过氧二硫酸盐
异质结
降级(电信)
催化作用
光催化
可见光谱
可重用性
猝灭(荧光)
辐照
材料科学
光化学
电子顺磁共振
反应速率常数
化学
光电子学
动力学
荧光
光学
核磁共振
有机化学
核物理学
物理
电信
程序设计语言
软件
量子力学
计算机科学
作者
Qi Yang,Chang‐Wei Bai,Yi-Jiao Sun,Yujie Liu,Kejun Hou,Fei Chen
标识
DOI:10.1016/j.cej.2023.145221
摘要
Heterogeneous iron materials show potential for activating peroxydisulfate (PDS). However, these systems may be constrained by low efficiency and secondary pollution. The visible-light-assisted activation has been demonstrated as a feasible and effective approach to enhance PDS activation by iron-based materials. In this study, a visible-light-responsive Bi2WO6/Fe2O3 heterojunction photocatalyst was synthesized to improve the ability of Fe2O3 for PDS activation through an effective Fe(III)/Fe(II) cycle. Rapid tetracycline (TC, a common antibiotic) removal (91.7% within 60 min at a concentration of 20 mg·L-1) was achieved in the constructed Bi2WO6/Fe2O3/PDS/vis system under conditions of 0.3 g·L-1 PDS and 0.3 g·L-1 catalyst. The corresponding pseudo-first-order rate constant reached 4.16 × 10-2 min-1, which was 8.42 and 16.38 times higher than those of Bi2WO6/Fe2O3/vis and Bi2WO6/Fe2O3/PDS systems, respectively. Moreover, the Bi2WO6/Fe2O3 exhibited favorable stability and reusability even after five cycles. Lastly, a catalytic mechanism for TC removal and PDS activation was proposed based on quenching experiments and electron spin resonance (ESR) tests. The SO4•- and •OH played a major role in TC removal, while •O2– and 1O2 contributed as auxiliary factors. This study presents a promising strategy for activating PDS using cost-effective and stable Fe(III)-based heterojunctions, and such an idea can be used to design catalysts for other high-value reactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI