微型多孔材料
聚合物
多孔性
选择性
胺气处理
替代(逻辑)
溶剂
化学工程
吸附
化学
材料科学
高分子化学
多孔介质
有机化学
程序设计语言
工程类
计算机科学
作者
Shuangshuang Hou,Bien Tan
出处
期刊:Macromolecules
[American Chemical Society]
日期:2018-04-04
卷期号:51 (8): 2923-2931
被引量:53
标识
DOI:10.1021/acs.macromol.8b00274
摘要
Exploring the effect of functional group substitution on the porous structure and gas adsorption performance of polymer materials is becoming much fascinating. Here, three novel polymers, based on various amine building blocks, were efficiently prepared by the solvent knitting method. It is intriguingly found that with the gradual functional group substitution of phenyl by naphthyl in building blocks both porosity and gas uptake capacity of these hyper-cross-linked polymers can be finely tuned, with SBET increased from 874 to 1717 m2 g–1, and CO2 adsorption capacity tuned from 12.76 to 18.85 wt % (273.15 K/1.00 bar). Besides, these polymers could reveal CO2/N2 selectivity up to 24.9 and CO2/CH4 selectivity of 6.3 at 298.15 K. This work has proved that increasing the number of naphthyl in precursors will be in favor of knitting microporous with improved porosity and enhanced gas uptake ability, and naphthyl outweighs phenyl in their contributions to bettering the porosity parameters and gas uptake capacity of synthesized polymers, which is crucially important for the further research.
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