Process for the preparation of microcapsules

Patent metadata

Field	Value
Publication number	US-12220677-B2
Application number	US-201917430943-A
Country	US
Kind code	B2
Filing date	Feb 13, 2019
Priority date	Feb 13, 2019
Publication date	Feb 11, 2025
Grant date	Feb 11, 2025

Abstract

The present invention relates to a process for the preparation of microcapsules, in particular isocyanate-based microcapsules with improved stability to carboxylic acid and aldehyde-containing active ingredients as core material. In addition, the present invention relates to microcapsules obtainable by the process according to the invention. In addition, the present invention relates to microcapsules, suspensions of such microcapsules, and the use of the microcapsules and suspensions as a component in detergents, fabric softeners, cleaning products, scent boosters (fragrance enhancers) in liquid or solid form, cosmetics, personal care products, agricultural products, or pharmaceutical products.

First claim

The invention claimed is:

1. A process for preparing isocyanate-based microcapsules comprising:
(a) providing an internal non-aqueous phase comprising at least one isocyanate having two or more isocyanate groups or at least one isothiocyanate having two or more isothiocyanate groups and a hydrophobic agent to be encapsulated;
(b) providing an external aqueous phase comprising at least one protective colloid and a catalyst;
(c) mixing the internal non-aqueous phase and the external aqueous phase, optionally in the presence of a stabilizer and/or an emulsifier, to obtain an oil-in-water emulsion;
(d) a first crosslinking by addition to the composition of step (c) of an amine reacting at an acidic pH;
(e) further crosslinking by addition to the composition of step (d) of an amine reacting at an alkaline pH to obtain microcapsules;
(f) curing the microcapsules obtained in step (e); and
optionally:
(g) separating the microcapsules from the reaction solution and further optionally drying of the microcapsules.

2. The process according to claim 1 , wherein the isocyanate having two or more isocyanate groups or the isothiocyanate having two or more isothiocyanate groups is selected from the group consisting of aliphatic, cycloaliphatic, hydroaromatic, aromatic or heterocyclic polyisocyanates or polyisothiocyanates, their substitution products and mixtures of the aforementioned compounds.

3. The process according to claim 1 , wherein the hydrophobic agent to be encapsulated is selected from one or more in the group of fragrances, aromatic substances, biocides, insecticides, a substance from the group of repellents, food additives, cosmetic active ingredients, pharmaceutical active ingredients, agrochemicals, dyes, luminous dyes, optical brighteners, solvents, waxes, silicone oils, lubricants.

4. The process of claim 1 , wherein the hydrophobic agent to be encapsulated is selected from one or more in the group of fragrances or flavoring agents having aldehyde, carboxylic acid or ester functionality.

5. The process according to claim 1 , wherein the at least one protective colloid is selected from one or more in the group of diols, ethanediol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, isomeric butanediol, 1,2-pentanediol, 1,2-hexanediol, 1,2-octanediol, 1,2-decanediol, 1,2-dodecanediol, polyols, triols, glycerol, ethoxylation products of glycerol, propoxylation products of glycerol, trimethylolpropane, ethoxylation products of trimethylolpropane, propoxylation products of trimethylolpropane, polyvinyl alcohol (PVOH), derivatives of PVOH, ammonium- or sulfonate-functionalized polyvinyl alcohols, polyphenols, 1,3,5-trihydroxybenzene, starch, chemically, mechanically and/or enzymatically modified starch, carboxymethylcellulose, and polyvinylpyrrolidone.

6. The process claim 1 , wherein the at least one protective colloid is used in combination with starch.

7. The process of claim 1 , wherein the catalyst is diazobicyclo[2.2.2]octane.

8. The process of claim 1 , wherein the first crosslinking by the amine reacting at an acidic pH occurs at a pH in a range of 2 to 7 and optionally at a temperature in a range of 20° C. to 30° C.

9. The process of claim 1 , wherein the amine reacting at an acidic pH is selected from one or more in the group of acidic amino acid hydrochlorides, lysine hydrochloride, and ornithine hydrochloride.

10. The process according to claim 1 , wherein the further crosslinking by the amine reacting at an alkaline pH is carried out at a pH in a range of 7 to 14 and optionally at a temperature in a range of 35° C. to 50° C.

11. The process of claim 1 , wherein the amine reacting at an alkaline pH is selected from one or more in the group of the di-, tri- and polyamines and guanidinium carbonate.

12. The process of claim 1 , wherein the curing of the microcapsules in step (f) is carried out at a temperature up to 70° C.

13. Microcapsules obtained according to claim 1 .

14. Isocyanate-based microcapsules comprising:
a core comprising at least one hydrophobic agent; and
a capsule shell comprising an isocyanate having two or more isocyanate groups which is crosslinked in the presence of a protective colloid and a catalyst in a first step by an amine reacting at an acidic pH and in a further step by an amine reacting at an alkaline pH.

15. The isocyanate-based microcapsules of claim 14 , wherein the capsule shell comprises: a first layer of polyurethane; and a second layer of polyurea.

16. A method of using the microcapsules according to claim 15 for the manufacture of one or more products in the group of detergents, fabric softeners, cleaning agents, scent boosters in liquid or solid form, cosmetics, personal care products, agricultural products, and pharmaceutical products.

17. The method of claim 16 , wherein the microcapsules are in suspension form.

18. The microcapsules of claim 14 , consisting of the core comprising at least one hydrophobic agent; and the capsule shell comprising an isocyanate having two or more isocyanate groups which is crosslinked in the presence of a protective colloid and a catalyst in a first step by an amine reacting at an acidic pH and in a further step by an amine reacting at an alkaline pH.

19. The microcapsules of claim 18 , wherein the capsule shell consists of a first layer of polyurethane and a second layer of polyurea.

20. The microcapsules of claim 15 , wherein the capsule shell consists of a first layer of polyurethane and a second layer of polyurea.

Assignees

• Symrise Ag

Inventors

• Georgi Julian Alexander
• Rost Benjamin
• Dröge Diane
• Bertram Ralf
• Böddeker Thorsten

Classifications

• C11D2111/12

  Soft surfaces, e.g. textile · CPC title

• C11D3/505

  encapsulated or adsorbed on a carrier, e.g. zeolite or clay · CPC title

• C11D3/001

  Softening compositions · CPC title

• B01J13/206

  Hardening; drying · CPC title

• A61K9/5089

  Processes · CPC title