位阻效应
胺气处理
化学
热重分析
吸附
介孔二氧化硅
介孔材料
傅里叶变换红外光谱
碳酸氢盐
铵
有机化学
化学工程
无机化学
催化作用
工程类
作者
Jason J. Lee,Chun‐Jae Yoo,Chia‐Hsin Chen,Sophia E. Hayes,Carsten Sievers,Christopher W. Jones
出处
期刊:Langmuir
[American Chemical Society]
日期:2018-09-24
卷期号:34 (41): 12279-12292
被引量:65
标识
DOI:10.1021/acs.langmuir.8b02472
摘要
Most studies exploring the capture of CO2 on solid-supported amines have focused on unhindered amines or alkylimine polymers. It has been observed in extensive solution studies that another class of amines, namely sterically hindered amines, can exhibit enhanced CO2 capacity when compared to their unhindered counterparts. In contrast to solution studies, there has been limited research conducted on sterically hindered amines on solid supports. In this work, one hindered primary amine and two hindered secondary amines are grafted onto mesoporous silica at similar amine coverages, and their adsorption performances are investigated through fixed bed breakthrough experiments and thermogravimetric analysis. Furthermore, chemisorbed CO2 species formed on the sorbents under dry and humid conditions are elucidated using in situ Fourier-transform infrared spectroscopy. Ammonium bicarbonate formation and enhancement of CO2 adsorption capacity is observed for all supported hindered amines under humid conditions. Our experiments in this study also suggest that chemisorbed CO2 species formed on supported hindered amines are weakly bound, which may lead to reduced energy costs associated with regeneration if such materials were deployed in a practical separation process. However, overall CO2 uptake capacities of the solid supported hindered amines are modest compared to their solution counterparts. The oxidative and thermal stabilities of the supported hindered amine sorbents are also assessed to give insight into their operational lifetimes.
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