Phase transition of Zr41Ti14Cu12.5Ni10Be22.5 bulk amorphous below glass transition temperature under high pressure

2001 ◽  
Vol 78 (5) ◽  
pp. 601-603 ◽  
Author(s):  
Ming Xiang Pan ◽  
Jing Guo Wang ◽  
Yu Shu Yao ◽  
De Qian Zhao ◽  
Wei Hua Wang
1995 ◽  
Vol 398 ◽  
Author(s):  
K. Nakayama ◽  
K. Kojima ◽  
N. Takahashi ◽  
Y. Masaki ◽  
A. Kitagawa ◽  
...  

ABSTRACTThe heating-rate dependence of crystallization temperature, Tc, and the glass transition temperature, Tg, is studied from the view points of nucleation and fragmentation processes in disordered structures. Tc and Tg are expected to increase monotonically with heating rate. Such behaviors of Tc and Tg are classified into four characteristic regions with respect to the heating rate. Results are summarized in the Transient Phase Diagram where Tc and Tg are given as a function of heating rate. The scaling rule in the Transient Phase Diagram is given.


2013 ◽  
Vol 130 (2) ◽  
pp. 1148-1157 ◽  
Author(s):  
Marion Dasriaux ◽  
Sylvie Castagnet ◽  
Ludovic Thilly ◽  
Laurence Chocinski-Arnault ◽  
Séverine A. E. Boyer

2021 ◽  
Author(s):  
Mitsuru Ishikawa ◽  
Taihei Takahashi ◽  
Yu-ichiro Hayashi ◽  
Maya Akashi ◽  
Takayuki Uwada

<p>Glass transition was primarily considered to be not phase transition; however, it has similarity to the second-order phase transition. Recent single-molecule spectroscopy developments have prompted re-investigating glass transition at the microscopic scale, revealing that glass transition includes phenomena similar to second-order phase transition. They are characterized by microscopic collective polymer motion and discontinuous changes in temperature dependent relaxation times, later of which is similar to critical slowing down, within a temperature window that includes the polymer calorimetric glass transition temperature. Considering that collective motion and critical slowing down are accompaniments to critical phenomena, second-order phase transition behavior was identified in polymer glass transition.</p>


2020 ◽  
Author(s):  
Mitsuru Ishikawa ◽  
Taihei Takahashi ◽  
Yu-ichiro Hayashi ◽  
Maya Akashi ◽  
Takayuki Uwada

Glass transition was primarily considered to be not phase transition; instead, regarded as pseudo secondorder phase transition due to its similarity to the ordinary second-order phase transition. Recent single-molecule spectroscopy developments have prompted re-investigating glass transition at the microscopic scale, confirming that the initial classification is correct and revealing that glass transition includes phenomena similar to second-order phase transition. They are characterized by microscopic collective polymer motion and discontinuous changes in temperature dependent relaxation times within a temperature window that includes the polymer calorimetric glass transition temperature. Generally, atom or molecule collective motion and discontinuous changes in physical quantities including relaxation times characterize critical phenomena associated with second-order phase transitions near specific temperatures. Thus, second-order phase transition phenomena are involved in polymer glass transition.


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