IP Library Granted Patent US 8,058,377
Granted Patent B1
US 8,058,377 · App. 12/822,284 · Granted Nov 15, 2011

Phosphate-containing polycarboxylate polymer dispersants

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,058,377
App. No.
12/822,284
Granted
Nov 15, 2011
Kind
B1
Abstract

Phosphate-containing polycarboxylate polymer dispersant compositions of the invention comprise a polymer made from polyoxyalkylene groups, acrylic acid groups, mono-ester groups, and optionally di-ester and tri-ester groups, all in specific molar ratios. The polymer dispersants of the invention achieve quick mix-in dispersibility, particularly within hydratable cementitious compositions such as concrete, in comparison with polycarboxylate polymer dispersants that do not contain phosphate groups, while having improved initial slump as well as slump retention compared to phosphate-containing polymers of the prior art.

Claims (41)

1. A polymer dispersant composition, comprising: a polymer made from the following monomer groups:

(a) polyoxyalkylene monomer represented by structural formula

wherein each of R 1 and R 2 individually represent a hydrogen atom or methyl group; R 3 represents hydrogen or —(CH 2 ) m (CO) n O(AO) p X 1 group; AO represents an oxyalkylene group having 2 to 4 carbon atoms; “m” represents an integer of 0 to 2; “n” represents an integer of 0 or 1; “p” represents an average number of the total oxyalkylene groups added and is an integer of from 5 to 200; and X 1 represents a hydrogen atom or alkyl group, respectively;

(b) acrylic acid monomer represented by structural formula

wherein each of R 4 , R 5 ′ and R 6 individually represent a hydrogen atom, a methyl group or —(CH 2 ) q C(O)OM 1 , respectively; “q” represents an integer from 0 to 2; M 1 represents a hydrogen atom, an alkali metal, or an alkali earth metal, respectively;

(c) phosphate monoester monomer represented by structural formula

wherein R 7 represents a hydrogen atom or a methyl group; R 8 represents an alkylene group having 2 to 4 carbon atoms; “r” is an integer of from 1 to 30; M 2 represents a hydrogen atom, an alkali metal or an alkali earth metal, respectively; and

(d) phosphate diester monomer represented by structural formula

wherein each of R 9 and R 11 individually represent a hydrogen atom or methyl group; each of R 10 and R 12 individually represent an alkylene group having 2 to 4 carbon atoms; each of “s” and “t” individually represent an integer of from 1 to 30; M 3 represents a hydrogen atom, an alkali metal or an alkali earth metal, respectively; and

(e) phosphate triester monomer represented by structural formula

wherein each of R 13 , R 15 , and R 17 individually represent a hydrogen atom or methyl group; R 14 , R 16 and R 18 each individually represent an alkylene group having 2 to 4 carbon atoms; each of “w”, “x” and “y” individually represent an integer of from 1 to 30, respectively; and

wherein the foregoing monomers (a), (b), (c), (d), and (e) are present in the following molar ratios, whereby the numerator and denominator numbers in a given range add up to 100, as follows:

(i) the molar ratio of monomers (a)+(b) to monomers (c)+(d)+(e) is in the range of 94-98/2-6;

(ii) the molar ratio of monomer (a) to monomer (b) is in the range of 20-60/40-80;

(iii) the molar ratio of monomer (c) to monomers (d)+(e) is in the range of 50-100/0-50; and

(iv) the molar ratio of monomers (d) and (e) to all monomers (a) through (e) is in the range of 0-2/98-100.

2. The polymer dispersant composition of claim 1 wherein, in monomer component (a), said AO represents an oxyalkylene group having 2 carbon atoms, and said “p” is an integer of from 5 to 100.

3. The polymer dispersant composition of claim 1 wherein, in monomer component (c), said R 8 represents an alkylene group having 2 carbon atoms and said “r” is an integer of 1 to 5.

4. The polymer dispersant composition of claim 1 wherein, in monomer component (d), said R 10 and R 12 each individually represent an alkylene group having 2 carbon atoms and said “s” and “t” each individually represent an integer of 1 to 5.

5. The polymer dispersant composition of claim 1 wherein, in monomer component (e), each of said R 14 , R 16 , and R 18 individually represent an alkylene group having 2 carbon atoms and each of said “w”, “x” and “y” individually represent an integer of from 1 to 5.

6. A method for modifying a cementitious composition comprising adding to a hydratable cementitious binder the polymer dispersant composition of claim 1 .

7. The method of claim 6 wherein said monomers are copolymerized in the presence of a chain transfer agent.

8. The method of claim 7 wherein said chain transfer agent is used in an amount of at least 3.5 mol percent based on said monomers.

9. The method of claim 8 wherein said monomers are copolymerized in the presence of a polymerization initiator in an amount of at least 2 mole percent based on total moles of all said monomers in said polymer dispersant composition.

10. A cement composition comprising a hydratable cementitious binder and the polymer dispersant composition of claim 1 .

11. A polymer dispersant composition, comprising: a polymer made from the following monomer groups:

(a) polyoxyalkylene monomer represented by structural formula

wherein each of R 1 and R 2 individually represent a hydrogen atom or methyl group; R 3 represents hydrogen or —(CH 2 ) m (CO) n O(AO) p X 1 group; AO represents an oxyalkylene group having 2 carbon atoms; “m” represents an integer of 0 to 2; “n” represents an integer of 0 or 1; “p” represents an average number of the total oxyalkylene groups added and is an integer of from 5 to 100; and X 1 represents a hydrogen atom or alkyl group, respectively;

(b) acrylic acid monomer represented by structural formula

wherein each of R 4 , R 5 ′ and R 6 individually represent a hydrogen atom, a methyl group or —(CH 2 ) q C(O)OM 1 , respectively; “q” represents an integer from 0 to 2; M 1 represents a hydrogen atom, an alkali metal, or an alkali earth metal, respectively;

(c) phosphate monoester monomer represented by structural formula

wherein R 7 represents a hydrogen atom or a methyl group; R 8 represents an alkylene group having 2 carbon atoms; “r” is an integer of from 1 to 5; M 2 represents a hydrogen atom, an alkali metal or an alkali earth metal, respectively; and

(d) phosphate diester monomer represented by structural formula

wherein each of R 9 and R 11 individually represent a hydrogen atom or methyl group; each of R 10 and R 12 individually represent an alkylene group having 2 carbon atoms; each of “s” and “t” individually represent an integer of from 1 to 5; M 3 represents a hydrogen atom, an alkali metal or an alkali earth metal, respectively; and

(e) phosphate triester monomer represented by structural formula

wherein each of R 13 , R 15 , and R 17 individually represent a hydrogen atom or methyl group; R 14 , R 16 and R 18 each individually represent an alkylene group having 2 carbon atoms; each of “w”, “x” and “y” individually represent an integer of from 1 to 5, respectively; and

wherein the foregoing monomers (a), (b), (c), (d), and (e) are present in the following molar ratios, whereby the numerator and denominator numbers in a given range add up to 100, as follows:

(i) the molar ratio of monomers (a)+(b) to monomers (c)+(d)+(e) is in the range of 94-98/2-6;

(ii) the molar ratio of monomer (a) to monomer (b) is in the range of 20-60/40-80;

(iii) the molar ratio of monomer (c) to monomers (d)+(e) is in the range of 50-100/0-50; and

(iv) the molar ratio of monomers (d) and (e) to all monomers (a) through (e) is in the range of 0-2/98-100.

Assignments (7)
RELEASE OF SECURITY INTEREST Recorded Sep 27, 2022
From: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
To: DE NEEF CONSTRUCTION CHEMICALS (US) INC.; VERIFI LLC; GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 061553/0521 →
RELEASE OF SECURITY AGREEMENT RECORDED AT REEL/FRAME NO.: 032159/0384 Recorded Apr 3, 2018
From: GOLDMAN SACHS BANK USA, AS THE COLLATERAL AGENT
To: W.R. GRACE & CO.-CONN.
Reel/Frame 045832/0887 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER 13353676 PREVIOUSLY RECORDED ON REEL 037701 FRAME 0396. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 17, 2016
From: W. R. GRACE & CO.-CONN.
To: GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 038289/0821 →
SECURITY INTEREST Recorded Mar 7, 2016
From: GCP APPLIED TECHNOLOGIES INC.
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
Reel/Frame 038012/0407 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2016
From: W. R. GRACE & CO.-CONN.
To: GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 037701/0396 →
RELEASE OF SECURITY INTEREST Recorded Feb 2, 2016
From: GOLDMAN SACHS BANK USA
To: W. R. GRACE & CO.-CONN.
Reel/Frame 037681/0323 →
SECURITY AGREEMENT Recorded Feb 4, 2014
From: W.R. GRACE & CO.-CONN.
To: GOLDMAN SACHS BANK USA, AS THE COLLATERAL AGENT
Reel/Frame 032159/0384 →