双金属片
选择性
吸附
X射线光电子能谱
金属
傅里叶变换红外光谱
金属有机骨架
化学
微型多孔材料
红外光谱学
化学工程
材料科学
无机化学
催化作用
有机化学
工程类
作者
Van Nhieu Le,Van Cuong Nguyen,Huu Trung Nguyen,Hieu Thuc Tran,Thach N. Tu,Woo‐Sik Kim,Jinsoo Kim
标识
DOI:10.1016/j.micromeso.2023.112716
摘要
Bimetallic metal-organic frameworks, having two different metal species in the framework metal sites, demonstrate higher effectiveness in CO2 capture and separation performance than their monometallic counterpart. For this reason, a series of bimetallic MIL-100(Fe, Al) was synthesized using a hydrothermal reaction system in the presence of Fe and Al metal precursors with various molar ratios. The physicochemical characterizations of the products were influenced by adding Al species in the starting materials, inducing the successful incorporation of a certain amount of Al species inside the framework. The effect of Al incorporation was analyzed by inductively coupled plasma, field-emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, NH3-temperature program desorption, and a N2 porosimetry. Among the investigated samples, MIL-100(Fe, Al)#2 showed the highest CO2 adsorption capacity of 3.27 mmol g−1 with an IAST-CO2/N2 selectivity of 76.5 at 25 °C and 1 bar. Compared to the MIL-100(Fe) parent sample, the results improved by approximately 26% for CO2 uptake amount and by 1.5-fold for CO2/N2 selectivity due to the increment of micropore volume and presence of the new adsorptive sites of unsaturated metal sites (Al3+) and H+ from the bridges between tiny particles of AlOOH and –COOH groups. This facile synthetic route for bimetallic MOFs has the potential to enhance CO2 adsorption performance.
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