IP Library Granted Patent US 11,634,664
Granted Patent B2
US 11,634,664 · App. 17/754,891 · Granted Apr 25, 2023

Method for preparing an inverse emulsion comprising two cationic polymers

Inventors: Céline Besset (Andrezieux Boutheon, FR); Frédéric Blondel (Andrezieux Boutheon, FR)
Assignee: SNF GROUP
C11D3/3773A61K8/064A61K8/8182C11D3/0015C11D3/3796C11D11/0017C11D17/0017
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 11,634,664
App. No.
17/754,891
Granted
Apr 25, 2023
Kind
B2
Abstract

This invention relates to a process for preparing an inverse emulsion comprising mixing an aqueous solution comprising a water-soluble (co)polymer A synthesized from at least one cationic monomer and an inverse EMI 2 emulsion comprising a water-soluble (co)polymer B synthesized from at least one cationic monomer, optionally followed by distillation. This invention also relates to the inverse emulsion thus obtained, a detergent or cosmetic or softening composition comprising such an inverse emulsion, as well as the use of such an inverse emulsion to improve the softening properties of a fabric softening composition.

Claims (28)

1. A process for preparing an inverse EMI 1 emulsion comprising the following step:

forming an inverse EMI 1 emulsion by mixing an aqueous solution of water-soluble (co)polymer A of at least one cationic monomer and an inverse EMI 2 emulsion of water-soluble (co)polymer B of at least one cationic monomer.

2. The process for the preparation of an inverse emulsion according to claim 1 , wherein water-soluble (co)polymers A and B are synthetic (co)polymers obtained, independently of each other, from at least one cationic monomer and at least one non-ionic monomer and/or of at least one anionic monomer.

3. The process for the preparation of an inverse emulsion according to claim 1 , wherein water-soluble (co)polymers A and B are, independently of each other, synthetic (co)polymers of at least one cationic monomer selected from quaternized dimethylaminoethyl acrylate (ADAME), quaternized dimethylaminoethyl methacrylate (MADAME), dimethyldiallylammonium chloride (DADMAC), acrylamido propyltrimethyl ammonium chloride (APTAC), methacrylamido propyltrimethyl ammonium chloride (MAPTAC), and mixtures thereof.

4. The process for the preparation of an inverse emulsion according to claim 1 , wherein water-soluble (co)polymer A and water-soluble (co)polymer B are, independently of each other, (co)polymers:

of at least one cationic monomer, and

of at least one non-ionic monomer and/or at least one anionic monomer, the non-ionic monomer being chosen from acrylamide, methacrylamide, N-isopropylacrylamide, N,N-dimethylacrylamide and N-methylolacrylamide, N-vinylformamide, N-vinyl acetamide, N-vinylpyridine and N-vinylpyrrolidone, acryloyl morpholine (ACMO), diacetone acrylamide, and mixtures thereof.

5. The process for the preparation of an inverse emulsion according to claim 1 , wherein water-soluble (co)polymer A and water-soluble (co)polymer B are, independently of each other, (co)polymers:

of at least one cationic monomer, and

of at least one anionic monomer and/or at least one non-ionic monomer the anionic monomer chosen from acrylic acid, methacrylic acid, itaconic acid, maleic acid, 2-acrylamido-2-methylpropane sulfonic acid (ATBS), vinylsulfonic acid, vinylphosphonic acid and mixtures thereof, said anionic monomer being non-salified, partially or totally salified, and the salts of 3-sulfopropyl methacrylate.

6. The process for the preparation of an inverse emulsion according to claim 1 , wherein water-soluble (co)polymer A is a water-soluble (co)polymer synthesized from at least one cationic monomer and from at least one anionic monomer, water-soluble (co)polymer A having an overall cationic charge.

7. The process for the preparation of an inverse emulsion according to claim 1 , wherein water-soluble (co)polymer B is a cross-linked water-soluble (co)polymer.

8. The process for the preparation of an inverse emulsion according to claim 1 , wherein the inverse EMI 1 emulsion comprises a total concentration of water-soluble (co)polymers A and B of between 5 and 50% weight relative to the total weight of the inverse EMI 1 emulsion.

9. The process for the preparation of an inverse emulsion according to claim 1 , wherein the process comprises a subsequent step of forming an inverse EMI 3 emulsion by distillation of the inverse EMI 1 emulsion.

10. The process for the preparation of an inverse emulsion according to claim 1 , wherein the process comprises a subsequent step of forming an inverse EMI 3 emulsion by distillation of the inverse EMI 1 emulsion, the inverse EMI 3 emulsion with a total concentration of water-soluble (co)polymers A and B of between 20 and 80% by weight relative to the total weight of the inverse EMI 3 emulsion.

11. The process for the preparation of an inverse emulsion according to claim 1 , wherein the process comprises a subsequent step of forming an inverse EMI 3 emulsion by distillation of the inverse EMI 1 emulsion, the inverse EMI 3 emulsion having a total concentration of water-soluble (co)polymers A and B of between 35 and 60% by weight relative to the total weight of the inverse EMI 3 emulsion.

12. The process for the preparation of an inverse emulsion according to claim 11 , wherein the inverse EMI 1 or EMI 3 emulsion has a mass ratio between the water-soluble (co)polymer B and water-soluble (co)polymer A between 1 and 100.

13. The process for the preparation of an inverse emulsion according to claim 6 , wherein water-soluble (co)polymer B is a cross-linked water-soluble (co)polymer.

14. The process for the preparation of an inverse emulsion according to claim 2 , wherein:

the at least one cationic monomer is selected from quaternized dimethylaminoethyl acrylate (ADAME), quaternized dimethylaminoethyl methacrylate (MADAME), dimethyldiallylammonium chloride (DADMAC), acrylamido propyltrimethyl ammonium chloride (APTAC), methacrylamido propyltrimethyl ammonium chloride (MAPTAC), and mixtures thereof;

the at least one non-ionic monomer is selected from acrylamide, methacrylamide, N-isopropylacrylamide, N,N-dimethylacrylamide and N-methylolacrylamide, N-vinylformamide, N-vinyl acetamide, N-vinylpyridine and N-vinylpyrrolidone, acryloyl morpholine (ACMO), diacetone acrylamide, and mixtures thereof; and

the at least one anionic monomer is selected from acrylic acid, methacrylic acid, itaconic acid, maleic acid, 2-acrylamido-2-methylpropane sulfonic acid (ATBS), vinylsulfonic acid, vinylphosphonic acid and mixtures thereof, said anionic monomer being non-salified, partially or totally salified, and the salts of 3-sulfopropyl methacrylate.

15. The process for the preparation of an inverse emulsion according to claim 14 , wherein water-soluble (co)polymer A is a water-soluble (co)polymer synthesized from at least one cationic monomer and from at least one anionic monomer, water-soluble (co)polymer A having an overall cationic charge.

16. The process for the preparation of an inverse emulsion according to claim 5 , wherein water-soluble (co)polymer B is a cross-linked water-soluble (co)polymer.

17. The process for the preparation of an inverse emulsion according to claim 16 , wherein:

the inverse EMI 1 emulsion comprises a total concentration of water-soluble (co)polymers A and B of between 5 and 50% weight relative to the total weight of the inverse EMI 1 emulsion;

the process comprises a subsequent step of forming an inverse EMI 3 emulsion by distillation of the inverse EMI 1 emulsion, the inverse EMI 3 emulsion with a total concentration of water-soluble (co)polymers A and B of between 35 and 60% by weight relative to the total weight of the inverse EMI 3 emulsion; and

the inverse EMI 1 or EMI 3 emulsion has a mass ratio between the water-soluble (co)polymer B and water-soluble (co)polymer A between 5 and 14.

Assignments (2)
CHANGE OF NAME Recorded Mar 8, 2023
From: SPCM SA
To: SNF GROUP
Reel/Frame 062923/0199 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2022
From: BESSET, CÉLINE; BLONDEL, FRÉDÉRIC
To: SPCM SA
Reel/Frame 059605/0736 →
Priority Claims (1)
FR 1912918 · Nov 19, 2019 · national
Continuity (1)
Related Publication 20220348847A1 · Nov 3, 2022