Comparative studies of organic contaminant removal in different calcium sulfite-enhanced oxidant/Fe(II) systems: Kinetics, mechanisms, and differentiated degradation pathways

The application of S(IV) for the regeneration of Fe(II) has been widely investigated. As the common S(IV) sources, sodium sulfite (Na 2 SO 3 ) and sodium bisulfite (NaHSO 3 ) are soluble in the solution, resulting in excessive SO 3 2− concentration and redundant radical scavenging problems. In this research, calcium sulfite (CaSO 3 ) was applied as the substitution for the enhancement of different oxidant/Fe(II) systems. The advantages of CaSO 3 could be summarized as follows: (1) it could sustainedly supplement SO 3 2− for Fe(II) regeneration, preventing radical scavenging and unnecessary reagent waste; (2) the cost and toxicity of CaSO 3 were extremely lower than that of other S(IV) sources; (3) the concentration of reactive species increased in the presence of CaSO 3 ; and (4) after the reaction, SO 4 2− would form CaSO 4 precipitate, which would not increase the burden of SO 4 2− in the solution. In the participation of CaSO 3 , the removal of trichloroethylene (TCE) and other organic contaminants were significantly promoted and different enhanced systems had high tolerance on complex solution conditions. The major reactive species in different systems were determined through qualitative and quantitative analyses. Eventually, the dechlorination and mineralization of TCE were measured and the differentiated degradation pathways in different CaSO 3 -enhanced oxidants/Fe(II) systems were elucidated.