Quest for an Optimal Methane Hydrate Formation in the Pores of Hydrolytically Stable Metal-Organic Frameworks

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Output type: Journal article

UM6P affiliated Publication?: Yes

Author list: Cuadrado-Collados, Carlos; Mouchaham, Georges; Daemen, Luke; Cheng, Yongqiang; Ramirez-Cuesta, Anibal; Aggarwal, Himanshu; Missyul, Alexander; Eddaoudi, Mohamed; Belmabkhout, Youssef; Silvestre-Albero, Joaquin

Publisher: American Chemical Society

Publication year: 2020

Journal: Journal of the American Chemical Society (0002-7863)

Volume number: 142

Issue number: 31

Start page: 13391

End page: 13397

Number of pages: 7

ISSN: 0002-7863

eISSN: 1520-5126

Languages: English (EN-GB)

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Porous metal-organic frameworks (MOFs) capable of storing a relatively high amount of dry methane (CH4) in the adsorbed phase are largely explored; however, solid CH4 storage in confined pores of MOFs in the form of hydrates is yet to be discovered. Here we report a rational approach to form CH4 hydrates by taking advantage of the optimal pore confinement in relatively narrow cavities of hydrolytically stable MOFs. Unprecedentedly, we were able to isolate methane hydrate (MH) nanocrystals with an sI structure encapsulated inside MOF pores with an optimal cavity dimension. It was found that confined nanocrystals require cavities slightly larger than the unit cell crystal size of MHs (1.2 nm), as exemplified in the experimental case study performed on Cr-soc-MOF-1 vs smaller cavities of Y-shp-MOF-5. Under these conditions, the excess amount of methane stored in the pores of Cr-soc-MOF-1 in the form of MH was found to be approximate to 50% larger than the corresponding dry adsorbed amount at 10 MPa. More importantly, the pressure gradient driving the CH4 storage/delivery process could be drastically reduced compared to the conventional CH4-adsorbed phase storage on the dry Cr-soc-MOF-1 (<= 3 MPa vs 10 MPa).


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Last updated on 2021-25-11 at 23:16