Facile synthesis of N-doped 3D graphene aerogel and its excellent performance in catalytic degradation of antibiotic contaminants in water

被引:131
|
作者
Wang, Jun [1 ]
Duan, Xiaoguang [2 ]
Dong, Qi [1 ]
Meng, Fanpeng [1 ]
Tan, Xiaoyao [1 ]
Liu, Shaomin [3 ]
Wang, Shaobin [2 ]
机构
[1] Tianjin Polytech Univ, Dept Chem Engn, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China
[2] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
[3] Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia
基金
中国博士后科学基金; 澳大利亚研究理事会;
关键词
EMERGING ORGANIC CONTAMINANTS; HETEROGENEOUS CATALYSIS; ACTIVE-SITES; METAL; ADSORPTION; OXIDATION; NITROGEN; ACTIVATION; GENERATION; OXIDE;
D O I
10.1016/j.carbon.2019.01.003
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
3D nitrogen-doped graphene aerogels (NGA) with hierarchically porous architectures and integrated macrostructures were facilely constructed by self-assembly of graphene oxide (GO) nanosheets and melamine. NGA exhibited excellent catalytic activities in peroxymonosulfate (PMS) activation for oxidative degradation of ibuprofen (IBP). NGA attained 44- and 8-fold enhancement in reaction rate over graphene aerogel (GA) and N-doped reduced graphene oxide (NrGO), respectively. Furthermore, the chemical reactivity of NGA could be facilely recovered by thermal annealing. The superior catalysis of NGA can be ascribed to the synergistic effects of 3D porous framework and N-doping in sp(2)-hybridized NGA. Graphitic N is demonstrated to be the intrinsic active sites in PMS activation. The 3D porous architecture is beneficial for adsorption and diffusion of the pollutant/oxidant and graphitic carbons within the conjugated pi system facilitate the electron transfer. Electron paramagnetic resonance and radical quenching tests indicate that NGA/PMS is a radical-based system, where SO4 center dot- and center dot OH with strong oxidative potentials account for the catalytic degradation of IBP. This study affords an innovative strategy for development of promising metal-free catalysts towards better advanced oxidation processes. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:781 / 790
页数:10
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