6. The method as claimed in claim 1 , further comprising the step of premixing the monovalent cation salt of a carboxylic acid with a latex composition.

7. The method as claimed in claim 6 , wherein the amount of the monovalent cation salt of a carboxylic acid, with respect to the total weight of dry latex, is between 0.1 and 20% by weight, with respect to the weight of the dry latex.

8. The method as claimed in 6 , wherein the monovalent cation salt of a carboxylic acid is added in the powder form to the latex composition in the form of a redispersible powder.

9. The method as claimed in claim 6 , wherein the monovalent cation salt of a carboxylic acid is added in the powder or solution form to the latex composition in the form of an aqueous dispersion during the polymerization or at the end of the polymerization.

10. The method as claimed in claim 6 , wherein the monovalent cation salt of a carboxylic acid is added in the powder form to the latex composition during a further step of drying by atomization of the latex.

11. The method as claimed in claim 6 , wherein the latex composition comprises:

at least one water-insoluble polymer,

from 0 to 35% by weight, with respect to the total weight of the polymer, of at least one protective colloid,

from 0 to 30% by weight, with respect to the total weight of the polymer, of anticaking agents, and

from 0.1 to 20% by weight, with respect to the total weight of the polymer, of at least one monovalent cation salt of a carboxylic acid.

12. The method as claimed in claim 11 , wherein the water-insoluble polymer is obtained by polymerization of vinyl esters, alkyl acrylates, alkyl methacrylates, whose alkyl group has from 1 to 10 carbon atoms, and/or vinylaromatic monomers.

13. The method as claimed in claim 12 , wherein the water-insoluble polymer is obtained by polymerization of monomers selected from the group consisting of: vinyl acetate,

methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, 2-ethylhexyl methacrylate, methyl acrylate, ethyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate, and styrene.

14. The method as claimed in claim 12 , wherein the monomers are further copolymerized with other monomers possessing ethylenic unsaturation being olefins, vinyl esters of saturated, branched or unbranched, monocarboxylic acids having from 1 to 12 carbon atoms, esters of branched C 9 -C 11 acids, vinyl pivalate or vinyl laurate; esters of unsaturated mono- or dicarboxylic acids having 3 to 6 carbon atoms with alkanols having 1 to 10 carbon atoms, vinylaromatic monomers, vinyl halides, diolefins, (meth)allyl esters of (meth)acrylic acid; (meth)allyl esters of the mono- and diesters of maleic, fumaric and itaconic acids; or alkene derivatives of amides of acrylic and methacrylic acids.

15. The method as claimed in claim 11 , wherein the anticaking agents are aluminum silicates, calcium carbonates, magnesium carbonates, silicas, aluminum hydrate, bentonite, talc, kaolin, barium sulfate, titanium oxide, or calcium sulfoaluminate (satin white).

16. The method as claimed in claim 1 , wherein the monovalent cation salt of a carboxylic acid has the formula C n H (2n-1) OO − X + wherein n=4 to 18 and X is sodium, potassium, lithium, ammonium or quaternary amines.

17. The method as claimed in claim 16 , wherein n=8 to 16.

18. The method as claimed in claim 1 , wherein the monovalent cation salt of a carboxylic acid is sodium laurate and/or potassium laurate.

19. The method as claimed in claim 1 , wherein the hydraulic binder is a cement, cement of Portland, high-alumina cement, blast-furnace cement, fly ash, calcined shale or pozzolan.

20. A grout, mortar or concrete comprising an inorganic hydraulic binder composition made by the process of claim 1 .

21. A method for enhancing the water repellency of an inorganic hydraulic binder composition, comprising the step of adding a sufficient amount of at least one monovalent cation salt of a carboxylic acid to said composition, said acid having an hydrocarbon chain optionally having halogens, hydroxyl groups, ether groups, thioether groups, ester groups, amide groups, carboxyl groups, sulfonic acid groups, carboxylic anhydride groups or carbonyl groups and the step of premixing the monovalent cation salt of a carboxylic acid with a latex composition

wherein the latex composition comprises:

at least one water-insoluble polymer,

from 0 to 35% by weight, with respect to the total weight of the polymer, of at least one protective colloid,

from 0 to 30% by weight, with respect to the total weight of the polymer, of anticaking agents wherein the anticaking agents are aluminum silicates, calcium carbonates, magnesium carbonates, silicas, aluminum hydrate, bentonite, talc, kaolin, barium sulfate, titanium oxide or calcium sulfoaluminate (satin white), and

from 0.1 to 20% by weight, with respect to the total weight of the polymer, of at least one monovalent cation salt of a carboxylic acid.

Assignments (21)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (030146/0970) Recorded Jul 9, 2019
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 049706/0264 →
RELEASE OF SECURITY INTEREST Recorded Feb 23, 2017
From: WILMINGTON TRUST, NATIONAL ASSOCIATION (SUCCESSOR BY MERGER TO WILMINGTON TRUST FSB), AS COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS HEXION SPECIALTY CHEMICALS INC.); BORDEN CHEMICAL FOUNDRY, LLC; HEXION INVESTMENTS INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INVESTMENTS, INC.); HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; HEXION INTERNATIONAL INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INTERNATIONAL INC.); OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
Reel/Frame 041793/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2017
From: HEXION INC.
To: SYNTHOMER USA LLC.
Reel/Frame 041057/0634 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039260/0011 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039260/0069 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 039260/0158 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC.
Reel/Frame 039259/0696 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC.
Reel/Frame 039258/0913 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST COMPANY
To: HEXION INC.
Reel/Frame 039259/0628 →
CHANGE OF NAME Recorded Jan 29, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034863/0264 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 030146/0946 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 030146/0970 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Mar 28, 2013
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE SPECIALTY CHEMICALS INC. (F/K/A HEXION SPECIALTY CHEMICALS, INC.)
Reel/Frame 030111/0021 →
CHANGE OF NAME Recorded Mar 5, 2012
From: HEXION SPECIALTY CHEMICALS, INC.
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 027808/0408 →
SECURITY AGREEMENT Recorded Feb 5, 2010
From: HEXION LLC; HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 023905/0451 →
SECURITY INTEREST Recorded Jan 29, 2010
From: HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: WILMINGTON TRUST FSB, AS COLLATERAL AGENT
Reel/Frame 023963/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2008
From: RHODIA CHIMIE
To: HEXION SPECIALTY CHEMICALS, INC.
Reel/Frame 020691/0991 →
SECURITY AGREEMENT Recorded Nov 21, 2006
From: HEXION SPECIALTY CHEMICALS, INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 018535/0701 →
SECURITY AGREEMENT Recorded Nov 21, 2006
From: HEXION SPECIALTY CHEMICALS, INC.
To: JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT
Reel/Frame 018535/0556 →
SECURITY AGREEMENT Recorded Jul 14, 2006
From: HEXION SPECIALTY CHEMICALS, INC.
To: JPMORGAN CHASE BANK, N.A. AS COLLATERAL AGENT
Reel/Frame 017946/0151 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2005
From: CASTAING, JEAN-CHRISTOPHE; BAKER, GARY; JOST, PHILIPPE
To: RHODIA CHIME
Reel/Frame 017413/0543 →