Zeolite screening for the separation of gas mixtures containing SO2, CO2 and CO

被引:82
|
作者
Matito-Martos, I. [1 ]
Martin-Calvo, A. [1 ]
Gutierrez-Sevillano, J. J. [2 ]
Haranczyk, M. [3 ]
Doblare, M. [4 ]
Parra, J. B. [5 ]
Ania, C. O. [5 ]
Calero, S. [1 ]
机构
[1] Univ Pablo Olavide, Dept Phys Chem & Nat Syst, Seville 41013, Spain
[2] Delft Univ Technol, Dept Proc & Energy, NL-2628 CA Delft, Netherlands
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[4] Abengoa Res, Seville 41014, Spain
[5] CSIC, Inst Nacl Carbon, INCAR, E-33080 Oviedo, Spain
基金
欧洲研究理事会;
关键词
METAL-ORGANIC FRAMEWORKS; X-RAY-DIFFRACTION; SI-29; MAS-NMR; CRYSTAL-STRUCTURE; CARBON-DIOXIDE; SULFUR-DIOXIDE; FLUE-GAS; ADSORPTION-ISOTHERMS; NEUTRON-DIFFRACTION; CATALYTIC-REDUCTION;
D O I
10.1039/c4cp00109e
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
We used a combination of experiments and molecular simulations to investigate at the molecular level the effects of zeolite structure on the adsorption and diffusion of sulfur dioxide, carbon dioxide and carbon monoxide as well as separation processes of their mixtures. Our study involved different zeolite topologies and revealed numerous structure-property trends depending on the temperature and pressure conditions. Sulfur dioxide, which has the strongest interactions with zeolites due to its size and polarity, showed the largest adsorption across investigated temperatures and pressures. Our results indicate that structures with channel-type pore topology and low pore volume are the most promising for selective adsorption of sulfur dioxide over carbon dioxide and carbon monoxide under room conditions, while structures with higher pore volume exhibit better storage capacity at higher pressure. Our results emphasize the need for considering both adsorption and diffusion processes in the selection of the optimal structure for a given separation process. Our findings help to identify the best materials for effective separation processes under realistic operating conditions.
引用
收藏
页码:19884 / 19893
页数:10
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