Please use this identifier to cite or link to this item:
|Title:||LaNiO3 perovskite catalyst precursor for rapid decomposition of methane: Influence of temperature and presence of H2 in feed stream|
Rapid decomposition of methane
|Citation:||Maneerung, T., Hidajat, K., Kawi, S. (2011-08-10). LaNiO3 perovskite catalyst precursor for rapid decomposition of methane: Influence of temperature and presence of H2 in feed stream. Catalysis Today 171 (1) : 24-35. ScholarBank@NUS Repository. https://doi.org/10.1016/j.cattod.2011.03.080|
|Abstract:||LaNiO3 perovskite has been successfully used as a crystalline catalyst precursor for the rapid decomposition of methane into carbon nanotubes (CNTs) and COx-free H2. The advantages of LaNiO 3 perovskite, when compared with Ni-supported La2O 3 catalyst, are as follows: (1) its ability to perform at higher reaction temperature to achieve higher CH4 conversion, ∼90% CH4 conversion at 800 °C vs. only 55% at 650 °C for NiO/La2O3 catalyst; (2) no significant deactivation of LaNiO3 catalyst; and (3) its ability to maintain catalytic activity for a long reaction time due to its ability to form CNTs even at high reaction temperature, while Ni-supported La2O3 catalyst mostly started forming encapsulating carbon species at 650 °C which caused rapid deactivation of catalyst. CNTs obtained from LaNiO3 perovskite have highly uniform diameter of 24 nm, which is the same size as Ni0 particles after the reduction of LaNiO3 perovskite catalyst. Moreover, the presence of H2 (10 vol%) in the feed stream not only reduces the deactivation rate of LaNiO3 perovskite catalyst at high reaction temperature, but also eliminates amorphous carbon on the surface of CNTs and improves the ordered graphitic structure of CNTs. © 2011 Elsevier B.V. All rights reserved.|
|Source Title:||Catalysis Today|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 18, 2018
WEB OF SCIENCETM
checked on Jul 9, 2018
checked on Jun 29, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.