Breathing effects of CO2 adsorption on a flexible 3D lanthanide metal-organic framework

被引:67
|
作者
Mu, Bin [1 ]
Li, Feng [2 ]
Huang, Yougui [1 ]
Walton, Krista S. [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[2] Xiangtan Univ, Sch Chem, Xiangtan 411105, Hunan, Peoples R China
关键词
LAYER COORDINATION POLYMER; HOST-GUEST INTERACTIONS; GAS-ADSORPTION; SELECTIVE SORPTION; THERMAL-STABILITY; DRUG-DELIVERY; POROUS SOLIDS; MOLECULES; VAPORS; NI-2(4,4'-BIPYRIDINE)(3)(NO3)(4);
D O I
10.1039/c2jm15721g
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
This work reports a new three-dimensional flexible lanthanide metal-organic framework [La(BTB)(H2O)center dot 3DMF](n) (BTB 1,3,5-tris(4-carboxyphenyl) benzene) that possesses a rare chiral space group (P6(5)22), very high thermal stability (560 degrees C), and high surface area (1014 m(2) g(-1)). This new MOF demonstrates a large adsorption hysteresis loop on the N-2 isotherm at 77K after activation at 300 degrees C. Powder X-ray thermodiffraction experiments reveal that structural transformation occurs upon removal of guest molecules. The as-synthesized material is the "open" form, while the activated sample is "closed". Adsorption isotherms of CO2 exhibit a dramatic step near a relative pressure of 0.3, which is similar to the location of the step in the N-2 isotherm at 77 K. Upon desorption, the material transforms to the closed form near a reduced pressure of 0.15, where it collapses back to the adsorption isotherm. Adsorption kinetic studies show that equilibrium is reached more slowly during the opening/closing steps compared to adsorption loadings measured on the static portion of the isotherm.
引用
收藏
页码:10172 / 10178
页数:7
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