Competitive Co-adsorption Of CO2 With H2O, NH3, SO2, NO ... - ArXiv

Condensed Matter > Materials Science arXiv:1503.04721 (cond-mat) [Submitted on 16 Mar 2015] Title:Competitive co-adsorption of CO2 with H2O, NH3, SO2, NO, NO2, N2, O2, and CH4 in M-MOF-74 (M= Mg, Co, Ni): the role of hydrogen bonding Authors:Kui Tan, Sebastian Zuluaga, Qihan Gong, Yuzhi Gao, Nour Nijem, Jing Li, Timo Thonhauser, Yves J Chabal View a PDF of the paper titled Competitive co-adsorption of CO2 with H2O, NH3, SO2, NO, NO2, N2, O2, and CH4 in M-MOF-74 (M= Mg, Co, Ni): the role of hydrogen bonding, by Kui Tan and 7 other authors View PDF

Abstract:The importance of co-adsorption for applications of porous materials in gas separation has motivated fundamental studies, which have initially focused on the comparison of the binding energies of different gas molecules in the pores (i.e. energetics) and their overall transport. By examining the competitive co-adsorption of several small molecules in M-MOF-74 (M= Mg, Co, Ni) with in-situ infrared spectroscopy and ab initio simulations, we find that the binding energy at the most favorable (metal) site is not a sufficient indicator for prediction of molecular adsorption and stability in MOFs. Instead, the occupation of the open metal sites is governed by kinetics, whereby the interaction of the guest molecules with the MOF organic linkers controls the reaction barrier for molecular exchange. Specifically, the displacement of CO2 adsorbed at the metal center by other molecules such as H2O, NH3, SO2, NO, NO2, N2, O2, and CH4 is mainly observed for H2O and NH3, even though SO2, NO, and NO2, have higher binding energies (~70-90 kJ/mol) to metal sites than that of CO2 (38 to 48 kJ/mol) and slightly higher than water (~60-80 kJ/mol). DFT simulations evaluate the barriers for H2O->CO2 and SO2->CO2 exchange to be - 13 and 20 kJ/mol, respectively, explaining the slow exchange of CO2 by SO2, compared to water. Furthermore, the calculations reveal that the kinetic barrier for this exchange is determined by the specifics of the interaction of the second guest molecule (e.g., H2O or SO2) with the MOF ligands.

Subjects:	Materials Science (cond-mat.mtrl-sci)
Cite as:	arXiv:1503.04721 [cond-mat.mtrl-sci]
(or arXiv:1503.04721v1 [cond-mat.mtrl-sci] for this version)
https://doi.org/10.48550/arXiv.1503.04721 Focus to learn more arXiv-issued DOI via DataCite
Journal reference:	Chem. Mater. 27, 2203 (2015)
Related DOI:	https://doi.org/10.1021/acs.chemmater.5b00315 Focus to learn more DOI(s) linking to related resources

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From: Pieremanuele Canepa [view email] [v1] Mon, 16 Mar 2015 16:42:12 UTC (4,306 KB) Full-text links:

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