Abstract
The pH value is easily monitored and widely used in real-time control processes. It is also a key parameter in removing Cr(VI) during electrocoagulation. We developed a theory of relations between initial pH (Oh) and chromic alkalinity (p[Cr(VI)1), and the final pH of a solution. That was, when p[Cr(VI)] = pH(i), the final pH was neutral; when p[Cr(VI)] < pH(i) the final pH was alkaline; and when p[Cr(VI)] > pH(i), the final pH was acidic. Response surface methodology confirmed that final pH was influenced by initial pH and initial Cr(VI) concentration rather than by current density. Subsequently, the relationship between pH evolution and Cr(VI) removal was investigated for the aforementioned final pH conditions. Our results suggested that the point of final pH can be detected by the features of pH evolution in case of p[Cr(VI)] = pH, and p[Cr(VI)] < Rapid Cr (VI) removal rate was achieved when p[Cr(VI)] > pH,. However, the major fraction of dissolved Cr (III) and the uncertain point of final pH were observed in this condition. Finally, we proposed a real-time control strategy for treating fluctuant (or stable) Cr(VI)-contaminated wastewater based on the features of pH evolution. (C) 2013 Elsevier B.V. All rights reserved.