Abstract
Hydrogen sulfide (H2S) is a hazardous contaminant in many industrial gases and wastewaters and a potential source of sulfur to be recovered, but effective and sustainable recovery technologies are still lacking. Here, we report a novel photoelectrochemical process for synchronous sulfur recovery and removal of organic pollutant, which typically coexist in waste streams, by using solar-simulating light as the sole driving force. In this system, sulfide was selectively converted into high-purity elemental sulfur (S0) particles at the photoanode, whereas efficient electrochemical oxidation of carbamazepine occurred at the cathode through Fe2+/Fe3+-mediated peroxymonosulfate activation. The formed sulfur particles with initial sizes of below one micrometer gradually grew into larger particles. Iodine ions were used as anodic redox mediator to favor a selective S0 production in the solution over the formation of sulfite/sulfate at the electrode surface. The practical feasibility of this system was demonstrated by using carbamazepine-spiked lake water samples. Our work suggests a great opportunity for sustainable recovery of sulfur resource with concomitant benefits of pollutant control by using the inexhaustible solar energy.
Original language | English |
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Pages (from-to) | 9591-9595 |
Number of pages | 5 |
Journal | ACS Sustainable Chemistry and Engineering |
Volume | 6 |
Issue number | 8 |
DOIs | |
Publication status | Published - 6 Aug 2018 |
Externally published | Yes |
Keywords
- Carbamazepine
- Hydrogen sulfide
- Photoelectrochemical system
- Selective oxidation
- Solar light
- Sulfur recovery