Encapsulates

Patent metadata

Field	Value
Publication number	US-9644174-B2
Application number	US-201213612994-A
Country	US
Kind code	B2
Filing date	Sep 13, 2012
Priority date	Sep 13, 2011
Publication date	May 9, 2017
Grant date	May 9, 2017

Abstract

The present application relates to encapsulated, preformed peracids and products comprising such encapsulates, as well as processes for making and using such encapsulates and products comprising such encapsulates. Such products deliver bleaching that results in superior whiteness and stain removal without the stability issues that are normally associated with certain bleaching systems.

First claim

What is claimed is:

1. A composition having a pH of from about 6.5 to about 14, said composition comprising an encapsulate having a diameter of from about 10 microns to about 450 microns, said encapsulate comprising a shell and a matrix composition, said shell encapsulating said matrix composition, said matrix composition having a pH from about 3.5 to about 6, said matrix composition comprising a matrix network material and matrix benefit agent cores, said matrix benefit agent cores being entrapped in said matrix network material,
wherein said matrix composition comprises, based on total matrix composition weight, from 0.01 wt % to 10 wt % of a matrix network material having a formula:

wherein R 1 and R 2 are aminofunctional end-groups; L is a backbone moiety having molecular weight from 14 to 500 g/mol; and at least one of L, R 1 or R 2 comprises a pH-sensitive group.

2. The composition of claim 1 , wherein said matrix composition comprises a self-assembled matrix network material having a molecular weight from about 150 g/mol to about 1,500 g/mol.

3. The composition of claim 1 , said matrix network material is in its neutral viscosity building form at a pH of from about 3.5 to about 6.

4. The composition of claim 1 , said matrix network material having a pKa of from about 1 to about 14.

5. The matrix network material from claim 1 , wherein R 1 and R 2 are amidofunctional end-groups.

6. The composition of claim 1 , wherein said matrix network material has a minimum gelling concentration (MGC) of from 0.1 to 100 mg/mL.

7. The composition of claim 1 , wherein said matrix composition comprises a buffer and/or buffer precursor.

8. The composition of claim 1 , wherein said matrix composition comprises a polysaccharide.

9. The composition of claim 1 , wherein said shell comprises a material selected from the group consisting of
a) a material comprising polyvinyl pyrrolidone;
b) polymers derived from hydrophilic monomers comprising diamines, triamines, diols and mixtures thereof;
c) polymers derived from hydrophobic monomers comprising di- and or tri-acyl chlorides, diisocyanates, bischloroformates and mixtures thereof;
d) a material comprising a polyvinyl alcohol derivative;
e) a material comprising a polymer with a cloud point from about 0° to about 120° C., or even from about 20° to about 60° C.;
f) a material comprising a cellulosic polymer;
g) a material comprising a wax, such wax having a melting point from about 35° C. to about 75° C.;
h) a material comprising a non-cellulosic, natural polymer;
and said matrix benefit agent cores comprise a material selected from the group consisting of a preformed peracid, a metal catalyst, a bleach activator, a bleach booster and a diacyl peroxide.

10. The composition of claim 9 , wherein:
a) said metal catalyst comprises a material selected from the group consisting of dichloro-1,4-diethyl-1,4,8,11-tetraaazabicyclo[6.6.2]hexadecane manganese(II); dichloro-1,4-dimethyl-1,4,8,11-tetraaazabicyclo[6.6.2]hexadecane manganese(II) and mixtures thereof;
b) said bleach booster comprises material selected from the group consisting of 2-[3-[(2-hexyldodecyl)oxy]-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 3,4-dihydro-2-[3-[(2-pentylundecyl)oxy]-2-(sulfooxy)propyl]isoquinolinium, inner salt; 2-[3-[(2-butyldecyl)oxy]-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 3,4-dihydro-2-[3-(octadecyloxy)-2-(sulfooxy)propyl]isoquinolinium, inner salt; 2-[3-(hexadecyloxy)-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 3,4-dihydro-2-[2-(sulfooxy)-3-(tetradecyloxy)propyl]isoquinolinium, inner salt; 2-[3-(dodecyloxy)-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 2-[3-[(3-hexyldecyl)oxy]-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 3,4-dihydro-2-[3-[(2-pentylnonyl)oxy]-2-(sulfooxy)propyl]isoquinolinium, inner salt; 3,4-dihydro-2-[3-[(2-propylheptyl)oxy]-2-(sulfooxy)propyl]isoquinolinium, inner salt; 2-[3-[(2-butyloctyl)oxy]-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 2-[3-(decyloxy)-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt; 3,4-dihydro-2-[3-(octyloxy)-2-(sulfooxy)propyl]isoquinolinium, inner salt; 2-[3-[(2-ethylhexyl)oxy]-2-(sulfooxy)propyl]-3,4-dihydroisoquinolinium, inner salt and mixtures thereof;
c) said bleach activator comprises a material selected from the group consisting of tetraacetyl ethylene diamine (TAED); benzoylcaprolactam (BzCL); 4-nitrobenzoylcaprolactam; 3-chlorobenzoyl caprolactam; benzoyloxybenzenesulphonate (BOBS); nonanoyloxybenzene sulphonate (NOBS); phenyl benzoate (PhBz); decanoyloxybenzoic acid (DOBA); (6-octanamidocaproyl)oxybenzenesulfonate; (6-nonanamidocaproyl) oxybenzenesulfonate; (6-decanamidocaproyl)oxybenzenesulfonate and mixtures thereof;
d) said preformed peracid comprises a material selected from the group consisting of peroxymonosulfuric acids; perimidic acids; percabonic acids; percarboxilic acids and salts of said acids; in one aspect said percarboxilic acids and salts thereof may be phthalimidoperoxyhexanoic acid, 1,12-diperoxydodecanedioic acid; or monoperoxyphthalic acid (magnesium salt hexahydrate); amidoperoxyacids, in one aspect, said amidoperoxyacids may be N,N′-terephthaloyl-di(6-aminocaproic acid), a monononylamide of either peroxysuccinic acid (NAPSA) or of peroxyadipic acid (NAPAA), N-nonanoylaminoperoxycaproic acid (NAPCA), and mixtures thereof; in one aspect, said preformed peracid comprises phthalimidoperoxyhexanoic acid;
e) said diacyl peroxide comprises a material selected from the group consisting of dinonanoyl peroxide, didecanoyl peroxide, diundecanoyl peroxide, dilauroyl peroxide, dibenzoyl peroxide, di-(3,5,5-trimethyl hexanoyl) peroxide and mixtures thereof; in one aspect, said diacyl peroxide is, clathrated.

11. The composition of claim 1 , wherein:
a) said encapsulate comprises two or more matrix compositions, said two or more matrix compositions being encapsulated by said encapsulate's shell; and/or
b) said composition comprises two or more different species of said encapsulate.

12. The composition of claim 1 , wherein said encapsulate has a stability index of from about 0.8 to about 1.

13. The composition of claim 1 , wherein said encapsulate has a release index of from about 0.25 to about 1.

14. The composition of claim 1 , wherein said encapsulate has a matrix composition to shell mass ratio of from about 1:99 to about 90:10.

15. The composition of claim 1 , said composition being a consumer product comprising said encapsulate and an adjunct ingredient.

16. A composition according to claim 1 , said composition comprising a material selected from
a) an anionic surfactant and/or a nonionic,
b) a solvent;
c) water,
d) an external structuring system
e) optionally one or more materials selected from the group consisting of:
(i) a bleach compatible clay clean polymer,
(ii) a brightener,
(iii) a builder,
(iv) a chelant.

17. A method of treating and/or cleaning a situs, said method comprising
a) optionally washing and/or rinsing said situs;
b) contacting said situs with a composition according to any preceding claim; and
c) optionally washing and/or rinsing said situs.

18. A situs treated with a composition according to claim 1 .

Assignees

• Miravet Celades Juan Felipe
• Escuder Gil Beatriu
• Nebot-Carda Vincent Josep
• Smets Johan
• Fernandez Prieto Susana
• Procter & Gamble

Inventors

• Miravet Celades Juan Felipe
• Escuder Gil Beatriu
• Nebot-Carda Vincent Josep
• Smets Johan
• Fernandez Prieto Susana

Classifications

• A61K8/38

  Percompounds, e.g. peracids · CPC title

• A61K8/42

  Amides · CPC title

• A61K8/8129

  Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers or esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers, e.g. polyvinylmethylether · CPC title

• A61Q5/08

  Preparations for bleaching the hair · CPC title

• A61K8/41

  Amines · CPC title