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A highly active, selective and stable copper/cobalt-structured nanocatalyst for methanol decomposition

Paper ID Volume ID Publish Year Pages File Format Full-Text
47235 46464 2010 8 PDF Available
Title
A highly active, selective and stable copper/cobalt-structured nanocatalyst for methanol decomposition
Abstract

A structured catalyst prepared by copper doping a support composed of mesoporous Co(OH)2/Co3O4 nanowire arrays hydrothermally grown on a stainless steel mesh was used for the methanol decomposition reaction. When copper doping was applied to an uncalcined cobalt-based support, followed by calcination in air, the catalytic activity of the resulting bimetallic catalyst was observed to increase by about one order of magnitude with respect to that of the catalyst obtained by copper doping a calcined support. This high activity, which is accompanied by a very high selectivity to CO and a fair stability, is thought to be due to the transformation of a large proportion of the copper precursor into Cu2O of a low crystal size during calcination. Comparison with other catalysts reported in the literature shows that the most active catalysts prepared in this work are better than the most active, selective and stable transition metal catalysts described in the reviewed literature.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights▶ Catalysts consist of CuOx/Co3O4 nanowire arrays supported on a stainless steel mesh. ▶ They are among the most active catalysts for methanol decomposition. ▶ These catalysts are highly selective to CO and H2. ▶ These catalysts are highly stable.

Keywords
Methanol decomposition; Hydrogen; CO; Co3O4; Cobalt; Cu2O; Copper; Spinel; Catalytic activity; Selectivity; Stability; Microreactor
First Page Preview
A highly active, selective and stable copper/cobalt-structured nanocatalyst for methanol decomposition
Publisher
Database: Elsevier - ScienceDirect
Journal: Applied Catalysis B: Environmental - Volume 99, Issues 1–2, 31 August 2010, Pages 257–264
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis