Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, 200 Xiao Ling Wei, Nanjing 210094, China.
Research Center for Environmental Nanotechnology (ReCENT), State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China.
Environ Sci Technol. 2022 Apr 5;56(7):4498-4506. doi: 10.1021/acs.est.1c08790. Epub 2022 Mar 17.
The environmentally benign Mn oxides play a crucial role in the transformation of organic contaminants, either through catalytically decomposing oxidants, e.g., peroxymonosulfate (PMS), or through directly oxidizing the target pollutants. Because of their dual roles and the complex surface chemical reactions, the mechanism involved in Mn oxide-catalyzed PMS activation processes remains obscure. Here, we clearly elucidate the mechanism involved in the MnO catalyzed PMS activation process by means of separating the PMS activation and the pollutant oxidation process. MnO acts as a shuttle that mediates the electron transfer from organic substrates to PMS, accompanied by the redox cycle of surface Mn(IV)/Mn(III). Multiple experimental results indicate that PMS is bound to the surface of MnO to form an inner-sphere complex, which then decomposes to form long-lived surface reactive Mn(IV) species, without the generation of sulfate radicals (SO) and hydroxyl radicals (HO). The surface reactive Mn(IV) species are proposed to be responsible for the degradation of organic contaminants (e.g., phenol) and the formation of singlet oxygen (O), followed by the regeneration of the surface Mn(III) sites on MnO. This study advances the fundamental understanding of the underlying mechanism involved in transition metal oxide-catalyzed PMS activation processes.
环境友好型的 Mn 氧化物在有机污染物的转化中起着至关重要的作用,无论是通过催化分解氧化剂(如过一硫酸盐(PMS)),还是通过直接氧化目标污染物。由于其双重作用和复杂的表面化学反应,Mn 氧化物催化 PMS 活化过程中涉及的机制仍然不清楚。在这里,我们通过分离 PMS 活化和污染物氧化过程,清楚地阐明了 MnO 催化 PMS 活化过程中涉及的机制。MnO 作为一种介体,介导有机底物向 PMS 的电子转移,同时伴随着表面 Mn(IV)/Mn(III)的氧化还原循环。多项实验结果表明,PMS 与 MnO 的表面结合形成内球络合物,然后分解形成长寿命的表面反应性 Mn(IV)物种,而不会生成硫酸盐自由基 (SO)和羟基自由基 (HO)。表面反应性 Mn(IV)物种被认为是降解有机污染物(如苯酚)和形成单线态氧(O)的原因,随后 MnO 表面的 Mn(III)位点得到再生。这项研究推进了对过渡金属氧化物催化 PMS 活化过程中涉及的潜在机制的基本理解。