IP Library Granted Patent US 8,609,757
Granted Patent B2
US 8,609,757 · App. 13/399,300 · Granted Dec 17, 2013

Cationic cross-linked polymers in water-in-water polymer dispersions

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Quick Facts
Patent No.
US 8,609,757
App. No.
13/399,300
Granted
Dec 17, 2013
Kind
B2
Abstract

The invention relates to water-in-water polymer dispersions containing cross-linked cationic polymers, methods for their preparation and their use. The water-in-water polymer dispersions are useful inter alia as flocculants, dewatering (drainage) aids and retention aids in papermaking.

Claims (73)

1. A method for manufacturing a water-in-water polymer dispersion, the method comprising:

free radical polymerizing an aqueous reaction mixture comprising

(i) a cationic polymeric dispersant, and

(ii) a monomer composition comprising

(ii-a) at least 5 wt.-% of a non-ionic monomer of formula (I)

wherein

R 1 means hydrogen or C 1 -C 3 -alkyl, and

R 2 and R 3 mean, independently of each other, hydrogen, C 1 -C 5 -alkyl or C 1 -C 5 -hydroxyalkyl,

based on a total weight of monomers;

(ii-b) at least 5 wt.-% of a cationic monomer according to general formula (II)

wherein

R 4 means hydrogen or C 1 -C 3 -alkyl,

Z 1 means O or NR 5 with R 5 being hydrogen or C 1 -C 3 -alkyl,

Y 0 means C 2 -C 6 -alkylene, optionally substituted with one or more hydroxy groups,

Y 1 , Y 2 , Y 3 , independently of each other, mean C 1 -C 6 -alkyl, and

X − means halogen, pseudo-halogen, acetate, or SO 4 CH 3 − ,

based on the total weight of monomers;

(ii-c) 0.0001 to 1.25 wt.-% of one or more cross-linkers, based on the total weight of monomers;

(ii-d) 0 to 1.25 wt.-% of one or more hydrophobic (meth)acrylic acid C 4-18 -alkyl esters, based on the total weight of monomers; and

(ii-e) optionally, a further ethylenically unsaturated monomer,

before, after, or before and after the free radical polymerizing, adding a water-soluble salt in a quantity of 0.1 to 5.0 wt.-%, based on a total weight of the aqueous reaction mixture, to the aqueous reaction mixture, to obtain a water-in-water polymer dispersion such that the water-in-water polymer dispersion comprises a cross-linked cationic copolymer.

2. The method of claim 1 , wherein the aqueous reaction mixture does not comprise any hydrophobic monomers.

3. The method of claim 1 , wherein the cross-linker comprises 2, 3, 4, or 5 ethylenically unsaturated groups.

4. The method of claim 1 , wherein the non-ionic monomer of formula (I) is selected from the group consisting of (meth)acrylamide, N-methyl(meth)acrylamide, N-isopropyl(meth)acrylamide, N,N-dimethyl(meth)-acrylamide, N,N-diethyl(meth)acrylamide, N-methyl-N-ethyl(meth)acrylamide, and N-hydroxyethyl(meth)acrylamide.

5. The method of claim 1 , wherein the cationic monomer of formula (II) is selected from the group consisting of a trimethylammoniumalkyl(meth)acrylate halide, a trimethylammoniumalkyl(meth)acrylamide halide, and a diallyldialkylammonium halide.

6. The method of claim 1 , wherein the cationic polymeric dispersant is a water-soluble polymer having a weight average molecular weight M w of at most 2.0×10 6 g/mol.

7. The method of claim 1 , wherein the cationic polymeric dispersant is a cationic polymer derived from at least one second cationic monomer selected from the group consisting of a trimethylammoniumalkyl(meth)acrylate halide, a trimethylammoniumalkyl(meth)acrylamide halide, and a diallyldialkylammonium halide.

8. The method of claim 7 , wherein the at least one second cationic monomer differs from the cationic monomer of formula (II).

9. A water-in-water polymer dispersion, comprising:

(i) a cationic polymeric dispersant; and

(ii) a cross-linked cationic copolymer derived from a monomer composition comprising

(ii-a) at least 5 wt.-% of a non-ionic monomer of formula (I)

wherein

R 1 means hydrogen or C 1 -C 3 -alkyl, and

R 2 and R 3 mean, independently of each other, hydrogen, C 1 -C 5 -alkyl, or C 1 -C 5 -hydroxyalkyl,

based on a total weight of monomers;

(ii-b) at least 5 wt.-% of a cationic monomer of formula (II)

wherein

R 4 means hydrogen or C 1 -C 3 -alkyl,

Z 1 means O or NR 5 with R 5 being hydrogen or C 1 -C 3 -alkyl,

Y 0 means C 2 -C 6 -alkylene, optionally substituted with one or more hydroxy groups,

Y 1 , Y 2 , Y 3 , independently of each other, mean C 1 -C 6 -alkyl, and

X − means halogen, pseudo-halogen, acetate, or SO 4 CH 3 − ,

based on the total weight of monomers;

(ii-c) 0.0001 to 1.25 wt.-% of one or more cross-linkers, based on the total weight of monomers;

(ii-d) 0 to 1.25 wt.-% of one or more hydrophobic (meth)acrylic acid C 4-18 -alkyl esters, based on the total weight of monomers;

(ii-e) optionally, a further ethylenically unsaturated monomer, and

(iii) 0.1 to 5.0 wt.-% of at least one selected from the group consisting of an acid and a salt, wherein an overall content of the acid and the salt amounts to a maximum of 5.0 wt.-%, based on a total weight of the dispersion, wherein the salt is present in an amount of from 0.1 wt.-% to 5.0 wt.-%.

10. The dispersion of claim 9 , obtained free radical polymerizing the monomer composition in the presence of (i) the cationic polymeric dispersant.

11. The dispersion of claim 9 , which has a polymer content of 40±20 based on a total weight of the dispersion.

12. The dispersion of claim 9 , where a relative weight ratio of cross-linked cationic copolymer to cationic polymeric dispersant is >1:1.

13. A flocculant,

a thickener,

a contaminant control,

a dry strength aid,

a retention agent, or drainage aid, comprising the dispersion of claim 9 .

14. The method of claim 2 , wherein the cross-linker comprises 2, 3, 4, or 5 ethylenically unsaturated groups.

15. The method of claim 1 , wherein the non-ionic monomer of formula (I) is (meth)acrylamide.

16. The method of claim 1 , wherein the non-ionic monomer of formula (I) is N-methyl(meth)acrylamide.

17. The method of claim 1 , wherein the non-ionic monomer of formula (I) is N-isopropyl(meth)acrylamide.

18. The method of claim 1 , wherein the non-ionic monomer of formula (I) is N,N-dimethyl(meth)-acrylamide.

19. The method of claim 1 , wherein the water-soluble salt is a salt of an inorganic acid.

20. The method of claim 1 , wherein the water-soluble salt is a salt of a saturated aliphatic organic acid.

21. The method of claim 1 , wherein the water-soluble salt is at least one selected from the group consisting of sodium chloride, ammonium sulfate and sodium sulfate.

22. The dispersion of claim 9 , wherein the water-soluble salt is a salt of an inorganic acid.

23. The dispersion of claim 9 , wherein the water-soluble salt is a salt of a saturated aliphatic organic acid.

24. The dispersion of claim 9 , wherein the water-soluble salt is at least one selected from the group consisting of sodium chloride, ammonium sulfate and sodium sulfate.

25. The dispersion of claim 9 , wherein the water-soluble salt is at least one salt of an organic acid selected from the group consisting of acetic acid, propionic acid, citric acid, oxalic acid, succinic acid, and malonic acid.

26. The dispersion of claim 9 , wherein the water-soluble salt is at least one of an ammonium, sodium, potassium, calcium or magnesium salt of at least one of sulfonic acid, phosphonic acid and a mineral acid.

27. The method of claim 1 , wherein the water-in-water polymer dispersion comprises an interpenetrating complex in which a cross-linked cationic copolymer formed by the free radical polymerizing is intercalated in the cationic polymeric dispersant.

28. The water-in-water polymer dispersion of claim 9 , wherein the cross-linked cationic copolymer is intercalated with the cationic polymeric dispersant to form an interpenetrating complex.

29. The method of claim 1 , wherein the water-soluble salt is at least one salt of an organic acid selected from the group consisting of acetic acid, propionic acid, citric acid, oxalic acid, succinic acid, and malonic acid.

30. The method of claim 1 , wherein the water-soluble salt is at least one of an ammonium, sodium, potassium, calcium or magnesium salt of at least one of sulfonic acid, phosphonic acid and a mineral acid.

Assignments (20)
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0838 →
RELEASE OF SECURITY INTEREST Recorded Nov 14, 2025
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
To: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 073564/0864 →
SECURITY AGREEMENT (NOTES) Recorded Oct 10, 2025
From: DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073061/0885 →
RELEASE OF 2023 NOTES PATENT SECURITY INTERESTS Recorded Oct 10, 2025
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
To: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 073074/0198 →
SECURITY AGREEMENT (2024 NOTES) Recorded Jun 24, 2024
From: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 067824/0278 →
2023 NOTES PATENT SECURITY AGREEMENT Recorded Jul 7, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE GLOBAL CORPORATION
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 064225/0170 →
SECURITY AGREEMENT (NOTES) Recorded Sep 14, 2022
From: SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A. AS COLLATERAL AGENT
Reel/Frame 061432/0821 →
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 →
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 →
RELEASE OF SECURITY INTEREST Recorded Nov 10, 2021
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 058856/0724 →
RELEASE OF SECURITY INTEREST Recorded Nov 10, 2021
From: CITIBANK, N.A.
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 058848/0636 →
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 →
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 →
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 →
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 →
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 →
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 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 23, 2012
From: BROECHER, MARKUS; KANTO OEQVIST, CHARLOTTA; SIEVERLING, NATHALIE; BOEKELO, CHRISTIAN
To: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC
Reel/Frame 028090/0460 →