CNT@Cu3(BTC)2 and Metal-Organic Frameworks for Separation of CO2/CH4 Mixture

被引:152
作者
Xiang, Zhonghua [1 ]
Peng, Xuan [2 ]
Cheng, Xuan [1 ]
Li, Xiujin [3 ]
Cao, Dapeng [1 ]
机构
[1] Beijing Univ Chem Technol, Div Mol & Mat Simulat, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Informat Sci, Beijing 100029, Peoples R China
[3] Beijing Univ Chem Technol, Dept Environm Engn, Beijing 100029, Peoples R China
关键词
CARBON-DIOXIDE; HYDROGEN STORAGE; HIGH-CAPACITY; ACTIVATED CARBON; METHANE STORAGE; GAS-MIXTURES; ADSORPTION; CO2; SIMULATION; CH4;
D O I
10.1021/jp206959k
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
Effectively separating CO2 from the natural gas, which is one of alternative "friendly" fuels, is a very important issue. A hybrid material CNT@Cu-3(BTC)(2) has been prepared to separate CO2 from the CO2/CH4 mixture. For comparison of separation efficiency, a series of representative metal organic frameworks (MOF-177, UMCM-1, ZIF-8, MIL-53 (Al), and Cu-3(BTC)(2)) have also been synthesized by the solvothermal method. Adsorption isotherms of CO2 and CH4 pure gases are measured by Hiden Isochema Intelligent Gravimetric Analyzer (IGA-003). The dual-site Langmuir-Freundlich (DSLF)-based ideal adsorption solution theory (IAST) is used to predict adsorption of each component in the CO2/CH4 mixture. The IAST-predicted results show that the hybrid material CNT@Cu-3(BTC)(2) exhibits the greatest selectivity among the six materials, and its selectivity keeps in the range of 5.5 to 7.0 for equimolar CO2/CH4 mixture at 1 < p < 20 bar, which is higher than activated carbons. Moreover, the selectivity of CNT@Cu-3(BTC)(2) for the CO2/CH4 mixture keeps almost no change with the composition of CH4, which is one of the excellent properties as a promising separation material. In short, this hybrid material CNT@Cu-3(BTC)(2) shows great potential in separation and purification of CO2 from various CO2/CH4 mixtures by adsorptive processes in important industrial systems.
引用
收藏
页码:19864 / 19871
页数:8
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