Photoelectrocatalytic Surfactant Pollutant Degradation and Simultaneous Green Hydrogen Generation

肺表面活性物质 化学工程 降级(电信) 化学 制氢 吸附 阳离子聚合 光催化 阴极 介孔材料 无机化学 有机化学 催化作用 电信 工程类 物理化学 计算机科学
作者
Katherine Rebecca Davies,Michael G. Allan,Sanjay Nagarajan,Rachel Townsend,Vijayshankar Asokan,Trystan Watson,A. Ruth Godfrey,M. Mercedes Maroto‐Valer,Moritz F. Kuehnel,Sudhagar Pitchaimuthu
出处
期刊:Industrial & Engineering Chemistry Research [American Chemical Society]
卷期号:62 (45): 19084-19094 被引量:11
标识
DOI:10.1021/acs.iecr.3c00840
摘要

High Resolution Image Download MS PowerPoint Slide For the first time, we demonstrate a photoelectrocatalysis technique for simultaneous surfactant pollutant degradation and green hydrogen generation using mesoporous WO 3 /BiVO 4 photoanode under simulated sunlight irradiation. The materials properties such as morphology, crystallite structure, chemical environment, optical absorbance, and bandgap energy of the WO 3 /BiVO 4 films are examined and discussed. We have tested the anionic type (sodium 2-naphthalenesulfonate (S2NS)) and cationic type surfactants (benzyl alkyl dimethylammonium compounds (BAC-C12)) as model pollutants. A complete removal of S2NS and BAC-C12 surfactants at 60 and 90 min, respectively, by applying 1.75 V applied potential vs RHE to the circuit, under 1 sun was achieved. An interesting competitive phenomenon for photohole utilization was observed between surfactants and adsorbed water. This led to the formation of H 2 O 2 from water alongside surfactant degradation (anode) and hydrogen evolution (cathode). No byproducts were observed after the direct photohole mediated degradation of surfactants, implying its advantage over other AOPs and biological processes. In the cathode compartment, 82.51 μmol/cm 2 and 71.81 μmol/cm 2 of hydrogen gas were generated during the BAC-C12 and S2NS surfactant degradation process, respectively, at 1.75 V RHE applied potential.
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