Photoelectrocatalytic degradation of Ag-cyanide complexes and synchronous recovery of metallic Ag driven by TiO nanorods array photoanode combined with titanium cathode.

Chemosphere

Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, PR China; University of Chinese Academy of Sciences, Beijing, 100049, PR China. Electronic address:

Published: March 2020

A photoelectrocatalytic (PEC) system for the decomposition of Ag-cyanide complexes synchronously with Ag recovery was established using the titanium dioxide nanorods (TiO NRs) as photoanode and the titanium plate as cathode. The removal efficiency of total cyanide was 76.58%, and the recovery ratio of Ag achieved 84.48% at the applied bias potential of 1.0 V vs SCE in the PEC process. During the reaction, the surface variations and photo-electric properties of TiO NRs photoanode or titanium cathode were characterized by SEM-EDS, XPS, and photoelectronic analyses. It was indicated that AgO and metallic Ag were deposited onto the TiO NRs photoanode and titanium cathode, respectively. Specifically, the in situ generated AgO on the TiO NRs photoanode facilitated the separation of the photogenerated charge carriers and enhanced the visible-light response, thus improving its PEC catalytic activity toward cyanide destruction. Combined with the results of active species quenching experiments, the mechanism of Ag-cyanide complexes decomposition and metallic Ag recovery by the PEC process was proposed.

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http://dx.doi.org/10.1016/j.chemosphere.2019.125156DOI Listing

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