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CuFeAl-composite catalysts of oxidation of gasification products of solid fuels : In situ XAS and XRD study. / Saraev, A. A.; Tsapina, A. M.; Fedorov, A. V. и др.
в: Radiation Physics and Chemistry, Том 175, 108071, 10.2020.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - CuFeAl-composite catalysts of oxidation of gasification products of solid fuels
T2 - In situ XAS and XRD study
AU - Saraev, A. A.
AU - Tsapina, A. M.
AU - Fedorov, A. V.
AU - Trigub, A. L.
AU - Bulavchenko, O. A.
AU - Vinokurov, Z. S.
AU - Zubavichus, Ya V.
AU - Kaichev, V. V.
N1 - Publisher Copyright: © 2019 Elsevier Ltd Copyright: Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/10
Y1 - 2020/10
N2 - The reduction of high-active FeAl and CuFeAl composite catalysts was investigated in situ by XRD and XAS in the temperature range between 100 and 600 °C. It was found that the fresh catalysts consist of Fe2O3 and Al2O3 phases only. The Al3+ cations partially dissolute in the Fe2O3 lattice. The addition of copper to the Fe-Al catalyst leads to formation of highly dispersed CuO nanoparticles and mixed oxide with a spinel-type crystalline structure similar to that of CuFe2O4. The low-temperature reduction of Cu2+ to Cu0 accelerates the Fe2O3 → Fe3O4 and FeO → Fe0 transformations. In the presence of oxygen we did not observe the reduction of Cu and Fe to the metallic state. This means that the oxidation of CO over FeAl and CuFeAl composite catalysts proceeds via a redox mechanism.
AB - The reduction of high-active FeAl and CuFeAl composite catalysts was investigated in situ by XRD and XAS in the temperature range between 100 and 600 °C. It was found that the fresh catalysts consist of Fe2O3 and Al2O3 phases only. The Al3+ cations partially dissolute in the Fe2O3 lattice. The addition of copper to the Fe-Al catalyst leads to formation of highly dispersed CuO nanoparticles and mixed oxide with a spinel-type crystalline structure similar to that of CuFe2O4. The low-temperature reduction of Cu2+ to Cu0 accelerates the Fe2O3 → Fe3O4 and FeO → Fe0 transformations. In the presence of oxygen we did not observe the reduction of Cu and Fe to the metallic state. This means that the oxidation of CO over FeAl and CuFeAl composite catalysts proceeds via a redox mechanism.
KW - Catalytic combustion
KW - CO oxidation
KW - CuFeAl-composite catalysts
KW - In situ XAS
KW - In situ XRD
KW - RAY-ABSORPTION SPECTROSCOPY
KW - REDUCTION
KW - COPPER
UR - http://www.scopus.com/inward/record.url?scp=85058150349&partnerID=8YFLogxK
U2 - 10.1016/j.radphyschem.2018.11.025
DO - 10.1016/j.radphyschem.2018.11.025
M3 - Article
AN - SCOPUS:85058150349
VL - 175
JO - Radiation Physics and Chemistry
JF - Radiation Physics and Chemistry
SN - 0969-806X
M1 - 108071
ER -
ID: 17822292