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Charcoal performance under accident conditions in light-water reactors. Final report

Technical Report ·
OSTI ID:6040146
Nuclear-grade carbons were systematically degraded by exposure to unfiltered outdoor air with decrease in radioactive methyl iodide trapping. Local meteorological conditions of high humidity combined with atmospheric pollutants in the test vicinity contributed jointly to the degradation. When service carbons were exposed to radiation levels of 10/sup 7/ to 10/sup 9/ rads, the iodine isotope exchange capacity was regenerated. The adsorptive properties were only slightly improved. It was possible to regenerate the iodine isotope-exchange efficiencies by reaction with airborne chemical reducing agents such as hydrazine for carbons removed from nuclear power operations. The depth profile in methyl iodide-131 penetration changed from simple exponentional through new carbons to a non-linear profile for weathered and service aged carbons. The behavior is attributed to the chromatographic distribution of the contaminants that accumulate in the bed. The removal of radioactive iodine depends on a minimum of 3 distinguishable processes: adsorption on the activated carbon, iodine isotope exchange with impregnated iodine-127, and chemical combination with impregnated tertiary amines when present. When a carbon is new, all 3 mechanisms are at peak performance. After the carbon is placed in service, the 3 mechanisms degrade at different rates; the adsorption process degrades faster than the others.
Research Organization:
Naval Research Lab., Washington, DC (USA)
OSTI ID:
6040146
Report Number(s):
NUREG/CR-3990; NRL-Memo-5528; ON: TI85901281
Country of Publication:
United States
Language:
English