Non-isothermal crystallization kinetics of some basaltic glass-ceramics containing CaF2 as nucleation agent

2009 ◽  
Vol 97 (2) ◽  
pp. 507-513 ◽  
Author(s):  
C. Păcurariu ◽  
R. I. Lazău ◽  
I. Lazău ◽  
R. Ianoş ◽  
B. Tiţa
2013 ◽  
Vol 830 ◽  
pp. 8-12
Author(s):  
Hui Ling Shen ◽  
Peng Cheng Zhou

The low density polyethylene (LDPE)/ethylene-octene copolymer (POE) blend films and LDPE/POE/inorganic particle composite films were prepared. By means of DSC method, the crystallization capability and the non-isothermal crystallization kinetics of LDPE composite films were investigated, the results show that the addition of DE can reduce the interfacial free energy of the crystal and the active energy of a nucleus, resulting in stable nuclei can be formed at lower supercooling, which makes the polymer crystallized successfully at high temperatures. By selecting data processing method of Mo ZS and modified Jeziorny, the results indicate that the DE play a role of heterogeneous nucleation agent in the process of crystallization and increased the crystalline rate of LDPE.


2017 ◽  
Vol 43 ◽  
pp. S407-S411 ◽  
Author(s):  
Surapong Panyata ◽  
Sukum Eitssayeam ◽  
Gobwute Rujijanagul ◽  
Tawee Tunkasiri ◽  
Kamonpan Pengpat

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.


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