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pH control for enhanced reductive bioremediation of chlorinated solvent source zones
Authors:Clare Robinson  DA Barry  Irina Kouznetsova
Affiliation:a Laboratoire de technologie écologique, Institut d'ingénierie de l'environnement, Station No. 2, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland
b Now at: Department of Civil and Environmental Engineering, University of Western Ontario, London, Canada N6A 5B9
c Department of Civil and Environmental Engineering, Stanford University, Stanford, CA 94305-4020, USA
d Institute for Infrastructure and Environment, University of Edinburgh, Edinburgh, EH9 3JL, UK
Abstract:Enhanced reductive dehalogenation is an attractive treatment technology for in situ remediation of chlorinated solvent DNAPL source areas. Reductive dehalogenation is an acid-forming process with hydrochloric acid and also organic acids from fermentation of the electron donors typically building up in the source zone during remediation. This can lead to groundwater acidification thereby inhibiting the activity of dehalogenating microorganisms. Where the soils' natural buffering capacity is likely to be exceeded, the addition of an external source of alkalinity is needed to ensure sustained dehalogenation. To assist in the design of bioremediation systems, an abiotic geochemical model was developed to provide insight into the processes influencing the groundwater acidity as dehalogenation proceeds, and to predict the amount of bicarbonate required to maintain the pH at a suitable level for dehalogenating bacteria (i.e., > 6.5). The model accounts for the amount of chlorinated solvent degraded, site water chemistry, electron donor, alternative terminal electron-accepting processes, gas release and soil mineralogy. While calcite and iron oxides were shown to be the key minerals influencing the soil's buffering capacity, for the extensive dehalogenation likely to occur in a DNAPL source zone, significant bicarbonate addition may be necessary even in soils that are naturally well buffered. Results indicated that the bicarbonate requirement strongly depends on the electron donor used and availability of competing electron acceptors (e.g., sulfate, iron (III)). Based on understanding gained from this model, a simplified model was developed for calculating a preliminary design estimate of the bicarbonate addition required to control the pH for user-specified operating conditions.
Keywords:Reductive dehalogenation  Dechlorination  Alkalinity  Trichloroethene  Bicarbonate  Electron donor  DNAPL  PHREEQC
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