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TY - JOUR
AU - Vasić, Milica M.
AU - Blagojević, Vladimir A.
AU - Begović, Nebojša N.
AU - Žák, Tomáš
AU - Pavlović, Vladimir B.
AU - Minić, Dragica M.
PY - 2015
UR - http://dais.sanu.ac.rs/123456789/3522
AB - The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate. © 2015 Elsevier B.V. All rights reserved.
PB - Elsevier
T2 - Thermochimica Acta
T1 - Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy
SP - 129
EP - 136
VL - 614
DO - 10.1016/j.tca.2015.06.015
ER -
@article{
author = "Vasić, Milica M. and Blagojević, Vladimir A. and Begović, Nebojša N. and Žák, Tomáš and Pavlović, Vladimir B. and Minić, Dragica M.",
year = "2015",
url = "http://dais.sanu.ac.rs/123456789/3522",
abstract = "The crystallization mechanism and kinetics of Fe40Ni40P14B6 amorphous alloy were studied under non-isothermal conditions. Thermal stabilization of this alloy manifests in DSC through two complex peaks, corresponding to crystallization and recrystallization, respectively. The complex crystallization DSC peak was deconvoluted into individual steps corresponding to crystallization of individual phases, where the results using both Gaussian-Lorentzian cross-product and Fraser-Suzuki function were compared. It was determined that the values of kinetic triplets of the individual steps did not exhibit any significant difference, depending on the deconvolution function. Anisotropic growth was indicated to be the prevailing type of impingement for all crystallization steps. Using the calculated values of the respective kinetic triplets and the mechanisms determined from the value of Avrami exponent, distinct values of activation energies for nucleation and crystal growth for crystallization of each individual phase were calculated, showing significantly higher values for nucleation than those for crystal growth. Alloy samples treated non-isothermally in the DSC cell exhibit inhomogeneous surface morphology with highly granulated structure dependent on heating rate. © 2015 Elsevier B.V. All rights reserved.",
publisher = "Elsevier",
journal = "Thermochimica Acta",
title = "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy",
pages = "129-136",
volume = "614",
doi = "10.1016/j.tca.2015.06.015"
}
Vasić MM, Blagojević VA, Begović NN, Žák T, Pavlović VB, Minić DM. Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy. Thermochimica Acta. 2015;614:129-136
Vasić, M. M., Blagojević, V. A., Begović, N. N., Žák, T., Pavlović, V. B.,& Minić, D. M. (2015). Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy.
Thermochimica ActaElsevier., 614, 129-136.
https://doi.org/10.1016/j.tca.2015.06.015
Vasić Milica M., Blagojević Vladimir A., Begović Nebojša N., Žák Tomáš, Pavlović Vladimir B., Minić Dragica M., "Thermally induced crystallization of amorphous Fe40Ni40P14B6 alloy" 614 (2015):129-136,
https://doi.org/10.1016/j.tca.2015.06.015 .
