Vše

Co hledáte?

Vše
Projekty
Výsledky výzkumu
Subjekty

Rychlé hledání

  • Projekty podpořené TA ČR
  • Významné projekty
  • Projekty s nejvyšší státní podporou
  • Aktuálně běžící projekty

Chytré vyhledávání

  • Takto najdu konkrétní +slovo
  • Takto z výsledků -slovo zcela vynechám
  • “Takto můžu najít celou frázi”

Microstructure, Thermal, and Magnetic Properties of Nanocrystalline/Amorphous Fe(Si,B,Nb) Powders Synthesized by Mechanical Alloying

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68407700%3A21340%2F25%3A00385776" target="_blank" >RIV/68407700:21340/25:00385776 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://doi.org/10.1007/s11665-025-11475-0" target="_blank" >https://doi.org/10.1007/s11665-025-11475-0</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s11665-025-11475-0" target="_blank" >10.1007/s11665-025-11475-0</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Microstructure, Thermal, and Magnetic Properties of Nanocrystalline/Amorphous Fe(Si,B,Nb) Powders Synthesized by Mechanical Alloying

  • Popis výsledku v původním jazyce

    In this work, two compositions Fe72Si16B5Nb7 and Fe75Si13B5Nb7 were elaborated by mechanical alloying (MA) of the elemental high-purity powder mixture. The morphological, microstructural, and thermal properties were analyzed using scanning electron microscopy (SEM) attached with energy dispersive spectroscopy (EDS), x-ray diffraction (XRD), and differential scanning calorimetry (DSC). The magnetic and hyperfine properties of the mixture elements during MA (0-64 h) were investigated by vibrating sample magnetometer (VSM) and Mössbauer spectroscopy (MS). Structural analysis by Rietveld refinement of the XRD pattern of the samples milled 4 h reveals the coexistence of various structures; Fe3Si, bcc-Fe, Fe23B6, and a small amount of Nb and Si, for the samples milled 16 h 32 h and 64 h the that the structure became much more and more amorphous, and the amorphous phase becomes the dominant phase. The DSC of the annealing of sample Fe72Si16B5Nb7 milled 64 h shows that the crystallization of the amorphous phases, and the activation energy determined using Kissinger's equation was 611.84 ± 10 KJ/mol. Mössbauer spectroscopy analysis confirmed a progressive amorphization of the material, accompanied by a reduction in the α-Fe crystalline phase content. In addition, for sample Fe75Si13B5Nb7 milled 64 h, the Mössbauer spectroscopy exhibits a paramagnetic doublet with a relatively small area fraction and a singlet, possibly assigned to the γ-Fe phase not detected by XRD. The VSM measurements show the hysteresis loops as a sigmoidal sharp, typically of nanomaterial or amorphous with little magnetic domain. The evolution of the coercivity and the saturation magnetization with milling time are discussed regarding different phenomena, such as residual stress, grain refinement, amorphous phase formation, surface anisotropy, defect density, and particle surface irregularities. ASM International 2025.

  • Název v anglickém jazyce

    Microstructure, Thermal, and Magnetic Properties of Nanocrystalline/Amorphous Fe(Si,B,Nb) Powders Synthesized by Mechanical Alloying

  • Popis výsledku anglicky

    In this work, two compositions Fe72Si16B5Nb7 and Fe75Si13B5Nb7 were elaborated by mechanical alloying (MA) of the elemental high-purity powder mixture. The morphological, microstructural, and thermal properties were analyzed using scanning electron microscopy (SEM) attached with energy dispersive spectroscopy (EDS), x-ray diffraction (XRD), and differential scanning calorimetry (DSC). The magnetic and hyperfine properties of the mixture elements during MA (0-64 h) were investigated by vibrating sample magnetometer (VSM) and Mössbauer spectroscopy (MS). Structural analysis by Rietveld refinement of the XRD pattern of the samples milled 4 h reveals the coexistence of various structures; Fe3Si, bcc-Fe, Fe23B6, and a small amount of Nb and Si, for the samples milled 16 h 32 h and 64 h the that the structure became much more and more amorphous, and the amorphous phase becomes the dominant phase. The DSC of the annealing of sample Fe72Si16B5Nb7 milled 64 h shows that the crystallization of the amorphous phases, and the activation energy determined using Kissinger's equation was 611.84 ± 10 KJ/mol. Mössbauer spectroscopy analysis confirmed a progressive amorphization of the material, accompanied by a reduction in the α-Fe crystalline phase content. In addition, for sample Fe75Si13B5Nb7 milled 64 h, the Mössbauer spectroscopy exhibits a paramagnetic doublet with a relatively small area fraction and a singlet, possibly assigned to the γ-Fe phase not detected by XRD. The VSM measurements show the hysteresis loops as a sigmoidal sharp, typically of nanomaterial or amorphous with little magnetic domain. The evolution of the coercivity and the saturation magnetization with milling time are discussed regarding different phenomena, such as residual stress, grain refinement, amorphous phase formation, surface anisotropy, defect density, and particle surface irregularities. ASM International 2025.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    20501 - Materials engineering

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LM2023073" target="_blank" >LM2023073: Jaderné experimentální centrum VR-1</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Journal of Materials Engineering and Performance

  • ISSN

    1059-9495

  • e-ISSN

    1544-1024

  • Svazek periodika

    34

  • Číslo periodika v rámci svazku

    19

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    18

  • Strana od-do

    22355-22372

  • Kód UT WoS článku

    001501993800001

  • EID výsledku v databázi Scopus

    2-s2.0-105007249966