GOLD LOADED TiO2 NANOTUBE-MULTIWALLED CARBON NANOTUBE COMPOSITES AS ACTIVE PHOTOCATALYSTS FOR CYCLOHEXANE OXIDATION
US-2016214087-A1 · Jul 28, 2016 · US
US11623866B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-11623866-B1 |
| Application number | US-202117371498-A |
| Country | US |
| Kind code | B1 |
| Filing date | Jul 9, 2021 |
| Priority date | Oct 16, 2018 |
| Publication date | Apr 11, 2023 |
| Grant date | Apr 11, 2023 |
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A method encapsulates nanoscale material by producing a suspension of the nanostructure material in a first solvent using a micelle surrounding the nanostructure material. The micelle surrounding the suspended nanostructure material is swollen by adding to and mixing with the suspension an immiscible phase second solvent containing a precursor. The precursor is then reduced by adding a reducing reactant selectively soluble in the first solvent that reacts to the precursor containing reactant selectively solvated in the second solvent to encapsulate the nanostructure material. A metal-nanostructure composite can be provided by collecting and mixing the metal-shell encapsulated nanostructure product produced by the aforementioned method into a metal matrix.
Opening claim text (preview).
We claim: 1. A method for encapsulating nanoscale material, comprising: (a) producing a suspension of the nanostructure material in a first solvent using a micelle surrounding the nanostructure material, (b) swelling the micelle surrounding the suspended nanostructure material by adding to and mixing with the suspension an immiscible phase second solvent containing a precursor, and (c) reducing the precursor by consisting of the step of adding a reducing reactant selectively soluble in the first solvent that reacts to the precursor containing reactant selectively solvated in the second solvent to encapsulate the nanostructure material; wherein the reducing reactant being used is hydrazine. 2. The method of claim 1 , further comprising: (d) collecting and mixing the encapsulated nanostructure material into a matrix. 3. The method of claim 2 , wherein the matrix is a metal matrix. 4. The method of claim 1 , wherein the nanostructure material is comprised of individual carbon nanotubes suspended in the first solvent. 5. The method of claim 1 , wherein the second solvent comprises an oil phase with the precursor. 6. The method of claim 1 , wherein the precursor is an organometallic precursor that is reduced to its base metal in step (c). 7. The method of claim 6 , wherein the second solvent comprises an oil phase with the precursor. 8. The method of claim 1 , wherein the surfactant is selected to provide a hydrophilic head and a hydrophobic head for producing an oleophilic micellar region around the suspended nanostructure material. 9. The method of claim 8 , wherein the nanostructure material is comprised of individual carbon nanotubes. 10. The method of claim 9 , wherein the nanostructure material is comprised of single-wall carbon nanotubes and the metal salt is iron (III) acetylacetonate (Fe(acac) 3 ) or copper (II) acetylacetonate (Cu(acac) 2 ) and with chloroform as the immiscible phase being used in step (b). 11. The method of claim 1 , wherein the precursor contains dissolved metal salt.
After-treatment · CPC title
obtained by TEM, STEM, STM or AFM · CPC title
by IR- or Raman-data · CPC title
Solid solutions · CPC title
Single-walled nanotubes · CPC title
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