Abstract
Vast numbers of unstudied hypothetical porous frameworks continue to spark interest in optimizing adsorption and catalytic processes. Evaluating the use of such materials depends on the accessibility of thermodynamic metrics such as the free energy, which, in turn, depend on the satisfactory estimation or calculation of the adsorption entropy, which often remains elusive. Previous works using simulations and experimental data have demonstrated relationships between the entropy and system descriptors, allowing for sensible predictions based on more-easily obtained physical parameters. However, the resultant conclusions were either based on experimental data for industrially relevant alkanes or lacked a significant sample size. In this paper, we evaluate correlations between gas-phase and adsorbed-phase entropies for a larger and more chemically diverse set of adsorbate molecules by using force fields and statistical mechanical expressions to calculate those entropies. In total, we perform calculations for 37 molecules across 10 chemical categories available in the TraPPE force field set, as adsorbed in five siliceous zeolites. Our results show that linear correlations between the gas- and adsorbed-phase entropies persist for the larger and diverse set of adsorbate molecules studied here, proving a broader applicability and justifying the use of simple correlations for many adsorbates and, presumably, adsorbent materials.