Modeling the adsorption of pure gases on coals with the SLD model

被引:115
作者
Fitzgerald, JE [1 ]
Sudibandriyo, M [1 ]
Pan, Z [1 ]
Robinson, RL [1 ]
Gasem, KAM [1 ]
机构
[1] Oklahoma State Univ, Sch Chem Engn, Stillwater, OK 74078 USA
关键词
coal; activated carbon; high pressure; adsorption properties; gas storage;
D O I
10.1016/S0008-6223(03)00202-1
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
The simplified local density/Peng-Robinson model (SLD-PR) was modified to improve its predictive capability when dealing with near-critical and supercritical adsorption systems of the type encountered in coalbed methane recovery and CO2 sequestration. The goal was to develop efficient equation-of-state (EOS) computational frameworks for representing adsorption behavior, as well as to improve our understanding of the phenomenon. The ability of the modified SLD-PR to correlate accurately data for supercritical adsorption systems is demonstrated using adsorption measurements on activated carbon, Illinois #6 coal, Fruitland coal, and Lower Basin Fruitland coal. The results indicate that the modified SLD-PR model, which incorporates a modified repulsive parameter "b" for the PR EOS, is capable of modeling the adsorption of pure methane, nitrogen, and CO2 at coalbed conditions. Inclusion of a slit geometry in the adsorbent matrix yields results superior to our previous two-dimensional EOS models for the adsorbates considered. The results also indicate that accounting for the adsorption surface structure within the SLD-EOS framework is effective in improving modeling capability for high-pressure adsorption phenomena. An explanation is offered as to why the adsorbed-phase densities are close to the EOS reciprocal co-volumes. Further, the model (a) generates direct estimates for the adsorbed-phase densities (which facilitate reliable prediction of absolute gas adsorption) and (b) readily describes the observed maximum in Gibbs-adsorption isotherms of CO2 at the temperatures and pressures encountered in coalbeds. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2203 / 2216
页数:14
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