Reduction behaviour of Fe<sup>3+</sup>/Al<sub>2</sub>O<sub>3</sub>obtained from the mixed oxalate precursor and the formation of the Fe<sup>0</sup>–Al<sub>2</sub>O<sub>3</sub>metal–ceramic composite — Christophe Laurent (1993) | RDL Network
Reduction behaviour of Fe<sup>3+</sup>/Al<sub>2</sub>O<sub>3</sub>obtained from the mixed oxalate precursor and the formation of the Fe<sup>0</sup>–Al<sub>2</sub>O<sub>3</sub>metal–ceramic composite
Journal of Materials Chemistry 3(5): 513-518
Article 1993 English
Authors
CL
Christophe Laurent
AR
A. Rousset
MV
M. Vérelst
Abstract
1 min read
Reduction behaviour of Fe3+/Al2O3 obtained by the decomposition of the oxalate precursor has been investigated by employing X-ray diffraction (XRD), Mössbauer spectroscopy and electron paramagnetic resonance (EPR) spectroscopy. Calcination of Fe3+/Al2O3 at or below 1070 K yields mainly a poorly ordered, fine particulate form of η-Al2–xFexO3. Calcination at or above 1220 K yields α-Al2–xFexO3. Reduction of Fe3+/Al2O3 samples calcined at or below 1070 K gives the FeAl2O4 spinel on reduction at 870 K; samples calcined at or above 1220 K give Al2-xFexO3 with a very small proportion of metallic iron. Fe3+/Al2O3 samples calcined at 1220 K or above yield metallic iron and a very small proportion of the spinel on reduction below 1270 K. In the samples reduced at or above 1270 K, the main product is metallic iron in both ferromagnetic and superparamagnetic forms. The oxalate precursor route yields more metallic iron than the sol–gel route.
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