IP Library Granted Patent US 7,271,214
Granted Patent B2
US 7,271,214 · App. 10/874,502 · Granted Sep 18, 2007

Cement dispersant and methods of making and using the same

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Quick Facts
Patent No.
US 7,271,214
App. No.
10/874,502
Granted
Sep 18, 2007
Kind
B2
Abstract

The present invention relates to cement dispersant that is a copolymerization product of a first monomer (A) comprising a carboxylic acid, a second monomer (B) comprising an alkoxylated allyl alcohol sulfate, and, optionally, a third monomer (C) comprising an alkoxylated allyl alcohol. The cement dispersant according to the invention provides improved slump life properties and water reduction properties in cement admixtures.

Claims (31)

1. A method of improving the slump properties of a cement admixture, the method comprising adding a dispersant composition to an admixture comprising cement and water, wherein the dispersant composition comprises a terpolymer comprised of a random combination of structural units (A), (B) and (C) remaining after polymerization, wherein:

(A) is one or more monomers having functional groups selected from the group consisting of carboxylic acids, amido carboxylic acids, C1-C6 alkyl esters of carboxylic acids, C1-C6 alkyl ester of amido carboxylic acids, hydroxylated C1-C6 alkyl esters of carboxylic acids, hydroxylated C1-C6 alkyl esters of amido carboxylic acids and sulfonic acids;

(B) is according to Formula (I):

 where “R1” is (CH 2 —CH 2 —O)n or (CH 2 —CH(CH 3 )—O)n or a mixture of both and “n” is an integer greater than 1; and “M” is sodium, potassium, calcium, ammonium or an organic amine; and

(C) is according to Formula (II):

 where “R2” is H or a C1-C4 straight or branched alkyl chain; “R3” is CH 2 or C═O; “R4” is (CH 2 —CH 2 —O)m or (CH 2 —CH(CH 3 )—O)m or a mixture of both and “in” is an integer greater than 1; and “R5” is H or a C1-C18 straight or branched alkyl chain.

2. The method according to claim 1 wherein (A) is one or more selected from the group consisting of acrylic acid, methacrylic acid, acrylamide, maleic acid, maleic anhydride, fumaric acid, itaconic acid, 2-acrylamido-2-methylpropanesulfonic acid, and water-soluble salts thereof.

3. The method according to claim 1 wherein (B) comprises an allyl alcohol that has been ethoxylated, propoxylated, or both, followed by the addition of sulfamic acid to form an end terminal sulfate group that is covalently bonded through an oxygen atom.

4. The method according to claim 1 wherein (B) is an ammonium allylpolyethoxy sulphate alkoxylated with an average of about 100 moles or more of ethylene oxide.

5. The method according to claim 1 wherein (B) is an ammonium allylpolyethoxy sulphate alkoxylated with an average of up to about 50 moles of ethylene oxide.

6. The method according to claim 1 wherein (C) is one or more selected from the group consisting of polyethylene glycol allyl ether (PEGAF), polypropylene glycol allyl ether (PPGAE), polyethylene glycol/polypropylene glycol allyl ether (PEGPGAE), hydroxyethyene glycol methylmethacrylate (HEME), and methoxyethyene glycol methylmethacrylate (MEME).

7. The method according to claim 1 wherein the molar ratio of (A) to (B) to (C) in the terpolymer is in a range of from about 1 to about 10 for (A), from about 1 to about 4 for (B), and from about 1 to about 10 for (C).

8. The method according to claim 1 wherein the molar ratio of (A) to (B) to (C) in the terpolymer is in a range of from about 2.5 to about 6 for (A), from about 1 to about 2 for (B), and from about 1 to about 3 for (C).

9. A cement admixture comprising:

a cementitious material;

water; and

a dispersant composition comprising a terpolymer comprised of a random combination of structural units (A), (B) and (C) remaining after polymerization, wherein:

(A) is one or more monomers having functional groups selected from the group consisting of carboxylic acids, amido carboxylic acids, C1-C6 alkyl esters of carboxylic acids, C1-C6 alkyl ester of amido carboxylic acids, hydroxylated C1-C6 alkyl esters of carboxylic acids, hydroxylated C1-C6 alkyl esters of amido carboxylic acids and sulfonic acids;

(B) is according to Formula (I):

 where “R1” is (CH 2 —CH 2 —O)n or (CH 2 —CH(CH 3 )—O)n or a mixture of both and “n” is an integer greater than 1; and “M” is sodium, potassium, calcium, ammonium or an organic amine; and

(C) is according to Formula (II):

where “R2” is H or a C1-C4 straight or branched alkyl chain; “R3” is CH 2 or C═O; “R4” is (CH 2 —CH 2 —O)m or (CH 2 —CH(CH 3 )—O)m or a mixture of both and “m” is an integer greater than 1; and “R5” is H or a C1-C18 straight or branched alkyl chain.

10. The cement admixture according to claim 9 wherein (A) is one or more selected from the group consisting of acrylic acid, methacrylic acid, acrylamide, maleic acid, maleic anhydride, fumaric acid, itaconic acid, 2-acrylamido-2-methylpropanesulfonic acid, and water-soluble salts thereof.

11. The cement admixture according to claim 9 wherein (B) comprises an allyl alcohol that has been ethoxylated, propoxylated, or both, followed by the addition of sulfamic acid to form an end terminal sulfate group that is covalently bonded through an oxygen atom.

12. The cement admixture according to claim 9 wherein (B) is an ammonium allylpolyethoxy sulphate alkoxylated with an average of about 100 moles or more of ethylene oxide.

13. The cement admixture according to claim 9 wherein (B) is an ammonium allylpolyethoxy sulphate alkoxylated with an average of up to about 50 moles of ethylene oxide.

14. The cement admixture according to claim 9 wherein (C) is one or more selected from the group consisting of polyethylene glycol allyl ether (PEGAF), polypropylene glycol allyl ether (PPGAE), polyethylene glycol/polypropylene glycol allyl ether (PEGPGAE), hydroxyethyene glycol methylmethacrylate (HEME), and methoxyethyene glycol methylmethacrylate (MEME).

15. The cement admixture according to claim 9 wherein the molar ratio of (A) to (B) to (C) in the terpolymer is in a range of from about 1 to about 10 for (A), from about 1 to about 4 for (B), and from about 1 to about 10 for (C).

16. The cement admixture according to claim 9 wherein the molar ratio of (A) to (B) to (C) in the terpolymer is in a range of from about 2.5 to about 6 for (A), from about 1 to about 2 for (B), and from about 1 to about 3 for (C).

17. The cement admixture according to claim 9 wherein (A) is acrylic acid and (B) is an allyloxypolyethylene glycol sulfate ammonium salt.

18. The method according to claim 1 wherein (A) is acrylic acid and (B) is an allyloxypolyethylene glycol sulfate ammonium salt.

Assignments (15)
RELEASE OF SECURITY INTEREST Recorded Jun 30, 2024
From: TWIN BROOK CAPITAL PARTNERS, LLC, AS ADMINISTRATIVE AGENT
To: RG DISPERSANTS USA LLC
Reel/Frame 067877/0761 →
RELEASE OF SECURITY INTEREST Recorded Sep 25, 2019
From: CITIZENS BANK, N.A.
To: GEO SPECIALTY CHEMICALS, INC.
Reel/Frame 050486/0061 →
RELEASE OF SECURITY INTEREST Recorded Sep 4, 2019
From: U.S. BANK NATIONAL ASSOCIATION
To: GEO SPECIALTY CHEMICALS, INC.
Reel/Frame 050264/0881 →
SECURITY INTEREST Recorded Aug 30, 2019
From: GEO SPECIALTY CHEMICALS, INC.
To: TWIN BROOK CAPITAL PARTNERS, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 050219/0608 →
SECURITY INTEREST Recorded Jan 11, 2019
From: GEO SPECIALTY CHEMICALS, INC.
To: CITIZENS BANK, N.A.
Reel/Frame 047968/0591 →
RELEASE OF SECURITY INTEREST Recorded Oct 19, 2017
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: GEO SPECIALTY CHEMICALS, INC.
Reel/Frame 043905/0673 →
SECURITY INTEREST Recorded Oct 18, 2017
From: GEO SPECIALTY CHEMICALS, INC.
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 043898/0392 →
RELEASE OF SECURITY INTEREST Recorded Feb 26, 2013
From: WELLS FARGO CAPITAL FINANCE, LLC
To: GEO SPECIALTY CHEMICALS, INC.; GEO SPECIALTY CHEMICALS LIMITED
Reel/Frame 029876/0076 →
RELEASE OF SECURITY INTEREST Recorded Oct 31, 2012
From: WELLS FARGO CAPITAL FINANCE, LLC
To: GEO SPECIALTY CHEMICALS, INC.; GEO SPECIALTY CHEMICALS LIMITED
Reel/Frame 029215/0137 →
SECURITY AGREEMENT Recorded Oct 31, 2012
From: GEO SPECIALTY CHEMICALS, INC.
To: CITIZENS BANK OF PENNSYLVANIA
Reel/Frame 029217/0707 →
RELEASE OF SECURITY INTEREST Recorded Mar 24, 2010
From: THE CIT GROUP/BUSINESS CREDIT, INC.
To: GEO SPECIALTY CHEMICALS, INC.
Reel/Frame 024128/0129 →
SECURITY AGREEMENT Recorded Mar 24, 2010
From: GEO SPECIALTY CHEMICALS, INC.; GEO SPECIALTY CHEMICALS LIMITED
To: WELLS FARGO CAPITAL FINANCE, LLC
Reel/Frame 024128/0355 →
SECURITY AGREEMENT Recorded Mar 17, 2006
From: GEO SPECIALTY CHEMICALS, INC.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 017314/0492 →
SECURITY INTEREST Recorded May 24, 2005
From: GEO SPECIALTY CHEMICALS, INC.
To: THE CIT GROUP/BUSINESS CREDIT, INC.
Reel/Frame 016263/0755 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 20, 2004
From: BAIR, KEITH A.; SAVOLY, ARPAD; VEAL, BENNIE
To: GEO SPECIALTY CHEMICALS, INC.
Reel/Frame 015799/0561 →