Redox Reaction Kinetics of Fe₂O₃ by Hydrogen and Water with Oxide Ion Conducting Supports and Oxygen Transport Modeling for Fe₂O₃ Reduction Process
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- Kosaka Fumihiko
- Department of Environment Systems, Graduate School of Frontier Sciences, The University of Tokyo
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- Isogai Syunsuke
- Department of Environment Systems, Graduate School of Frontier Sciences, The University of Tokyo
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- Hatano Hiroyuki
- Department of Integrated Science and Engineering for Sustainable Society, Faculty of Science and Engineering, Chuo University
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- Oshima Yoshito
- Department of Environment Systems, Graduate School of Frontier Sciences, The University of Tokyo
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- Otomo Junichiro
- Department of Environment Systems, Graduate School of Frontier Sciences, The University of Tokyo
書誌事項
- タイトル別名
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- Redox Reaction Kinetics of Fe<sub>2</sub>O<sub>3</sub> by Hydrogen and Water with Oxide Ion Conducting Supports and Oxygen Transport Modeling for Fe<sub>2</sub>O<sub>3</sub> Reduction Process
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Improvement in the reduction kinetics and stabilities resulting in longer lifetimes are required for practical application of energy conversion and storage systems using redox reaction of metal oxides such as chemical looping systems. It has been previously reported that using oxide ion conductors as supports can improve the redox reactions of metal oxides. To evaluate which physical properties (such as oxide ion transport and electron transport) can affect the redox reaction kinetics of Fe2O3, reduction kinetic analyses of Fe2O3 reduction by hydrogen were performed. The experiments were conducted using various supports such as CaTi1–xFexO3 (CTFO, as a mixed ionic and electronic conductor), yttlia-stabilized zirconia (YSZ, as a pure oxide ionic conductor) and Al2O3 as a reference (insulator). The results showed that reduction of Fe2O3 with CTFO or YSZ as a support was greatly improved compared with Al2O3. Oxidation measurements of the Fe/supports by water vapor, i.e. hydrogen production by a steam-iron reaction, showed that CTFO was highly effective at increasing oxidation. Modeling analyses based on the oxygen chemical potential distributions of the Fe2O3/supports were also performed to analyze the effect of the supports quantitatively. Calculations assuming high electron and oxygen transport at the interface supported the experimental results. The results suggest that the transport properties at the interface were derived from a highly conducting phase and that oxide ionic conductivity is the predominant factor in the improvement. Sensitivity analysis using various parameters was also conducted and the mechanism for the improvements was discussed.
収録刊行物
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- JOURNAL OF CHEMICAL ENGINEERING OF JAPAN
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JOURNAL OF CHEMICAL ENGINEERING OF JAPAN 49 (3), 243-250, 2016
公益社団法人 化学工学会
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詳細情報 詳細情報について
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- CRID
- 1390282679544178176
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- NII論文ID
- 130005137822
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- NII書誌ID
- AA00709658
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- ISSN
- 18811299
- 00219592
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- NDL書誌ID
- 027204166
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
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- KAKEN
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- 抄録ライセンスフラグ
- 使用不可