Composition, Structure and Reduction Reactivity of Composite Materials of the α-Fe2O3–СaFe2O4 System by Hydrogen

IF 0.5 Q4 CHEMISTRY, MULTIDISCIPLINARY
V. Vladimir, P. Nadezhda, N. Nina, V. Yuriy, M. Z. Anatoly, A. Leonid
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引用次数: 2

Abstract

In this paper, α-Fe2O3–CaFe2O4 composite materials obtained by high-temperature solid-phase synthesis from Ca and Fe (III) oxides with varying molar ratio CaO/Fe2O3 in the range 0.15-1.00 were investigated. The materials are characterized by Х-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray microanalysis (SEM-EDS) and simultaneous thermal analysis (STA) in the hydrogen temperature-programmed reduction mode (H2-TPR). SEM-EDS studies of the specimens were revealed a formation of the “core-shell” type complex microstructure of material with the hematite phase as the “core”. H2-TPR of the specimens allowed to establish a decrease of the contribution of low-temperature forms of lattice oxygen in areas of 350-510 °С (up to 2.6 times) and 510-650 °С (up to 1.7 times), and the growth of the contribution of the high-temperature oxygen form in the range of 650-900 °С (up to 2 times) with an increase in the content of the phase CaFe2O4 from 33.4 to 97.5 wt. %. Relying on the assessment of lattice oxygen mobility, it was suggested, that the samples with content of CaFe2O4 phase more than 55.4 wt. % are promising for use as oxygen carriers in chemical looping processes of syngas production.
α-Fe2O3 -СaFe2O4体系复合材料的组成、结构及氢还原反应性
以CaO/Fe2O3摩尔比在0.15 ~ 1.00范围内变化的Ca和Fe (III)氧化物为原料,采用高温固相合成法制备了α-Fe2O3-CaFe2O4复合材料。通过Х-ray衍射(XRD)、SEM-EDS (SEM-EDS)扫描电镜和H2-TPR同步热分析(STA)对材料进行表征。对试样进行SEM-EDS分析,发现材料形成以赤铁矿相为“核心”的“核-壳”型复合微观结构。样品的H2-TPR允许建立在350-510°С(高达2.6倍)和510-650°С(高达1.7倍)区域的低温形式的晶格氧的贡献减少,在650-900°С(高达2倍)范围内的高温形式的贡献增加,CaFe2O4相的含量从33.4%增加到97.5 wt. %。通过对晶格氧迁移率的评价,认为CaFe2O4相含量大于55.4 wt. %的样品有望作为合成气化学环工艺中的氧载体。
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CiteScore
1.10
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13
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