Thermal stability of the solvothermal-synthesized MnFe2O4 nanopowder

被引:23
作者
Stoia, Marcela [1 ,2 ]
Pacurariu, Cornelia [1 ]
Muntean, Eliza-Cornelia [1 ]
机构
[1] Politehn Univ Timisoara, Fac Ind Chem & Environm Engn, 6 Pirvan Blvd, Timisoara 300223, Romania
[2] Politehn Univ Timisoara, Res Inst Renewable Energy, P Ta Victoriei 2, Timisoara 300006, Romania
关键词
Manganese ferrite; Nanopowder; Solvothermal; 1,2-Propanediol; Thermal stability; MANGANESE FERRITE MNFE2O4; MAGNETIC-PROPERTIES; NANOPARTICLES;
D O I
10.1007/s10973-016-5249-5
中图分类号
O414.1 [热力学];
学科分类号
摘要
Manganese ferrite nanopowder was prepared by a new solvothermal method, using 1,2 propanediol as solvent and KOH as precipitant. The as-synthesized powder, by solvothermal treatment in autoclave at 195 A degrees C, for 12 h, consisted of fine manganese ferrite nanoparticles. The further thermal treatment of the initial manganese ferrite powder to higher temperature resulted in manganese ferrite decomposition due to Mn(II) oxidation to Mn(III), as observed by X-ray diffraction. FT-IR spectroscopy has evidenced that the oxidation takes place even at 400 A degrees C. The oxidation of Mn(II) to Mn(III) was studied by TG/DSC simultaneous thermal analysis. It was shown that Mn(II) oxidation takes place in a very small extent up to 400 A degrees C. The main oxidation step occurs around 600 A degrees C, when a clear mass gain is registered on TG curve, associated with a sharp exothermic effect on DSC curve. The exothermic effect is smaller in case of the powder annealed at 400 A degrees C, confirming the superficial oxidation of Mn(II) up to 400 A degrees C. In order to avoid Mn(II) oxidation, the powder obtained at 400 A degrees C was further annealed at 800 A degrees C in argon atmosphere, without degassing, when manganese ferrite MnFe2O4 was obtained as major crystalline phase (69 %). All manganese ferrite powders showed a superparamagnetic behavior, with maximum magnetization of 51 emu g(-1) in case of the as-synthesized powder, characteristic of magnetic ferrite nanopowders.
引用
收藏
页码:155 / 162
页数:8
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