IP Library Granted Patent US 7,323,510
Granted Patent B2
US 7,323,510 · App. 10/432,624 · Granted Jan 29, 2008

Method for the production of water-in-water polymer dispersions

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Quick Facts
Patent No.
US 7,323,510
App. No.
10/432,624
Granted
Jan 29, 2008
Kind
B2
Abstract

The invention relates to methods for manufacturing a water-in-water polymer dispersion containing polymer A and at least one polymer dispersant B, according to which monomers, which are dispersed in an aqueous phase containing water-soluble dispersant B, are subjected to radical polymerization, possibly following the addition of a water-soluble salt, and, after polymerisation, a water-soluble acid is added to the water-soluble and/or water-swellable polymer A obtained in this way, where the acid is added in quantities of 0.1 to 5% by weight and the salt in quantities of up to a maximum of 3% by weight, each referred to the total dispersion, and the total quantity of salt and acid amounts to a maximum of 5% by weight, referred to the total dispersion.

Claims (116)

1. A method for manufacturing a water-in-water polymer dispersion containing a water-soluble and/or water-swellable polymer A and at least one polymeric dispersant B, comprising:

a) dispersing monomers in an aqueous phase containing the water-soluble dispersant B to form a monomer dispersion, wherein said monomers consist of one or more of the monomers (i), (ii), and (iii):

(i) a non-ionic monomer of formula (I)

where

R 1 is a hydrogen or a methyl residue, and

R 2 and R 2 are, independently of each other, hydrogen, an alkyl or a hydroxyalkyl residue with 1 to 5 C atoms;

(ii) a cationic monomer of formula (II)

where

R 1 is a hydrogen or a methyl residue,

Z 1 is O, NH or NR 4 wherein R 4 is an alkyl residue with 1 to 4 C atoms, and

Y is one of

wherein Y 0 and Y 1 are an alkylene residue with 2 to 6 C atoms, optionally substituted with hydroxy groups,

Y 2 , Y 3 , Y 4 , Y 5 , Y 6 , Y 7 , independently of each other, are each an alkyl residue with 1 to 6 C atoms; and

Z − is a halogen, acetate, or SO 4 CH 3 − ; and

(iii) an amphiphilic monomer of formula (III) or (IV)

where

Z 1 is O, NH, NR 4 wherein R 4 is an alkyl residue with 1 to 4 carbon atoms,

R 1 is a hydrogen or a methyl residue,

R 8 is an alkylene residue with 1 to 6 carbon atoms,

R 5 and R 6 are, independently of each other, an alkyl residue with 1 to 6 carbon atoms,

R 7 is an alkyl residue with 8 to 32 carbon atoms, and

Z − is a halogen, pseudo-halogen, SO 4 CH 3 or acetate, or

where

Z 1 is O, NH, NR 4 wherein R 4 is an alkyl residue with 1 to 4 carbon atoms,

R 1 is a hydrogen or a methyl residue,

R 10 is a hydrogen, alkyl, aryl and/or aralkyl residue with 8 to 32 carbon atoms,

R 9 is an alkylene residue with 2 to 6 carbon atoms,

and

n is an integer between 1 and 50;

b) adding a water-soluble salt;

c) subjecting the monomer dispersion formed in b) to a radical polymerization to form a dispersion of the water-soluble or water-swellable polymer A, and, after polymerization;

d) adding a water-soluble acid to the dispersion of the water-soluble and/or water-swellable polymer A;

wherein the polymeric dispersant B is a cationic polymer comprising at least 30% by weight of polymerized cationic monomer, and

the acid is added in an amount of from 0.1 to 5% by weight and the salt is added in an amount of up to 3% by weight, where the total quantity of salt and acid is a maximum of 5% by weight; wherein % by weight is based on the total weight of the dispersion.

2. The method of claim 1 , wherein the acid is added in an amount of 0.2 to 3.5% by weight, based on the total weight of the dispersion.

3. The method of claim 1 , wherein the salt is added in an amount of up to a maximum of 2.0% by weight, based on the total weight of the dispersion.

4. The method of claim 1 , wherein the acid and the salt are added in a total amount of a maximum of 3.5% by weight, based on the total weight of the dispersion.

5. The method of claim 1 , wherein the water-soluble acid is at least one of an organic acid and an inorganic acid.

6. The method of claim 5 , wherein the water-soluble acid is at least one selected from the group consisting of aliphatic or an aromatic monocarboxylic acid, dicarboxylic acid, polycarboxylic acid and a hydroxycarboxylic acid.

7. The method of claim 5 , wherein the water-soluble acid is at least one selected from the group consisting of hydrochloric acid, sulphuric acid, nitric acid and phosphoric acid.

8. The method of claim 1 , wherein the water-soluble salt is at least one selected from the group consisting of an ammonium salt, an alkaline metal salt and an alkaline-earth metal salt.

9. The method of claim 8 , wherein the water-soluble salt is at least one selected from the group consisting of an ammonium salt, sodium salt, potassium salt, calcium salt and magnesium salt.

10. The method of claim 8 , wherein the water-soluble salt is a salt of an inorganic acid or an organic acid.

11. The method of claim 10 , wherein the water-soluble salt is at least one selected from the group consisting of a salt of an aliphatic or aromatic monocarboxylic, dicarboxylic or polycarboxylic acid, and a hydroxycarboxylic acid.

12. The method of claim 11 , wherein the water-soluble salt is at least one selected from the group consisting of sodium chloride, ammonium sulphate and sodium sulphate.

13. The method of claim 1 , wherein the polymeric dispersant B is a water-soluble polymer with a maximum M w of 2.0×10 6 .

14. The method of claim 13 , wherein polymeric dispersant B contains at least one functional group selected from the group consisting of ether, carboxyl, sulpho, sulphate ester, amino, amido, imido, tertiary amino and quaternary ammonium groups.

15. The method of claim 14 , wherein the polymeric dispersant B is at least one selected from the group consisting of a cellulose derivative, polyvinyl acetate, starch, starch derivative, dextran, polyvinylpyrrolidone, polyvinylpyridine, polyethylene imine, polyamine, polyvinyl imidazole, polyvinyl succinimide, polyvinyl-2-methylsuccinimide, polyvinyl-1,3-oxazolidone-2, polyvinyl-2-methylimidazoline, a copolymer thereof with maleic acid, maleic anhydride, famaric acid, itaconic acid, itaconic anhydride, (meth)acrylic acid, salts of (meth)acrylic acid and a (meth)acrylic acid amide compound.

16. The method of claim 1 , wherein the cationic monomer is at least one selected from the group consisting of a diallyl dimethylammonium chloride, a dialkylaminoalkyl(meth)acrylate and dialkylaminoalkyl(meth)acrylamide with C 1 -C 3 in the alkyl or alkylene groups and protonated or quaternised as an ammonium salt.

17. The method of claim 13 , wherein the polymeric dispersant B further comprises at least one polyfunctional alcohol selected from the group consisting of a polyalkylene glycol, a block polymer of propylene/ethylene oxide with a molecular weight of 1,500 to 50,000, glycerin, ethylene glycol, propylene glycol, pentaerythritol and sorbitol.

18. The method of claim 13 , wherein the polymeric dispersant B and a polyfunctional alcohol are added in quantities of 5 to 50% by weight, based on the total weight of the dispersion.

19. The method of claim 13 , wherein the polymeric dispersant B further comprises a polyfunctional alcohol and the weight ratio of polymeric dispersant B to the polyfunctional alcohol is 1:0.01 to 0.5.

20. The method of claim 1 , wherein the polymerizing forms the polymer A having an M w of >1.0×10 6 g/mol.

21. The method of claim 1 , wherein the polymer A comprises from 1 to 99% by weight, of one or more cationic monomers.

22. The method of claim 1 , wherein the polymer A is present in quantities of 5 to 60% by weight, based on the total weight of the composition.

23. The method of claim 1 , further comprising:

continuously adding an initiator system during the entire course of polymerisation.

24. A water-in-water polymer dispersion obtained by the method of claim 1 .

25. The water-in-water polymer dispersion of claim 24 which is a flocculant in the sedimentation of solids, the conditioning of water and process water, in waste water treatment, in raw materials extraction, in coal extraction, in aluminium extraction, in petroleum extraction, an auxiliary in papermaking or a demulsifier in the separation of water mixtures containing at least one oil and fat.

26. The water-in-water polymer dispersion of claim 24 , which is a thickener.

27. The water-in-water polymer dispersion of claim 24 , which is a retention agent and drainage aid in papermaking.

28. The water-in-water polymer dispersion of claim 24 , which is an additive for a crop protection agent.

29. The water-in-water polymer dispersion of claim 24 , which is an additive for an anti-erosion agent.

30. The method of claim 1 , wherein the acid is added in a quantity of from 0.3 to 2.0% by weight based on the total weight of the dispersion.

31. The method of claim 1 , wherein the salt is added in a quantity of from 0.5 to 1.5% by weight based on the total weight of the dispersion.

32. The method of claim 1 , wherein the water-soluble acid is at least one selected from the group consisting of an organic carboxylic acid, sulfonic acid, phosphonic acid and a mineral acid.

33. The method of claim 1 , wherein the water-soluble acid is at least one selected from the group consisting of acetic acid, propionic acid, citric acid, oxalic acid, succinic acid, malonic acid, adipic acid, fumaric acid, maleic acid, and benzoic acid.

34. The method of claim 1 , wherein the carboxylic acid is at least one selected from the group consisting of citric acid, adipic acid and benzoic acid.

35. The method of claim 8 , wherein the salt is a salt of at least one selected from the group consisting of an organic carboxylic acid, a sulphonic acid, a phosphonic acid, and a mineral acid.

36. The method of claim 10 , wherein the water-soluble salt is at least one selected from the group consisting of acetic acid, propionic acid, citric acid, oxalic acid, succinic acid, malonic acid, adipic acid, fumaric acid, maleic acid, benzoic acid, sulphuric acid, hydrochloric acid and phosphoric acid.

37. The method of claim 11 , wherein the polymeric dispersant B is a water-soluble polymer having a maximum M w of from 50,000 to 1.2×10 6 g/mol and may be present as a mixture with one or more of a polyfunctional alcohol and a conversion product of a polyfunctional alcohol with a fatty amine.

38. The method of claim 13 , wherein the dispersant B is a cationic polymer comprising at least 50% by weight of a cationic monomer.

39. The method of claim 13 , wherein the polymeric dispersant B is a cationic polymer consisting of a cationic monomer.

40. The method of claim 1 , wherein the cationic monomer is at least one selected from the group consisting of a methyl chloride quaternised ammonium salt of dimethylaminoethyl(meth)acrylate, dimethylaminopropyl(meth)acrylate and dimethylaminopropyl(meth)acrylamide.

41. The method of claim 1 , wherein the cationic monomer is a diallyl dimethylammonium chloride.

42. The method of claim 13 , wherein the polyfunctional alcohol is a polyethylene glycol.

43. The method of claim 1 , wherein the polymeric dispersant B and a polyfunctional alcohol are added in a quantity of from 10 to 20% by weight based on the total weight of the dispersion.

44. The method of claim 19 , wherein the weight ratio of the polymeric dispersant B to the polyfunctional alcohol is 1:0.01 to 0.3.

45. The method of claim 1 , wherein the polymer A comprises one or more water-soluble monomers.

46. The method of claim 1 , wherein Y 0 and Y 1 are substituted with one or more hydroxy groups.

47. The method of claim 1 , wherein the polymer A comprises from 20 to 80% by weight of one or more cationic monomers.

48. The method of claim 1 , wherein the polymer A is present in a quantity of from 10 to 50% by weight based on the total weight of the dispersion.

49. The water-in-water polymer dispersion of claim 28 , further comprising one or more biologically effective substances.

50. A method for making a water-in-water polymer dispersion comprising a polymer A and at least one polymeric dispersant B, the method comprising:

a) dispersing one or more monomers in an aqueous phase comprising the polymeric dispersant, wherein said monomers consist of one or more of monomers (i), (ii), and (iii):

(i) a non-ionic monomer of formula (I)

where

R 1 is a hydrogen or a methyl residue, and

R 2 and R 2 are, independently of each other, hydrogen, an alkyl or a hydroxyalkyl residue with 1 to 5 C atoms;

(ii) a cationic monomer of formula (II)

where

R 1 is a hydrogen or a methyl residue,

Z 1 is O, NH or NR 4 wherein R 4 is an alkyl residue with 1 to 4 C atoms, and

Y is one of

wherein Y 0 and Y 1 are an alkylene residue optionally substituted with hydroxy groups, with 2 to 6 C atoms,

Y 2 , Y 3 , Y 4 , Y 5 , Y 6 , Y 7 , independently of each other, are each an alkyl residue with 1 to 6 C atoms; and

Z − is a halogen, acetate, or SO 4 CH 3 − ; and

(iii) an amphiphilic monomer of formula (III) or (IV)

where

Z 1 is O, NH, NR 4 wherein R 4 is an alkyl residue with 1 to 4 carbon atoms,

R 1 is a hydrogen or a methyl residue,

R 8 is an alkylene residue with 1 to 6 carbon atoms,

R 5 and R 6 are, independently of each other, an alkyl residue with 1 to 6 carbon atoms,

R 7 is an alkyl residue with 8 to 32 carbon atoms, and

Z − is a halogen, pseudo-halogen, SO 4 CH 3 or acetate, or

where

Z 1 is O, NH, NR 4 wherein R 4 is an alkyl residue with 1 to 4 carbon atoms,

R 1 is a hydrogen or a methyl residue,

R 10 is a hydrogen, an alkyl, aryl and/or aralkyl residue with 8 to 32 carbon atoms,

R 9 is an alkylene residue with 2 to 6 carbon atoms, and

n is an integer between 1 and 50,

b) adding a water-soluble salt;

c) polymerizing the monomers in the aqueous phase formed in b) by radical polymerization to form a mixture of a water-soluble or water-swellable polymer A and the polymeric dispersant B; then

d) adding a water-soluble acid to the mixture to form the water-in-water dispersion;

wherein the polymeric dispersant B is a cationic polymer comprising at least 30% by weight of polymerized cationic monomer, and

the water-soluble acid is added to the mixture in an amount of from 0.1 to 0.5% by weight based on the total weight of the dispersion.

Assignments (20)
TERM LOAN PATENT SECURITY AGREEMENT Recorded Nov 10, 2021
From: INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: GOLDMAN SACHS BANK USA
Reel/Frame 058102/0407 →
NOTES SECURITY AGREEMENT Recorded Nov 10, 2021
From: INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 058103/0066 →
ABL PATENT SECURITY AGREEMENT Recorded Nov 10, 2021
From: INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: BANK OF AMERICA, N.A.
Reel/Frame 058102/0122 →
RELEASE OF SECURITY INTEREST Recorded Nov 10, 2021
From: CITIBANK, N.A.
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 058848/0636 →
RELEASE OF SECURITY INTEREST Recorded Nov 10, 2021
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 058856/0724 →
INTELLECTUAL PROPERTY SECOND LIEN SECURITY AGREEMENT RELEASE Recorded Jul 20, 2018
From: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 047058/0800 →
FIRST LIEN NOTICE AND CONFIRMATION OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Jul 20, 2018
From: SOLENIS TECHNOLOGIES, L.P.
To: CITIBANK, N.A., COLLATERAL AGENT
Reel/Frame 046595/0241 →
SECOND LIEN NOTICE AND CONFIRMATION OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Jul 20, 2018
From: SOLENIS TECHNOLOGIES, L.P.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 046629/0213 →
INTELLECTUAL PROPERTY FIRST LIEN SECURITY AGREEMENT RELEASE Recorded Jul 20, 2018
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 046594/0252 →
NOTICE AND CONFIRMATION OF GRANT OF SECURITY INTEREST IN PATENTS (FIRST LIEN) Recorded Aug 14, 2014
From: SOLENIS TECHNOLOGIES, L.P.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH, AS COLLATERAL AGENT
Reel/Frame 033535/0806 →
NOTICE AND CONFIRMATION OF GRANT OF SECURITY INTEREST IN PATENTS (SECOND LIEN) Recorded Aug 14, 2014
From: SOLENIS TECHNOLOGIES, L.P.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 033535/0847 →
U.S. ASSIGNMENT OF PATENTS Recorded Aug 4, 2014
From: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 033471/0048 →
RELEASE OF PATENT SECURITY AGREEMENT Recorded Mar 18, 2013
From: THE BANK OF NOVA SCOTIA
To: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC; AQUALON COMPANY; ISP INVESTMENTS INC.; HERCULES INCORPORATED
Reel/Frame 030025/0320 →
SECURITY AGREEMENT Recorded Sep 16, 2011
From: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC; HERCULES INCORPORATED; AQUALON COMPANY; ISP INVESTMENT INC.
To: THE BANK OF NOVA SCOTIA, AS ADMINISTRATIVE AGENT
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RELEASE OF PATENT SECURITY AGREEMENT Recorded Sep 15, 2011
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To: ASHLAND, INC.; ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC; AQUALON COMPANY; HERCULES INCORPORATED
Reel/Frame 026927/0247 →
SECURITY AGREEMENT Recorded Apr 14, 2010
From: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC; AQUALON COMPANY; HERCULES INCORPORATED
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024225/0289 →
RELEASE OF SECURITY INTEREST Recorded Apr 13, 2010
From: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
To: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC; AQUALON COMPANY; HERCULES INCORPORATED
Reel/Frame 024218/0928 →
SECURITY AGREEMENT Recorded Dec 3, 2008
From: ASHLAND LICENSING AND INTELLECTUAL PROPERTY...; AQUALON COMPANY; HERCULES INCORPORATED
To: BANK OF AMERICA, N.A. AS ADMINISTRATIVE AGENT
Reel/Frame 021924/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 5, 2006
From: STOCKHAUSEN GMBH
To: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC
Reel/Frame 017870/0643 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2003
From: FISCHER, ULRICH; SCHROERS, OTTO; WOEBEL, WOLFGANG
To: STOCKHAUSEN GMBH & CO. KG
Reel/Frame 014721/0313 →