Direct comparison of surface crystal growth kinetics in chalcogenide glass measured by microscopy and DSC

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F23%3A39920258" target="_blank" >RIV/00216275:25310/23:39920258 - isvavai.cz</a>

Výsledek na webu

<a href="https://ceramics.onlinelibrary.wiley.com/doi/10.1111/jace.19204" target="_blank" >https://ceramics.onlinelibrary.wiley.com/doi/10.1111/jace.19204</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1111/jace.19204" target="_blank" >10.1111/jace.19204</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Direct comparison of surface crystal growth kinetics in chalcogenide glass measured by microscopy and DSC

Popis výsledku v původním jazyce

Surface crystallization in fine powder Se70Te30 chalcogenide glass was studied by differential scanning calorimetry (DSC) and optical microscopy. A complex kinetic analysis of these experimental data reveals that the contracting sphere mechanism (R3 model) is the rate determining step of crystal growth, and the conventional Johnson-Mehl-Avrami-Kolmogorov model cannot be used in this case. Moreover, it is clearly shown that the particle size distribution should be considered in crystallization studies. Actually, when the particle size effect is taken into account, the simulated DSC curves for the R3 model agree very well with the experimental data over the entire temperature range. The crystallization kinetics determined from the nonisothermal DSC data are consistent with previously reported isothermal crystallization data for the same powder fraction. The crystal growth rate calculated from isothermal and nonisothermal DSC data agrees very well with the microscopically measured surface and bulk crystal growth rate.

Název v anglickém jazyce

Direct comparison of surface crystal growth kinetics in chalcogenide glass measured by microscopy and DSC

Popis výsledku anglicky

Surface crystallization in fine powder Se70Te30 chalcogenide glass was studied by differential scanning calorimetry (DSC) and optical microscopy. A complex kinetic analysis of these experimental data reveals that the contracting sphere mechanism (R3 model) is the rate determining step of crystal growth, and the conventional Johnson-Mehl-Avrami-Kolmogorov model cannot be used in this case. Moreover, it is clearly shown that the particle size distribution should be considered in crystallization studies. Actually, when the particle size effect is taken into account, the simulated DSC curves for the R3 model agree very well with the experimental data over the entire temperature range. The crystallization kinetics determined from the nonisothermal DSC data are consistent with previously reported isothermal crystallization data for the same powder fraction. The crystal growth rate calculated from isothermal and nonisothermal DSC data agrees very well with the microscopically measured surface and bulk crystal growth rate.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

20504 - Ceramics

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2023

Kód důvěrnosti údajů

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

Název periodika

Journal of the American Ceramic Society

ISSN

0002-7820

e-ISSN

1551-2916

Svazek periodika

106

Číslo periodika v rámci svazku

10

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

11

Strana od-do

6051-6061

Kód UT WoS článku

000994676200001

EID výsledku v databázi Scopus

2-s2.0-85160636828