Effects of Milling Variables in Amorphous Phase Formation of Fe78Si9B13 Alloy Produced by Mechanical Alloying

In this study, amorphous Fe78Si9B13 alloy was successfully synthesized by mechanical alloying (MA) of pure elemental powders which were milled under an argon gas atmosphere. Effects of milling time on the phase transformation, microstructure and morphological evolution were studied by X-ray diffraction (XRD), laser diffraction (Granulometry), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Results showed that by increasing the milling time, the nanocrystalline and amorphous phase content increases and alloys with good properties are obtained at 100 h of milling.

Influence of Cu Content on Structure and Magnetic Properties in Fe86-xCuxB14 Alloys

Influence of Cu content on thermodynamic parameters (configurational entropy, Gibbs free energy of mixing, Gibbs free energy of amorphous phase formation), crystallization kinetics, structure and magnetic properties of Fe86-xCuxB14 (x = 0, 0.4, 0.55, 0.7, 1) alloys is investigated. The chemical composition has been optimized using a thermodynamic approach to obtain a minimum of Gibbs free energy of amorphous phase formation (minimum at 0.55 at.% of Cu). By using differential scanning calorimetry method the crystallization kinetics of amorphous melt-spun ribbons was analyzed. It was found that the average activation energy of α-Fe phase crystallization is in the range from 201.8 to 228.74 kJ/mol for studied samples. In order to obtain the lowest power core loss values, the isothermal annealing process was optimized in the temperature range from 260 °C to 400 °C. Materials annealed at optimal temperature had power core losses at 1 T/50 Hz—0.13–0.25 W/kg, magnetic saturation—1.47–1.6 T and coercivity—9.71–13.1 A/m. These samples were characterized by the amorphous structure with small amount of α-Fe nanocrystallites. The studies of complex permeability allowed to determine a minimum of both permeability values at 0.55 at.% of Cu. At the end of this work a correlation between thermodynamic parameters and kinetics, structure and magnetic properties were described.

Thermopolarization Phenomena in the Temperature Range of Glass Transition of Amorphous Polydiethylsiloxane

The transition from the glass to the highly elastic state in polydiethylsiloxane (PDES) is not reflected on the temperature dependences of the relative permittivity, the dielectric loss tangent, and the specific volumetric electrical conductivity. But, the peak of the current of thermostimulated depolarization (TSD) is fixed in the temperature range of the transition to the highly elastic state. The peak of the TSD current at T ~ 130K indicates a continuous amorphous phase formation in the experimental conditions. The maximum value of the TSD current directly depends on the content of the amorphous phase in the polymer. The cooling of the polymer in an electric field reduces the magnitude of the peak. Exposure in the mesophase leads to an almost complete absence of thermopolarization effects near the glass transition temperature. This peak of the TSD current in the absence of preliminary polarization is characteristic, presumably, only for flexible-chain polymers where structural units have pyroelectric properties. Under certain conditions, PDES demonstrates itself as an active dielectric in the temperature range of 90 - 180K.

How similar are amorphous calcium carbonate and calcium phosphate? A comparative study of amorphous phase formation conditions

Precipitation domains of ACP and ACP increase with the complexity of the system, the ACP one being always larger.