摘要
The abatement of chlorophenols is of great environmental importance. Though Fe 0 can activate persulfate (PS) to improve performance, our findings proved that pre-magnetized Fe 0 (Pre-Fe 0 ) could significantly enhanced the degradation and dechlorination of 2,4-dichlorophenol (2,4-DCP), and this Pre-Fe 0 /PS process was more efficient than Fe(II)/PS. The Fe 0 before and after magnetization was characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD), suggesting the acceleration of Fe 2+ release after magnetization. The effects of some important operating parameters such as Fe 0 dosage, PS dosage, pH, and initial 2,4-DCP concentration on the 2,4-DCP degradation and dechlorination by Pre-Fe 0 /PS were investigated and compared with that of Fe 0 /PS, observing a 1.9–5.2-fold enhancement in the degradation rate of 2,4-DCP. Although SO 4 − was the dominant active species responsible for 2,4-DCP degradation in two processes, pre-magnetization could promote more OH generation. Identified by GC–MS and IC, the degradation intermediates such as 4-chlorophenol (4-CP), 2-chlorophenol (2-CP), phenol, and some carboxylic acids were detected, and possible degradation pathway was proposed. This Pre-Fe 0 /PS process was also efficient for 4-chlorophenol and chlorobenzene degradation, obtaining a 5.2 and 3.2 folds enhancement, respectively. This work demonstrated that such a Pre-Fe 0 /PS would be very promising and environmental-friendly for organics degradation and dechlorination since pre-magnetization required no extra energy source while the introduction of Pre-Fe 0 was rather simple and no need to change the present treatment system.
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