How does periodic polarity reversal affect the faradaic efficiency and electrode fouling during iron electrocoagulation?

结垢 法拉第效率 法拉第电流 电极 电解质 极性反转 化学 电凝 电化学 可逆氢电极 化学工程 无机化学 电极电位 分析化学(期刊) 材料科学 工作电极 色谱法 电压 物理 工程类 量子力学 物理化学 生物化学
作者
Héline Chow,Markus Ingelsson,Edward P.L. Roberts,Anh Le‐Tuan Pham
出处
期刊:Water Research [Elsevier]
卷期号:203: 117497-117497 被引量:32
标识
DOI:10.1016/j.watres.2021.117497
摘要

Electrocoagulation (EC) is a promising electrochemical water treatment technology. However, a major challenge to sustaining effective long-term EC operation is controlling the precipitation of materials on the electrodes, commonly referred to as fouling. Periodically reversing electrode polarity has been suggested as an in-situ fouling mitigation strategy and is often implemented in EC field applications. However, the utility of this approach has not been investigated in detail. In this study, the effect of polarity reversal (PR) on the performance of EC using iron electrodes was examined under different water chemistry conditions and at a range of reversal frequencies. It was observed that the faradaic efficiency in PR-EC was always lower than that in the EC systems operated with a direct current (i.e., DC-EC). It was also observed that the faradaic efficiency progressively decreased as the current reversal frequency increased, with the faradaic efficiency dropping as low as 10% when the PR interval was 0.5 min. Results from fouling layer, chronopotentiometric, and cyclic voltammetric investigations indicated that the decrease in the faradaic efficiency was caused by (i) increased electrode fouling by iron precipitates and (ii) electrochemical side reactions at the electrode-electrolyte interface. The extent of these effects was dependent on the solution chemistry; oxyanions and sulfide were found to be particularly detrimental to the performance of PR-EC, causing severe electrode fouling while decreasing the faradaic efficiency. Fouling could be mitigated by increasing the solution convection rate, resulting in a shear on the electrode surface that removed iron and other electrochemically reactive species from the electrodes.
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