US2018214842A1PendingUtilityA1
Photo-responsive macro- and micro- liquid marbles
Est. expiryFeb 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
C05G 5/30A61K 9/4808C05G 5/23B82Y 30/00B01J 2219/12A61K 41/0028C05G 5/35B82Y 5/00B01J 2219/089A61K 9/5015G21K 5/02A61K 9/501C05G 3/0041B01J 19/12C05G 3/0005C05G 3/0076C05G 3/0017C05G 5/18
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Claims
Abstract
The invention relates to macro- and micro-liquid marbles (i.e. droplets of liquid with a particulate-based shell), and in particular, to photo-responsive macro- and micro-liquid marbles encapsulating a substance therein. Methods for forming the macro- and micro-liquid marbles, and use of the macro- and micro-liquid marbles, in controlled release applications are also disclosed.
Claims
exact text as granted — not AI-modified1 . A method for releasing a substance from a macro- or micro-liquid marble, wherein the macro- or micro-liquid marble is formed by a plurality of nanoparticles and/or mixture of plurality of nanoparticles and said substance is encapsulated therein, the method comprising:
irradiating the plurality of nanoparticles at a wavelength of between about 200 nm and about 2,000 nm, wherein each of the plurality of the nanoparticles is hydrophobic and/or oleophobic, wherein the plurality of nanoparticles comprises a material selected from the group consisting of an organic compound, a polymer, and a mixture thereof.
2 . The method as recited in claim 1 , wherein the hydrophobic and/or oleophobic groups or molecules are selected from the group consisting of a silane, a silicone-based polymer, a fatty acid or a derivative thereof, an alkyl amine, and a mixture thereof.
3 . The method as recited in claim 2 , wherein the hydrophobic molecules comprise a silane of formula RSi(OR′) 3 ,
wherein
R is a C 6 -C 18 alkyl; and
R′ is a C 1 -C 3 alkyl.
4 . The method as recited in claim 2 , wherein the hydrophobic molecules comprise a silane of formula RSiX 3 , R 2 SiX 2 , or R 3 SiX,
wherein R is a C 1 -C 18 alkyl; and X is a halogen.
5 . The method as recited in claim 2 , wherein the oleophobic molecules comprise a fluorinated or a perfluorinated fatty acid of formula RCOOH,
wherein R is a fluorinated or a perfluorinated C 6 -C 18 alkyl.
6 . The method as recited in claim 2 , wherein the oleophobic molecules comprise a fluorinated or a perfluorinated fatty acid chloride of formula RCOC 1 ,
wherein R is a fluorinated or a perfluorinated C 6 -C 18 alkyl.
7 . The method as recited in claim 5 , wherein R in RCOOH or RCOC 1 is CF 3 (CF 2 ) 5 CH 2 CH 2 — or CF 3 (CF 2 ) 7 CH 2 CH 2 —.
8 . The method as recited in claim 1 , wherein the plurality of nanoparticles is comprised of a hydrophobic and/or an oleophobic polymer.
9 . The method as recited in claim 1 , wherein the plurality of nanoparticles is comprised of an organic compound selected from the group consisting of an azo-containing compound, a stilbene-containing compound, and a mixture thereof.
10 . The method as recited in claim 1 comprising:
irradiating the plurality of nanoparticles at the wavelength of between about 200 nm and about 2,000 nm with an intensity of more than 0.01 mW/cm 2 .
11 . The method as recited in claim 1 , wherein the substance encapsulated by the macro- or micro-liquid marble is in liquid phase.
12 . The method as recited in claim 11 , wherein the substance comprises water or an aqueous solution.
13 . The method as recited in claim 12 , wherein the substance further comprises a pharmaceutical active ingredient, an anti-oxidant, a dispersant, a fertilizer, a pesticide, a herbicide, or a mixture thereof.
14 . The method as recited in claim 11 , wherein the substance comprises oil or an organic liquid.
15 . The method as recited in claim 14 , wherein the substance further comprises a pharmaceutical active ingredient, an anti-oxidant, a dispersant, a fertilizer, a pesticide, a herbicide, or a mixture thereof.Cited by (0)
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