¹H NMR signal broadening in spectra of alkane molecules adsorbed on MFI-type zeolites

Abstract

The anisotropic behavior of C₁–C₆ alkane molecules adsorbed in MFI zeolite was studied by ¹H nuclear magnetic resonance (NMR) using single-pulse excitation, Carr–Purcell–Meiboom–Gill (CPMG) pulse sequence, Hahn echo (HE) pulse sequence, and magic-angle spinning. The molecular order parameter was obtained by both static ²H NMR spectroscopy and molecular simulations. This yields an order parameter in the range of 0.28–0.42 for linear alkanes in MFI zeolite, whereas the parameter equals zero for FAU zeolite with a cubic symmetry. Thus, in the case of a zeolite with a non-cubic symmetry like MFI, the mobility of the molecules in one crystallite cannot fully average the dipolar interaction. As a consequence, transverse nuclear magnetization as revealed in the echo attenuation notably deviates from a mono-exponential decay. This information is of particular relevance for the performance of pulsed field gradient (PFG) NMR diffusion experiments, since the occurrence of non-exponential magnetization attenuation could be taken as an indication of the existence of different molecules or of molecules in different states of mobility.