Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Ethanol, niobium(5+) salt (5:1) | HCID 160675 | — |
| Reactant | Cerium 2-ethyl hexanoate | HCID 86749478 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Niobium | HCID 23936 | — |
| Product | Ethanol, niobium(5+) salt (5:1) | HCID 160675 | — |
| Product | cerium (III) 2-ethyl hexanoate | HCID 20151587 | — |
Reaction Steps
NbxCe1-xO2 where x is from about 0.02 to about 0.05 was prepared by the following procedure. A solution of niobium ethoxide was prepared in n-butanol solvent in a low moisture and low oxygen environment to prevent hydrolysis of the niobium ethoxide with moisture present in the air. A partial solution/emulsion of cerium (III) 2-ethyl hexanoate in n-butanol was prepared. Then, the niobium ethoxide solution is admixed with the cerium 2-ethyl hexanoate solution/emulsion in an amount to provide a desired solid solution of about 2 to 5 mole percent niobium dopant. Then, the solution/emulsion mixture was then dried at about 110° C. in air to begin to transform the gel into powder. Next, the dried material was thermally decomposed by calcination at about 650° C. in air to form the solid solution of metal oxides powder agglomerate. The metal oxide powder was then deagglomerated by high frequency vibration through sonication in a MEK-ethanol solution containing a small amount of fish oil to result in an average particle size powder of about 0.8 microns.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516597 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-5009623d3cc54f6ea58cdc8812a82ab0 |
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| Source note | uspto-grants-1996_05 |
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