化学
传质
丙烷
吸附
多孔性
分辨率(逻辑)
体积流量
色谱法
化学工程
有机化学
热力学
计算机科学
物理
人工智能
工程类
作者
Yuan-Xiao Gao,Xuannuo Yi,Zhe-Chen Tang,Yang Han,Wei Wang,Ming Xu,Zhi‐Yuan Gu
标识
DOI:10.1021/acs.analchem.4c00880
摘要
Modulating mass transfer is crucial for optimizing the catalytic and separation performances of porous materials. Here, we systematically developed a series of continuously tunable MOFs (CTMOFs) that exhibit incessantly increased mass transfer. This was achieved through the strategic blending of ligands with different lengths and ratios in MOFs featuring the fcu topology. By employing a proportional mixture of two ligands in the synthesis of UiO-66, the micropores expanded, facilitating faster mass transfer. The mass transfer rate was evaluated by dye adsorption, dark-field microscopy, and gas chromatography (GC). The GC performance proved that both too-fast and too-slow mass transfer led to low separation performance. The optimized mass transfer in CTMOFs resulted in an exceptionally high separation resolution (5.96) in separating p-xylene and o-xylene. Moreover, this study represents the first successful use of MOFs for high-performance separation of propylene and propane by GC. This strategy provides new inspiration in regulating mass transfer in porous materials.
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