Yang Yang, Yao Tongjie, Balasubramanian Rajasekhar, Chen J Paul
Department of Civil and Environmental Engineering, National University of Singapore, 10 Kent Ridge, Singapore; State Key Laboratory of Urban Water Resource and Environment, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, PR China.
State Key Laboratory of Urban Water Resource and Environment, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, PR China.
J Colloid Interface Sci. 2025 Apr;683(Pt 2):496-506. doi: 10.1016/j.jcis.2024.12.145. Epub 2024 Dec 19.
Fenton reaction technology has worked well in water and wastewater treatment; however it is often limited by such problems as continuous external supply of HO, slow Fe/Fe cycle rate, high energy requirements, and maintenance of low pH during operation. Herein, a novel self-sufficient heterogeneous Fenton system based on Fe/MoS was designed, fabricated, and optimized to effectively address these problems. The combined presence of Fe and sulfur vacancies sites in MoS played a pivotal role in the generation of HOvia two-step single-electron reduction process without any energy consumption. The existence of dual active sites resulted in a considerable increase in the HO yield (up to 0.6 mM/g/h) in a pH-neutral aqueous solution. Furthermore, the Fe/Fe cycle rate was accelerated by Mo/Mo/Mo sites. The factors collectively contributed to the impressive performance of the reaction in degrading complex pollutants (e.g., polyethylene, a model plastic matter) under pH-neutral conditions. In addition to its outstanding catalytic performance, Fe/MoS exhibited superior reusability and stability. Notably, the catalyst reactivity was well sustained in the presence of common competitive factors such as inorganic anions and dissolved organic pollutants, and for other polymer types. This study demonstrates that Fe/MoS with impressive self-sufficient Fenton reaction capacity has greater potentials for water and wastewater treatment.
芬顿反应技术在水和废水处理中效果良好;然而,它常常受到诸如羟基自由基(HO)的持续外部供应、铁(Fe)/亚铁(Fe)循环速率缓慢、高能量需求以及运行过程中低pH值的维持等问题的限制。在此,设计、制备并优化了一种基于铁/二硫化钼(Fe/MoS)的新型自给自足的非均相芬顿体系,以有效解决这些问题。二硫化钼中Fe和硫空位的共同存在,在无需任何能量消耗的两步单电子还原过程中羟基自由基的生成中起关键作用。双活性位点的存在导致在pH中性水溶液中羟基自由基产率显著提高(高达0.6 mM/g/h)。此外,钼(Mo)/钼(Mo)/钼(Mo)位点加速了铁(Fe)/亚铁(Fe)循环速率。这些因素共同促成了该反应在pH中性条件下降解复杂污染物(如聚乙烯,一种典型塑料物质)时的出色性能。除了其出色的催化性能外,铁/二硫化钼还表现出卓越的可重复使用性和稳定性。值得注意的是,在存在无机阴离子和溶解有机污染物等常见竞争因素以及其他聚合物类型的情况下,催化剂的反应活性仍能很好地维持。这项研究表明,具有令人印象深刻的自给自足芬顿反应能力的铁/二硫化钼在水和废水处理方面具有更大的潜力。