Water recovery system for use in confined spaces
US-2015353401-A1 · Dec 10, 2015 · US
US10717664B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10717664-B2 |
| Application number | US-201414910202-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 4, 2014 |
| Priority date | Aug 5, 2013 |
| Publication date | Jul 21, 2020 |
| Grant date | Jul 21, 2020 |
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The invention provides a process for the preparation of bismuth oxyhalide, comprising a precipitation of bismuth oxyhalide in an acidic aqueous medium in the presence of a reducing agent. Also provided are bismuth oxyhalide compounds doped with elemental bismuth Bi (0) . The use of Bi (0) doped bismuth oxyhalide as photocatalysts in water purification is also described.
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The invention claimed is: 1. A process for the preparation of bismuth oxyhalide, comprising combining at least one bismuth salt and at least one halide source in an acidic aqueous medium in the presence of a reducing agent, and isolating a precipitate formed, wherein the so-formed bismuth oxyhalide is doped with elemental bismuth Bi (0) , wherein the so-formed bismuth oxyhalide is doped with elemental bismuth Bi (0) at a doping level of not more than 7 molar %, relative to the total amount of the bismuth. 2. A process according to claim 1 , wherein the halide source is an organic halide salt. 3. A process according to claim 2 , wherein the organic halide salt is selected from the group consisting of quaternary ammonium salts represented by the formulas N + R 1 R 2 R 3 R 4 C − , N + R 1 R 2 R 3 R 4 Br − and their mixture, wherein R 1 , R 2 , R 3 and R 4 are alkyl groups, which may be the same or different. 4. A process according to claim 1 , wherein the reducing agent comprises hydride. 5. A process according to claim 4 , wherein the reducing agent is borohydride. 6. A process according to claim 1 , wherein the acidic aqueous medium comprises an organic acid. 7. A process according to claim 1 , wherein the bismuth oxyhalide is selected from the group consisting of BiOCl, BiOBr and BiOCl y Br 1-y wherein y is in the range from 0.5 to 0.95. 8. A process according to claim 7 , wherein the bismuth oxyhalide is BiOCl y Br 1-y wherein y is in the range from 0.6 to 0.95. 9. A process according to claim 1 , wherein the bismuth oxyhalide is selected from the group consisting of: Bi (0) doped-BiOCl; Bi (0) doped-BiOBr; and Bi (0) doped-BiOCl y Br 1-y wherein y is in the range from 0.5 to 0.95. 10. A process according to claim 1 , wherein the doping level of Bi(0) is from 0.1 to 3 molar %. 11. A process for the preparation of bismuth oxyhalide, comprising combining at least one bismuth salt and at least one halide source in an acidic aqueous medium in the presence of a reducing agent, and isolating a precipitate formed, wherein the so-formed bismuth oxyhalide is doped with elemental bismuth Bi (0) , wherein the halide source is an organic halide salt. 12. A process for the preparation of bismuth oxyhalide, comprising combining at least one bismuth salt and at least one halide source in an acidic aqueous medium in the presence of a reducing agent, and isolating a precipitate formed, wherein the so-formed bismuth oxyhalide is doped with elemental bismuth Bi (0) , wherein the reducing agent comprises hydride.
Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title
Scanning electron microscopy; Transmission electron microscopy · CPC title
X-ray diffraction · CPC title
characterised by their crystalline properties, e.g. semi-crystalline (catalysts comprising carbon B01J21/18; molecular sieves B01J29/00) · CPC title
of particles · CPC title
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