Investigations of Ni-Bi-Sn system were performed in order to inquire the phase diagram and to assess some diffusion kinetic parameters. For this purpose diffusion couples consisting of solid nickel (preliminary electroplated with tin) and liquid Bi-Sn phase were annealed at 370 °C. Three compositions (0.8, 0.6 and 0.4 mole fractions Sn) of the Bi-Sn melts were chosen. Annealing times from 24 to 216 h were applied. The phase and chemical compositions of the contact zone were determined by means of electron scanning microscope. It was confirmed that the diffusion layers consist mainly of Ni3Sn4 but other intermetallic phases grow as well. For the first time metastable Ni-Sn phases as NiSn and NiSn8 (NiSn9) were observed in metallurgical alloys (i.e. not in electroplated samples). The existence of a ternary compound previously reported in the literature was confirmed. More than one ternary Ni-Bi-Sn compounds might possibly be admitted. A growth coefficient of (2.29 ± 0.02) x 10-15 m2 s-1 was obtained. It was found that the apparent activation energy for diffusion layers growth (18 ± 8 kJ mol-1) is inferior to that one assessed at growth from solid state Bi-Sn mixtures (88 ± 12 kJ mol-1)
Anodic aluminum oxide films modified by silver incorporation (Al-O-Ag) under specific electrodeposition conditions were produced and their biocompatibility was analyzed by in vitro assays using mammalian cell lines. The results obtained demonstrate that Al-O-Ag substrates are well tolerated by human dermal fibroblasts. The alumina pads doped with silver for short time-period (30 seconds) showed the highest biocompatibility among all modified metal substrates and in comparison with three dental alloys.
A typical modification technique of the functional properties of Al–Si based alloys is the addition of some third element in trace level. In the present work, ternary Al–Si–Zr bulk and ribbon alloys have been prepared. The kinetics of high-temperature surface oxidation has been studied by thermogravimetric method. It was found that at the start of the experiment the chemical reaction velocity is rate-controlling while for longer times the (oxygen) diffusion is the rate-controlling process. Activation energy of the two stages of oxidation has been obtained. Additional studies such as thermochemical analysis, optical and electron microscopy, and microhardness tests have been done.
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