共查询到19条相似文献,搜索用时 140 毫秒
1.
本文报道利用单辊方法制备的非晶Nd3Fe81B16合金的晶化及其对磁性和M?ssbauer谱的影响。发现在非晶Fe81B19合金中用3at%Nd取代B,使非晶Fe81B19合金的晶化温度提高88℃。在适当的退火条件下晶化后样品在室温下的磁性是:σs=189emu/g,σr/σs=0.7,iHc=2.15kOe,Br≈12kG,bHc=2kOe,(BH)max≈8MGOe。与目前广泛使用的六角铁氧体相比,bHc相近,但Br和(BH)max远比六角铁氧体高。这种材料仅含有少量的Nd,因此可能开发为一种新的廉价永磁材料。本文对少量Nd的添加对非晶FeB合金的晶化温度,磁性和M?ssbauer谱的影响进行了讨论。初步探讨了高矫顽力的来源,认为它的磁化和反磁化过程可以用畴壁钉扎理论解释。
关键词: 相似文献
2.
3.
4.
YTi(Fe1-xCox)11在012型四方结构,居里温度随Co含量的增加而提高,本文为了揭示YTi(Fe1-xCox)11磁性与微观结构的联系,对这一系列化合物进行穆斯堡尔谱研究,在室温下,测量YTi(Fe1-xCox)11(其中x=0.0,0.2,0.4)的穆斯堡尔谱,最佳拟合结果证实在这种化合物中,Co原子优先占据j和f晶位,在所测样品中,超精细场在x=0.2处出现极值,这与YTi(Fe1-xCox)11饱和磁化强度测量结果相符合。并对YTi(Fe1-xCox)11,Y2(Fe1-xCox)14和YTi(Fe1-xCox)11的穆斯堡尔谱的实验结果进行比较,分析在YTiFe11中与Y2Fe14B中的3d电子能带结构的差异。
关键词: 相似文献
5.
6.
7.
通过熔体快淬方法获得Pr(Fe1-xCox)2合金条带,经过X射线衍射、差示扫描量热计和磁性测量对其结构、磁性和热稳定性进行了研究.发现当Co的含量x大于0.2时才可能获得Pr(Fe,Co)2立方Laves相化合物.对Pr(Fe0.6Co0.4)2合金,在快淬速度为30m/s时,条带由Pr2(Fe,Co)17,Pr(Fe,Co)2和富稀土相组成;在速度为40m/s时,获得了几乎单相的Pr(Fe0.6Co0.4)2化合物,其居里温度为305℃;在速度为45m/s时,除了Pr(Fe0.6Co0.4)2化合物外,还存在少量的非晶相.Pr(Fe0.6Co0.4)2化合物在770℃以上发生分解.用40m/s快淬纳米晶粉胶粘磁体有大的磁致伸缩系数(λ∥-λ⊥=140×10-6)和高的硬磁性能(iHc=398kA/m).
关键词: 相似文献
8.
本文对Nd-Fe-Si三元系富铁区域相的结构和磁性进行了研究。结果表明,Nd-Fe-Si三元系富铁区域(Fe>40at%),除出现NdFe2Si2三元金属间化合物外(Si>20at%),同时只出现Nd2(Fe,Si)17赝二元金属间化合物,其中Si取代9d位的Fe原子,而不能形成类似于Nd2Fe14B的三元金属间化合物,Si取代Nd2Fe17中的9d位Fe原子后,使晶胞体积缩小;使饱和磁化强度减小;同时使Fe次晶格的铁磁相互作用增强,导致居里温度增高;还使得Fe次晶格的易面各向异性减弱,造成室温下各向异性场减小。
关键词: 相似文献
9.
10.
运用微磁学方法结合物质参数探究了垂直取向Nd2Fe14B/α-Fe磁性三层膜的磁化反转过程,计算出成核场、钉扎场以及磁滞回线随Ls(软磁相厚度)的变化,并与相关的实验和理论数据进行比较.由于考虑了退磁能量项,垂直取向的成核场比平行取向时低,在外磁场还没有反向时就发生了成核.随着软磁相厚度的增加,理论矫顽力从等于成核场(同时也等于钉扎场),到等于钉扎场,再到小于钉扎场,矫顽力机理由成核变为钉扎.
关键词:
成核场
钉扎场
矫顽力
磁滞回线 相似文献
11.
MAGNETIC PROPERTIES AND CRYSTALLIZATION OF THE RAPIDLY QUENCHED (Fe1-xNdx) 81.5B18.5 ALLOYS 总被引:1,自引:0,他引:1 下载免费PDF全文
Magnetic properties and crystallization behaviors of amorphous (Fe1-xNdx) 81.5B18.5 alloys were studied. The crystallization temperature is found to rise at first and then drop monotonically with x, having a maximum value of 976K at x=0.11 (9at% Nd). The (Fe1-xNdx) 81.5B18.5 alloys prepared at a quenching rate of vs = 6.6m /s are amorphous, and exhibit good glass formability. Both the coercive field Hc and energy product (BH)max depend strongly on Nd concentration. Amorphous (Fe1-xNdx) 81.5B18.5 alloys with higher Nd concentration have a high coercive field at low temperature, due to the large random uniaxial anisotropy of Nd. The room-temperature Hc and (BH)max obtained on optimal annealing con-ditions show two maxima as a function of Nd concentration x. The highest room-temperature coercive field Hc =22 kOe within the Nd concentrations around x=0.368 and the maximum energy product(RH)max= 13.3 MG·Oe at x =0.055 are observed. The hard magnetic properties of these crystallized samples are related to the presence of the bard magnetic Nd2Fe14B phase. 相似文献
12.
13.
The magnetic properties of (Cox Fe1-x)A (Zn1-x Fe1+x)B O4 are studied using mean-field theory and the probability distribution law to obtain the saturation magnetization, the coercive field, the critical temperature, and the exchange interactions with different values of D (nm) and x. High-temperature series expansions (HTSEs) combined with the Pade approximant are used to calculate the critical temperature of (CoxFe1-x)A(Znl-xFe1+x)BO4, and the critical exponent associated with magnetic susceptibility is obtained. 相似文献
14.
15.
A systematic investigation of nitrides R3Fe29-xCrxN4(R=Y, Ce, Nd, Sm, Gd, Tb, and Dy) has been performed. The nitrogen concentration in the nitride R3Fe29-xCrxNy was determined to be y=4. Nitrogenation leads to a relative volume expansion of about 5.3%. The lattice constants and unit cell volume decrease with in creasing rare earth atomic number from Nd to Dy, reflecting the lanthanide contraction. In average, the increase of Curie temperature upon nitrogenation is about 200 K, compared with its parent compound. The nitrogenation also results in a remarkable improvement in the saturation magnetization and anisotropy fields for R3Fe29-xCrxN4 at 4.2 K and room temperature, comp ared with their parent compounds. A spin reorientation of Nd3Fe24.5 Cr4.5N4 occurs at around 368 K, which is 138 K higher than that of Nd3Fe24.5Cr4.5.Magnetohistory effects of R3Fe29-xCrxN4(R=Nd and Sm) are observed in a low field of 0.04 T. First order magneti zation process occurs in Sm3Fe24.0Cr5.0N4 in magnetic fields of around 3.0 T at 4.2 K. After nitrogenation the easy magnetization direction of Sm3Fe24.0Cr5.0 is changed from the easy cone structure to the uniaxial. The excellent intrinsic magnetic properties of Sm3Fe24.0Cr5.0N4 make this compound a hopeful candidate for new high performance permanent magnets. 相似文献
16.
The magnetic properties of Nd4.5Fe77−xMnxB18.5 (x=0, 1 and 2) nanocomposites prepared by the crystallization of amorphous precursors were investigated. Addition of Mn is found to decrease the crystallization temperature of the amorphous ribbons. The intrinsic coercivity iHc and maximum energy product (BH)max increase from 2.6 kOe and 9.1 MGOe for x=0 to 3.1 kOe and 10.3 MGOe for x=1, respectively, and the remanence ratio Mr/Ms increases from 0.70 to 0.72. The effect of Mn on Curie temperature TC and the thermal stability of Mr and iHc were also studied. 57Fe Mössbauer spectra have been recorded for x=0, 1 and 2 ribbons at room temperature and site preference of the Mn atoms in Fe3B and Nd2Fe14B phases is discussed using the Mössbauer spectroscopy. 相似文献
17.
用直拉单晶生长系统制备TbyDy1-x(Fe1-xTx)2(T=Al,Mn)单晶,并测量其磁致伸缩.用电弧炉合成多晶TbyDy1-y(Fe1-xTx)2(T=Al,Mn),并用X射线衍射方法测量拟合得到内禀磁致伸缩.结果表明,Al和Mn替代后饱和磁场降低,说明Al和Mn的替代明显地降低了各向异性能.随Al和Mn替代量的增加,总的趋势是材料的内禀磁致伸缩λ111降低.对Tb0.5Dy0.5(Fe0.9Mn0.1)2单晶,在不加压情况下的磁致伸缩效果并不明显,但当施加压力时,磁致伸缩变化显著,尤其在12—26MPa压力下,磁致伸缩变化很大,且低场效果很好.
关键词: 相似文献
18.
通过x射线衍射及磁测量手段研究了Y2(Fe1-y-x,Coy,C rx)17化合物的结 构及居里温度.研究结果表明Y2(Fe1-y-x,Coy,Crx)17化合物具有六 角相的Th2Ni17型结构.随着x的增加,Y2(Fe
关键词:
2(Fe1-y-x')" href="#">Y2(Fe1-y-x
y')" href="#">Coy
x)1 7化合物')" href="#">Crx)1 7化合物
x射线衍射
居里温度 相似文献
19.
The magnetic property of double doped manganite Nd0.5(1+x)Ca0.5(1−x)Mn(1−x)CrxO3 with a fixed ratio of Mn3+:Mn4+=1:1 has been investigated. For the undoped sample, it undergoes one transition from charge disordering to charge ordering (CO) associated with paramagnetic (PM)-antiferromagnetic (AFM) phase transition at T<250 K. The long range AFM ordering seems to form at 35 K, rather than previously reported 150 K. At low temperature, an asymmetrical M-H hysteresis loop occurs due to weak AFM coupling. For the doped samples, the substitution of Cr3+ for Mn3+ ions causes the increase of magnetization and the rise of Tc. As the Cr3+ concentration increases, the CO domain gradually becomes smaller and the CO melting process emerges. At low temperature, the FM superexchange interaction between Mn3+ and Cr3+ ions causes a magnetic upturn, namely, the second FM phase transition. 相似文献