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Toste, A.P.; Kirby, L.J.; Pahl, T.R.
Pacific Northwest Lab., Richland, WA (USA)1984
Pacific Northwest Lab., Richland, WA (USA)1984
AbstractAbstract
[en] The subsurface migration of radionuclides has been studied at a commercial, shallow-land burial site of low-level nuclear waste at Maxey Flats, Kentucky. A variety of radionuclides including 3H, 238239240Pu, 60Co, 137Cs and 90Sr have migrated short distances on-site (meters to tens of meters). A number of the mobile radionuclides, notably plutonium and 60Co, appear to exist as anionic species with organic properties. As a result, we have studied the organic geochemistry of radioactive leachates pumped from a number of waste burial trenches throughout the site. The major aim of the organic research is to elucidate the role of organic compounds in mediating the subsurface migration of the mobile radionuclides in groundwater. A survey study of the hydrophilic and hydrophobic organic content of the waste leachates has revealed that organic compounds are readily leached from the buried waste. Organic chelating agents like EDTA, HEDTA and ED3A are the major hydrophilic organic compounds in the leachates, their concentrations ranging from 78 ppB to 19,511 ppB. A number of carboxylic acids are also present in the leachates, ranging from 675 ppB to 8757 ppB, collectively. A variety of hydrophobic organic compounds including barbiturates and other aromatic compounds, presumably waste-derived, are also present in the leachates, generally at lower ppB concentrations. A detailed chemical speciation study, aimed at determining whether any of the organic compounds identified in the survey study are associated with the mobile radionuclides, was undertaken using leachate from one of the waste trenches. It is clear that EDTA is chelated to plutonium and 60Co in the leachate, potentially mobilizing these radionuclides. Other radionuclides, 137Cs and 90Sr, may be associated with polar organic compounds such as carboxylic acids. 14 references, 2 figures, 2 tables
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Secondary Subject
Source
Jan 1984; 8 p; Waste management '84; Tucson, AZ (USA); 11-15 Mar 1984; CONF-840307--33; Available from NTIS, PC A02; 3 as DE84011361
Record Type
Report
Literature Type
Conference; Numerical Data
Report Number
Country of publication
CESIUM 137, CHELATING AGENTS, CHEMICAL COMPOSITION, COBALT 60, ENVIRONMENTAL TRANSPORT, EXPERIMENTAL DATA, GAS CHROMATOGRAPHY, GEOCHEMISTRY, GEOLOGIC DEPOSITS, GROUND WATER, INTERNAL CONVERSION RADIOISOTO, KENTUCKY, LEACHATES, LEACHING, LOW-LEVEL RADIOACTIVE WASTES, MASS SPECTROSCOPY, ORGANIC COMPOUNDS, PLUTONIUM 238, PLUTONIUM 239, PLUTONIUM 240, RADIOACTIVE WASTE DISPOSAL, RADIONUCLIDE MIGRATION, STRONTIUM 90, TRITIUM, UNDERGROUND DISPOSAL
ACTINIDE NUCLEI, ALPHA DECAY RADIOISOTOPES, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CESIUM ISOTOPES, CHROMATOGRAPHY, COBALT ISOTOPES, DATA, DEVELOPED COUNTRIES, DISPERSIONS, DISSOLUTION, EVEN-EVEN NUCLEI, EVEN-ODD NUCLEI, HEAVY NUCLEI, HOMOGENEOUS MIXTURES, HYDROGEN COMPOUNDS, HYDROGEN ISOTOPES, INFORMATION, INTERMEDIATE MASS NUCLEI, ISOMERIC TRANSITION ISOTOPES, ISOTOPES, LIGHT NUCLEI, MANAGEMENT, MASS TRANSFER, MATERIALS, MINUTES LIVING RADIOISOTOPES, MIXTURES, NORTH AMERICA, NUCLEI, NUMERICAL DATA, ODD-EVEN NUCLEI, ODD-ODD NUCLEI, OXYGEN COMPOUNDS, PLUTONIUM ISOTOPES, RADIOACTIVE MATERIALS, RADIOACTIVE WASTES, RADIOISOTOPES, SEPARATION PROCESSES, SOLUTIONS, SPECTROSCOPY, STRONTIUM ISOTOPES, USA, WASTE DISPOSAL, WASTE MANAGEMENT, WASTES, WATER, YEARS LIVING RADIOISOTOPES
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