吸附
六氟化硫
化学工程
气体分离
整体
氮气
选择性
多孔性
硫黄
材料科学
多孔介质
温室气体
选择性吸附
分子筛
重新使用
分离(统计)
化学
空气分离
活性炭
环境压力
二氧化硫
合成气
比表面积
分辨率(逻辑)
作者
Julio E. Sosa,Rui P. P. L. Ribeiro,Srđana Kolaković,Inês Matos,María Bernardo,José P. B. Mota,João M. M. Araújo,Ana B. Pereiro
标识
DOI:10.1002/cplu.202500376
摘要
Developing technologies to capture, purify, and reuse potent greenhouse gases such as sulfur hexafluoride (SF 6 ) is crucial because of their high global warming potential. Porous solid matrices are promising candidates for this purpose, due to their high surface areas and pore volumes. Herein, two coconut shell–derived activated carbons (AC) (CS‐CO 2 and CS‐ZnCl 2 ), obtained through physical and chemical activation, are evaluated and compared with two commercial adsorbents: an AC monolith (ACM) and a metal‐organic framework. The adsorption capacities for SF 6 and nitrogen (N 2 ) are measured gravimetrically at three temperatures: 283.15, 303.15, and 323.15 K. The experimental data are fitted using the Toth model, and the impact of temperature and pressure on the adsorption performance is analyzed. The order of SF 6 adsorption capacity is: ACM > CS‐ZnCl 2 > Fe‐BTC > CS‐CO 2 , reflecting dependence on surface area. Selectivity for SF 6 /N 2 separation is evaluated using Ideal Adsorbed Solution Theory, with ACM exhibiting the highest adsorption capacity due to its selective separation properties. These findings contribute to the understanding and selection of efficient adsorbent materials for SF 6 separation and recovery, providing valuable insights for their future implementation in industrial gas treatment and environmental management applications.
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