Nuclear magnetic resonance studies of carbon dioxide capture

被引:7
|
作者
Pugh, Suzi M. [1 ]
Forse, Alexander C. [1 ]
机构
[1] Yusuf Hamied Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
关键词
Carbon Capture; In situ NMR; Operando NMR; Carbon Dioxide Capture; CO2; capture; Metal-organic framework; Nuclear magnetic resonance; Diffusion NMR; adsorption; METAL-ORGANIC FRAMEWORK; SOLID-STATE NMR; OF-THE-ART; CO2; CAPTURE; CHEMISORBED CO2; FLUE-GAS; MAS NMR; OXIDATIVE-DEGRADATION; DIFFUSION ANISOTROPY; DYNAMICS;
D O I
10.1016/j.jmr.2022.107343
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Carbon dioxide capture is an important greenhouse gas mitigation technology that can help limit climate change. The design of improved capture materials requires a detailed understanding of the mechanisms by which carbon dioxide is bound. Nuclear magnetic resonance (NMR) spectroscopy methods have emerged as a powerful probe of CO2 sorption and diffusion in carbon capture materials. In this article, we first review the practical considerations for carrying out NMR measurements on capture materials dosed with CO2 and we then present three case studies that review our recent work on NMR studies of CO2 binding in metal-organic framework materials. We show that simple 13C NMR experiments are often inadequate to determine CO2 binding modes, but that more advanced experiments such as multi-dimensional NMR experiments and 17O NMR experiments can lead to more conclusive structural assign-ments. We further discuss how pulsed field gradient (PFG) NMR can be used to explore diffusion of adsorbed CO2 through the porous framework. Finally, we provide an outlook on the challenges and opportunities for the further development of NMR methodologies that can improve our understanding of carbon capture. (c) 2022 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
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页数:11
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