This study deals with an investigation of the catalytic performance of a bimetallic system based on Ni and Cu prepared by two different methods. It was found that the oxalate method permits to obtain crystallites with lower dimension compared to the sol-gel method, even after the calcination of powders carried out at the same temperature. Furthermore, the catalytic behavior of the two samples was different. The Ni-Cu prepared by oxalate method showed higher performance and stability than the Ni-Cu prepared by sol-gel in autothermal reforming (ATR) of methane achieving a fuel conversion of about 80%. (C) 2014 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.

Ni-Cu based catalysts prepared by two different methods and their catalytic activity toward the ATR of methane / Lo Faro, M; Antonucci, Pierluigi; Arico, As; Frontera, Patrizia. - In: CHEMICAL ENGINEERING RESEARCH & DESIGN. - ISSN 0263-8762. - 93:(2015), pp. 269-277. [10.1016/j.cherd.2014.05.014]

Ni-Cu based catalysts prepared by two different methods and their catalytic activity toward the ATR of methane

ANTONUCCI, Pierluigi;FRONTERA, Patrizia
2015-01-01

Abstract

This study deals with an investigation of the catalytic performance of a bimetallic system based on Ni and Cu prepared by two different methods. It was found that the oxalate method permits to obtain crystallites with lower dimension compared to the sol-gel method, even after the calcination of powders carried out at the same temperature. Furthermore, the catalytic behavior of the two samples was different. The Ni-Cu prepared by oxalate method showed higher performance and stability than the Ni-Cu prepared by sol-gel in autothermal reforming (ATR) of methane achieving a fuel conversion of about 80%. (C) 2014 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
2015
Autothermal reforming;
Ba-doped catalyst;
Ni-Cu bimetallic catalyst
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12318/1306
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