Interface-Promoted Direct Oxidation of p-Arsanilic Acid and Removal of Total Arsenic by the Coupling of Peroxymonosulfate and Mn-Fe-Mixed Oxide

化学 吸附 氧化物 氧化法 污染物 高级氧化法 无机化学 催化作用 核化学 化学工程 有机化学 工程类
作者
Ming‐Kun Ke,Gui‐Xiang Huang,Shu‐Chuan Mei,Zhaohua Wang,Yingjie Zhang,Tian-Wei Hua,Lirong Zheng,Han‐Qing Yu
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:55 (10): 7063-7071 被引量:50
标识
DOI:10.1021/acs.est.1c00386
摘要

As one of the extensively used feed additives in livestock and poultry breeding, p-arsanilic acid (p-ASA) has become an organoarsenic pollutant with great concern. For the efficient removal of p-ASA from water, the combination of chemical oxidation and adsorption is recognized as a promising process. Herein, hollow/porous Mn–Fe-mixed oxide (MnFeO) nanocubes were synthesized and used in coupling with peroxymonosulfate (PMS) to oxidize p-ASA and remove the total arsenic (As). Under acidic conditions, both p-ASA and total As could be completely removed in the PMS/MnFeO process and the overall performance was substantially better than that of the Mn/Fe monometallic system. More importantly, an interface-promoted direct oxidation mechanism was found in the p-ASA-involved PMS/MnFeO system. Rather than activate PMS to generate reactive oxygen species (i.e., SO4·–, ·OH, and 1O2), the MnFeO nanocubes first adsorbed p-ASA to form a ligand–oxide interface, which improved the oxidation of the adsorbed p-ASA by PMS and ultimately enhanced the removal of the total As. Such a direct oxidation process achieved selective oxidation of p-ASA and avoidance of severe interference from the commonly present constituents in real water samples. After facile elution with dilute alkali solution, the used MnFeO nanocubes exhibited superior recyclability in the repeated p-ASA removal experiments. Therefore, this work provides a promising approach for efficient abatement of phenylarsenical-caused water pollution based on the PMS/MnFeO oxidation process.
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