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负载型位阻伯胺用于 CO2 捕集。

Silica-Supported Sterically Hindered Amines for CO Capture.

机构信息

School of Chemical & Biomolecular Engineering , Georgia Institute of Technology , 311 Ferst Drive , Atlanta , Georgia 30332 , United States.

Department of Chemistry , Washington University , One Brookings Drive , Saint Louis , Missouri 63130 , United States.

出版信息

Langmuir. 2018 Oct 16;34(41):12279-12292. doi: 10.1021/acs.langmuir.8b02472. Epub 2018 Oct 8.

Abstract

Most studies exploring the capture of CO 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 CO 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 CO 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 CO adsorption capacity is observed for all supported hindered amines under humid conditions. Our experiments in this study also suggest that chemisorbed CO 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 CO 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.

摘要

大多数研究探索固体支撑胺对 CO 的捕集都集中在无阻碍胺或烷基亚胺聚合物上。在广泛的溶液研究中观察到,另一类胺,即空间位阻胺,与无阻碍的胺相比,其 CO 容量可以得到增强。与溶液研究相比,在固体载体上对空间位阻胺的研究有限。在这项工作中,将一种受阻伯胺和两种受阻仲胺以相似的胺覆盖率接枝到介孔硅上,并通过固定床穿透实验和热重分析研究它们的吸附性能。此外,还使用原位傅里叶变换红外光谱法阐明了在干燥和潮湿条件下在吸附剂上形成的化学吸附 CO 物种。在潮湿条件下,所有负载的受阻胺都观察到碳酸氢铵的形成和 CO 吸附容量的增强。我们在这项研究中的实验还表明,负载的受阻胺上形成的化学吸附 CO 物种结合较弱,如果这些材料在实际分离过程中得到应用,可能会降低与再生相关的能源成本。然而,与溶液相比,固体支撑受阻胺的 CO 总吸附容量适中。还评估了负载的受阻胺吸附剂的氧化和热稳定性,以深入了解其运行寿命。

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