This study intends to reinvent classical Fenton chemistry by enabling the Fe(II)/Fe(III) redox cycle to occur on a newly developed FeOCl nanosheet catalyst for facile hydroxyl radical ( • OH) generation from H 2 O 2 activation. This approach overcomes challenges such as low operating pH and large sludge production that have prevented a wider use of otherwise attractive Fenton chemistry for practical water treatment, in particular, for the destruction of recalcitrant pollutants through nonselective oxidation by • OH. We demonstrate that FeOCl catalysts exhibit the highest performance reported in the literature for • OH production and organic pollutant destruction over a wide pH range. We further elucidate the mechanism of rapid conversion between Fe(III) and Fe(II) in FeOCl crystals based on extensive characterizations. Given the low-cost raw material and simple synthesis and regeneration, FeOCl catalysts represent a critical advance toward application of iron-based advanced oxidation in real practice.
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Sun et al. (2018) studied this question.
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