Synthesis, Structure, and Selective Gas Adsorption of a Single-Crystalline Zirconium Based Microporous Metal-Organic Framework

被引:24
|
作者
Wang, Hao [1 ]
Wang, Qining [1 ]
Teat, Simon J. [2 ]
Olson, David H. [1 ]
Li, Jing [1 ]
机构
[1] Rutgers State Univ, Dept Chem & Chem Biol, 610 Taylor Rd, Piscataway, NJ 08854 USA
[2] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
关键词
CARBON-DIOXIDE CAPTURE; COMMENSURATE ADSORPTION; CO2; CAPTURE; SEPARATION; STABILITY; FLUOROCARBONS; HYDROCARBONS; PERFORMANCE; MIXTURES; UIO-66;
D O I
10.1021/acs.cgd.7b00030
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porous metal organic framework (MOP) materials with high thermal and water stability are desirable for various adsorption based applications. Early transition metal based MOFs such as those built on zirconium metal have been well recognized for their excellent stability toward heat and/or moisture. However, the difficulty growing large single crystals makes their structural characterization challenging. Herein we report a porous Zr-MOF, [Zr6O4(OH)(4)(cca)(6)] (Zr-cca), which is assembled from zirconium and 4-carboxycinnamic acid (H(2)cca) under solvothermal conditions. Single crystal X-ray diffraction analysis reveals that the structure of Zr-cca is isoreticular to the prototype zirconium based MOF, UiO-66. Zr-cca shows permanent porosity upon removal of solvent molecules initially residing inside the pores, with a BET surface area of 1178 m(2)/g. As expected, it exhibits good thermal stability (stable up to 400 degrees C) and high resistance to acidity over a wide pH range. Evaluation of its gas adsorption performance on various hydrocarbons and fluorocarbons indicates that it preferentially adsorbs C-3 and C-4 hydrocarbons over C-2 analogues. At 30 degrees C Zr-cca takes up more than 50 wt % of perfluorohexane and the adsorption-desorption process is fully recyclable. We have compared this material with UiO-66 and studied the underlying reasons for the difference in their adsorption performance toward perfluorohexane.
引用
收藏
页码:2034 / 2040
页数:7
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