Enhancement of Activity of Activated Carbon Fiber for Electro-Fenton Process by Loading it with SiO2 having Tunable Hydrophobic/Hydrophilic Moieties

Electro-Fenton (EF) process is promising for achieving satisfactory oxidation of organic contaminants. However, the sluggish kinetics of in situ production of H2O2 and slow rate of Fe2+ regeneration remain its limitations. In this work, SiO2 with tunable methyl and hydroxyl moieties on the surface (...

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Published inIndustrial & engineering chemistry research Vol. 63; no. 5; pp. 2126 - 2138
Main Authors Tang, Juntao, Zhou, Taotao, Cao, Mengyi, Wang, Da, He, Zhiqiao, Song, Shuang
Format Journal Article
LanguageEnglish
Published American Chemical Society 07.02.2024
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Summary:Electro-Fenton (EF) process is promising for achieving satisfactory oxidation of organic contaminants. However, the sluggish kinetics of in situ production of H2O2 and slow rate of Fe2+ regeneration remain its limitations. In this work, SiO2 with tunable methyl and hydroxyl moieties on the surface (M x OHSiO2; x denotes the mass ratio of diethoxydimethylsilane to tetraethyl orthosilicate) was successfully loaded onto activated carbon fiber (ACF) to construct an ACF-supported cathode (M x OHSiO2/ACF) for the degradation of bisphenol A (BPA). The M x OHSiO2/ACF exhibited substantially higher activity than bare ACF in the EF process. The removal of BPA proceeded most rapidly with M0.75OHSiO2/ACF with an initial pH of 3.0, an electrolyzing voltage of 20 V, and an Fe2+ dosage of 0.5 mM. The mineralization efficiency was 79.3% after 360 min, with the complete disappearance of BPA recorded at 60 min during the EF process. In addition, the M0.75OHSiO2/ACF catalytic electrode remained stable for five successive cycling tests. Because of the synergistic effect of the hydrophobic methyl moiety and electron-rich hydroxyl moiety on SiO2, the H2O2 electro-generation and Fe2+ regeneration at M0.75OHSiO2/ACF were simultaneously improved. This work provides an effective strategy for the application of EF technology in future.
ISSN:0888-5885
1520-5045
DOI:10.1021/acs.iecr.3c03629