Non-isothermal crystallization kinetics of the Zr50Cu34Al8Ag8 amorphous alloy

2022 ◽  
Vol 307 ◽  
pp. 130996
Author(s):  
Shan Zhang ◽  
Chao Wei ◽  
Jingwang Lv ◽  
Haoran Zhang ◽  
Zhilin Shi ◽  
...  
2011 ◽  
Vol 522 (1-2) ◽  
pp. 166-172 ◽  
Author(s):  
L.H. Kong ◽  
Y.L. Gao ◽  
T.T. Song ◽  
G. Wang ◽  
Q.J. Zhai

2013 ◽  
Vol 1 (3) ◽  
pp. 251-257 ◽  
Author(s):  
Bing-Ge Zhao ◽  
Ling-Hong Kong ◽  
Ting-Ting Song ◽  
Qi-Jie Zhai ◽  
Yu-Lai Gao

2014 ◽  
Vol 587 ◽  
pp. 11-17 ◽  
Author(s):  
Sirui Cheng ◽  
Chunju Wang ◽  
Mingzhen Ma ◽  
Debin Shan ◽  
Bin Guo

2012 ◽  
Vol 706-709 ◽  
pp. 1311-1317 ◽  
Author(s):  
S.A. Hasheminezhad ◽  
M. Haddad-Sabzevar ◽  
S. Sahebian

Non-isothermal crystallization kinetics of Co67Fe4Cr7Si8B14amorphous ribbons was studied by differential scanning calorimetry (DSC) technique under 10, 20, 30, 40 and 80 °Cmin-1heating rates. It is found that Co67Fe4Cr7Si8B14amorphous alloy exhibits two-stage crystallization on heating. The two crystallization peaks shift to higher temperatures with increasing heating rate. The apparent activation energies (EC) for the first stage of crystallization were determined as 443.44 and 434.47 kJmol-1by using the Kissinger and Ozawa equations, respectively. Frequency factor (A) estimated to be 1.084×1026s-1using Kissinger equation. Kinetics parameters such as Crystallization exponent (n) and dimensionality of growth (Ndim) were determined using JMA (Johnson-Mehl-Avrami) method. Details of the nucleation and growth behaviours during the non-isothermal crystallization were studied in terms of local activation energy EC(x) by the OFW (Ozawa, Flynn and Wall) method. Also the activation energy for nucleation (En) and growth (Eg) separately estimated.


Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 648
Author(s):  
Xiangning Wen ◽  
Yunlan Su ◽  
Shaofan Li ◽  
Weilong Ju ◽  
Dujin Wang

In this work, the crystallization kinetics of poly(ethylene oxide) (PEO) matrix included with poly(ethylene glycol) (PEG) grafted silica (PEG-g-SiO2) nanoparticles and bare SiO2 were systematically investigated by differential scanning calorimetry (DSC) and polarized light optical microscopy (PLOM) method. PEG-g-SiO2 can significantly increase the crystallinity and crystallization temperature of PEO matrix under the non-isothermal crystallization process. Pronounced effects of PEG-g-SiO2 on the crystalline morphology and crystallization rate of PEO were further characterized by employing spherulitic morphological observation and isothermal crystallization kinetics analysis. In contrast to the bare SiO2, PEG-g-SiO2 can be well dispersed in PEO matrix at low P/N (P: Molecular weight of matrix chains, N: Molecular weight of grafted chains), which is a key factor to enhance the primary nucleation rate. In particular, we found that the addition of PEG-g-SiO2 slows the spherulitic growth fronts compared to the neat PEO. It is speculated that the interfacial structure of the grafted PEG plays a key role in the formation of nuclei sites, thus ultimately determines the crystallization behavior of PEO PNCs and enhances the overall crystallization rate of the PEO nanocomposites.


2017 ◽  
Vol 48 (6) ◽  
pp. 2949-2960 ◽  
Author(s):  
Lejun Zhou ◽  
Huan Li ◽  
Wanlin Wang ◽  
Zhaoyang Wu ◽  
Jie Yu ◽  
...  

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