Migration of transuranic elements in groundwater from the near-surface radioactive waste site
- 1. Ukrainian Institute of Agricultural Radiology UIAR NUBiP of Ukraine, Mashinobudivnykiv Str. 7, Chabany, Kyiv-Svjatoshin Distr, Kyiv Reg. 08162 (Ukraine)
- 2. IRSN, DEI/SARG/LR2S, POB 17, F-92262 Fontenay-aux-Roses (France)
Description
Field experiments and laboratory studies were performed to investigate migration processes of plutonium isotopes from a near-surface radioactive waste trench to the underlying sandy aquifer at the Red Forest waste dump in the Chernobyl zone. The objectives of these experiments were to characterize the spatial distribution and possible migration mechanisms of plutonium in the aquifer. During 2002–2007 experimental investigations were carried out and spatial distributions of plutonium isotopes (239,240Pu, 238Pu), 90Sr and major ions in the aquifer in the direction of the groundwater flow were obtained. Specific activities of radionuclides in groundwater depended on the location of the piezometer and varied in the range of 1–360 mBq kg−1 for 239,240Pu, 0.5–180 mBq kg−1 for 238Pu and n–n·104 Bq kg−1 for 90Sr. It was found that the spatial features of the distributions of plutonium and strontium specific activities in the upper eolian aquifer were similar, i.e. there was a correlation between the positions of the activity maxima of the radionuclides. The Pu isotopes plume in the aquifer spreads about 15 m downstream of the radionuclides source. Characterization of the initial radionuclide composition of the waste showed that all plutonium in the aquifer originated from the trench. The ratio of plutonium isotopes (239,240Pu/238Pu) at the sampling time was the same in waste material and in groundwater samples. In situ ultrafiltration of several groundwater samples was carried out. The size fractionation data obtained suggest that a significant part of plutonium (50–98%) in the groundwater sampled close to the source from the upper part of the aquifer is associated with a very low molecular weight fraction (<1 kDa).
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apgeochem.2012.01.002Additional details
Identifiers
- DOI
- 10.1016/j.apgeochem.2012.01.002;
- PII
- S0883-2927(12)00005-4;
Publishing Information
- Journal Title
- Applied Geochemistry
- Journal Volume
- 27
- Journal Issue
- 7
- Journal Page Range
- p. 1339-1347
- ISSN
- 0883-2927
- CODEN
- APPGEY
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44106190
- Subject category
- S54: ENVIRONMENTAL SCIENCES; S58: GEOSCIENCES;
- Descriptors DEI
- AQUIFERS; ENVIRONMENTAL EFFECTS; GROUND WATER; PLUTONIUM; PLUTONIUM 238; PLUTONIUM 240; RADIOACTIVE WASTES; RADIOECOLOGICAL CONCENTRATION; RADIONUCLIDE MIGRATION; SPATIAL DISTRIBUTION; STRONTIUM 90
- Descriptors DEC
- ACTINIDE NUCLEI; ACTINIDES; ALKALINE EARTH ISOTOPES; ALPHA DECAY RADIOISOTOPES; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; DISTRIBUTION; ECOLOGICAL CONCENTRATION; ELEMENTS; ENVIRONMENTAL TRANSPORT; EVEN-EVEN NUCLEI; HEAVY ION DECAY RADIOISOTOPES; HEAVY NUCLEI; HYDROGEN COMPOUNDS; INTERMEDIATE MASS NUCLEI; ISOTOPES; MASS TRANSFER; MATERIALS; METALS; NUCLEI; OXYGEN COMPOUNDS; PLUTONIUM ISOTOPES; RADIOACTIVE MATERIALS; RADIOISOTOPES; SILICON 32 DECAY RADIOISOTOPES; SPONTANEOUS FISSION RADIOISOTOPES; STRONTIUM ISOTOPES; TRANSURANIUM ELEMENTS; WASTES; WATER; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.