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New insights into reaction mechanisms of ethanol steam reforming on Co–ZrO2

Paper ID Volume ID Publish Year Pages File Format Full-Text
45630 46418 2015 8 PDF Available
Title
New insights into reaction mechanisms of ethanol steam reforming on Co–ZrO2
Abstract

•More than 90% carbon goes through acetone intermediate during ESR on Co–ZrO2.•The possible active site for each reaction step has been identified.•This work provides new fundamental understanding of the ESR on Co–ZrO2.•This work sheds light on the rational design of selective and durable ESR catalysts.

The reaction pathway of ethanol steam reforming on Co–ZrO2 has been identified and the active sites associated with each step are proposed. Ethanol is converted into acetaldehyde and then into acetone, followed by acetone steam reforming. More than 90% of carbon was found to follow this reaction pathway. N2 sorption, X-ray diffraction (XRD), temperature-programmed reduction (TPR), in situ X-ray photoelectron spectroscopy (XPS), transmission electron microscopy, as well as theoretical density functional theory (DFT) calculations have been employed to identify the structure and functionality of the catalysts, which was further used to correlate their performance in ethanol steam reforming (ESR). It was found that metallic cobalt is mainly responsible for the acetone steam-reforming reactions, while CoO and basic sites on the support play a key role in converting ethanol into acetone via dehydrogenation and condensation/ketonization reaction pathways. The current work provides fundamental understanding of the ethanol steam-reforming reaction mechanisms on Co–ZrO2 catalysts and sheds light on the rational design of selective and durable ethanol steam-reforming catalysts.

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Keywords
Ethanol steam reforming; Cobalt; Reaction pathway; Acetone; Oxidation state
First Page Preview
New insights into reaction mechanisms of ethanol steam reforming on Co–ZrO2
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis B: Environmental - Volume 162, January 2015, Pages 141–148
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis