Selective gas adsorption and separation in metal-organic frameworks

被引:7863
作者
Li, Jian-Rong [1 ]
Kuppler, Ryan J. [1 ]
Zhou, Hong-Cai [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
基金
美国国家科学基金会;
关键词
ZEOLITIC IMIDAZOLATE FRAMEWORKS; MICROPOROUS METAL; HYDROGEN STORAGE; COORDINATION POLYMERS; MOLECULAR-DYNAMICS; CARBON-DIOXIDE; CU-BTC; PERMANENT POROSITY; POROUS MATERIAL; D-2; ADSORPTION;
D O I
10.1039/b802426j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Adsorptive separation is very important in industry. Generally, the process uses porous solid materials such as zeolites, activated carbons, or silica gels as adsorbents. With an ever increasing need for a more efficient, energy-saving, and environmentally benign procedure for gas separation, adsorbents with tailored structures and tunable surface properties must be found. Metal-organic frameworks (MOFs), constructed by metal-containing nodes connected by organic bridges, are such a new type of porous materials. They are promising candidates as adsorbents for gas separations due to their large surface areas, adjustable pore sizes and controllable properties, as well as acceptable thermal stability. This critical review starts with a brief introduction to gas separation and purification based on selective adsorption, followed by a review of gas selective adsorption in rigid and flexible MOFs. Based on possible mechanisms, selective adsorptions observed in MOFs are classified, and primary relationships between adsorption properties and framework features are analyzed. As a specific example of tailor-made MOFs, mesh-adjustable molecular sieves are emphasized and the underlying working mechanism elucidated. In addition to the experimental aspect, theoretical investigations from adsorption equilibrium to diffusion dynamics via molecular simulations are also briefly reviewed. Furthermore, gas separations in MOFs, including the molecular sieving effect, kinetic separation, the quantum sieving effect for H-2/D-2 separation, and MOF-based membranes are also summarized (227 references).
引用
收藏
页码:1477 / 1504
页数:28
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