jp903788n_si_024.cif (16.95 kB)

Correlation between Brønsted Acid Strength and Local Structure in Zeolites

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posted on 2009-11-05, 00:00 authored by Naonobu Katada, Katsuki Suzuki, Takayuki Noda, German Sastre, Miki Niwa
As an index of acid strength, ammonia adsorption energies (Eads) were calculated with density functional theory on cluster models of Brønsted acid sites belonging to FAU, BEA, MFI, FER, MWW, and MOR structures, which were selected because of the availability of experimental data and industrial importance. The calculated Eads were reasonably consistent with experimental results from the ammonia IRMS-TPD (infrared mass spectroscopy−temperature-programmed desorption) method. The calculated value was slightly (10−20 kJ mol−1) lower than the observed value, and its change with varying structure was approximately in agreement with the experiments. A thorough study was carried out to find the geometric parameters of the zeolite clusters (in the H and NH4 forms) relevant to Eads and to discuss parameters controlling the acidic property. Hydrogen bonding interactions between ammonium cations and neighboring zeolitic oxygens were found to affect Eads observed in small cavities. When NH4+ was stabilized in relatively open spaces (large cavities), acid strength was controlled by the local geometry of the Brønsted acid site, indicating a contribution of strain around Si(OH)Al to acid strength. In these cases, a shorter Al−O distance (a) gave a higher Eads. This is consistent with the explanation that Lewis acidic Al withdraws the electron charge of the SiOH contributing to Brønsted acid strength. A relationship was found between a and the distance (b) and planar angle (ω) between two triangles consisting of three oxygens each, which surrounded the Si(OH)Al unit, and finally, a relationship was found in which a smaller b and ω brought a higher Eads. The strain (compression) on atoms surrounding the Si(OH)Al unit is reflected in the extent of b and ω, and this contributes to vary Brønsted acid strength.