文献类型：期刊文献

英文题名：Adsorption Equilibrium and Kinetics of Methane and Nitrogen on Carbon Molecular Sieve

作者：Yang, Ying[1,2];Ribeiro, Ana M.[2];Li, Ping[1];Yu, Jian-Guo[1];Rodrigues, Alirio E.[2]

机构：[1]E China Univ Sci & Technol, Coll Chem Engn, State Key Lab Chem Engn, Shanghai 20037, Peoples R China;[2]Univ Porto, Fac Engn, Dept Chem Engn, LSRE,Associated Lab LSRE LCM, P-4200465 Oporto, Portugal

年份：2014

卷号：53

期号：43

起止页码：16840

外文期刊名：INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH

收录：;EI(收录号：20144600180828);WOS:【SCI-EXPANDED(收录号:WOS:000344042700027)】；

基金：Y.Y. is grateful for the fellowship from the China Scholarship Council (201306740026). This work was financed by the Program of International S&T Cooperation (S2015GR1004). This work was financed by FCT under the Cooperation Project FCT/CHINA 441.00. This work was cofinanced by FCT and FEDER under Programme COMPETE (Project PEst-C/EQB/LA0020/2013). This work was cofinanced by QREN, ON2, and FEDER (Projects NORTE-07-0162-FEDER-000050 and NORTE-07-0124-FEDER-0000006).

语种：英文

外文关键词：Methane - Adsorption - Microporosity - Sieves - Kinetics - Molecular sieves - Carbon - Adsorption isotherms

摘要：Knowledge of adsorption equilibrium and kinetic data is essential for the design of an adsorption process. In this work, the adsorption equilibrium isotherms of methane and nitrogen are reported at 303, 323, and 343 K over the pressure range from 0 to 700 kPa by a gravimetric system on a carbon molecular sieve (CMS-131510). Methane is preferentially adsorbed. The adsorption capacity at 303 K and 700 kPa is 1.91 mol/kg for methane and 1.01 mol/kg for nitrogen. Experimental data obtained were fitted with the multisite Langmuir model and Toth model. The adsorption kinetics of pure gas was studied by a batch uptake experiment at several different surface coverages within the pressure range of 0100 kPa and in the same temperature range covered by the equilibrium isotherm. The adsorption rate of both gases is found to be controlled by the surface barrier resistance at the mouth of the micropore and diffusion in the micropore interior. The dual resistance model employed in the simulation can successfully describe the uptake curves. The temperature and concentration dependences of kinetic parameters were also studied. A very high kinetic selectivity was observed. The effect of micropore distribution on the transport parameters is discussed in detail. Binary breakthrough curves were determined, and an enrichment of 50% for methane in the first few seconds was observed. The data reported in this work can be used for the future modeling of adsorption process for the separation of methane and nitrogen on this CMS material.