• Rane, N. J.
• Overweg, A. R.
• Kazansky, V. B.
• Hensen, Emiel, J. M.
• Van Santen, Rutger

Abstract

The reduction of Ga(CH3)3/ZSM-5 was closely followed by Fourier transform infrared spectroscopy and Ga K-edge X-ray absorption near-edge spectroscopy. Chemical vapor deposition of trimethylgallium on HZSM-5 (TMG/ZSM-5) resulted in the replacement of nearly all Brønsted acid protons by dimethylgallium species. Removal of the methyl ligands from the cationic Ga clusters gave charge-compensating Ga+ and species. At high temperatures and in the absence of hydrogen, the Ga+ species were the most stable, although decomposition of the species was very slow. Ga+ ions can be oxidized by nitrous oxide at low temperature (473 K), resulting in the formation of gallyl (GaO+) cations. A detailed comparison of the reactivity of Brønsted acid protons (HZSM-5) and Ga+ ions (reduced TMG/ZSM-5) in propane dehydrogenation showed that the former converted propane via protolytic cracking with methane, ethane, and propene as hydrocarbon products, whereas monovalent Ga+ ions produced propene almost exclusively. The reaction data suggest that propane was converted over Ga+ cations but not over cations. The initial rate of propane dehydrogenation was highest for GaO+ ions, although rapid deactivation was observed, due to the higher barrier for regeneration of GaO+ ions than for formation of less active Ga+ ions.ERRATUM : Journal of Catalysis, Volume 240, Issue 1, 15 May 2006, Page 85,

Topics

• cluster
• laser emission spectroscopy
• Hydrogen
• Fourier transform infrared spectroscopy
• chemical vapor deposition
• decomposition