Performance and mechanism of efficient activation of peroxymonosulfate by Co-Mn-ZIF derived layered double hydroxide for the degradation of enrofloxacin

被引:38
|
作者
Yang, Yiqiong [1 ]
Jie, Borui [1 ]
Zhai, Yixuan [1 ]
Zeng, Yijie [1 ]
Kang, Jingyan [1 ]
Cheng, Geng [1 ]
Zhang, Xiaodong [1 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Environm & Architecture, Shanghai 200093, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Co-Mn-Ni layered double hydroxide (Co-Mn-Ni LDH); Co-Mn-zeolitic imidazolate framework (Co-Mn-ZIF); PMS activation; Enrofloxacin (ENR); GRAPHENE OXIDE; NANOPARTICLES; OXIDATION; PATHWAYS; REMOVAL; FRAMEWORKS; CATALYST; WATER;
D O I
10.1016/j.molliq.2023.123723
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
Due to the uncontrolled synthesis of layered double hydroxides (LDHs), a simple and efficient strategy was needed to construct high-performance LDHs. Herein, Co-Mn-ZIF was used as the sacrificial template to form cobalt-manganese-nickel LDH (M-Co-Mn-Ni LDH) through the process of deconstruction and reconstruction. Due to the sufficient in-situ etching of the Co-Mn-ZIF template, M-Co-Mn-Ni LDH exhibited a larger specific surface area (482.4 m(2)/g) and pore volume (3.3 x 10(-2) cm(3)/g) as well as easier diffusion and interaction with reaction sites of organic molecules. The prepared M-Co-Mn-Ni LDH showed high catalytic performance for the degradation of enrofloxacin (ENR) by activating peroxymonosulfate (PMS), with the removal rate of 88.5 % within 30 min. The quenching reaction and electron paramagnetic resonance (EPR) analysis results indicated that SO4 center dot- and O-1(2) were main active substances in the oxidation process of ENR. In addition, the Co-Mn-Ni LDH/PMS system was stable and almost unaffected by pH values, organic and inorganic substances, and it could achieve high removal efficiency in various pollutant samples. This work provided a convenient and efficient approach for the construction of high-performance MOFs derived LDHs catalysts.
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页数:13
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