論文

基本情報

氏名 牧 涼介
氏名(カナ) マキ リョウスケ
氏名(英語) Maki Ryosuke
所属 工学部 応用化学科
職名 講師
researchmap研究者コード R000007789
researchmap機関 岡山理科大学

題名

Spinodal Decomposition in the Mg-Al-Fe-O System

単著・共著の別

共著

著者

Y. Kusano, T. Furuta, R. Maki, T. Ogawa, T. Fujii

概要

A supersaturated spinel solid solution having a nominal compositional ratio of Mg/Al/Fe = 0.5:1.0:1.5 was prepared
using a conventional solid-state reaction at 1573 K in air followed by quenching in ice water. The formula of the resulting spinel
structure compound (the spinel) was determined to be (Mg0.50AlFe0.262+Fe1.243+)0.97O4 based on a Rietveld refinement and
thermogravimetry, indicating a cation-deficient spinel structure having mixed valences of Fe. This spinel was found to decompose to
γ-Fe2O3 and a modified, Fe-poor spinel structure compound via a spinodal decomposition below 855 K. The spinodal temperature
was estimated using the sidebands appearing in X-ray diffraction patterns in addition to the temperature dependence of
magnetization values. This spinodal decomposition was accompanied by the oxidation of Fe2+ to Fe3+ and produced a unique grid-
like microstructure (with a grid width of approximately 25 nm) along with enhancement of the saturated magnetization of the
material. A sample cooled to room temperature in a furnace after heating at 1573 K in air had a lamella structure having a width of
approximately 0.1 μm and comprised particles with a mixture of γ-Fe2O3 and the Fe-poor spinel compound on their surfaces.
Subsequent heating of this same material to 1373 K in air formed ε-Fe2O3 in the particles. The crystallographic relationship between
ε-Fe2O3 and the modified spinel structure compound was aε // [112̅]s, bε // [1̅10]s, and cε // [111]s (where ε and s indicate the ε-Fe2O3 and spinel, respectively).

発表雑誌等の名称

Inorganic Chemistry

出版者

American Chemical Society

61

45

開始ページ

18170

終了ページ

18180

発行又は発表の年月

2022/11

査読の有無

有り

招待の有無

無し

記述言語

英語

掲載種別

研究論文(学術雑誌)

ISSN

ID:DOI

ID:NAID(CiNiiのID)

ID:PMID

URL

JGlobalID

arXiv ID

ORCIDのPut Code

DBLP ID