Sustainable Preparation of MIL-100(Fe) and Its Photocatalytic Behavior in the Degradation of Methyl Orange in Water

光催化 甲基橙 热重分析 材料科学 漫反射红外傅里叶变换 降级(电信) 金属有机骨架 化学工程 解吸 扫描电子显微镜 核化学 化学 催化作用 纳米技术 吸附 有机化学 复合材料 工程类 电信 计算机科学
作者
Kiros Guesh,Clarice A. D. Caiuby,Álvaro Mayoral,Manuel Díaz‐García,Isabel Dı́az,Manuel Sánchez‐Sánchez
出处
期刊:Crystal Growth & Design [American Chemical Society]
卷期号:17 (4): 1806-1813 被引量:326
标识
DOI:10.1021/acs.cgd.6b01776
摘要

The real industrial establishment of metal–organic frameworks (MOFs) requires significant advances in economic and chemical sustainability. This work describes a novel and simple method to prepare one of the most widely studied MOF materials, i.e., MIL-100(Fe), which significantly improves the sustainability of the conventional process in several aspects. This MOF material is prepared (i) at room temperature (instead of 150 °C used in the conventional method), (ii) after a few hours (instead of 6 days), (iii) in the absence of any inorganic corrosive acid (significant amounts of HF and HNO3 are used in the conventional method), and (iv) it is washed at room temperature (unlike the washing at 80 °C for 3 h). Interestingly, the only difference in the preparation method of MIL-100(Fe) compared with that of semiamorphous Fe-BTC (MOF material commercialized as Basolite F300 having the same metal and linker, and which can be also prepared under similar sustainable conditions) is to start from Fe(II) or Fe(III) sources, respectively, which opens certain versatility options in the room temperature synthesis procedures of MOF materials. The prepared samples were characterized using X-ray diffraction, thermogravimetric analysis, N2 adsorption/desorption isotherms, Cs-aberration corrected scanning transmission electron microscopy, and UV–vis diffuse reflectance spectroscopy. These two room-temperature-made Fe-BTC materials were tested in the industrially demanded photocatalytic degradation of methyl orange under both ultraviolet and solar light radiation. MIL-100(Fe) was a very active photocatalyst in comparison with its homologue. That difference was mainly attributed to the presence of larger cavities within its structure.
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