Recovery of Rhenium from Uranium In-Situ Leach Liquor (890ecaea-a864-45b5-8b04-768ebe877fac)

The American Institute of Mining, Metallurgical, and Petroleum Engineers
J. B. Goddard
Organization:
The American Institute of Mining, Metallurgical, and Petroleum Engineers
Pages:
5
File Size:
362 KB
Publication Date:
Jan 1, 1984

Abstract

The discovery of rhenium on the ion exchange resin used at the uraniun in-situ leach operations at Palangana, TX, led to a laborabory study of possible recovery methods. Rhenium was present in small amounts in the ammonium carbonate leach liquors as the perrhenate anion, ReO4-. It concentrated on the anion exchange resin, which was a factor of 10 more selective for rhenium than for uranium. Various elution systems were investigated for stripping the rhenium from the columns after the uranium had been eluted with chloride or nitrate solutions. Although the per-chlorate ion was most efficient on a molar basis, nitrate ion combined the benefits of efficiency and low cost. A 3N or stronger concentration of nitrate containing up to 0. 5N H + was found to be the system of choice. A rhenium sulfide concentrate containing up to 14010 Re was obtained from these effluents by hydrogen sulfide precipitation. Preliminary experiments were run to produce rhenium metal powder by oxidation of the concentrate to NH4ReO4 followed by hydrogen reduction at elevated temperature.
Citation

APA: J. B. Goddard  (1984)  Recovery of Rhenium from Uranium In-Situ Leach Liquor (890ecaea-a864-45b5-8b04-768ebe877fac)

MLA: J. B. Goddard Recovery of Rhenium from Uranium In-Situ Leach Liquor (890ecaea-a864-45b5-8b04-768ebe877fac). The American Institute of Mining, Metallurgical, and Petroleum Engineers, 1984.

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