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Phase Formation and Magnetic Properties of Nanocomposite Nd-Fe-B Adjusted by Small Amount of Dy and Co

机译:少量Dy和Co调节的纳米复合Nd-Fe-B的相形成和磁性能

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In order to improve and stabilize the magnetic properties of nanocomposite Nd_2Fe_(14)B/α-Fe magnetic alloys by a compositional adjustment, small amount of Dy and/or Co was added to Nd_9Fe_(84)B_7 alloys. DTA analysis on the amorphous Nd_(9-x)Dy_xFe_(84)B_7(x = 0 ~ 1.5) and Nd_9Fe_(84-y)Co_yB_7(y = 0~3.0) both melt spun at 40 m·s~(-1) revealed that crystallization of the alloys took place as the soft magnetic phases were crystallized, and then the hard magnetic Nd_2Fe_(14)B was precipitated from them. While α-Fe and a metastable 1:7 ( TbCu_7-type) phase were formed simultaneously in Dy and Co-free alloys, they were crystallized separately at different temperatures after Dy or Co was added. This phase separation occurred more clearly in the Dy-treated alloys and the other soft magnetic phase Fe_3B was also stabilized by Dy and/or Co. The 1:7 phase that was stabilized by Dy and/or Co was not eliminated at 700℃, decreasing magnetic properties of the alloys. It was eventually disappeared above 725℃, but Fe_3B was not eliminated even at 750℃ when Dy was added more than 0.5 at % or Co was added more than 2.0 at %. Amount of Nd_2Fe_(14)B in the alloys tended to increase as Dy addition increased, whereas Co addition did not lead to any appreciable change in the ratio of α-Fe and Nd_2Fe_(14)B. Moreover, Dy addition apparently increased coercivity of an alloy while Co addition had a beneficial effect on remanence. The grains in the Dy-treated alloys were usually finer than those in the Co-treated alloys. The grain size of both α-Fe and Nd_2Fe_(14)B in the alloys exhibiting mr ≥ 0.72 was in the range of 20 ~ 40 nm or even larger 50 nm, which is larger than the theoretical optimum size ( ~ 10 nm). Typical magnetic properties obtained from a Nd_(7.5)Dy_(1.5)Fe_(82.5)Co_(1.5)B_7 alloy annealed for 12 min at 725℃ were ~iH_c = 4.85 kOe, B_r=11.32 kG, (BH)_(max) = 15.73 MGOe, and m_r = 0.73.
机译:为了通过组成调整来改善和稳定纳米复合Nd_2Fe_(14)B /α-Fe磁性合金的磁性能,向Nd_9Fe_(84)B_7合金中添加了少量的Dy和/或Co。非晶态Nd_(9-x)Dy_xFe_(84)B_7(x = 0〜1.5)和Nd_9Fe_(84-y)Co_yB_7(y = 0〜3.0)的DTA分析都在40 m·s〜(-1 )显示出合金的结晶是在软磁性相结晶后发生的,然后从其中析出了硬磁性Nd_2Fe_(14)B。虽然在Dy和无Co合金中同时形成了α-Fe和亚稳的1:7(TbCu_7型)相,但在加入Dy或Co之后,它们在不同的温度下分别结晶。在Dy处理的合金中,这种相分离更明显,另一种软磁相Fe_3B也被Dy和/或Co稳定。在700℃下,由Dy和/或Co稳定的1:7相没有消除。降低合金的磁性。最终在725℃以上消失,但即使在750℃下,当Dy添加量大于0.5 at%或Co添加量大于2.0 at%时,Fe_3B仍未消除。随着Dy添加量的增加,合金中Nd_2Fe_(14)B的含量趋于增加,而Co添加并未导致α-Fe和Nd_2Fe_(14)B的比例发生任何明显的变化。而且,Dy添加显然增加了合金的矫顽力,而Co添加对剩磁具有有益的作用。 Dy处理的合金中的晶粒通常比Co处理的合金中的晶粒细。 mr≥0.72的合金中α-Fe和Nd_2Fe_(14)B的晶粒尺寸都在20〜40 nm甚至更大的50 nm范围内,这比理论上的最佳尺寸(〜10 nm)大。在725℃下退火12分钟的Nd_(7.5)Dy_(1.5)Fe_(82.5)Co_(1.5)B_7合金获得的典型磁性能为〜iH_c = 4.85 kOe,B_r = 11.32 kG,(BH)_(max) = 15.73 MGOe,并且m_r = 0.73。

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