IP Library Granted Patent US 9,687,424
Granted Patent B2
US 9,687,424 · App. 13/969,038 · Granted Jun 27, 2017

Polyurea capsules prepared with aliphatic isocyanates and amines

Inventors: Yabin Lei (Holmdel, NJ); Li Xu (Newark, NJ); Carol Joyce (Toms River, NJ); Lewis Michael Popplewell (Morganville, NJ)
Assignee: INTERNATIONAL FLAVORS & FRAGRANCES
A61K8/11A61K8/731A61K8/84A61Q5/00A61Q5/02A61Q5/12A61Q19/10B01J13/14B01J13/16B01J13/206C11D3/505C11D17/0039A61K2800/412A61K2800/624
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Quick Facts
Patent No.
US 9,687,424
App. No.
13/969,038
Granted
Jun 27, 2017
Kind
B2
Abstract

Polyurea capsules that encapsulate active materials in polymeric walls resulting from the polymerization of an aliphatic polyisocyanate and a cross-linking agent such as a diamine, amphoteric amine or guanidine amine/salt are provided as are consumer products containing said polyurea capsules and for methods for producing such capsules.

Claims (17)

1. A method for preparing a polyurea capsule composition comprising:

(a) preparing an oil phase comprising an active material and a polyisocyanate in which the active material is a fragrance oil;

(b) preparing a surfactant solution containing a capsule formation aid that is a mixture of polyvinyl alcohol and carboxymethyl cellulose;

(c) emulsifying the oil phase into the surfactant solution to form a fragrance emulsion;

(d) adding a cross-linking agent to the fragrance emulsion to form a capsule slurry; and

(e) curing the capsule slurry,

wherein the active material is present at a level of 5% to 80% of the polyurea capsule composition; the polyisocyanate is present at a level of 1% to 7.5% of the polyurea capsule composition; the capsule formation aid is present at a level of 0.25% to 2% of the polyurea capsule composition; the cross-linking agent, being a guanidine salt, is present at a level of 0.25% to 3% of the polyurea capsule composition; the polyurea capsule composition contains a microcapsule having an encapsulating polymer that encapsulates the active material; and the encapsulating polymer is the polymerization product between the polyisocyanate and the cross-linking agent in the presence of the capsule formation aid.

2. The method of claim 1 , wherein the polyisocyanate is an aromatic polyisocyanate or aliphatic polyisocyanate.

3. The method of claim 2 , wherein the aliphatic polyisocyanate is a dimer, biuret, symmetric trimer, or asymmetric trimer of hexamethylene diisocyanate.

4. The method of claim 1 , wherein the guanidine salt is 1,3-diaminoguanidine monohydrochloride, 1,1-dimethylbiguanide hydrochloride, guanidine carbonate or guanidine hydrochloride.

5. The method of claim 4 , further comprising addition of sodium carbonate to the fragrance emulsion.

6. The method of claim 1 , wherein the step of adding the cross-linking agent to the fragrance emulsion is at a temperature of 35° C.

7. The method of claim 1 , wherein the step of adding the cross-linking agent to the fragrance emulsion is at a temperature of 22° C.

8. The method of claim 1 , wherein the capsule slurry is cured at a temperature greater than 55° C., 65° C., 75° C., 85° C. or 95° C.

9. The method of claim 1 , wherein the step of curing the capsule slurry is carried out in the presence of a catalyst.

10. The method of claim 1 , further comprising the step of washing the cured capsule slurry with water.

11. The method of claim 10 , further comprising the step of adding a salt to the cured capsule slurry before washing the capsule slurry with water.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 21, 2014
From: LEI, YABIN; XU, LI; JOYCE, CAROL; POPPLEWELL, LEWIS MICHAEL
To: INTERNATIONAL FLAVORS & FRAGRANCES INC.
Reel/Frame 032006/0267 →
Continuity (4)
Continuation In Part 13163320 · Jun 17, 2011
Continuation In Part 12883337 · Sep 16, 2010
Continuation In Part 12562578 · Sep 18, 2009
Related Publication 20130337023A1 · Dec 19, 2013