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首页> 外文期刊>Materials Characterization >Coercivity and superparamagnetic evolution of high energy ball milled (HEBM) bulk CoFe_2O_4 material
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Coercivity and superparamagnetic evolution of high energy ball milled (HEBM) bulk CoFe_2O_4 material

机译:高能球磨(CoCo_2O_4)块体材料的矫顽力和超顺磁演化

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摘要

Ball milling (BM) of bulk CoFe_2O_4 powder material carried out in order to study its structural stability and attendant property changes with respect to coercivity enhancements and superparamagnetic behaviors, showed that drastic crystallite size reduction occurred within the first 1 h of ball milling. Crystallite size dropped from 74 nm for the as-received material to a value of 11.6 nm for 600 min of ball milling. Combined X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses confirmed crystallite size reduction with corresponding increase in interparticle agglomeration/pores with increasing milling time. The maximum coercivity of 0.46 T and the crystallite size of 15.6 nm were recorded with 20 min, while peak residual strain of 0.0066 mm/mm was for 180 min of BM. Material with peak coercivity value did not have peak residual strain, or minimum crystallite size, thereby suggesting that other structural defects contributed to coercivity enhancement. The saturation magnetization (M_s) value de creased continuously with increasing milling time, while remanence magnetization (M_r) and coercivity decreased with increasing BM time, after an initial increase. Mossbauer spectroscopy (MS) measurements confirmed both particle size distribution and decomposition/disordering of the material together with superparamagnetism as BM time increased. The degree of inversion ranged from 41% to 71.7% at different milled states from Mossbauer spectroscopy. The internal magnetic fields of the Fe sites associated with the tetrahedral and octahedral sites were 507.4 kOe and 492 kOe respectively in the unmilled state, while 484 kOe and 468.5 kOe in the 600 min milled state correspondingly.
机译:为了研究球状CoFe_2O_4粉末材料的结构稳定性以及随之而来的矫顽力增强和超顺磁性行为的特性变化,进行了球磨(BM),结果表明,在球磨的前1 h内,晶粒尺寸急剧减小。对于球磨600分钟,微晶尺寸从接收时的材料的74 nm下降到11.6 nm。结合X射线衍射(XRD)和扫描电子显微镜(SEM)分析确认,晶粒尺寸减小,且随着研磨时间的增加,颗粒间附聚/孔的数量相应增加。在20分钟内记录的最大矫顽力为0.46 T,微晶尺寸为15.6 nm,而BM的180分钟峰值残余应变为0.0066 mm / mm。具有矫顽力峰值的材料没有峰值残余应变或最小的微晶尺寸,因此表明其他结构缺陷有助于矫顽力的提高。在初始增加之后,饱和磁化强度(M_s)值随研磨时间的增加而连续降低,而剩余磁化强度(M_r)和矫顽力随BM时间的增加而降低。 Mossbauer光谱(MS)测量结果证实,随着BM时间的增加,材料的粒度分布和分解/无序性都与超顺磁性一起出现。根据Mossbauer光谱,在不同研磨状态下,反演度的范围从41%到71.7%。在未铣削状态下,与四面体和八面体位置相关的Fe位置的内部磁场分别为507.4 kOe和492 kOe,而在600 min铣削状态下分别为484 kOe和468.5 kOe。

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