吸附
化学工程
材料科学
离子键合
气体分离
活性炭
多孔性
原位
化学
离子
微型多孔材料
碳纤维
有机化学
膜
复合材料
复合数
工程类
生物化学
作者
Peixin Zhang,Jun Wang,Wei Fan,Yao Zhong,Yan Zhang,Qiang Deng,Zheling Zeng,Shuguang Deng
标识
DOI:10.1016/j.cej.2019.121931
摘要
Developing highly selective, cycle reliable, and moisture resistant adsorbents is of great importance for gas separation. It is very challenging to control and optimize pore sizes within the ultramicroporous ranges (<0.7 nm), especially for biomass-derived carbons. Moreover, porous carbons featured with random micropore sizes usually exhibited inferior gas separation performances. Herein, we developed an in-situ ionic activation method, in which the chemically bonded K+ ions that are uniformly distributed in the carbon precursor are able to create ultramicroporous carbons with uniform and narrow pore size distributions. Thus, the obtained carbons exhibited high CO2 uptakes (4.17 mmol g−1) and selectivities (333.2 and 34.9) for CO2/N2 (15v/85v) and CO2/CH4 (40v/60v) separation at ambient conditions. The dynamic breakthrough experiments clearly demonstrate their superior and applicable gas-mixture separation performances. Upon the detailed evaluation of vacuum swing adsorption (VSA) working parameters, a record-high adsorbent selective parameter (S) of 1906.4 is obtained. Hence, the in-situ ionic activation approach is an effective method for preparing ultramicroporous carbons with narrow and uniform pore size distributions.
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