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Effect of ball milling time on microstructure and magnetic properties of Fe-W nanocrystalline composite synthesised by hydrogen reduction and sintering

机译:球磨时间对氢还原烧结法制备的Fe-W纳米晶复合材料微观结构和磁性能的影响

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摘要

Sintered nanocrystalline Fe–W composites were synthesised by isothermal reduction of a Fe2O3–nWO3 powder mixture in pure hydrogen at 900uC. Before reduction, a 1:1 mixture of the powdersnwas ball milled thoroughly for 3, 9 or 15 h, then compacted and dried at 90uC for 24 h. Thenreduced powders were re-compacted and sintered at 1000uC for 2 h in hydrogen. The reductionnbehaviour was studied by thermogravimetric analysis. The microstructure, phase composition,npore distribution and magnetic properties of the initial oxide mixtures and of the reduced andnsintered products were characterised. Complete reduction was achieved in all cases, to give annanocrystalline homogenous composite with Fe of 13 nm crystallite size and W of 38 nm. A densencrystalline structure was observed within sintered samples having a total porosity of 52–54%. Thenmagnetic coercivity (Hc) of the sintered Fe–W specimens increased with increasing milling time,nwhereas magnetisation (Ms) decreased.
机译:烧结的纳米晶Fe–W复合材料是通过在900uC的纯氢气中等温还原Fe2O3-nWO3粉末混合物而合成的。还原前,将1:1的粉末混合物充分球磨3、9或15小时,然后压实并在90°C下干燥24小时。然后将还原的粉末重新压实,并在氢气中1000uC烧结2小时。通过热重分析研究还原行为。表征了初始氧化物混合物和还原烧结烧结产物的微观结构,相组成,孔分布和磁性能。在所有情况下均完全还原,得到具有13 nm微晶尺寸的Fe和38 nm W的胭脂红均质复合材料。在烧结样品中观察到了致密晶体结构,总孔隙率为52–54%。然后,随着铣削时间的增加,烧结的Fe-W试样的矫顽力(Hc)增大,而磁化强度(Ms)减小。

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