Adsorption equilibria and kinetics of CH4 and N2 on commercial zeolites and carbons

被引:39
作者
Xiao, Gongkui [1 ]
Li, Zhikao [1 ]
Saleman, Thomas L. [1 ]
May, Eric F. [1 ]
机构
[1] Univ Western Australia, Sch Mech & Chem Engn, Fluid Sci & Resources Div, 35 Stirling Hwy, Crawley, WA 6009, Australia
来源
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY | 2017年 / 23卷 / 01期
基金
澳大利亚研究理事会;
关键词
Adsorption kinetics; Rate of adsorption; Helium calibration; Non-isothermal model; Effective sorption rates; ACTIVATED CARBON; DIFFUSION MECHANISM; MOLECULAR-SIEVE; CO2; METHANE; 13X; NITROGEN; SORPTION; GAS; ADSORBENTS;
D O I
10.1007/s10450-016-9840-7
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
Adsorption equilibria and kinetics are two sets of properties crucial to the design and simulation of adsorption based gas separation processes. The adsorption equilibria and kinetics of N-2 and CH4 on commercial activated carbon Norit RB3, zeolite 13X, zeolite 4A and molecular sieving carbon MSC-3K 172 were studied experimentally at temperatures of (273 and 303) K in the pressure range of (5-120) kPa. These measurements were in part motivated by the lack of consistent adsorption kinetic data available in the literature for these systems, which forces the use of empirical estimates with large uncertainties in process designs. The adsorption measurements were carried out on a commercial volumetric apparatus. To obtain reliable kinetic data, the apparatus was operated in its rate of adsorption mode with calibration experiments conducted using helium to correct for the impact of gas expansion on the observed uptake dynamics. Analysis of the corrected rate of adsorption data for N2 and CH4 using the nonisothermal Fickian diffusion (FD) model was also found to be essential; the FD model was able to describe the dynamic uptake observed to better that 1% in all cases, while the more commonly applied isothermal linear driving force model was found to have a relative root mean square deviation of around 10%. The measured sorption kinetics had no dependence on gas pressure but their temperature dependence was consistent with an Arrhenius-type relation. The effective sorption rates extracted using the FD model were able to resolve inconsistencies in the literature for similar measurements.
引用
收藏
页码:131 / 147
页数:17
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