The role of combined addition of Ti and B in magnetic hardening of devitrified Pr2Fe14B/(Fe3B,α‐Fe) nanocomposite magnets
The role of combined addition of Ti and B in magnetic hardening of devitrified Pr2Fe14B/(Fe3B,α‐Fe) nanocomposite magnets
复制标题
Ti和B联合添加对失透Pr2Fe14B/(Fe3B,α-Fe)纳米复合磁体磁硬化的作用
DOI:
10.1002/pssa.200622546
复制
发表时间:
2008
期刊:
影响因子:
--
通讯作者:
H. Ehrenberg
中科院分区:
文献类型:
--
作者:
W. Zhang;M. Stoica;J. Eckert;H. Chang;W. Chang;H. Ehrenberg
Pr2Fe14B/(Fe3B,α‐Fe) nanocomposite magnets with high coercivity have been prepared by devitrification of Pr9Fe88.5–x Ti2.5Bx (x = 7, 9, 11, 13, and 15) amorphous ribbons. Similar to Zr and Nb, Ti substitutes rare earth sites and participates in forming the (Pr,Ti)2Fe14B phase. The increasing amount of nonmagnetic TiB2 with increasing x in the nanocomposite magnets may precipitate along the grain boundaries and refine the microstructure by inhibiting the grain growth, and results in a continuous increase of coercivity. It also leads to an increase of the fraction of soft phases in the nanocomposites, which enhances the remanence. The squareness of the demagnetization curves is also improved by appropriate B addition. As a result, the energy product attains a maximum value of 129.6 kJ/m3 for x = 13. A more obvious shoulder and significantly enhanced coercivity (2424 kA/m) in the hysteresis curves at 70 K was observed for the sample with x = 15 in comparison with the ribbon with x = 7. This further demonstrates that B addition promotes the formation of TiB2 and the Fe3B soft phase in good agreement with XRD results. Accordingly, the introduction of a proper amount of nonmagnetic phases can enhance the magnetic properties of the nanocomposite magnets. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)
影响因子:
2.7
作者:
S. Hirosawa;H. Kanekiyo;T. Miyoshi
通讯作者:
S. Hirosawa;H. Kanekiyo;T. Miyoshi
影响因子:
3.2
作者:
Bauer, J;Seeger, M;Kronmuller, H
通讯作者:
Kronmuller, H
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
Naruse K;Sakai Y;Guo L;Natori T;Shindoh J;Karasawa Y;Iida Y;Kojima K;Michishita K;Makuuchi M.;邵 勇
通讯作者:
邵 勇