Published April 15, 2016 | Version v1
Journal article

Microscopic characterization of changes in the structure of KCo/CeO2 catalyst used in the steam reforming of ethanol

Description

The cobalt catalyst with a support of CeO2 and potassium promoted (KCo/CeO2) was prepared by an impregnation method and used in the steam reforming of ethanol (SRE). The catalyst was characterized in its initial oxide form and after its work in the SRE by electron microscopy and EDS methods. Microscopic characterization of the catalyst allowed for identification of the active phase (in Co3O4 form) and the CeO2 support phase (O-terminated), existing in the fresh catalyst, and also the active phase (at various forms, Co and CoO), support phase as well as various carbonaceous phases in the used catalyst. STEM-EDS studies allowed to determine the distribution of constituent elements in the catalyst before reaction and besides of them - also carbon deposit after the SRE. Microscopic studies of used catalyst proved that it was largely covered with carbonaceous deposit which was the main reason of deactivation of the catalyst. Carbon deposit growing during the reaction causes destruction of the support and the active phase into smaller particles which are sunked in the carbonaceous structures. - Highlights: • CeO2 and K promoter do not prevent cobalt catalyst from carbon formation in the SRE. • Carbon deposit was present in three forms: fibrous, encapsulates, partly surrounding. • Two types of carbon deposit structures: amorphous and hexagonal graphite were found. • Metallic cobalt and ceria support crystallites are present with K in fibrous carbon. • Cobalt active phase is present under SRE conditions as metallic Co and CoO.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2016.02.008

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2016.02.008;
PII
S0254-0584(16)30078-5;

Publishing Information

Journal Title
Materials Chemistry and Physics
Journal Volume
173
Journal Page Range
p. 219-237
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.