双金属片
X射线光电子能谱
纳米孔
催化作用
扫描电子显微镜
材料科学
金属有机骨架
透射电子显微镜
化学工程
傅里叶变换红外光谱
吸附
过氧二硫酸盐
核化学
红外光谱学
化学
无机化学
纳米技术
有机化学
复合材料
工程类
作者
Huanxuan Li,Jian Zhang,Yue Yao,Xiangrui Miao,Jiale Chen,Junhong Tang
标识
DOI:10.1016/j.envpol.2019.113337
摘要
In this work, we report on the synthesis and characterization of nanoporous bimetallic metal-organic frameworks (FeCo-BDC). Effects of synthesis time and temperature on the structures, morphology, and catalytic performance of FeCo-BDC were investigated. Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM) and Brunauer-Emmett-Teller (BET) were used to reveal the morphological and textural characteristics. The crystal structure and chemical composition of FeCo-BDC were determined by means of X-ray powder diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray Photoelectron Spectroscopy (XPS), and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) measurements. Interestingly, FeCo-BDC grew into the same crystal structure with different morphology in the temperature of 110–150 °C with 12–48 h. The heterogeneous catalytic activity of FeCo-BDC was tested to activate peroxydisulfate (PDS) and peroxymonosulfate (PMS) for removal of methylene blue (MB). The results found that FeCo-BDC synthesized at 150 °C with 24 h exhibited the best catalytic performance for PMS and obtained 100% of MB removal within 15 min. The abundant unsaturated metal active sites of Fe(II) and Co(II) in the skeleton of FeCo-BDC made a great contribution to the generation of sulfate () and hydroxyl radicals (OH), which resulted in the excellent performance for MB degradation.
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