Issue 29, 2014

A porous metal–organic framework with an elongated anthracene derivative exhibiting a high working capacity for the storage of methane

Abstract

We have developed a new porous metal–organic framework (MOF) (UTSA-80) with an elongated anthracene derivative as a linker. The activated UTSA-80a has a pore volume of 1.03 cm3 g−1 and a gravimetric Brunauer–Emmett–Teller surface area of ca. 2280 m2 g−1, higher than those of PCN-14. The volumetric methane storage capacity of UTSA-80a at 35 bar and 298 K is 192 cm3 (STP) cm−3, which makes it one of the few porous MOFs with a storage capacity >190 cm3 (STP) cm−3 at 35 bar. The volumetric uptake of methane by UTSA-80a reaches 233 cm3 (STP) cm−3 at room temperature and 65 bar; this is 88.6% of the new volumetric target of the US Department of Energy if the packing density loss is ignored. This capacity is comparable with that of PCN-14. However, as a result of the lower methane uptake of UTSA-80a at 5 bar, it has a much higher methane storage working capacity (deliverable amount of methane between 65 and 5 bar) of 174 cm3 (STP) cm−3 compared with PCN-14 [157–160 cm3 (STP) cm−3]. This value is slightly lower than the 190 cm3 (STP) cm−3 achieved by HKUST-1, suggesting that it is a promising material for methane storage in transport applications. Such an exceptionally high working capacity can probably be attributed to the elongated anthracene derivative used as a linker within UTSA-80a, which adjusts the pore sizes/cages and interactions with the methane molecules to optimize the methane working capacity.

Graphical abstract: A porous metal–organic framework with an elongated anthracene derivative exhibiting a high working capacity for the storage of methane

Supplementary files

Article information

Article type
Paper
Submitted
15 Apr 2014
Accepted
27 May 2014
First published
28 May 2014

J. Mater. Chem. A, 2014,2, 11516-11522

A porous metal–organic framework with an elongated anthracene derivative exhibiting a high working capacity for the storage of methane

H. Wen, B. Li, D. Yuan, H. Wang, T. Yildirim, W. Zhou and B. Chen, J. Mater. Chem. A, 2014, 2, 11516 DOI: 10.1039/C4TA01860E

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