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Deposition of inorganic bronze coatings over ceramic foams

Published online by Cambridge University Press:  03 March 2011

M. Mann
Affiliation:
Department of Chemical Engineering, Technion–Israel Institute of Technology, Haifa 32000, Israel
G.E. Shter
Affiliation:
Department of Chemical Engineering, Technion–Israel Institute of Technology, Haifa 32000, Israel
G.S. Grader*
Affiliation:
Department of Chemical Engineering, Technion–Israel Institute of Technology, Haifa 32000, Israel
*
a)Address all correspondence to this author.e-mail: grader@tx.technion.ac.il
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Abstract

A method for applying conductive inorganic tungsten bronze (NaxWO3) coatings over ceramic foams is presented. The general basis of bronze coating involves an intermediate layer between the ceramic surface and the redox external agent (liquid or gas phase). The intermediate layer is a multifunctional element and its function depends on the agents involved in redox reaction. The bronze film is formed either on the intermediate layer or in place of it. The initial melt included Na2WO4, WO3, and NaCl. The reticulated ceramic foams, made from pure alumina (Al2O3), were prepared by a standard impregnation method. In all depositions, the temperature was above the melting point of the Na2WO4/WO3 system. The effect of NaCl content on the final coating properties was investigated in the 10–40 mol% range. The best results were obtained with hydrogen reduction of 40% NaCl in the melt. The bronze crystals size in the coating was 0.8–1.6 μm. The bronze layer was continuous throughout the foam. The obtained coating has a bright yellow-gold color, consistent with a stoichiometric parameter value (x) of 0.85–0.95. The resistivity of coated foams decreased from above 12 Ω mm to below 1 Ω mm when the NaCl concentration in the melts increased from 10% to 40%, respectively, due to improved continuity of the bronze crystals. These highly conductive, bronze-coated alumina foams, can potentially serve as high-temperature electrodes in aggressive conditions.

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Articles
Copyright
Copyright © Materials Research Society 2005

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