Hydrogen absorption of NdDyFeCoNbCuB sintered magnets

Hydrogen absorption and desorption characteristics for high coercivity NdDyFeCoNbCuB sintered bulk magnets were studied, by differential scanning calorimetry （DSC） measurement and hydrogenation kinetics measurement. The DSC measurements showed that hydrogenation of Nd-rich phase occurred in the temperature range of 40-185 ℃, hydrogenation of the tetragonal （Ф） phase in the temperature range of 185-220 ℃, as well as the disproportionation of the Ф phase that occurred in a broad temperature range from around 500 to 800 ℃. The hydrogenation kinetics measurements indicated that hydrogen absorption of the bulk magnets at 50 ℃ absorbed more hydrogen than at 150 ℃, although this procedure was slower at 50 ℃ than at 150℃. This phenomenon was discussed by means of pressure-concentration-temperature （p-c-T） diagrams.

Enhancing magnetic properties of anisotropic NdDyFeCoNbCuB powder by applying magnetic field at high temperature during hydrogen desorption

Anisotropic powder was prepared with precursor （NdDy）-（FeCoNbCu）-B sintered magnets by hydrogen decrepitation, desorption, and subsequent annealing treatment. The hydrogen desorption was performed in magnetic fields of 0, 1, 3, and 5 T. The orientation of tetragonal phase grains of the powder was evaluated from the hysteresis loops measured by extraction magnetometer. Residual hydrogen content of the powder was evaluated by thermal-magnetic analysis. The powder with Hcj, Br, and （BH）max of 1138 kA.m^-1, 1.029 T, and 172.5 kJ.m^-3, respectively, was achieved under the condition of the magnetic field of 3 T. Magnetic properties of the powder, especially, the remanence of the powder, are enhanced upon magnetic fields, which is due to better orientation of powder particles and less residual hydrogen in the powder resulted from the magnetic field during the hydrogen desorption process.

Magnetic and specific heat studies of the frustrated Er_2Mn_2O_7 compound

A new ErzMn207 compound was synthesized by the ceramic method and its crystal structure was characterized LJsing powder X-ray diffraction （XRD） and observed by scanning electron microscopy （SEM）. The magnetic properties were investigated using a BS2 magnetometer and the heat capacity was studied using a quantum design （PPMS）. The structural study revealed that this compound was monophasic and crystallized in the monoclinic system with the P2/M space group. Magnetization measurements were carried out in the temperature range of 1.8-200 K under an applied magnetic field of 0.05 T. A crossover from a room temperature para- magnetic phase to an antiferromagnetic one at low temperature was detected from the magnetic study. The magnetic susceptibility, in the paramagnetic region above 40 K, was found to present a simple Curie-Weiss type behavior. From the specific heat （G,） measurements in magnetic fields up to 5 T, we noted the presence of a wide peak characteristic of a second order magneto-structural transition.