Fe/Fe3C@N-doped porous carbon hybrids derived from nano-scale MOFs: robust and enhanced heterogeneous catalyst for peroxymonosulfate activation

被引:145
作者
Zeng, Tao [1 ]
Yu, Mingdong [1 ]
Zhang, Haiyan [1 ]
He, Zhiqiao [1 ]
Chen, Jianmeng [1 ]
Song, Shuang [1 ]
机构
[1] Zhejiang Univ Technol, Coll Environm, Hangzhou 310032, Zhejiang, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; ADVANCED OXIDATION PROCESSES; NITROGEN-DOPED GRAPHENE; HIGHLY EFFICIENT; ORANGE II; FACILE SYNTHESIS; BISPHENOL-A; DEGRADATION; SULFATE; WATER;
D O I
10.1039/c6cy02130a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study subtly integrates eco-friendly and cost-effective Fe-based nanoparticles (Fe/Fe3C NPs) with N-doped porous carbon (NC) to effectively activate peroxymonosulfate (PMS) and decompose target organic compounds in water. The Fe/Fe3C@NC hybrids can be facilely fabricated through one-pot pyrolysis of an Fe, N-containing nano-scale metal-organic framework (MOF). Benefiting from the excellent enrichment ability of NC matrix and abundant accessible sites arising from NPs and catalyst support, Fe/Fe3C@NC outperformed common oxides such as Co3O4 and Fe3O4 for PMS activation and organic compound degradation. With high saturation magnetization, the catalyst can then be easily recycled for subsequent runs without significant capacity or activity loss. The applicability of this catalyst was also systematically assessed by means of the influence of the main factors and extent of mineralization. Through the mechanistic study, the active species in the system were identified as sulfate radicals (SO4-) and hydroxyl radicals (OH center dot), and the variable chemical valences of Fe NPs as well as pyridinic N and graphitic N in support contribute to the outstanding catalytic activity. Such findings elucidated a new opportunity for the design of a feasible platform to improve the overall catalytic activity in environmental remediation.
引用
收藏
页码:396 / 404
页数:9
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