SPECIATION OF URANIUM IN SEEPAGE WATERS OF A MINE TAILING PILE STUDIED BY TIME-RESOLVED LASER-INDUCED FLUORESCENCE SPECTROSCOPY (TRLFS)

Citation
G. Bernhard et al., SPECIATION OF URANIUM IN SEEPAGE WATERS OF A MINE TAILING PILE STUDIED BY TIME-RESOLVED LASER-INDUCED FLUORESCENCE SPECTROSCOPY (TRLFS), Radiochimica Acta, 74, 1996, pp. 87-91
Citations number
10
Categorie Soggetti
Nuclear Sciences & Tecnology","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00338230
Volume
74
Year of publication
1996
Pages
87 - 91
Database
ISI
SICI code
0033-8230(1996)74:<87:SOUISW>2.0.ZU;2-4
Abstract
Chemical speciation of U(VI) in natural seepage water and correspondin g model solutions was investigated by time-resolved laser-induced fluo rescence spectroscopy. Calculations of uranium speciation in this medi um show that UO2(CO3)(3)(4-) and UO2(CO3)(2)(2-) should be the major i ndividual components. Due to the very low fluorescence intensity, the pure uranyl carbonate complexes could not be measured directly by TRLF S. However, a uranium fluorescence spectrum was recorded from seepage water samples. The TRLFS investigations show that the main component o f uranium in this seepage water is a calcium uranium carbonate complex . The main fluorescence wavelengths of this complex are at 463.9, 483. 6, 502.8, 524.3 and 555.4 nm. The fluorescence lifetime of the species is 64+/-17 ns. This study shows that the calcium content of the water has a great influence on the uranium speciation. For the first time, the existence of a calcium uranium carbonate complex - {Ca-2[UO2(CO3)3 ]}((ag.)) - is reported. The stability constant was determined to be l og beta = 26.8+/-0.7. Existing thermodynamic data bases do not contain this species and modeling calculation must lead to erroneous results in the medium under investigation.