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Simultaneous electrochemical degradation of organophosphorus pesticides and recovery of phosphorus: Synergistic effect of anodic oxidation and cathodic precipitation
Journal of the Taiwan Institute of Chemical Engineers ( IF 5.7 ) Pub Date : 2021-07-18 , DOI: 10.1016/j.jtice.2021.06.039
Yanan Ning 1 , Kai Li 1 , Zekun Zhao 1 , Dong Chen 1 , Yifan Li 1 , Yijie Liu 1 , Qipeng Yang 1 , Bo Jiang 1
Affiliation  

To address future phosphorus scarcity and organophosphorus pesticides discharge associated environmental problems, a filter-press type electrochemical system was developed for acephate, a typical organophosphorus pesticide, degradation and simultaneous recovery of phosphorus. In this reaction system, boron-doped diamond (BDD) mediated anodic oxidation could transform acephate into ortho-phosphate (o-PO4) and then o-PO4 was precipitated with Ca2+ at the cathode surface in the form of hydroxyapatite induced by the local basic environment. The phosphorus recovery efficiency raised from 57 % to 92 % within 180 min by elevating current density from 5 to 30 mA/cm2, accompanying the enhanced acephate mineralization efficiency from 77% to 97%. These enhancement trends were attributed to the increased yield of BDD(OH) and higher local pH near the cathode, respectively, at higher current density applied. Phosphorus recovery efficiency swelled by 15% with solution pH decreasing from 9.0 to 4.0 since anodic oxidation of acephate into o-PO4 was favorable in the acid solution. Moreover, phosphorus recovery was seriously depressed in the initial reaction stage with the presence of Mg2+, whereas bicarbonate posed the negative effect over the whole reaction process. Unexpectedly, the presence of Cl inhibited the degradation of acephate since highly oxidative OH was consumed by Cl. In general, the electrochemical strategy of “anodic oxidation-cathodic precipitation” has been demonstrated practicable for phosphorus recovery from the organophosphorus wastewater.



中文翻译:

有机磷农药的同步电化学降解和磷的回收:阳极氧化和阴极沉淀的协同作用

为了解决未来磷稀缺和有机磷农药排放相关的环境问题,开发了一种压滤式电化学系统,用于降解和同时回收磷的典型有机磷农药乙酰甲胺磷。在该反应体系中,掺硼金刚石 (BDD) 介导的阳极氧化可将乙酰磷灰石转化为正磷酸盐 (o-PO 4 ),然后 o-PO 4与 Ca 2+在阴极表面以羟基磷灰石诱导的形式沉淀。由当地的基本环境决定。通过将电流密度从 5 mA/cm 2提高到 30 mA/cm 2,磷回收效率在 180 分钟内从 57 % 提高到 92 %,伴随着乙酰甲胺磷矿化效率从 77% 提高到 97%。这些增强趋势分别归因于在施加更高电流密度时BDD( OH)产量增加和阴极附近更高的局部 pH 值。由于在酸溶液中乙酰甲胺磷阳极氧化为 o-PO 4是有利的,磷回收效率随着溶液 pH 值从 9.0 降低到 4.0 增加了 15% 。此外,Mg 2+的存在在初始反应阶段严重抑制了磷的回收率,而碳酸氢盐对整个反应过程产生了负面影响。出乎意料的是,Cl -的存在抑制了乙酰甲胺磷的降解,因为它具有高度氧化性OH 被 Cl -消耗。总的来说,“阳极氧化-阴极沉淀”的电化学策略已被证明可用于从有机磷废水中回收磷。

更新日期:2021-08-03
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