Mutual-activation between Zero-Valent iron and graphitic carbon for Cr(VI) Removal: Mechanism and inhibition of inherent Side-reaction

The low reactivity of zero-valent iron (ZVI) usually limits its application for pollutant remediation. Therefore, a microscopic galvanic cell (mGC) with short-circuited cathode and anode was synthesized to intensify its galvanic corrosion. The prepared mGC exhibited 7.14 times higher Fe(II) release performance than ordinary nanoscale-ZVI (nZVI), rendering efficient Cr(VI) removal performance. Density functional theory (DFT) revealed mutual-activation of the cathode and anode due to close proximity, dramatically enhancing the galvanic corrosion of Fe(0) in mGC. The corrosion potential of mGC was measured as −0.77 V, which was 100 mV more negative than nZVI. The released electrons and surface-bond Fe(II) from anode in mGC was proved to be the dominant reductive species. More importantly, Cr(VI) reduction was slightly inhibited by hydroxyl radicals generated by a series of inherent side-reactions in the system, which could be well eliminated by low concentrations of 4-acetamido phenol. This study provides a promising strategy for ZVI activation, and sheds light on its environmental applications.