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Synthesis of MIL-53(Fe) Metal-Organic Framework Material and Its Application as a Catalyst for Fenton-Type Oxidation of Organic Pollutants

机译:MIL-53(Fe)金属 - 有机骨架材料的合成及其作为有机污染物氧化型氧化催化剂的应用

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The iron (III) benzene dicarboxylate metal-organic framework material (MIL-53(Fe)) was synthesized with either the solvent-thermal or hydrothermal method under different conditions. The influence of the type of solvents, molar ratio of precursors and solvent, temperature, and reaction time on the structure of MIL-53(Fe) was investigated. The material was characterized by using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), and N 2 adsorption/desorption isotherm. The MIL-53(Fe) structure formed in N′, N-dimethylformamide (DMF) and methanol (MeOH) but not in water. In DMF, the molar ratio of precursors and solvent, temperature, and reaction time had a significant effect on the crystal structure of MIL-53(Fe). Under optimal conditions, MIL-53(Fe) has high crystallinity and a large specific surface area ( ?=?88.2?m 2 /g). The obtained MIL-53(Fe) could serve as a potential heterogeneous catalyst to oxidize phenol (PhN), rhodamine B (RhB), and methylene blue (MtB) in the Fenton-like reaction system at the different solution pHs.
机译:铁(III)苯二羧酸金属 - 有机骨架材料(MIL-53(Fe))在不同条件下用溶剂 - 热或水热法合成。研究了溶剂类型,前体和溶剂,温度和反应时间对MIL-53(Fe)结构的影响。该材料的特征在于使用X射线衍射(XRD),傅里叶变换红外光谱(FT-IR),扫描电子显微镜(SEM),高分辨率透射电子显微镜(HR-TEM),X射线光电子谱( XPS),N 2吸附/解吸等温线。在N',N-二甲基甲酰胺(DMF)和甲醇(MeOH)中形成的MIL-53(Fe)结构但不在水中。在DMF中,前体和溶剂,温度和反应时间的摩尔比对MIL-53(Fe)的晶体结构具有显着影响。在最佳条件下,MIL-53(Fe)具有高结晶度和大的比表面积(α=88.2μm2 / g)。所得MIL-53(Fe)可以用作潜在的异质催化剂,以在不同溶液pH下氧化在芬顿的反应体系中的苯酚(PHN),罗丹明B(MTB)和亚甲基蓝(MTB)。

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