Title of article
Evolution of strong acidity and high-alkane-cracking activity in ammonium-treated USY zeolites Original Research Article
Author/Authors
Kazu Okumura c، نويسنده , , Takuya Tomiyama، نويسنده , , Nami Morishita، نويسنده , , Takashi Sanada، نويسنده , , Kazuhiro Kamiguchi، نويسنده , , Naonobu Katada، نويسنده , , Miki Niwa، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2011
Pages
10
From page
8
To page
17
Abstract
USY zeolites prepared by steam treatment of NH4-Y zeolites were treated with ammonium nitrate solutions. Treatment with ammonium nitrate solutions resulted in a significant enhancement of the octane-cracking activity of the USY zeolites. We found by infrared spectroscopy/mass spectrometry-temperature programmed desorption (IRMS-TPD) of NH3 that the prepared USY zeolites have acidity strong enough to catalyze alkane cracking. The acid strength (ΔH) values of the enhanced Brønsted OH on the USY are found to be ca. 150 kJ mol−1. A linear correlation between ΔH and the activation energy in alkane cracking was obtained when Y-type zeolites were used for the reaction. The heats of adsorption of octane and hexane were almost constant over various types of FAU zeolites. This means that the higher the strength of the acid site, the smaller the intrinsic activation energy of the alkane cracking. This study clearly indicated that treatment with NH4+ was the key to creating very strong acidity in USY zeolites. Furthermore, the origin of the high catalytic activity of the ammonium-treated USY zeolites was attributed to the evolution of strong acidity rather than changes in the adsorption energies of the alkanes, based on the measurements of acid strength, heat of alkane adsorption, and activation energy.
Keywords
Ultra-stable Y zeolite , IRMS-TPD , Alkane cracking , Ammonium salts
Journal title
Applied Catalysis A:General
Serial Year
2011
Journal title
Applied Catalysis A:General
Record number
1156506
Link To Document