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AbstractAbstract
[en] Chemical complexities of ruthenium in nitric acid solution cause difficulties in removing this element from waste solution arising from reprocessing of spent nuclear fuel. The waste solution from the 99Mo production process by means of 235U(n,f)99Mo reaction has similar chemical composition to that of spent nuclear fuel reprocessing. Chemical species and their relative abundance are supposed to be quite similar in the both waste solutions. Various ruthenium species in the waste solution arising from 99Mo production process were separated by high performance liquid chromatography for the both high level (VH-1) and medium level (MH-1) aqueous waste solutions. Up to fifty species of ruthenium were separated by cation exchange chromatography with nitric acid. It is confirmed by the cation exchange behaviors that most of these species are anionic and neutral ones. The transformation of chemical species of ruthenium and their relative abundance are determined after each waste treatment. The effectiveness of charcoal-zinc column treatment is ascribed to that the column removes not only positively charged ruthenium species but also negatively charged ruthenium species and neutral ruthenium species from slightly acidic solution. (author)
Source
May 1986; 34 p
Record Type
Report
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ACTINIDE NUCLEI, ALPHA DECAY RADIOISOTOPES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CHROMATOGRAPHY, COMPLEXES, DAYS LIVING RADIOISOTOPES, DISPERSIONS, EVEN-ODD NUCLEI, HEAVY NUCLEI, HOMOGENEOUS MIXTURES, HYDROGEN COMPOUNDS, INORGANIC ACIDS, INORGANIC COMPOUNDS, INTERMEDIATE MASS NUCLEI, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, MATERIALS, MINUTES LIVING RADIOISOTOPES, MIXTURES, MOLYBDENUM ISOTOPES, NITROGEN COMPOUNDS, NUCLEI, OXYGEN COMPOUNDS, RADIOACTIVE MATERIALS, RADIOACTIVE WASTES, RADIOISOTOPES, SEPARATION PROCESSES, SOLUTIONS, TRANSITION ELEMENT COMPLEXES, URANIUM ISOTOPES, WASTES, YEARS LIVING RADIOISOTOPES
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