亚硫酸盐在无金属阳极上的电化学活化促进卡马西平的降解

IF 4.3 Q1 ENVIRONMENTAL SCIENCES
Qiufang Yao, Jiabin Chen*, Zewei Hao, Libin Yang, Yalei Zhang and Xuefei Zhou*, 
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引用次数: 0

摘要

本研究开发了一种使用活性石墨毡(GF-400)阳极的无金属电亚硫酸盐(ES)系统,以克服活性亚硫酸盐过程中金属二次污染的持续挑战[S(IV)]。GF-400阳极在活化亚硫酸盐(S(IV))降解卡马西平(CBZ)方面表现优异,在中性ph下的速率常数为0.056 min-1,是传统电氧化(0.001 min-1)的50倍。猝灭实验和电子自旋共振(ESR)光谱验证了SO4•-和•OH是优势反应物质。DFT计算确定羧基(−COOH)为主要活性位点(吸附能:−1.78 eV),通过低能途径实现高效S(IV)活化:SO32 -→SO3•-→SO5•- /H SO5•-→SO4•- (ΔG =−3.9424 eV)。实际废水试验表明,该系统对CBZ的去除率达到83.6%以上,进一步证明了ES系统的优越性。ES系统在18个循环中保持了稳定的CBZ降解性能,同时将废SO2转化为增值氧化剂。该技术为同时进行烟气净化和水处理提供了可持续的双重方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced Carbamazepine Degradation by Electrochemical Activation of Sulfite on a Metal-free Anode

Enhanced Carbamazepine Degradation by Electrochemical Activation of Sulfite on a Metal-free Anode

This study developed a metal-free electrosulfite (ES) system using active graphite felt (GF-400) anode to overcome persistent challenges of metal secondary pollution in activated sulfite [S(IV)] procedures. The GF-400 anode demonstrated excellent performance in activating sulfite (S(IV)) to degradation of carbamazepine (CBZ) with a rate constant of 0.056 min–1, which was 50-fold higher than conventional electro-oxidation (0.001 min–1) at neutral pH. Quenching experiments and electron spin resonance (ESR) spectroscopy verified SO4•– and •OH as dominant reactive species, contributing to 93.1% CBZ removal within 60 min. DFT calculations identified carboxyl groups (−COOH) as the primary active sites (adsorption energy: −1.78 eV), enabling efficient S(IV) activation through a low-energy pathway: SO32– → SO3•–→ SO5•–/H SO5•–→ SO4•–G = −3.9424 eV). Real wastewater tests with more than 83.6% CBZ removal further demonstrated the superiority of the ES system. The ES system maintained stable performance for CBZ degradation over 18 cycles while converting waste SO2 into value-added oxidants. This technology offers a sustainable dual approach for simultaneous flue gas purification and water treatment.

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CiteScore
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