Microcapsules with functional reactive groups for binding to fibres and process of application and fixation

• US 8,404,345 B2
• Filed: 02/27/2006
• Issued: 03/26/2013
• Est. Priority Date: 04/22/2005
• Status: Active Grant

• Current Assignee: Devan Micropolis, S.A.
• Original Assignee: Devan Micropolis, S.A.
• Inventors: Magalhaes Vaz Vieira, Raquel Maria, Pinto Cerqueira Barros, Sandra Maria, Naylor Rocha Gomes, Jamie Isidoro
• Primary Examiner(s): Gulakowski, Randy
• Assistant Examiner(s): WASHVILLE, JEFFREY D
• Application Number:
  US11/912,118
• Publication Number:
  US 20080193761A1
• Time in Patent Office: 2,584 Days
• Field of Search: 428402-40224, 4272133-21336, 264 4- 47
• US Class Current: 428/402.21
• CPC Class Codes: D06M 23/12 Processes in which the treating agent is incorporated in microcapsules making microcapsules B01J13/02
• CPC Class Codes: D06P 1/0016 Dye baths containing a dyeing agent in a special form such as for instance in melted or solid form, as a floating film or gel, spray or aerosol, or atomised dyes
• CPC Class Codes: Y10T 428/2985 Solid-walled microcapsule from synthetic polymer

Abstract

Microcapsules for smart textile materials, containing an active product and with reactive groups, with the objective of chemically binding the microcapsules to the fibers. The microcapsules contain active products such as PCM (phase change materials), or can be of controlled release of products such as fragrances, essential oils, antibacterial and others with the objective to add specific functional properties to the textile materials. They can be applied by padding and spraying followed by thermofixation. In case of products such as knitwear the application process can also be by exhaustion process, given that the microcapsules acquire affinity towards the fibers and react with the fibers during the process. The chemical bond of the controlled release microcapsules with the fibers confers them a higher resistance to washing than the existing microcapsules glued to the fabric by printing or padding.

Claims

1. A process for directly chemically binding microcapsules having a sole or outer shell of urea-formaldehyde, melamine-formaldehyde, polyamide or chitosan to fibres, comprising reacting free amino (—

NH) or hydroxyl (—

OH) groups of the shell with a first functional group of a bifunctional compound and reacting a second functional group of the same bifunctional compound with the fibres, whereby the microcapsule is directly bonded to the fibre, through the bifunctional compound, by covalent chemical binding, wherein the bifunctional compound comprises first and second reactive functional groups, the first reactive function group is selected from the group consisting of epoxy group, halogen-substituted alkyl group, and vinyl group and wherein the second reactive functional group is a functional group selected for reaction with the fibres.

2. The process for directly chemically binding microcapsules according to claim 1, wherein the first and second reactive functional groups of the bifunctional compound comprise at least one of the following:

two or more epoxy groups,

an epoxy group of epichlorydrin or derivatives,

a —

CO—

(CH₂)_nCl group,

di-chloro or tri-chlorotriazine group,

a —

CO—

CH═

CHR group, where R is a hydrogen or a halogen.

3. The process for directly chemically binding microcapsules according to claim 1, wherein the bifunctional compound is epichlorohydrin, and the free amino (—

NH) or hydroxyl (—

OH) groups present in the shell react with the —

CO—

(CH)Cl group of the epichlorydrin, leaving the remaining epoxy group free to react with the fibre.

4. The process for directly chemically binding microcapsules according to claim 1, wherein the bifunctional compound comprises two or more epoxy groups, and the free amino (—

NH) or hydroxyl (—

OH) groups present in the shell react with one of the epoxy group of the bifunctional compound, leaving a remaining epoxy group free to react with the fibre.

5. The process for directly chemically binding microcapsules according to claim 1, wherein the bifunctional compound is epichlorohydrin, and the free amino (—

NH) or hydroxyl (—

OH) groups react with the epoxy group of the epichlorohydrin leaving the remaining —

CO—

(CH₂)_nCl group free to react with the fibre.

6. The process for directly chemically binding microcapsules according to claim 1, wherein the free amino (—

NH) or hydroxyl (—

OH) groups react with a di-chloro or tri-chlorotriazine group of a bifunctional compound, in which one of the chlorine atoms is substituted in the reaction by the amino (—

NH) or hydroxyl (—

OH) group of the shell and the other chorine atom is substituted in the reaction by the fibre.

7. The process for directly chemically binding microcapsules according to claim 1, wherein the microcapsules are applied to the textile fibres by an exhaustion process.

8. The process for directly chemically binding microcapsules according to claim 1, wherein the microcapsules are applied to the textile fibres by a padding process.

9. The process for directly chemically binding microcapsules according to claim 1, wherein the microcapsules are applied to the textile fibres by a spray process.

10. The process for directly chemically binding microcapsules according to claim 1, wherein the textile fibre used is a cellulosic fibre, a polyamide fibre, a wool fibre, an acrylic fibre or a modacrylic fibre.

11. Microcapsules binding to textile fibres obtainable by the process according to any one of claims 1-10.

12. The microcapsules according claim 11 characterised by containing in the interior an active product.

13. The microcapsules according to claim 12, wherein the active product is a phase change material (PCM) for temperature regulation selected from the group consisting of n-octacosane, n-heptacosane, n-hexacosane, n-pentacosane, n-tetracosane, n-tricosane, n-docosane, n-heneicosane, n-eicosane, n-nonadecane, n-octadecane, n-heptadecane, n-hexadecane, n-pentadecane, n-tetradecane, n-tridecane, and n-dodecane.

14. The microcapsules according to claim 12, wherein the active product is a ther-mochromic or photochromic material.

15. The microcapsules according to claim 12, wherein the active product is an aroma, an essential oil, a fragrance, an antimicrobial, an insect repellent, an insecticide, a disinfectant, a hydrant, an anti-cellulite, aloe-vera, an antioxidant or a vitamin for controlled release by rupture of the wall caused by friction, or another process of solubilization or degradation of the shell, of the type that is applied on fibres so that they produce a controlled release of the microencapsulated product.

16. Textile materials having microcapsules covalently bound thereto by the process of any one of claims 1-10.

17. The process for directly chemically binding microcapsules according to claim 1, wherein the second reactive functional group is selected from the group consisting of epoxy group, halogen-substituted alkyl group and vinyl group.