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Mertz, C.; Chamberlain, D.B.; Chen, L.; Conner, C.; Vandegrift, G.F.; Drockelman, D.; Kaminski, M.; Landsberger, S.; Stubbins, J.
Argonne National Lab., IL (United States). Funding organisation: USDOE, Washington, DC (United States)1996
Argonne National Lab., IL (United States). Funding organisation: USDOE, Washington, DC (United States)1996
AbstractAbstract
[en] Seven in situ decontamination processes were evaluated as possible candidates to reduce radioactivity levels in nuclear facilities throughout the DOE complex. These processes were tested using stainless steel coupons (Type 304) contaminated with actinides (Pu and Am) or fission products (a mixture of Cs, Sr, and Gd). The seven processes were decontamination with nitric acid, nitric acid plus hydrofluoric acid, fluoboric acid, silver(II) persulfate, hydrogen peroxide plus oxalic acid plus hydrofluoric acid, alkaline persulfate followed by citric acid plus oxalic acid, and electropolishing using nitric acid electrolyte. Of the seven processes, the nitric acid plus hydrofluoric acid and fluoboric acid solutions gave the best results; the decontamination factors for 3- to 6-h contacts at 80 degree C were as high as 600 for plutonium, 5500 for americium, 700 for cesium, 15000 for strontium, and 1100 for gadolinium
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1996; 8 p; American Nuclear Society (ANS) topical meeting on decontamination and decommissioning; Chicago, IL (United States); 14-17 Apr 1996; CONF-960443--5; CONTRACT W-31109-ENG-38; Also available from OSTI as DE96008402; NTIS; US Govt. Printing Office Dep
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