Synthesis, characterization, infrared studies, and thermal analysis of Mn0.6Zn0.4Fe2(C4H2O4)3•6N2H4 and its decomposition product Mn0.6Zn0.4Fe2O4

被引:18
作者
Gawas, U. B. [2 ]
Mojumdar, S. C. [1 ,2 ]
Verenkar, V. M. S.
机构
[1] Univ New Brunswick, Dept Engn, St John, NB E2L 4L5, Canada
[2] Goa Univ, Dept Chem, Taleigao Plateau 403206, Goa, India
关键词
Hydrazine precursor; Ultrafine oxide; Autocatalytic decomposition; DSC; TG; XRD; METAL-CONTAINING MONOMERS; FERRITES PREPARATION; MAGNETIC-PROPERTIES; CRYSTAL-STRUCTURE; HYDRAZINE METHOD; PRECURSOR METHOD; COMPLEXES; GAMMA-FE2O3; REACTIVITY; POLYMERIZATION;
D O I
10.1007/s10973-010-0720-1
中图分类号
O414.1 [热力学];
学科分类号
摘要
Manganese zinc ferrous fumarato-hydrazinate precursor, Mn0.6Zn0.4Fe2(C4H2O4)(3)center dot 6N(2)H(4) was synthesized for the first time and characterized by chemical analysis, infrared spectral studies, and thermal analysis. Infrared studies show band at 977 cm(-1) indicating bidentate bridging nature of the hydrazine in the complex. Thermogravimetric (TG) studies show two steps dehydrazination followed by two steps total decarboxylation. The precursor on touching with burning splinter undergoes self propagating autocatalytic decomposition yielding ultrafine Mn0.6Zn0.4Fe2O4. XRD studies confirms single phase formation as well as nanosize nature of "as prepared" Mn0.6Zn0.4Fe2O4. The saturation magnetization of the "as prepared" Mn0.6Zn0.4Fe2O4 was found to be 31.46 emu gm(-1), which is lower than the reported, confirms the ultrafine nature of the oxide.
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页码:867 / 871
页数:5
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