Evaluation of synthetic methods for microporous metal-organic frameworks exemplified by the competitive formation of [Cu2(btc)3(H2O)3] and [Cu2(btc)(OH)(H2O)]

被引:234
作者
Schlesinger, Maik [1 ]
Schulze, Steffen [2 ]
Hietschold, Michael [2 ]
Mehring, Michael [1 ]
机构
[1] Tech Univ Chemnitz, Inst Chem, D-09111 Chemnitz, Germany
[2] Tech Univ Chemnitz, Inst Phys, D-09126 Chemnitz, Germany
关键词
Metal-organic frameworks; Solvothermal; Microwave; Ultrasonication; Mechanochemical; HYDROGEN STORAGE; GAS-ADSORPTION; CU-3(BTC)(2); SEPARATION; PRESSURE; INSIGHTS; SOLIDS; DESIGN; GROWTH; MOFS;
D O I
10.1016/j.micromeso.2010.02.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Six different synthetic methods (solvothermal, microwave-assisted, atmospheric pressure and reflux, ultrasonic and mechanochemical conditions) for the metal-organic framework [Cu-3(btc)(2)(H2O)(3)] (btc = benzene-1,3,5-tricarboxylate) were compared. The advantages and disadvantages of the various synthetic methods were discussed including the influence of different solvents and reaction conditions on product formation, microporosity and crystallisation. Therefore, pressure and temperature for the solvothermal synthesis (autoclave and microwave) were monitored during the reaction. The characterization of the samples was performed by X-ray powder diffraction, scanning electron microscopy, infrared-spectroscopy, thermogravimetric analysis and specific surface determination using the BET method. The experimental results show that microwave-assisted solvothermal synthesis is the best method to produce crystalline [Cu-3(btc)(2)(H2O)(3)] in a short time associated with high purity, high specific pore volume (0.79 cm(3)/g) and quantitative yield. Noteworthy, the solvent-assisted mechanochemical approach gave a comparable specific pore volume of 0.74 cm(3)/g. Furthermore, synthesis conditions were explored which enable to control the product formation of either [Cu-3(btc)(2)(H2O)(3)] or [Cu-2(btc)(OH)(H2O)]. Finally, it is shown that water stability of [Cu-3(btc)(2)(H2O)(3)] at higher temperatures is low, if the adsorbed and coordinated water is not removed rapidly upon heating. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:121 / 127
页数:7
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