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Catalysts 2014, 4(2), 196-214;

Deactivation Pattern of a “Model” Ni/MgO Catalyst in the Pre-Reforming of n-Hexane

Dipartimento di Ingegneria Elettronica, Chimica e Ingegneria Industriale, Università degli Studi di Messina, Viale F. Stagno D'Alcontres 31, I-98166 Messina, Italy
Istituto CNR-ITAE "Nicola Giordano", Salita S. Lucia 5, I-98126 Messina, Italy
Dedicated to Professor Adolfo Parmaliana, who died five years ago (2 October 2008), for his passionate contribution to the research topic of hydrocarbon reforming.
Author to whom correspondence should be addressed.
Received: 14 August 2013 / Revised: 20 January 2014 / Accepted: 5 June 2014 / Published: 19 June 2014
(This article belongs to the Special Issue Advances in Catalyst Deactivation)
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The deactivation pattern of a “model” Ni/MgO catalyst in the pre-reforming of n-hexane with steam (T, 450 °C; P, 5–15 bar) is reviewed. The influence of the steam-to-carbon ratio (S/C, 1.5–3.5) on the rate of catalyst fouling by coking is ascertained. Catalyst fouling leads to an exponential decay in activity, denoting 1st-order dependence of the coking process on active sites availability. Hydrogen hinders the coking process, though slight activity decay is due to sintering of the active Ni phase. Deactivation by thiophene causes a sharp, almost linear, drop to nearly zero activity within only 6 h; this deactivation is likely due to dissociative adsorption of thiophene with subsequent strong, irreversible chemical adsorption of S-atoms on active Ni sites, i.e., irreversible poisoning. Modeling of activity decay curves (α, at/a0) by proper kinetic equations allows assessing the effects of temperature, pressure, S/C, H2 and thiophene feed on the deactivation pattern of the model Ni/MgO catalyst by coking, sintering, and poisoning phenomena. View Full-Text
Keywords: pre-reforming; activity decay; poisoning; sintering pre-reforming; activity decay; poisoning; sintering

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Trunfio, G.; Arena, F. Deactivation Pattern of a “Model” Ni/MgO Catalyst in the Pre-Reforming of n-Hexane. Catalysts 2014, 4, 196-214.

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