Phenylene ether oligomer composition
US-12173118-B2 · Dec 24, 2024 · US
US10315177B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10315177-B2 |
| Application number | US-201515517324-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 8, 2015 |
| Priority date | Oct 10, 2014 |
| Publication date | Jun 11, 2019 |
| Grant date | Jun 11, 2019 |
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Embodiments of the present disclosure provide for substrates having an oxide shell layer (e.g., a silica shell layer), methods of making an oxide shell layer, and the like.
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We claim: 1. A method for forming a hollow metal oxide shell layer, comprising: providing a substrate having a hydrophobic surface with a plurality of nucleation sites and a water vapor source, a catalyst vapor source, and a hydrolyzable metal oxide precursor vapor source in a closed chamber; saturating the atmosphere of the closed chamber with the water vapor, the catalyst vapor and the hydrolyzable metal oxide precursor vapor; condensing the water vapor at the nucleation sites on the surface of the substrate to form a plurality of water droplets; hydrolyzing the hydrolyzable metal oxide precursor at an air-water interface of the water droplets in the presence of the catalyst vapor to immobilize each water droplet in a metal oxide shell; and removing the water to produce a substrate having a layer comprising a plurality of hollow metal oxide shells disposed on the hydrophobic surface. 2. The method of claim 1 , wherein the hydrolyzable metal oxide precursor is a hydrolyzable silica precursor, hydrolyzable titanium oxide precursor, hydrolyzable zirconium oxide precursor, hydrolyzable tantalum oxide precursor, or a combination thereof. 3. The method of claim 1 , wherein the plurality of nucleation sites comprises an array of organosilane aggregates. 4. The method of claim 3 , wherein the organosilane is perfluorooctyltrichlorosilane (PTCS). 5. The method of claim 4 , further comprising forming the organosilane aggregates by vapor-depositing the PTCS on the substrate at a temperature of 30° C., 60° C., 90° C., or 120° C. 6. The method of claim 2 , wherein the hydrolyzable metal oxide precursor includes a hydrolyzable silica precursor is selected from the group consisting of tetrapropyl orthosilicate, silicon tetrachloride, and tetraethyl orthosilicate (TEOS). 7. The method of claim 1 , wherein the water vapor source and catalyst vapor source is a first solution comprising an aqueous ammonium solution and the hydrolyzable metal oxide vapor source is a second solution comprising TEOS. 8. The method of claim 1 , wherein the hydrophobic substrate is selected from the group consisting of glass, borosilicate glass, soda lime glass, hydrated glass, dehydrated glass, perfluorodecyltriethoxysilane-modified zinc-oxide nanorod arrays, silicon substrates with a thermally oxidized layer, and flexible plastics. 9. The method of claim 7 , wherein the aqueous ammonia solution comprises 20% w/v ammonium hydroxide. 10. The method of claim 1 , wherein the condensing and hydrolyzing occur concurrently. 11. The method of claim 4 , wherein the PTCS aggregates have an average size within a range of 22.6±9.7 nm. 12. The method of claim 5 , wherein the substrate is glass and the method further comprises preparing the substrate for vapor-deposition by dehydrating the glass. 13. The method of claim 7 , wherein the metal oxide shells are 20-30 nm thick.
Using Hydrolysis · CPC title
Preparation of silica of undetermined type · CPC title
Preparation of particles, e.g. dispersion of droplets in an oil bath · CPC title
of the thin-film type · CPC title
Coating on a liquid substrate · CPC title
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