微型多孔材料
吸附
碳化
碳纤维
体积热力学
多孔性
比表面积
材料科学
活性炭
产量(工程)
化学工程
化学
有机化学
工程类
复合材料
催化作用
复合数
物理
量子力学
作者
Seok Min Hong,Hyung Jin Yoon,Yeji Choi,Yung-Zun Cho,Sungyong Mun,Vilas G. Pol,Ki Bong Lee
标识
DOI:10.1016/j.cej.2019.122219
摘要
Highly porous carbon microsheets (CMS) were prepared by the bulk carbonization and activation of waste packing peanuts, and applied to CO2 capture and release. Two different activation methods, physical activation using CO2 and chemical activation using KOH, were used for the preparation of porous CMS, and the effects of different activation methods were compared. Chemical activation functioned better than the physical activation, successfully producing highly microporous carbon structures with higher carbon yield. Textural properties such as specific surface area and total pore volume increased proportionally to the mass ratio of KOH/carbon because of the development of the porous structure and enlargement of pore size through KOH activation. Among the samples prepared, the highest CO2 adsorption capacities of 6.51 mol kg−1 at 0 °C and 4.07 mol kg−1 at 25 °C were obtained at 1 bar in the packing-peanut-derived CMS prepared with a KOH/carbon ratio of 3 (CMS-K3). It is noteworthy that the CO2 adsorption uptake was significantly dependent on the volume of narrow micropores of pore sizes less than 0.8 nm rather than the specific surface area or total pore volume. CMS-K3 also exhibited excellent cyclic stability, good CO2/N2 selectivity, fast adsorption kinetics, and low heat of adsorption, being regarded as a promising adsorbent for CO2 capture.
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