http://hdl.handle.net/20.500.12128/19251
Tytuł: | Investigations of crystallization behaviour of Co80Si9B11 amorphous alloy |
Autor: | Lesz, S. Nowosielski, R. Zajdel, A. Kostrubiec, Beata Stokłosa, Zbigniew |
Słowa kluczowe: | Materials; Amorphous Materials; Nanomaterials; Heat treatment; Crystallization behavior; Magnetic properties |
Data wydania: | 2007 |
Źródło: | Archives of Materials Science and Engineering, Vol. 28, iss. 2 (2007), s. 91-97 |
Abstrakt: | Purpose: This paper describes crystallization kinetics and changes of magnetic properties involved by process of crystallization of the amorphous Co80Si9B11 alloy. Design/methodology/approach: The following experimental techniques were used: X-ray diffraction (XRD), electrical resistivity in situ measurements (four-point probe), static and dynamic measurements of magnetic properties (magnetic balance, fluxmeter, Maxwell-Wien bridge). Findings: In this work has been performed influence of thermal annealing on crystallization kinetics and magnetic properties amorphous Co80Si9B11 alloy. Practical implications: The attractive properties of Co-Si-B alloy are of special interest for basic research on the materials as well as for their potential applications, like magnetic sensors. The Co soft magnetic material is used in noise filters, saturable reactors, miniature inductance elements for abating spike noise, mains transformers, choke coils, zero-phase current transformers, and magnetic heads etc., i.e., devices which are expected to exhibit high levels of permeability at high frequencies. Originality/value: It has been shown that thermal annealing at temperature close to the crystallization temperature leads to a significant increase of the initial magnetic permeability. The maximum permeability for examined alloy in as quenched state is about 11300. |
URI: | http://hdl.handle.net/20.500.12128/19251 |
ISSN: | 1897-2764 2300-8679 |
Pojawia się w kolekcji: | Artykuły (WNŚiT) |
Plik | Opis | Rozmiar | Format | |
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Lesz_Investigations_of_crystallization_behaviour.pdf | 1,23 MB | Adobe PDF | Przejrzyj / Otwórz |
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