Computational study of the interplay between intermolecular interactions and CO 2 orientations in type I hydrates

• Published in: Physical chemistry chemical physics : PCCP Vol. 19; no. 4; pp. 3384 - 3393
• Main Authors: Pérez-Rodríguez, M, Vidal-Vidal, A, Míguez, J M, Blas, F J, Torré, J-P, Piñeiro, M M
• Format: Journal Article
• Language: English
• Published: England 25.01.2017
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/C6CP07097C

Carbon dioxide (CO ) molecules show a rich orientation landscape when they are enclathrated in type I hydrates. Previous studies have described experimentally their preferential orientations, and some theoretical works have explained, but only partially, these experimental results. In the present paper, we use classical molecular dynamics and electronic density functional theory to advance in the theoretical description of CO orientations within type I hydrates. Our results are fully compatible with those previously reported, both theoretical and experimental, the geometric shape of the cavities in hydrate being, and therefore, the steric constraints, responsible for some (but not all) preferential angles. In addition, our calculations also show that guest-guest interactions in neighbouring cages are a key factor to explain the remaining experimental angles. Besides the implication concerning equation of state hydrate modeling approximations, the conclusion is that these guest-guest interactions should not be neglected, contrary to the usual practice.