Method for modifying acid group containing polymers

• US 6,846,882 B2
• Filed: 03/27/2001
• Issued: 01/25/2005
• Est. Priority Date: 03/29/2000
• Status: Expired due to Term

• Current Assignee: BASF AG (BASF SE)
• Original Assignee: BASF AG (BASF SE)
• Inventors: Perner, Johannes, Wild, Jochen, Kroner, Matthias, Pfister, Jürgen, Büchner, Karl-Heinz
• Primary Examiner(s): Lipman, Bernard
• Application Number:
  US10/239,053
• Publication Number:
  US 20030050404A1
• Time in Patent Office: 1,400 Days
• Field of Search: 525/330.1, 525/384
• US Class Current: 525/330.1
• CPC Class Codes: C04B 2103/408 Dispersants
• CPC Class Codes: C04B 24/2658 containing polyether side chains
• CPC Class Codes: C08G 81/025 containing polyether sequences

Abstract

Polymers containing acid groups are modified by reaction of

• • (a) polymers which comprise at least 5% by weight of a copolymerized monoethylenically unsaturated monomer containing acid groups, have molar masses of from 200 to 100,000 and are obtainable by free-radical polymerization of monoethylenically unsaturated acids in aqueous solution in the presence or absence of other monoethylenically unsaturated monomers and in the presence of at least 4% by weight, based on the monomers used in the polymerization, of a water-soluble sulfur compound in which the sulfur is in the oxidation state +4,
    with
  • (b) polyalkylene glycols which are end-capped at one end, alkylpolyalkylene glycol amines or mixtures thereof, or mixtures of at least one of the two compounds specified with up to 30% by weight, based on the mixtures, of ammonia, amines, alcohols, hydroxycarboxylic acids or aminocarboxylic acids
    at up to 250° C.

Claims

1. A process for modifying polymers containing acid groups by reaction of

(a) polymers comprising at least 5% by weight of a copolymerized monoethylenically unsaturated monomer containing acid groups and having molar masses of from 200 to 100,000 with

(b) polyalkylene glycols which are end-capped at one end, alkylpolyalkylene glycol amines or mixtures thereof, or mixtures of at least one of the two compounds specified with up to 30% by weight, based on the mixtures, of ammonia, amines, alcohols, hydroxycarboxylic acids or aminocarboxylic acids

at up to 250°

C., wherein the polymers used as component (a) are ones which are obtained by free-radical polymerization of monoethylenically unsaturated acids in aqueous solution in the presence or absence of other monoethylenically unsaturated monomers and in the presence of at least 4% by weight, based on the monomers used in the polymerization, of a water-soluble sulfur compound in which the sulfur is in the oxidation state +4.

2. A process as claimed in claim 1, wherein the water-soluble sulfur compound used is sulfur dioxide, sulfurous acid, an alkali metal, alkaline earth metal or ammonium salt of sulfurous acid or of disulfurous acid, a sodium, potassium or ammonium formaldehyde sulfoxylate, a dialkyl sulfite or a mixture thereof.

3. A process as claimed in claim 1, wherein the water-soluble sulfur compound used is sodium, potassium or ammonium sulfite, sodium, potassium, calcium or ammonium disulfite, sodium, potassium, calcium or ammonium hydrogensulfite or a mixture thereof.

4. A process as claimed in claim 1, wherein the water-soluble sulfur compound is used in an amount of from 4 to 15% by weight, based on the monomers used in the polymerization.

5. A process as claimed in claim 1, wherein the compounds used in component (a) are homopolymers or copolymers of acrylic acid, methacrylic acid, maleic acid, maleic anhydride, vinylsulfonic acid, acrylamidomethyl-propanesulfonic acid, methallylsulfonic acid or alkali metal or ammonium salts of the monomers specified.

6. A process as claimed in claim 1, wherein the component (a) used comprises copolymers of from 5 to 95% by weight of acrylic acid, methacrylic acid, maleic acid, maleic anhydride, vinylsulfonic acid, acrylamidomethylpropanesulfonic acid, methallylsulfonic acid and/or their alkali metal or ammonium salts and from 95 to 5% by weight of acrylic, methacrylic or maleic esters of monohydric alcohols having 1 to 8 carbon atoms in the molecule.

7. A process as claimed in claim 1, wherein the component (a) used comprises homopolymers of acrylic acid, homopolymers of methacrylic acid, copolymers of acrylic acid and methacrylic acid, copolymers of methacrylic acid and vinylsulfonic acid, copolymers of acrylic acid and maleic acid, copolymers of methacrylic acid and maleic acid, copolymers of acrylic acid and an ester of a monoethylenically unsaturated carboxylic acid, copolymers of methacrylic acid and an ester of a monoethylenically unsaturated carboxylic acid and/or alkali metal or ammonium salts of the copolymers specified.

8. A process as claimed in claim 1, wherein the molar mass of the polymers of component (a) is from 1000 to 10,000.

9. A process as claimed in claim 1, wherein the component (a) used comprises homopolymers of acrylic acid or methacrylic acid or copolymers of methacrylic acid and acrylic acid.

10. A process as claimed in claim 1, wherein the component (b) used comprises polyalkylene glycols which are end-capped at one end and have the formula

R¹—

O—

(CHR²—

CHR³—

O)_nH 

 

(I)

or

R¹—

O—

(CH₂—

CH₂—

CH₂—

CH₂—

O)_n—

H 

 

(II), or

where

R¹=C₁-C₅₀-alkyl,

R², R³=H, methyl or ethyl

and

n=1 to 100.

11. A process as claimed in claim 1, wherein the compounds used in component (b) are methylpolyethylene glycols or methylpolyalkylene glycols comprising ethylene oxide and propylene oxide, in each case having molar masses of from 200 to 10,000.

12. A process as claimed in claim 1, wherein the water-soluble sulfur compound is sodium bisulfite.

13. A method comprising carrying out the process as claimed in claim 1, followed by incorporating modified polymers obtained from said process in a cement slurry.

14. A modified polymer obtained by the process of claim 1.

15. A cement slurry obtained by the method of claim 13.