Zhang Yue, Zhao Bangcheng, Wang Caijie, Huang Yuyu, Liu Xiang, Wang Ruikun, Wang ChunBo
Department of Energy Power & Mechanical Engineering, North China Electric Power University, Baoding 071003, China; Hebei Key Laboratory of Low Carbon and High Efficiency Power Generation Technology, North China Electric Power University, Baoding 071003, Hebei, China.
Department of Energy Power & Mechanical Engineering, North China Electric Power University, Baoding 071003, China.
J Hazard Mater. 2023 Oct 5;459:132079. doi: 10.1016/j.jhazmat.2023.132079. Epub 2023 Jul 17.
Arsenic oxidation plays a crucial role in its removal, which has been identified in numerous studies. However, the mechanisms, especially reaction pathways of arsenic oxidation on sorbent surfaces remain inadequately explored. In this work, the effects of Mn doping on arsenic adsorption and oxidation were first verified by adsorption experiments. Subsequently, DFT calculations were carried out to identify alterations in the adsorption energies, active sites, and oxidation pathways. By integrating the experimental and simulation results, a dual-functional framework encompassing adsorption and catalysis of Mn-modified Fe-based material was distinctly established. For adsorption, the introduction of manganese into iron-based sorbent considerably enhanced AsO adsorption owing to the increased active sites available for AsO chemisorption and the promotion of surface nucleophilicity. Concerning oxidative catalysis, the incorporation of MnO augmented surface catalytic oxidation and provided a substantial amount of active O. Consequently, the arsenic oxidation occurring on the Mn-modified sorbent surfaces possessed a lower oxidation RDS energy barrier and a shorter oxidation pathway than those on the bare sorbent surfaces. These experimental and simulation results provide a theoretical basis for the design and application of efficient gaseous arsenic adsorbents.
砷的氧化在其去除过程中起着关键作用,这一点已在众多研究中得到证实。然而,其机制,尤其是砷在吸附剂表面的氧化反应途径仍未得到充分探索。在这项工作中,首先通过吸附实验验证了锰掺杂对砷吸附和氧化的影响。随后,进行了密度泛函理论(DFT)计算,以确定吸附能、活性位点和氧化途径的变化。通过整合实验和模拟结果,明确建立了一个包含锰改性铁基材料吸附和催化功能的双功能框架。对于吸附而言,由于可用于AsO化学吸附的活性位点增加以及表面亲核性的促进,将锰引入铁基吸附剂显著增强了AsO的吸附。关于氧化催化,MnO的掺入增强了表面催化氧化并提供了大量活性氧。因此,与未改性吸附剂表面相比,锰改性吸附剂表面发生的砷氧化具有更低的氧化速率决定步骤(RDS)能垒和更短的氧化途径。这些实验和模拟结果为高效气态砷吸附剂的设计和应用提供了理论依据。