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优化MOF-74的铜浸渍以改善CO/N和CO/CO分离。

Optimisation of Cu impregnation of MOF-74 to improve CO/N and CO/CO separations.

作者信息

Evans Arwyn, Cummings Matthew, Decarolis Donato, Gianolio Diego, Shahid Salman, Law Gareth, Attfield Martin, Law David, Petit Camille

机构信息

Barrer Centre, Department of Chemical Engineering, Imperial College London UK

School of Chemistry, The University of Manchester UK.

出版信息

RSC Adv. 2020 Jan 31;10(9):5152-5162. doi: 10.1039/c9ra10115b. eCollection 2020 Jan 29.

Abstract

Carbon monoxide (CO) purification from syngas impurities is a highly energy and cost intensive process. Adsorption separation using metal-organic frameworks (MOFs) is being explored as an alternative technology for CO/nitrogen (N) and CO/carbon dioxide (CO) separation. Currently, MOFs' uptake and selectivity levels do not justify displacement of the current commercially available technologies. Herein, we have impregnated a leading MOF candidate for CO purification, M-MOF-74 (M = Co or Ni), with Cu sites. Cu allows strong π-complexation from the 3d electrons with CO, potentially enhancing the separation performance. We have optimised the Cu loading procedure and confirmed the presence of the Cu sites using X-ray absorption fine structure analysis (XAFS). XAFS and diffuse reflectance infrared Fourier Transform spectroscopy analyses have demonstrated Cu-CO binding. The dynamic breakthrough measurements showed an improvement in CO/N and CO/CO separations upon Cu impregnation. This is because Cu sites do not block the MOF metal sites but rather increase the number of sites available for interactions with CO, and decrease the surface area/porosity available for adsorption of the lighter component.

摘要

从合成气杂质中提纯一氧化碳(CO)是一个能源和成本密集型的过程。利用金属有机框架材料(MOF)进行吸附分离正在作为一种用于CO/氮气(N)和CO/二氧化碳(CO₂)分离的替代技术进行探索。目前,MOF的吸附量和选择性水平尚不足以取代现有的商业可用技术。在此,我们用铜位点对用于CO提纯的一种领先的MOF候选材料M-MOF-74(M = Co或Ni)进行了浸渍。铜能通过3d电子与CO形成强π络合,有可能提高分离性能。我们优化了铜负载程序,并使用X射线吸收精细结构分析(XAFS)确认了铜位点的存在。XAFS和漫反射红外傅里叶变换光谱分析已证明存在Cu-CO键合。动态突破测量表明,浸渍铜后CO/N和CO/CO₂的分离性能有所改善。这是因为铜位点不会阻塞MOF的金属位点,而是增加了可用于与CO相互作用的位点数量,并减少了可用于吸附较轻组分的表面积/孔隙率。

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