Phenol driven changes onto MnO(2) surface for efficient removal of methyl parathion: The role of adsorption.
Phenol driven changes onto MnO(2) surface for efficient removal of methyl parathion: The role of adsorption.
复制标题
苯酚驱动的 MnO(2) 表面变化可有效去除甲基对硫磷:吸附的作用。
DOI:
10.1016/j.chemosphere.2020.128695
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发表时间:
2021
期刊:
影响因子:
8.8
通讯作者:
Hu Lisong
中科院分区:
文献类型:
--
作者:
Liao Xiaoping;Zhang Caixiang;Nan Chao;Lv You;Fan Zenghui;Hu Lisong
Manganese oxides (MnO2), important environmental oxides, have drawn significant attention in areas such as detoxification of micro-hazardous organic contaminants with electron-donating functional groups such as –OH. However, studies on whether these oxidized processes might further impact the fate of some esters like organophosphorus pesticide (OPPs) remain poorly understood. Herein, we propose a new mechanism involved in the enhanced removal of methyl parathion in mixtures of MnO2and phenol. Specifically, the removal of methyl parathion (up to 73.7%) was significantly higher for a binary system than for MnO2alone (approximately 9.3%) and was primarily due to adsorption rather than degradation. The extent of methyl parathion adsorption was dependent significantly on pH, reactant loading and metal ion co-solutes (such as Ca2+, Mg2+, Fe3+and Mn2+). Both spectroscopic (FT-IR, SEM-EDX and XPS) and chromatographic (LC/HRMS) analyses showed that the remarkable increase in the number of organics (e.g., polymers) onto the MnO2surface dominated methyl parathion adsorption via hydrogen bonding, n-π and π-π interactions, van der Waals forces and pore-diffusion. The results from this study provided evidence for the role of manganese oxides in adsorption of methyl parathion in soil-aquatic environments involving phenolic compounds.