Published June 15, 2010 | Version v1
Journal article

Prediction of uranium and technetium sorption during titration of contaminated acidic groundwater

  • 1. Institute of Tibetan Plateau Research, Chinese Academy of Sciences, 18 Shuangqing Road, P.O. Box 2871, Beijing 100085 (China)
  • 2. Department of Civil and Environmental Engineering, University of Tennessee, Knoxville, TN 37996 (United States)
  • 3. Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6038 (United States)
  • 4. Biosystems Engineering and Soil Science Department, University of Tennessee, Knoxville, TN 37996 (United States)

Description

This study investigates uranium and technetium sorption onto aluminum and iron hydroxides during titration of acidic groundwater. The contaminated groundwater exhibits oxic conditions with high concentrations of NO3-, SO42-, U, Tc, and various metal cations. More than 90% of U and Tc was removed from the aqueous phase as Al and Fe precipitated above pH 5.5, but was partially resolublized at higher pH values. An equilibrium hydrolysis and precipitation reaction model adequately described variations in aqueous concentrations of metal cations. An anion exchange reaction model was incorporated to simulate sulfate, U and Tc sorption onto variably charged (pH-dependent) Al and Fe hydroxides. Modeling results indicate that competitive sorption/desorption on mixed mineral phases needs to be considered to adequately predict U and Tc mobility. The model could be useful for future studies of the speciation of U, Tc and co-existing ions during pre- and post-groundwater treatment practices.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2010.01.040

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2010.01.040;
PII
S0304-3894(10)00056-7;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
178
Journal Issue
1-3
Journal Page Range
p. 42-48
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.