Adsorbate/adsorbent interactions in microporous zeolites: mechanistic insights from NMR relaxation and DFT calculations

C. D'Agostino, P. Bräuer, J. Zheng, N. Robinson, A. P.E. York, L. Song, X. Fan

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Nuclear magnetic resonance (NMR) relaxation is an effective and non-invasive technique for probing guest-host interactions in porous materials. In particular, the ratio of longitudinal-to-transverse nuclear spin relaxation time constants T1/T2 has been demonstrated as a robust indicator of adsorbate/adsorbent interactions in mesoporous media. However, the use of NMR relaxation times in microporous materials to probe interactions and dynamics remains relatively unexplored. Herein, we investigate and describe the effect of the aluminium content in microporous HZSM-5 zeolites on the NMR relaxation times of a range of common liquid probe molecules. In particular, we discuss the NMR relaxation time behavior of liquids with hydrophilic (water, methanol) and hydrophobic (toluene, methyl cyclohexane) properties adsorbed over HZSM-5 samples with varying silica-to-alumina ratios (SAR = SiO2/Al2O3). Our results demonstrate that highly polar molecules show high sensitivity to aluminium content (i.e., surface acidity), with T1/T2 ratios increasing significantly for higher acidity zeolites. Conversely, for molecules with low polarity, the T1/T2 ratio as a function of SAR remains approximately constant, and in the zeolites with low SAR is much lower compared to that of water and methanol. Density functional theory (DFT) calculations are employed to contrast the surface interaction mechanisms of water and toluene within model zeolite structures of varying SAR, and provide molecular level insights into the observed trends in NMR relaxation behavior.

Original languageEnglish
Article number101443
JournalMaterials Today Chemistry
Volume29
DOIs
Publication statusPublished - Apr 2023

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