Measurements were made of the tracer diffusivity in amorphous samples which had been prepared by melt-spinning in a vacuum. The diffusivity in as-quenched material was enhanced by the presence of quasi-vacancies. That is, excess free volume. During annealing, the quasi-vacancies were removed and the diffusivity tended to a constant value which depended only upon the temperature. The tracer self-diffusion of 57Co, at 513 to 693K, in relaxed amorphous material (table 77) could be described by:
D(m2/s) = 8.03 x 10-7 exp[-147(kJ/mol)/RT]
Appreciable atomic motion took place at temperatures where solid-state amorphization reactions occurred. This suggested that diffusion-limited growth of an amorphous phase could take place without nucleation of the more stable intermetallic compounds. The activation enthalpy for crystallization (335kJ/mol) was much higher than that for Co diffusion.
W.Dorner, H.Mehrer: Physical Review B, 1991, 44[1], 101-14
Figure 13
Diffusivity of Co in CoxZr1-x
Table 76
Diffusion of 195Au in Annealed Amorphous Co89Zr11
Temperature (K) | D (m2/s) |
684 | 9.69 x 10-22 |
674 | 4.23 x 10-22 |
664 | 2.04 x 10-22 |
653 | 9.08 x 10-23 |
643 | 4.50 x 10-23 |
633 | 1.84 x 10-23 |
Table 77
Diffusion of 57Co in Annealed Amorphous Co89Zr11
Temperature (K) | D (m2/s) |
693 | 7.16 x 10-18 |
682 | 4.53 x 10-18 |
673 | 3.46 x 10-18 |
654 | 1.46 x 10-18 |
633 | 6.58 x 10-19 |
613 | 3.30 x 10-19 |
602 | 1.75 x 10-19 |
583 | 5.68 x 10-20 |
574 | 2.86 x 10-20 |
552 | 6.99 x 10-21 |
533 | 3.03 x 10-21 |
513 | 1.49 x 10-21 |