School of Chemical Engineering, Northeast Electric Power University, Jilin 132012, China; Lanhe Zhang and Qi Zhang are co-first authors.
School of Chemical Engineering, Northeast Electric Power University, Jilin 132012, China.
Water Sci Technol. 2024 Apr;89(7):1860-1878. doi: 10.2166/wst.2024.076. Epub 2024 Mar 11.
The activated persulfate (PS) process could produce sulfate radical (SO) and rapidly degrade organic pollutants. The application of FeO as a promising PS activator was limited due to the rapid conversion of Fe to Fe on its surface. Mo on MoS surface could be used as a reducing site to convert Fe to Fe, but the separation and recovery of MoS was complex. In this study, MoS/FeO was prepared to accelerate the Fe/Fe cycle on FeO surface and achieved efficient separation of MoS. The results showed that MoS/FeO was more effective for PS activation compared to FeO or MoS, with a removal efficiency of 91.8% for 20 mg·L tetracycline (TC) solution under the optimal conditions. Fe and Mo on MoS/FeO surface acted as active sites for PS activation with the generation of SO, •OH, •O, and O. Mo acted as an electron donor to promote the Fe/Fe cycling and thus improved the PS activation capability of MoS/FeO. The degradation pathways of TC were inferred as hydroxylation, ketylation of dimethylamino group and C-N bond breaking. This study provided a promising activated persulfate-based advanced oxidation process for the efficient degradation of TC by employing MoS/FeO as an effective activator.
过硫酸盐活化(PS)过程可以产生硫酸根自由基(SO),并迅速降解有机污染物。由于其表面的铁迅速转化为铁,因此将 FeO 作为一种有前途的 PS 活化剂的应用受到限制。MoS 表面上的 Mo 可以作为还原位点将 Fe 转化为 Fe,但 MoS 的分离和回收很复杂。本研究制备了 MoS/FeO 以加速 FeO 表面上的 Fe/Fe 循环,并实现了 MoS 的有效分离。结果表明,与 FeO 或 MoS 相比,MoS/FeO 对 PS 活化更有效,在最佳条件下,20mg·L 四环素(TC)溶液的去除效率达到 91.8%。MoS/FeO 表面上的 Fe 和 Mo 作为 PS 活化的活性位点,生成 SO、•OH、•O 和 O。Mo 作为电子供体促进 Fe/Fe 循环,从而提高了 MoS/FeO 的 PS 活化能力。TC 的降解途径推断为羟基化、二甲氨基的酮化和 C-N 键断裂。本研究提供了一种有前途的基于过硫酸盐的高级氧化工艺,通过使用 MoS/FeO 作为有效的活化剂,可有效降解 TC。