PREPARATION OF MANGANESE FERRITE FINE PARTICLES FROM AQUEOUS-SOLUTION

被引:122
作者
TANG, ZX
SORENSEN, CM
KLABUNDE, KJ
HADJIPANAYIS, GC
机构
[1] KANSAS STATE UNIV AGR & APPL SCI,DEPT PHYS,MANHATTAN,KS 66506
[2] KANSAS STATE UNIV AGR & APPL SCI,DEPT CHEM,MANHATTAN,KS 66506
[3] UNIV DELAWARE,DEPT PHYS & ASTRON,NEWARK,DE 19716
基金
美国国家科学基金会;
关键词
D O I
10.1016/0021-9797(91)90004-R
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fine manganese ferrite particles have been prepared by a coprecipitation method and subsequent digestion process (below 100°C). Manganous salts mixed with either ferric or ferrous salts were coprecipitated with sodium hydroxide. Particles produced from ferric salts were MnFe2O4 with relatively smaller sizes (5 to 25 nm) while ferrous salts created MnxFe3-xO4 (0.2 < × < 0.7) with bigger sizes up to 180 nm. In either case, the particle size appeared to be a unique function of the ratio of metal ion concentration to hydroxide ion concentration when the digestion conditions were fixed. For the system with ferric salts, the undigested samples were polycrystals with crystallite sizes of about 2 nm. Digestion, which could be described as an Ostwald ripening process, did not change the crystalline structure but increased both the crystallite size and the particle size. A basic solution was essential for an effective digestion process in this system. The system with ferrous salts, on the contrary, needed an acidic solution to create a single ferrite phase. Digestion changed both the crystalline structure and the particle size of the precipitated precursors. This process involved a dissolution and renucleation/growth mechanism. Cation and anion effects on the particle size and the evolution during digestion were also studied. © 1991.
引用
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页码:38 / 52
页数:15
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