Journal
APPLIED GEOCHEMISTRY
Volume 24, Issue 1, Pages 32-43Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.apgeochem.2008.10.004
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Funding
- German Science Foundation [KE508/6]
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Experimental closed-system AT acid-base titrations between 10 degrees C and 75 degrees C were used to constrain a temperature-dependent 1-pK basic Stern model of the goethite surface complexation reactions. Experimental data for the temperature dependence of pH(PZC) determined by the one-term Van't Hoff extrapolation yield a value for goethite surface protonation enthalpy of -49.6 kJ mol(-1) in good agreement with literature data. Batch titration data between 10 degrees C and 75 degrees C with arsenite concentrations between 10 mu M and 100 mu M yield adsorption curves, which increases with pH, peak at a pH of 9, and decrease at higher pH values. The slope of this bend becomes steeper with increasing temperature. A 1-pK charge distribution model in combination with a basic Stern layer option could be established for the pH-dependent arsenite adsorption. Formation of two inner-sphere bidentate surface complexes best matched the experimental data in agreement with published EXAFS spectroscopic information. The temperature behaviour of the thus derived intrinsic equilibrium constants can be well represented by the linear Van't Hoff log K-T(int) vs. 1/T plot. Adsorption of arsenite on the goethite surface is exothermic (negative Delta H-r(298) values) and therefore becomes weaker with increasing temperature. Application of the new constants with the aqueous speciation code VMINTEQ predicts that the As(III) concentration in presence of goethite sorbent decreases by 10 times once the hydrothermal solution is cooled from 99 degrees C to 1 degrees C. The model curve matches data from a natural thermal water spring system. The increase of adsorption efficiency for As along the temperature gradient may well serve as an additional process to prevent ecosystem contamination by As-rich water seepage from geothermal energy generation facilities. (C) 2008 Elsevier Ltd. All rights reserved.
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