Use of an ampholyte copolymer as colloidal stabilizer

Patent metadata

Field	Value
Publication number	US-10406498-B2
Application number	US-201615737601-A
Country	US
Kind code	B2
Filing date	Jun 22, 2016
Priority date	Jun 22, 2015
Publication date	Sep 10, 2019
Grant date	Sep 10, 2019

Abstract

The invention relates to the use of an ampholyte copolymer as a colloidal stabilizer in the preparation of aminoplast core-shell microcapsules containing an active material, wherein the ampholyte copolymer comprises:
2 to 99 mol % of cationic monomer having at least one quaternary ammonium group, 1 to 98 mol % of acrylic based monomer, 0 to 97 mol % of non-ionic monomer,

and wherein the ampholyte copolymer has more cationic charges than anionic charges, wherein the cationic charges of the ampholyte copolymer are exclusively due to the at least one quaternary ammonium group of the cationic monomer.

First claim

The invention claimed is:

1. A method of preparing aminoplast core-shell microcapsules containing an active material, the method comprising using an ampholyte copolymer as a colloidal stabilizer, wherein the ampholyte copolymer comprises:
2 to 99 mol % of cationic monomer having at least one quaternary ammonium group,
1 to 98 mol % of acrylic based monomer,
0 to 97 mol % of non-ionic monomer,

and wherein the ampholyte copolymer has more cationic charges than anionic charges, wherein the cationic charges of the ampholyte copolymer are exclusively due to the at least one quaternary ammonium group of the cationic monomer.

2. The method according to claim 1 , wherein the cationic monomer is chosen from the group consisting of quaternized dimethylaminoethyl acrylate (ADAME), quaternized dimethylaminoethyl methacrylate (MADAME), dimethyldiallylammonium chloride (DADMAC), acrylamidopropyltrimethylammonium chloride (APTAC) and methacrylamidopropyltrimethylammonium chloride (MAPTAC).

3. The method according to claim 1 , wherein the cationic monomer is methacrylamidopropyltrimethylammonium chloride (MAPTAC).

4. The method according to claim 1 , wherein the acrylic based monomer is chosen from the group consisting of acrylic acid, methacrylic acid, itaconic acid, crotonic acid, maleic acid, fumaric acid, 2-acrylamido-2-methylpropane sulfonic acid, vinylsulfonic acid, vinylphosphonic acid, allylsulfonic acid, allylphosphonic acid, styrene sulfonic acid, and their water-soluble salts of an alkali metal, alkaline-earth metal or ammonium.

5. The method according to claim 1 , wherein the acrylic based monomer is (meth)acrylic acid or a water soluble salt thereof.

6. The method according to claim 1 , wherein the non-ionic monomer is chosen from the group consisting of acrylamide, methacrylamide, N-isopropylacrylamide, N N-dimethylacrylamide, N-methylolacrylamide, N-vinylformamide, N-vinyl acetamide, N-vinylpyridine and N-vinylpyrrolidone.

7. The method according to claim 1 , wherein the non-ionic monomer is acrylamide.

8. The method according to claim 1 , wherein the ampholyte copolymer comprises 30 to 95 mol % of cationic monomer.

9. The method according to claim 1 , wherein the ampholyte copolymer comprises 60 to 90 mol % of cationic monomer.

10. The method according to claim 1 , wherein the ampholyte copolymer comprises 5 to 70 mol % of acrylic based monomer.

11. The method according to claim 1 , wherein the ampholyte copolymer comprises 10 to 40 mol % of acrylic based monomer.

12. The method according to claim 1 , wherein the ampholyte copolymer comprises:
30 to 95 mol % of methacrylamidopropyltrimethylammonium chloride (MAPTAC) %;
5 to 70 mol % of acrylic acid or a water soluble salt thereof; and
0 to 80 mol % of acrylamide.

13. The method according to claim 1 , wherein the ampholyte copolymer has a molecular weight of at least 100,000 g/mol.

14. The method according to claim 1 , wherein the ampholyte copolymer has a molecular weight of at least 500,000 g/mol.

15. The method according to claim 1 , wherein the ampholyte copolymer is linear, branched, star-shaped, or comb-shaped.

16. The method according to claim 2 , wherein the acrylic based monomer is chosen from the group consisting of acrylic acid, methacrylic acid, itaconic acid, crotonic acid, maleic acid, fumaric acid, 2-acrylamido-2-methylpropane sulfonic acid, vinyl sulfonic acid, vinylphosphonic acid, allylsulfonic acid, allylphosphonic acid, styrene sulfonic acid, and their water-soluble salts of an alkali metal, alkaline-earth metal or ammonium.

17. The method according to claim 2 , wherein the acrylic based monomer is (meth)acrylic acid or a water soluble salt thereof.

18. The method according to claim 2 , wherein the non-ionic monomer is chosen from the group consisting of acrylamide, methacrylamide, N-isopropylacrylamide, N N-dimethylacrylamide, N-methylolacrylamide, N-vinylformamide, N-vinyl acetamide, N-vinylpyridine and N-vinylpyrrolidone.

19. The method according to claim 16 , wherein the non-ionic monomer is chosen from the group consisting of acrylamide, methacrylamide, N-isopropylacrylamide, N N-dimethylacrylamide, N-methylolacrylamide, N-vinylformamide, N-vinyl acetamide, N-vinylpyridine and N-vinylpyrrolidone.

20. The method according claim 1 , wherein the ampholyte copolymer comprises:
60 to 90 mol % of methacrylamidopropyltrimethylammonium chloride (MAPTAC);
10 to 40 mol % of acrylic acid or a water soluble salt thereof; and
0 to 50 mol % of acrylamide.

Assignees

• Spcm Sa

Inventors

• Blondel Frédéric
• Jeanson Guillaume
• Harrison Ian
• Aussant Emmanuel

Classifications

• C11D3/3796

  Amphoteric polymers or zwitterionic polymers · CPC title

• A61Q13/00

  Formulations or additives for perfume preparations (essential oils or perfumes per se C11B9/00) · CPC title

• A61K2800/5428

  amphoteric or zwitterionic · CPC title

• A61K8/8158

  Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers · CPC title

• C11D17/0039

  Coated compositions or coated components in the compositions, (micro)capsules · CPC title