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Preparation of submicron-sized Sm2Fe17N3 fine powder with high coercivity by reduction-diffusion process
Submicron-sized Sm2Fe17N3 powders having high coercivity were prepared by a newly-developed synthesis procedure for submicron-sized Sm2Fe17 powders and nitridation process with a proper post-process for the powders. It was revealed that the washing step, which is performed to remove excess Ca, suppl...
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Published in: | Journal of alloys and compounds 2017-02, Vol.695, p.1617-1623 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Submicron-sized Sm2Fe17N3 powders having high coercivity were prepared by a newly-developed synthesis procedure for submicron-sized Sm2Fe17 powders and nitridation process with a proper post-process for the powders. It was revealed that the washing step, which is performed to remove excess Ca, supplied hydrogen into the Sm2Fe17N3 crystal structure, and elongation of the crystal structure along the c-axis by the supplied hydrogen reduced coercivity. This phenomenon was observed clearly in powder with a smaller size and good dispersity. When the powders were subjected to dehydrogenation treatment, they showed high coercivity, as expected from the particle size, and coercivity of 24.7 kOe was achieved with the 0.5 μm powder. The fact that the intrinsic good thermal stability of Sm2Fe17N3 is maintained at the submicron-scale was also confirmed. In addition, the obtained powder exhibited a high maximum energy product after disintegration treatment under appropriate conditions. This study demonstrated the high potential of Sm2Fe17N3 for surpassing the performance of NdFeB magnets under hot environments.
•Sm2Fe17N3 powders having high coercivity, up to 24.7 kOe, were obtained.•Temperature coefficient of coercivity of submicron-sized powder was demonstrated.•Anisotropic Sm2Fe17N3 powder having a high maximum energy product was obtained. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2016.10.306 |