Boosting micropollutants removal over bimetallic Fe-Mo catalyst via peracetic acid activation: Mo doping enhanced generation of reactive oxygen species

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Journal of Hazardous Materials Pub Date : 2025-03-21 DOI:10.1016/j.jhazmat.2025.138013
Congcong Guo, Chao Yu, Yiran Zhang, Yuyou Li, Jun Wan, Lei Wang, Jingwen Pan
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Abstract

Herein, a range of bimetallic Fe-Mo catalysts (FexMoy@C) were successfully synthesized to explore the effect of Mo doping on the activity of Fe-based catalyst (Fe@C) for peracetic acid (PAA) activation. Mo doped during Fe@C preparation process introduced more low-valent metal species into Fe@C with the potential to promote PAA activation and Fe(III)/Fe(II) cycling. Compared to single Fe catalyst, Fe4Mo1@C exhibited outstanding performance in PAA activation for ultrafast degradation of bisphenol A (BPA), with the degradation rate of 0.88 min-1, which exceeded most reported heterogeneous catalysts. Mechanism results indicated that the Mo doping promoted the generation of reactive species and accelerated Fe(III)/Fe(II) conversion on the surface of Fe4Mo1@C to ensure the continuous PAA activation. Further analysis revealed that incorporated Mo not only promoted electron transfer and accelerated transform of Fe(III) to Fe(II), but also lowered the energy barrier for PAA activation. Moreover, the toxicity of BPA and its intermediates could be effectively reduced in Fe4Mo1@C/PAA system, guaranteeing the safety of treatment process. This study clarified the mechanism of Mo doping to enhance the Fe-based catalysts activity for organic micropollutant degradation, and the new insights obtained would further promote the application of bimetallic catalysts in PAA-based advanced oxidation processes.

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通过过氧乙酸活化促进双金属Fe-Mo催化剂去除微污染物:Mo掺杂增强活性氧的产生
本文成功合成了一系列双金属Fe-Mo催化剂(FexMoy@C),以探索Mo掺杂对fe基催化剂(Fe@C)过氧乙酸(PAA)活化活性的影响。在Fe@C制备过程中掺杂Mo将更多的低价金属引入Fe@C中,有可能促进PAA活化和Fe(III)/Fe(II)循环。与单一Fe催化剂相比,Fe4Mo1@C在PAA活化双酚A (BPA)的超快降解中表现出优异的性能,降解速率为0.88 min-1,超过了目前报道的大多数多相催化剂。机理结果表明,Mo掺杂促进了反应物质的生成,加速了Fe4Mo1@C表面Fe(III)/Fe(II)的转化,保证了PAA的持续活化。进一步分析表明,Mo的加入不仅促进了Fe(III)向Fe(II)的电子转移,加速了Fe(III)向Fe(II)的转变,而且降低了PAA活化的能垒。同时,Fe4Mo1@C/PAA体系可以有效降低BPA及其中间体的毒性,保证处理过程的安全性。本研究阐明了Mo掺杂增强fe基催化剂降解有机微污染物活性的机理,获得的新见解将进一步促进双金属催化剂在paas基高级氧化工艺中的应用。
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来源期刊
Journal of Hazardous Materials
Journal of Hazardous Materials 工程技术-工程:环境
CiteScore
25.40
自引率
5.90%
发文量
3059
审稿时长
58 days
期刊介绍: The Journal of Hazardous Materials serves as a global platform for promoting cutting-edge research in the field of Environmental Science and Engineering. Our publication features a wide range of articles, including full-length research papers, review articles, and perspectives, with the aim of enhancing our understanding of the dangers and risks associated with various materials concerning public health and the environment. It is important to note that the term "environmental contaminants" refers specifically to substances that pose hazardous effects through contamination, while excluding those that do not have such impacts on the environment or human health. Moreover, we emphasize the distinction between wastes and hazardous materials in order to provide further clarity on the scope of the journal. We have a keen interest in exploring specific compounds and microbial agents that have adverse effects on the environment.
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