A novel catalyst of MIL-101(Fe) doped with Co and Cu as persulfate activator: synthesis, characterization, and catalytic performance

催化作用 过硫酸盐 材料科学 扫描电子显微镜 金属有机骨架 兴奋剂 拉曼光谱 傅里叶变换红外光谱 吸附 金属 透射电子显微镜 无机化学 核化学 化学工程 化学 纳米技术 物理化学 有机化学 冶金 光电子学 物理 光学 复合材料 工程类
作者
Meijuan Duan,Zeyu Guan,Yongwen Ma,Jinquan Wan,Yan Wang,Yanfei Qu
出处
期刊:Chemical Papers [Springer Science+Business Media]
卷期号:72 (1): 235-250 被引量:64
标识
DOI:10.1007/s11696-017-0276-7
摘要

In this work, effective and novel heterogeneous catalysts of Metal–organic framework MIL-101(Fe) doped with cobalt (Co2+) or copper (Cu2+) have been synthesized by post-synthesis method, namely Co–MIL-101(Fe) and Cu–MIL-101(Fe). The initial and metal-doped samples were tested to activate persulfate (PS) for removal of Acid Orange 7 (AO7) in water. The surface of samples were characterized using X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, N2 adsorption, scanning electron microscopy and transmission electron microscopy. The addition of Cu2+ and Co2+ could alter structure characteristics of MIL-101(Fe) in crystal structure and morphology. The unusual octahedron morphology of MIL-101(Fe) turned to be irregular, disorder and a rod-like morphology was shaped. What is more, Co doping caused greater changes in structure characteristics in comparison with Cu doping. The alteration was reflected in the catalytic capacity of PS activation. An interesting note was that, whether Co or Cu doping, metal-doped MIL-101(Fe) greatly improved the PS activation as compared to unmodified MIL-101(Fe). The removal rate of AO7 was about 66, 92, 98% in MIL-101(Fe)/PS, 6%wtCu–MIL-101(Fe)/PS and 6%wtCo–MIL-101(Fe)/PS system, respectively. Some results also suggested the performance of Co–MIL-101(Fe) was superior to that of Cu–MIL-101(Fe). Additionally, a series of parameters were designed to achieve maximum capacity of PS activation. Such an enhancement in activity may be attributed to the main reasons: the new active sites created by metal additives; an increase in number of active Fe sites produced by Co and Cu doping which results in alteration of morphology and structure of catalysts.
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