461684 The Degradation Mechanism of MOFs during Acid Gas Exposure: An Experimental and Computational Study

Wednesday, November 16, 2016: 12:30 PM
Cyril Magnin I (Parc 55 San Francisco)
William P. Mounfield III1, Chu Han1, Simon H. Pang1, Uma Tumuluri2, Souryadeep Bhattacharyya1, Yang Jiao1, Sankar Nair1, Zili Wu2, Ryan P. Lively1, David S. Sholl1 and Krista S. Walton1, (1)School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, (2)Chemical Sciences Division and Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN

Developing sorbents for the adsorption of acid gases has garnered much research attention in the field of porous materials. Impregnated activated carbons have been widely explored for acid gas separation applications; however, metal-organic frameworks (MOFs) have emerged as a promising class of materials for acid gas separations. MOFs are characterized by metal clusters and organic linkers, large surface areas, and tunable chemical properties that make them excellent candidates for these gas adsorption applications.[1] Several MOFs using titanium for the metal source have shown promising adsorption properties for CO2, water, and H2S.[2] However, MOFs often degrade and are unable to retain their performance in the presence of SO2, NO2 or other acid gases that are commonly present in industrial applications of interest.[3-5] In this study, MIL-125 and MIL-125-NH2 were investigated with SO2 exposure in dry, humid, and aqueous environments using in situ IR experiments and timed, controlled exposures. MIL-125 was found to be unstable in both humid and aqueous environments while the amine functionalized MIL-125-NH2 was stable under all conditions for extended time periods, showing no change in textural properties or visual degradation as observed through SEM. Both materials were found to be stable under pure water and pure dry SO2, thereby suggesting the formation of sulfurous acid and the associated bisulfite ion is likely a key step in the degradation mechanism. In situ IR experiments confirmed the presence of sulfite species supporting the hypothesis that the presence of the bisulfite ion likely leads to the degradation of the MIL-125 structure. Computational investigation of several potential reaction mechanisms in the MIL-125 framework indicated the reaction involving the bisulfite ion is favored over reaction with pure water or pure SO2. DFT simulations support the observation that MIL-125-NH2 is stable in humid and aqueous conditions as all reactions are less favorable with the functionalized framework compared to the unfunctionalized framework. This study advances the fundamental understanding of MOF degradation mechanisms during acid gas exposure.

[1] K. Sumida, D.L. Rogow, J.A. Mason, T.M. McDonald, E.D. Bloch, Z.R. Herm, T.H. Bae, J.R. Long, Chem. Rev., 112 (2012) 724-781.

[2] S. Vaesen, V. Guillerm, Q. Yang, A.D. Wiersum, B. Marszalek, B. Gil, A. Vimont, M. Daturi, T. Devic, P.L. Llewellyn, C. Serre, G. Maurin, G. De Weireld, Chem. Commun., 49 (2013) 10082-10084.

[3] S.G. Han, Y.G. Huang, T. Watanabe, S. Nair, K.S. Walton, D.S. Sholl, J.C. Meredith, Micro. Meso. Mater., 173 (2013) 86-91.

[4] C. Petit, B. Levasseur, B. Mendoza, T.J. Bandosz, Micro. Meso. Mater., 154 (2012) 107-112.

[5] W.P. Mounfield III, U. Tumuluri, Y. Jiao, M. Li, S. Dai, Z. Wu, K.S. Walton, Micro. Meso. Mater., 227 (2016) 65-75.

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See more of this Session: Adsorbent Materials: MOFs
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