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The interaction of naturally occurring minerals with H 2 O 2 affects the remediation efficiency of polluted sites in in situ chemical oxidation (ISCO) treatments. However, interactions between vanadium(V) minerals and H 2 O 2 have rarely been explored. In this study, H 2 O 2 decomposition by various vanadium-containing minerals including V(III), V(IV), and V(V) oxides was examined, and the mechanism of hydroxyl radical ( • OH) generation for contaminant degradation was studied. Vanadium minerals were found to catalyze H 2 O 2 decomposition efficiently to produce • OH for diethyl phthalate (DEP) degradation in both aqueous solutions with a wide pH range and in soil slurry. Electron paramagnetic resonance (EPR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) analyses, and free radical quenching studies suggested that • OH was produced via single electron transfer from V(III)/V(IV) to H 2 O 2 followed a Fenton-like pathway on the surface of V 2 O 3 and VO 2 particles, whereas the oxygen vacancy (OV) was mainly responsible for • OH formation on the surface of V 2 O 5 particles. This study provides new insight into the mechanism of interactions between vanadium minerals and H 2 O 2 during H 2 O 2 -based ISCO.
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Fang et al. (2018) studied this question.
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