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Title: In situ carbonyl extraction of Ni from gaseous diffusion cells

Conference ·
OSTI ID:210374
 [1];  [2];  [3]
  1. USBM Salt Lake Research Center, Salt Lake City, UT (United States)
  2. Battelle Pacific Northwest Lab., Richland, WA (United States)
  3. Battelle Memorial Institute, Oak Ridge, TN (United States)

This paper discusses the use of carbonyl processing technology for recovery of nickel from uranium isotope separation diffusion cells, and potential applications to recover nickel, iron, chromium, cobalt, and other carbonyl forming metals from nuclear waste while reducing the volume of the high level residue for more economic disposal. Nickel powder was carbonylated under static and dynamic conditions using only carbon monoxide to determine if the nickel powder would react rapidly enough to require no promoter. Nickel to Ni(CO){sub 4} conversion was realized in all cases and nickel metal was vapor deposited in the thermal decomposer, but the conversion rates in all cases the reaction were too slow for practical recovery. Addition of hydrogen sulfide gas as a promoter increased the conversion rate more than 500-fold over conversion with no promoter. Test summaries are provided in the paper; results indicate that promoter activated carbonylation is a viable approach for recovery of nickel from uranium isotope diffusion cells.

OSTI ID:
210374
Report Number(s):
CONF-9509139-; TRN: 95:008324-0216
Resource Relation:
Conference: 7. ACS special symposium: emerging technologies in hazardous waste management, Atlanta, GA (United States), 17-20 Sep 1995; Other Information: PBD: 1995; Related Information: Is Part Of Emerging technologies in hazardous waste management VII; Tedder, D.W. [ed.]; PB: 1352 p.
Country of Publication:
United States
Language:
English