STRUCTURAL AND MAGNETIC-PROPERTIES OF PRFE10MO2NY PREPARED BY NATION-DISPROPORTIONATION-DESORPTION-RECOMBINATION AND NITROGENATION PROCESSES

Citation
Zq. Jin et al., STRUCTURAL AND MAGNETIC-PROPERTIES OF PRFE10MO2NY PREPARED BY NATION-DISPROPORTIONATION-DESORPTION-RECOMBINATION AND NITROGENATION PROCESSES, Journal of magnetism and magnetic materials, 187(2), 1998, pp. 231-236
Citations number
12
Categorie Soggetti
Material Science","Physics, Condensed Matter
ISSN journal
03048853
Volume
187
Issue
2
Year of publication
1998
Pages
231 - 236
Database
ISI
SICI code
0304-8853(1998)187:2<231:SAMOPP>2.0.ZU;2-2
Abstract
nation-disproportionation-desorption-recombination (HDDR) process has been used as a pretreatment to prepare isotropic Pr(Fe,Mo)(12)N-y comp ounds. The phase component, microstructure and magnetic properties of the nitrided powders have been investigated systematically Pr(Fe,Mo)(1 2) absorbs interstitial hydrogen on heating at 200-350 degrees C and f orms isostructural Pr(Fe,Mo)(12)H-x hydrides accompanied with a slight lattice expansion corresponding to 0.9% of the cell volume. The dispr oportionation reaction of hydrogen with Pr(Fe,Mo)(12) above 580 degree s C results in the occurrences of PrHdelta, Fe2Mo and alpha-Fe. As the samples hydrogenated at 750 degrees C are degassed at 650 degrees C i n a vacuum, a metastable phase with TbCu7-type crystal structure forms . With increasing dehydrogenation temperature to 750 degrees C, the Tb Cu7-type phase transforms into Pr(Fe,Mo)(12) compounds. Above 850 degr ees C, Pr(Fe,Mo)(12) partially decomposes and the amount of alpha-Fe i ncreases. The optimum temperature for the HDDR process is 750 degrees C for preparing the isotropic Pr(Fe,Mo)(12)N-y, magnets. Upon nitrogen ation at 425 degrees C, the Curie temperatures of 1 : 7 and 1 : 12 typ e nitrides are found to be about 395 and 303 degrees C, respectively, and a best coercivity of 3.4 kOe with a magnetization up to 122 emu/g at a field of 2 T is obtained for 1 : 12 compounds without fine millin g. The coercivity is probably arised by the reverse domain nucleation mechanism. (C) 1998 Elsevier Science B.V. All rights reserved.