Environmental and Energy Engineering
Thermal dissociation of compressed ZnO and SnO2 powders in a moving-front solar thermochemical reactor
Article first published online: 2 NOV 2010
DOI: 10.1002/aic.12432
Copyright © 2010 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Chambon, M., Abanades, S. and Flamant, G. (2011), Thermal dissociation of compressed ZnO and SnO2 powders in a moving-front solar thermochemical reactor. AIChE J., 57: 2264–2273. doi: 10.1002/aic.12432
Publication History
- Issue published online: 12 JUL 2011
- Article first published online: 2 NOV 2010
- Accepted manuscript online: 14 SEP 2010 09:24AM EST
- Manuscript Revised: 6 SEP 2010
- Manuscript Received: 18 JUN 2010
Funded by
- CNRS
- The Languedoc-Roussillon Regional Council
- The Energy program of CNRS. Grant Number: DISCO2 project
- ANR. Grant Number: ANR-09-JCJC-0004-01
- Abstract
- Article
- References
- Cited By
Keywords:
- thermochemical cycles;
- zinc;
- tin oxide;
- dissociation;
- solar reactor;
- kinetics
Abstract
The high-temperature thermal dissociation reaction of ZnO and SnO2 was investigated, as part of a two-step thermochemical water-splitting cycle for H2 production. A lab-scale solar reactor (1 kW) was designed, built, and operated for continuous dissociation of volatile oxides under reduced pressure. In this reactor, compressed oxide powders placed in a vertical ceramic cavity are irradiated by highly concentrated solar energy. The reactor design allows moving the reaction front for achieving continuous reactant feeding. ZnO and SnO2 thermal dissociations were successfully performed at about 1900 K, with the recovery of up to 50% of products as nanopowders with high specific surface area (in the range 20–60 m2/g) and with mass fractions of reduced species up to 48 wt % for Zn and 72 wt % for SnO. The performed O2 measurements confirmed the kinetics of ZnO dissociation and gave an activation energy of 380 ± 16 kJ/mol, based on an ablation regime of the ZnO surface. © 2010 American Institute of Chemical Engineers AIChE J, 2011

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