Abstract

The Ta 2O 5 or Ta (99.99%, Aldrich) was carburized using pure CH 4 in a temperature-programmed manner. The BET surface areas of these materials varied with different molar hourly space velocity, suggesting that the sorption properties of these materials were strong functions of space velocity employed. The tantalum carbides proved to be active NH 3 decomposition catalysts. The ammonia decomposition activities of tantalum carbides normalized by the oxygen uptake increased with increasing surface area, suggesting that NH 3 decomposition over these materials is structure-sensitive. This behavior may be ascribed to variations in the surface stoichiometry with surface area as confirmed by XPS results. The ammonia decomposition activation energies for all the tantalum carbides were similar and averaged 39 kcal/mol, which is in good agreement with those reported in the literature. The activities of the tantalum carbides were much lower than those of vanadium and molybdenum carbide catalysts. This difference was probably due to the degree of electron transfer between metals and carbon in transition metal carbides.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.