Adsorption and separation of n-hexane and cyclohexane on the UiO-66 metal-organic framework

被引:56
作者
Bozbiyik, Belgin [1 ]
Duerinck, Tim [1 ]
Lannoeye, Jeroen [2 ]
De Vos, Dirk E. [2 ]
Baron, Gino V. [1 ]
Denayer, Joeri F. M. [1 ]
机构
[1] Vrije Univ Brussel, Dept Chem Engn, B-1050 Brussels, Belgium
[2] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, B-3001 Louvain, Belgium
关键词
Adsorption; MOF; Hexane; Cyclohexane; Breakthrough; ZIRCONIUM TEREPHTHALATE UIO-66(ZR); INVERSE SHAPE SELECTIVITY; MODULATED SYNTHESIS; CYCLIC PARAFFINS; MOLECULAR-SIEVES; XYLENE ISOMERS; MIXTURES; SILICALITE; RETENTION; ALKANES;
D O I
10.1016/j.micromeso.2013.07.035
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Adsorption and separation of n-hexane and cyclohexane on the UiO-66 metal organic framework was studied by pulse gas chromatography and vapour phase breakthrough experiments. Vapour phase breakthrough experiments were performed with mixtures of both components, diluted in helium. Experiments were carried out at temperatures between 50 and 200 degrees C, at partial pressures between 0.0024 and 0.05 bar and varying mixture composition. In all conditions, separation between both components is observed, with cyclohexane being the most strongly retained component. This unusual preference for adsorbing the more bulky cyclic alkane isomer was further studied by pulse GC measurements at low coverage, at temperatures between 200 and 300 degrees C. These experiments confirm the inverse shape selective behaviour of UiO-66 in the adsorption of linear and cyclic alkanes. Cyclohexane fits better in the cages of UiO-66, leading to a more negative adsorption enthalpy, together with a lower loss of entropy during adsorption as compared to n-hexane. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
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