The ability to determine the types and concentrations of acid sites in zeolites and fluid-catalytic cracking systems is important for an increased understanding of structure/performance relationships in these materials. Currently, a variety of thermal methods exist that allow quantitative measurement of the Brønsted acid site concentration. In addition, numerous spectroscopic methods using probe molecules are available for qualitative and quantitative detection of both Brønsted and Lewis acid sites. In studies utilizing solid-state NMR spectroscopy, probe molecules containing 31 P nuclei present substantial advantages over probes isotopically enriched with 13 C and 15 N nuclei. These advantages include increased sensitivity and chemical shift dispersion. While a number of phosphorus-based experiments have probed the interaction of trimethylphosphine with solid acid catalysts, initial studies of the more stable trimethylphosphine oxide (TMPO) have only been reported on amorphous silica-alumina surfaces. We now report the successful completion of TMPO studies of acid sites in several systems including γ-alumina; HY, USY, and dealuminated Y zeolites; and a silica-alumina catalyst with an aluminum concentration of 13%. Comprehensive and consistent assignments to particular types of sites are made for all resonance lines in the 31 P MAS NMR signals from TMPO. Based on results from dehydroxylated γ-alumina, new chemical shift assignments are made for the TMPO/Lewis acid complex. The assignments of 31 P resonances from molecules not directly associated with nearby 27 Al nuclei (such as crystalline or physisorbed TMPO species) are supported using 1 H/ 31 P/ 27 Al triple-resonance NMR methods. The concentrations of Brønsted acid sites from the NMR results are compared with concentrations obtained from isopropylamine/temperature-programmed-desorption measurements, and substantial agreement between the methods is found.

The coverage of H-MFI zeolite acid sites by light alkanes (C3-C7) at monomolecular cracking reaction conditions was determined using infrared operando spectroscopy. At such conditions, alkane adsorption through H-bonding leads to a fully reversible perturbation of the zeolite νOH band at 3600 cm-1. This was used to assess the coverage at various temperatures and pressures, allowing for the determination of the adsorption thermodynamic parameters at reaction