Hierarchical porous graphite-like carbon nanosheet cooperated with Fe/Fe3C@Fe-N-C nanocomposites toward catalytic oxidation process

单线态氧 催化作用 激进的 电子顺磁共振 化学 羟基自由基 纳米片 碳纤维 石墨 氧气 活性氧 纳米复合材料 光化学 无机化学 材料科学 纳米技术 有机化学 物理 复合材料 复合数 生物化学 核磁共振
作者
Haoyang Wu,Zhilong Tan,Bin Miao,Hailong Hu,Sanying Hou
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:11 (1): 109204-109204 被引量:17
标识
DOI:10.1016/j.jece.2022.109204
摘要

In this work, Fe, N co-doped hierarchical porous graphite-like carbon with carbon-encapsulated Fe/Fe3[email protected] Fe-N-C was synthesized by a facile solid-phase synthesis strategy, and was employed as an efficient catalyst to activate peroxymonosulfate (PMS) for oxidation of tetracycline (TC). The optimal Fe-N/C 800 outlined a highly catalytic performance in activating peroxymonosulfate (PMS) with TC decomposition rate reaching 89.2 % in 20 min at ultra-low catalyst dosage. Meanwhile, the effect of operating parameters was also investigated in order to evaluate the potential of using Fe-N/C 800 in practical applications. In addition, the characterization analysis and experiments results elucidated that graphitic N, pyridinic N, CO, Fe3C, Fe0 and FeN4 were considered as the main reactive species promoting the PMS activation to generate reactive oxygen species (ROS) (including singlet oxygen (1O2), sulfate radical (SO4•-) and hydroxyl radical (•OH)). The electron paramagnetic resonance (EPR) experiments and radicals quenching analyses further demonstrated that the non-radical species singlet oxygen (1O2) was the dominant reactive oxygen species. Moreover, the TC degradation pathways were presented by LC-MS. Ultimately, the toxicity of the intermediate products were also investigated by ECOSAR system.

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