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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的纳米复合ND-FE-B的相形成和磁性。

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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°C, decreasing magnetic properties of the alloys. It was eventually disappeared above 725°C, but Fe_3B was not eliminated even at 750°C 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°C were ~iH_c = 4.85 kOe, B_r=11.32 kG, (BH)_(max) = 15.73 MGOe, and m_r = 0.73.
机译:为了通过组合物调节改善和稳定纳米复合材料Nd_2Fe_(14)B /α-Fe磁性合金的磁性,将少量DY和/或CO加入ND_9FE_(84)B_7合金中。在非晶ND_(9-X)DY_XFE_(84)B_7(x = 0〜1.5)和ND_9FE_(84-Y)CO_YB_7(Y = 0〜3.0)上的DTA分析(y = 0〜3.0),熔体纺丝在40 m·s〜(-1 )显示,随着软磁相结晶,合金的结晶发生,然后将硬磁ND_2FE_(14)B从它们中沉淀出来。虽然在Dy和无共同合金中同时形成α-Fe和亚稳态1:7(TBCU_7型)相,但在加入Dy或CO后,它们在不同温度下分别结晶。在Dy处理的合金中更清楚地发生这种相分离,并且其他软磁性相Fe_3b也通过Dy和/或Co.1:7的稳定,通过Dy和/或Co稳定在700°C下未消除,降低合金的磁性。它最终消失在725°C以上,但即使在750°C中加入大于0.5以0.5%,也不会消除Fe_3B,加入大于2.0以%。合金中的ND_2FE_(14)B的量趋于增加,随着DY的增加而增加,而CO补充不会导致α-Fe和ND_2FE_(14)B的比率的任何明显变化。此外,由于Co加入对剩磁有益的效果,Dy添加显然增加了合金的矫顽力。当治疗的合金中的晶粒通常比共同处理合金中的晶粒更精细。表现出MR≥0.72的合金中α-Fe和Nd_2Fe_(14)B的晶粒尺寸在20〜40nm或甚至较大的50nm的范围内,其大于理论最佳尺寸(〜10nm)。从ND_(7.5)DY_(1.5)FE_(82.5)的典型磁性(82.5)CO_(1.5)B_7合金在725°C时退火12分钟,〜IH_C = 4.85 KOE,B_R = 11.32千克,(BH)_(最大)= 15.73 mgoe,M_R = 0.73。

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