The invention discloses a method for preparing a heavy
rare earth hydride nano-particle doped sintered NdFeB permanent
magnet, which belongs to the technical field of magnetic materials. The prior preThe invention discloses a method for preparing a heavy
rare earth hydride nano-particle doped sintered NdFeB permanent
magnet, which belongs to the technical field of magnetic materials. The prior preparation method improves the coercive force and the temperature stability of magnets by adding heavy
rare earth elements, namely
terbium or
dysprosium into master
alloy, but the method can cause the rparation method improves the coercive force and the temperature stability of magnets by adding heavy rare earth elements, namely
terbium or
dysprosium into master
alloy, but the method can cause the residual
magnetism of the magnets, the reduction of
magnetic energy product and the increase of manufacturing cost. The method adopts heavy rare earth
terbium hydride and
dysprosium hydride nano-powderesidual
magnetism of the magnets, the reduction of
magnetic energy product and the increase of manufacturing cost. The method adopts heavy rare earth terbium hydride and dysprosium hydride nano-
powder doping technology to prepare the sintered NdFeB permanent
magnet with high coercive force and excellent magnetic property. The method comprises the following steps: preparing NdFeB
powder by a rapidldoping technology to prepare the sintered NdFeB permanent magnet with high coercive force and excellent magnetic property. The method comprises the following steps: preparing NdFeB
powder by a rapidly solidified flake process and a
hydrogen decrepitation process; preparing the terbium hydride or the dysprosium hydride nano-powder by
physical vapor deposition technology; mixing the two powders, any solidified flake process and a
hydrogen decrepitation process; preparing the terbium hydride or the dysprosium hydride nano-powder by
physical vapor deposition technology; mixing the two powders, and performing
magnetic field orientation and press forming; and performing
dehydrogenation treatment,
sintering and heat treatment on a green compact at different temperatures, and obtaining the sinterd performing
magnetic field orientation and press forming; and performing
dehydrogenation treatment,
sintering and heat treatment on a green compact at different temperatures, and obtaining the sintered magnet. The coercive force of the magnet prepared by the method is higher than that of the prior sintered magnet with the same ingredients; and compared with the sintered magnet with the equivalented magnet. The coercive force of the magnet prepared by the method is higher than that of the prior sintered magnet with the same ingredients; and compared with the sintered magnet with the equivalent coercive force, the proportion of the terbium and dysprosium needed by the magnet prepared by the method is remarkably reduced.coercive force, the proportion of the terbium and dysprosium needed by the magnet prepared by the method is remarkably reduced.