Removal of 2,4-dichlorophenoxyacetic acid by the boron-nitrogen co-doped carbon nanotubes: Insights into peroxymonosulfate adsorption and activation

被引:52
作者
Luo, Haopeng [1 ]
Zhou, Xin [1 ]
Chen, Quanyuan [1 ,2 ]
Zhou, Juan [1 ,2 ]
机构
[1] Donghua Univ, Coll Environm Sci & Engn, Shanghai 201620, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
2,4-D; AOPs; PMS activation; Adsorption; Synergistic effect; CATALYTIC HYDRODECHLORINATION; ORGANIC POLLUTANTS; MESOPOROUS CARBON; PERSULFATE ACTIVATION; AQUEOUS-SOLUTION; OXIDATION; GRAPHENE; DEGRADATION; NITRIDE; PERFORMANCE;
D O I
10.1016/j.seppur.2020.118196
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
B, N co-doped CNTs were synthesized by a simple one-step thermal process and the advanced oxidation processes (AOPs) of 2,4-dichlorophenoxyacetic acid (2,4-D) over the catalyst involved peroxymonosulfate (PMS) activation was investigated. The co-doped catalysts showed higher isoelectric points (IEPs) than those of CNTs and single doped CNTs, facilitating the adsorption of PMS anion (HSO5-) on the catalyst surface, and the AOPs of 2,4-D depended on PMS concentration could be illustrated by the Langmuir-Hinshelwood model. The removal efficiency of 2,4-D over CNTs, CB450, CN450 and CBN450-2 was 20%, 23%, 34% and 68%, respectively. The enhancement of catalytic activity was due to the synergistic effect between B and N dopants and both the pyrrolic N and B-N complex played roles in the catalytic reaction. The quenching test and electron paramagnetic resonance (EPR) results showed that O-1(2) contributed most to the oxidation of 2,4-D and the reaction experienced both the free radical and non-radical pathways. Additionally, the DFT calculation results showed that the adsorption energy of PMS on the surface N dopants decreased by B co-doping, implying that a moderate adsorption energy may facilitate the release of active species generated by PMS activation.
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页数:11
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