Comparison of molecular simulation of adsorption with experiment

被引:59
作者
Myers, AL
Calles, JA
Calleja, G
机构
[1] UNIV PENN, DEPT CHEM ENGN, PHILADELPHIA, PA 19104 USA
[2] UNIV COMPLUTENSE MADRID, DEPT CHEM ENGN, E-28040 MADRID, SPAIN
来源
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY | 1997年 / 3卷 / 02期
基金
美国国家科学基金会;
关键词
adsorption; molecular simulation; isosteric heat;
D O I
10.1007/BF01650234
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
Experimental measurements of adsorption yield the surface excess. The Gibbs surface excess is the actual or absolute amount of gas contained in the pores less the amount of gas that would be present in the pores in the absence of gas-solid intermolecular forces. Molecular simulation of adsorption yields the absolute amount adsorbed. Comparison of simulated adsorption isotherms and heats of adsorption with experiment requires a conversion from absolute to excess variables. Molecular simulations of adsorption of methane in slit pores at room temperature show large differences between absolute and excess adsorption. The difference between absolute and excess adsorption may be ignored when the pore volume of the adsorbent is negligible compared to the adsorption second virial coefficient (V << B-1s).
引用
收藏
页码:107 / 115
页数:9
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