Major ion and electrical potential distribution in soil under electrokinetic remediation

To assess the effect of pore water chemistry on the contaminant removal rat e, we monitored major ion concentrations in the pore water and the electric al potential distribution of a soil during electrokinetic remediation treat ment. On application of the voltage, the soil near the anode became acidic due to the electrolytic generation of Hf, and the acid region gradually spr ead toward the cathode. The major cation in the acid region was, however, n ot Hf but Al3+ that arose from the acid-induced dissolution of soil mineral s, and it migrated very slowly toward the cathode. The measured pH and acco mpanying ion concentrations indicated that the anomalously slow migration o f Al3+ was due to its precipitation-dissolution reaction at the acid front. The stagnancy of Al3+ increased the ionic concentration, flattened the ele ctrical potential profile, and in turn, diminished electromigration in the acid region. This seems to be one of the causes of the relatively low remov al rate of cationic and anionic contaminants in electrokinetic treatments.