Description of Carbon Dioxide Adsorption and Desorption onto Malaysian Coals under Subcritical Condition

被引:36
|
作者
Abunowara, Mustafa [1 ]
Bustam, Mohamad Azmi [1 ]
Sufian, Suriati [1 ]
Eldemerdash, Usama [2 ]
机构
[1] Univ Teknol PETRONAS, Chem Engn Dept, Tronoh 31750, Perak, Malaysia
[2] Benha Univ, Benha Fac Engn, Chem Engn Dept, Banha, Egypt
关键词
CO2 adsorption and desorption; coal; hystersis; isother medols; METHANE RECOVERY; CO2; SEQUESTRATION; ISOTHERMS; SORPTION;
D O I
10.1016/j.proeng.2016.06.521
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Coal bed seams have been considered as promising sequestration reservoirs for CO2 disposal to mitigate the green house gas emissions. The CO2 adsorption and desorption attributes of CO2 on dry Malaysian coals (Sarawak, volatile bituminous) were performed using a sorptomat apparatus (ASAP 2010, Micromeritics, USA) and BELSORP-mini II machine (BEL Japan, Inc.) at 273 K, 298 K and pressure up to 1 bar. The CO2 adsorption was favourable at low temperature and dry coal conditions. However, S3 and S4 coals have the highest adsorption capacity by 0.71 and 0.73 mmol/g respectively. According to IUPAC classification of adsorption isotherms, CO2 adsorption isotherm of all coal samples follow type I which most probably describe the adsorption limited to a few molecular layers (micropores). The results of adsorption and desorption isotherm demonstrate a positive hysteresis in all coal samples. The S1 coal and S2 coal have the highest hysteresis between adsorption and desorption isotherm compared to S3 coal and S4 coal. According to hysteresis classifications, the hysteresis during CO2 adsorption and desorption process for all coal samples follows type H-3 which describes micropores and mesopores. The evaluation of the equilibrium adsorption data where fitted using by Langmuir, Freundlich, Redlich-Peterson, Koble-Corrigan, Toth and Sips models. Toth model provided the best fit for all adsorption experimental data that predicting all coals having heterogeneous surface properties. (C) 2016 Published by Elsevier Ltd.
引用
收藏
页码:600 / 608
页数:9
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