Adsorption and Separation of Xylene Isomers and Ethylbenzene on Two Zn-Terephthalate Metal-Organic Frameworks

被引:173
作者
Gu, Zhi-Yuan [1 ]
Jiang, Dong-Qing [1 ]
Wang, He-Fang [1 ]
Cui, Xiao-Yan [1 ]
Yan, Xiu-Ping [1 ]
机构
[1] Nankai Univ, Coll Chem, Res Ctr Analyt Sci, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
VAPOR-PHASE ADSORPTION; FIXED-BED ADSORPTION; GAS-CHROMATOGRAPHY; COORDINATION POLYMERS; SELECTIVE ADSORPTION; STATIONARY PHASES; HYDROGEN STORAGE; ZEOLITE; DESIGN; DIFFUSION;
D O I
10.1021/jp9063017
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metal-organic frameworks (MOFs) with metal-containing secondary building units and organic linkers have great potential for the separation of isomers. In this work, the adsorption and separation of xylene isomers and ethylbenzene (EB) on two Zn-terephthalate MOFs (MOF-5 and MOF-monoclinic) were studied by means of pulse gas chromatography, static vapor-phase adsorption, and breakthrough adsorption. The two studied Zn-terephthalate MOFs showed different selectivity and efficiency for the separation of xylene isomers and EB. On MOF-5, EB eluted first, while other isomers eluted at the same time. MOF-monoclinic showed a preferable adsorption of p-xylene over other isomers. The adsorption and separation of xylene isomers and EB were equilibrium-constant-controlled on MOF-5 and diffusion-dominated on MOF-monoclinic. On the basis of the measured McReynolds constants, MOF-5 was characterized as a stationary phase of nonpolarity, whereas MOF-monoclinic as a stationary phase of intermediate polarity for gas chromatography.
引用
收藏
页码:311 / 316
页数:6
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