Trends in the Adsorption of Volatile Organic Compounds in a Large-Pore Metal−Organic Framework, IRMOF-1

Abstract

Metal-organic frameworks have been proposed as useful sorbents for the capture of a variety of compounds. In this work, inverse gas chromatography (IGC) utilizing micropacked capillary columns was used to probe the adsorption of more than 30 volatile organic compounds (VOCs) on IRMOF-1. In an attempt to study the effect of structural degradation upon VOC adsorption, multiple samples of IRMOF-1 with widely ranging properties were investigated. Trends in the differential enthalpies and equilibrium constants for the adsorption of VOCs were determined on the basis of the molecular properties of the adsorbate and the structural properties of the MOF sample. The results indicate that samples of IRMOF-1 that are affected by a moderate amount of structural degradation interact with adsorbed species more strongly than does a sample with fewer defects, resulting in higher heats of adsorption. Samples of IRMOF-1 with specific surface areas of around 1000 m(2)/g show heats of adsorption for alkanes that are higher than those estimated previously via Monte Carlo calculations. Although the data for nonpolar (and weakly polar) species showed many of the anticipated trends for the interactions with IRMOF-1, the equilibrium behavior of polar VOCs did not correlate well with the molecular properties of the adsorbate (i.e., vapor pressure and deformation polarizability), leaving some uncertainty about the nature of the interaction mechanism. The equilibrium data and the heats of adsorption were found to fit well to a small group of molecular descriptors through the application of the Abraham linear free-energy relationship, thus providing insight into the complex interactions between the MOF structure and the VOC compounds. Hydrogen bonding interactions were determined to be the primary contributors to specific interactions between adsorbates and the MOF surface. Size exclusion also seems to play a role in the adsorption of larger species. These results show that the interaction of VOCs with MOFs is more complex than previously assumed and that more work is needed to probe the mechanisms of these processes.