Adsorption separation of CO2, CH4, and N2 on microwave activated carbon

被引:138
|
作者
Yi, Honghong [1 ]
Li, Fenrong [1 ,2 ]
Ning, Ping [1 ]
Tang, Xiaolong [1 ]
Peng, Jinhui [3 ]
Li, Yundong [1 ]
Deng, Hua [1 ]
机构
[1] Kunming Univ Sci & Technol, Coll Environm Sci & Engn, Kunming 650500, Peoples R China
[2] Kunming Univ Sci & Technol, Coll Architectural Engn, Kunming 650500, Peoples R China
[3] Kunming Univ Sci & Technol, Coll Met & Energy Engn, Kunming 650093, Peoples R China
关键词
Adsorption; Microwave-activated carbon; Separation factor; Carbon dioxide; Methane; Nitrogen; SELECTIVE ADSORPTION; BIOGAS COMPONENTS; PILLARED CLAYS; DIOXIDE; METHANE; NITROGEN; EQUILIBRIUM; GAS; MIXTURES; BETA;
D O I
10.1016/j.cej.2012.11.050
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, the adsorption equilibrium isotherms of carbon dioxide, methane and nitrogen on microwave activated carbon (MAC) at three temperatures (298, 308 and 323 K) have been obtained by a static volume instrument. The adsorption equilibrium data of CO2, CH4 and N-2 at various temperatures were fitted to Langmuir and Toth isotherm models. It was found that the fitting results of Toth model were fine. The capacities of pure gas CO2, CH4 and N-2 were 2.13, 0.98 and 0.33 mmol g(-1) at 298 K and the partial pressure of 100 kPa. The competition adsorption behavior of multi component was predicted by the extend Langmuir and Toth model. The results indicated that CO2 still dominate the adsorption system in the ternary mixtures. Additionally, the separation factors of the binary mixtures CO2/CH4, CO2/N-2 and CH4/N-2 were calculated from the isotherms data. The results showed that the separation factors (S) of different binary mixtures at 298 K and the total pressure of 100 kPa were as follows: CO2/N-2 (14.6) > CO2/CH4 (4.37) > CH4/N-2 (3.33). Finally, thermodynamic functions integral Gibbs' free energy (Delta G), integral molar enthalpy change (Delta H) and entropy change (Delta S) were calculated to characterize adsorption behavior. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:635 / 642
页数:8
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