Titanium dioxide fine particle-dispersed composite particles and cosmetic
US-2019000726-A1 · Jan 3, 2019 · US
US10836901B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10836901-B2 |
| Application number | US-201716076580-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 13, 2017 |
| Priority date | Feb 12, 2016 |
| Publication date | Nov 17, 2020 |
| Grant date | Nov 17, 2020 |
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According to the present disclosure, a hydrophobic polymeric composite comprising a hydrophobic polymer matrix with hydrophobically modified particles dispersed therein is provided. The hydrophobically modified particles may be derived from hydrophilic particles modified with organic moieties. The hydrophobically modified particles may also take in the form of core-shell fibers with hydrophilic particles encapsulated inside the core of said fibers or in the form of monolithic fibers embedded with hydrophilic particles. The method for making hydrophobic polymeric composite comprising each of the various hydrophobically modified particles is also provided. The hydrophobic polymer matrix can be chosen from poly(alpha-hydroxyesters), of carbonates, polyurethanes or polyalkanoates. For example, hydrophilic particles, such as barium sulphate, zirconium oxide, tantalum oxide or bismuth oxide, are dispersed in the hydrophobic biodegradable polymers, such as poly-(L-lactide) (PLLA).
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The invention claimed is: 1. A hydrophobic polymeric composite comprising a hydrophobic polymer matrix with hydrophobically modified particles dispersed therein, wherein the hydrophobically modified particles each comprises a hydrophilic particle comprising an organic moiety which changes the hydrophilic particle into a hydrophobically modified particle, and wherein the hydrophilic particle comprises barium sulphate, zirconia, tantalum oxide, or bismuth oxide, wherein the organic moiety comprises a conjugating group and a functional group, wherein the conjugating group is derived from an aluminate coupling agent, and wherein the functional group is derived from L-lactic acid. 2. The hydrophobic polymeric composite according to claim 1 , wherein the hydrophobic polymer matrix comprises poly(alpha-hydroxyesters), polycarbonates, polyurethanes, or polyalkanoates. 3. The hydrophobic polymeric composite according to claim 2 , wherein the poly(alpha-hydroxyesters) are selected from the group consisting of polylactic acid, poly-(l-lactide), poly-(d,l-lactide), poly(glycolic) acid, poly(lactide-co-glycoside acid), polycaprolactone, poly(p-dioxanone), and poly(lactide-co-trimethylene carbonate). 4. The hydrophobic polymeric composite according to claim 2 , wherein the polyalkanoates comprise poly(3-hydroxybutyrate). 5. The hydrophobic polymeric composite according to claim 1 , wherein the hydrophobically modified particles are 1 nm to 100 μm. 6. The hydrophobic polymeric composite according to claim 1 , wherein the hydrophobically modified particles comprise 1 wt % to 40 wt % of the hydrophobic polymeric composite. 7. A method of synthesizing a hydrophobic polymeric composite comprising a hydrophobic polymer matrix with hydrophobically modified particles dispersed therein, wherein the hydrophobically modified particles each comprises a hydrophilic particle comprising an organic moiety which changes the hydrophilic particle into a hydrophobically modified particle, and wherein the hydrophilic particle comprises barium sulphate, zirconia, tantalum oxide, or bismuth oxide, the method comprising the steps of: separately contacting hydrophilic particles with a conjugating agent and then a functionalizing agent to change the hydrophilic particles into the hydrophobically modified particles, wherein the hydrophilic particles comprise barium sulphate, zirconia, tantalum oxide, or bismuth oxide, wherein the conjugating agent comprises a conjugating group derived from an aluminate coupling agent, and wherein the functionalizing agent comprises a functional group comprising L-lactic acid; and blending the hydrophobically modified particles with a hydrophobic polymer matrix to form the hydrophobic polymeric composite. 8. The method according to claim 7 , wherein the blending is carried out by directly mixing the hydrophobic polymer matrix with the hydrophobically modified particles or by mixing the hydrophobically modified particles with a hydrophobic polymer matrix solution. 9. The method according to claim 8 , wherein the hydrophobic polymer matrix and the hydrophobic polymer matrix solution comprise poly(alpha-hydroxyesters), polycarbonates, polyurethanes, or polyalkanoates. 10. The method according to claim 9 , wherein the poly(alpha-hydroxyesters) are selected from the group consisting of polylactic acid, poly-(l-lactide), poly-(d, l-lactide), poly(glycolic) acid, poly(lactide-co-glycoside acid), polycaprolactone, poly(p-dioxanone), and poly(lactide-co-trimethylene carbonate). 11. The method according to claim 9 , wherein the polyalkanoates comprise poly(3-hydroxybutyrate). 12. The method according to claim 8 , wherein the hydrophobic polymer matrix solution comprising the mixed hydrophobically modified particles is casted on a substrate and then allowed to evaporate at 25° C. for up to 24 hours to form the hydrophobic polymeric composite, wherein the substrate comprises a glass surface. 13. The method according to claim 7 , further comprising a step of annealing the hydrophobic polymeric composite at a temperature of 70° C. to 140° C. for up to 24 hours.
Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties · CPC title
the material being a polymer melt · CPC title
with at least one other macromolecular compound obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds as constituent · CPC title
Treatment with low-molecular-weight {non-polymer} organic compounds {(C09C3/006, C09C3/048 take precedence)} · CPC title
Treatment with organosilicon compounds {(C09C3/006 takes precedence)} · CPC title
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