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New insights into iron/nickel-carbon ternary micro-electrolysis toward 4-nitrochlorobenzene removal: Enhancing reduction and unveiling removal mechanisms

三元运算 电解 阴极 材料科学 无机化学 阳极 活性炭 碳纤维 零价铁 氧化还原 化学 化学工程 冶金 电极 物理化学 复合材料 复合数 工程类 吸附 电解质 程序设计语言 计算机科学
作者
Mengmeng Xiong,Siyi Gu,Gu He,Daofang Zhang,Chenyang Ma,Zhihua Xu
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:612: 308-322 被引量:11
标识
DOI:10.1016/j.jcis.2021.12.116
摘要

The ternary micro-electrolysis material iron/nickel-carbon (Fe/Ni-AC) with enhanced reducibility was constructed by introducing the trace transition metal Ni based on the iron/carbon (Fe/AC) system and used for the removal of 4-nitrochlorobenzene (4-NCB) in solution. The composition and structures of the Fe/Ni-AC were analyzed by various characterizations to estimate its feasibility as reductants for pollutants. The removal efficiency of 4-NCB by Fe/Ni-AC was considerably greater than that of Fe/AC and iron/nickel (Fe/Ni) binary systems. This was mainly due to the enhanced reducibility of 4-NCB by the synergism between anode and double-cathode in the ternary micro-electrolysis system (MES). In the Fe/Ni-AC ternary MES, zero-iron (Fe0) served as anode involved in the formation of galvanic couples with activated carbon (AC) and zero-nickel (Ni0), respectively, where AC and Ni0 functioned as double-cathode, thereby promoting the electron transfer and the corrosion of Fe0. The cathodic and catalytic effects of Ni0 that existed simultaneously could not only facilitate the corrosion of Fe0 but also catalyze H2 to form active hydrogen (H*), which was responsible for 4-NCB transformation. Besides, AC acted as a supporter which could offer the reaction interface for in-situ reduction, and at the same time provide interconnection space for electrons and H2 to transfer from Fe0 to the surface of Ni0. The results suggest that a double-cathode of Ni0 and AC could drive much more electrons, Fe2+ and H*, thus serving as effective reductants for 4-NCB reduction.

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