Crystalization in the glass-forming materials: [KNO[sub 3]][sub X][Ca(NO[sub 3])[sub 2]][sub 1−X] and Brillouin scattering study of glass transition in X=0.64 mixture

1999 ◽  
Author(s):  
Yasunari Takagi ◽  
Toshiki Watanabe
1986 ◽  
Vol 55 (3) ◽  
pp. 981-986 ◽  
Author(s):  
Masanori Cho ◽  
Masao Kodama ◽  
Toshirou Yagi

2006 ◽  
Vol 442 (1-2) ◽  
pp. 379-382 ◽  
Author(s):  
S. Tsukada ◽  
Y. Ike ◽  
J. Kano ◽  
S. Kojima

2021 ◽  
Author(s):  
Khalil Akkaoui ◽  
Joe Schlenoff

Abstract Though the strong transformation in mechanical properties of glass-forming materials near the glass transition, Tg, has been recognized and exploited for millenia, efforts to understand and predict this phenomenon at a molecular level continue to this day. Close to Tg, where relaxation is considerably slower than predicted by the well-known Arrhenius equation, one of the most versatile and widely-used expressions to describe the dynamics or relaxation of glass formers is that of Vogel, Fulcher and Tammann (VFT). The VFT equation, introduced nearly 100 years ago, contains three adjustable fit parameters. In this work the dynamics of the polymer repeat units are related to macroscopic dynamics in polyelectrolyte complexes, which are hydrated amorphous blends of charged polymers. A simple expression, containing no freely adjustable fit parameters, is derived to quantitatively model relaxation from Tg to temperatures well into the Arrhenius region. The new expression, which also fits a selection of three common neutral polymers, will advance the understanding and use of the glass-forming phenomenon.


2018 ◽  
Vol 4 (12) ◽  
pp. eaau5423 ◽  
Author(s):  
Heedong Yoon ◽  
Gregory B. McKenna

A major challenge to understanding glass-forming materials is obtaining equilibrium data far below the laboratory glass transition temperatureTg. The challenge arises because it takes geologic aging times to achieve the equilibrium glassy state when temperatures are well belowTg. Here, we finesse this problem through measurements on an ultrastable amorphous Teflon with fictive temperatureTfnear to its Kauzmann temperatureTK. In the window betweenTfandTg, the material has a lower molecular mobility than the equilibrium state because of its low specific volume and enthalpy. Our measurements show that the determined scaled relaxation times deviate strongly from the classical expectation of divergence of time scales at a finite temperature. The results challenge the view of an ideal glass transition at or near toTK.


2007 ◽  
Vol 1048 ◽  
Author(s):  
Oleg N. Senkov ◽  
Daniel B. Miracle

AbstractCorrelations between three characteristic temperatures: glass transition, Tg, Kauzmann, Tk, and Vogel-Fulcher-Tammann, To, were identified from the analysis of more than 60 metallic and non-metallic glass-forming materials. It was found that Tg ≥ Tk ≥ To and Tk is the geometric mean of Tg and To. The relation Tk ≥ To indicates that the excess total entropy of a super-cooled liquid ΔS approaches zero at a higher temperature than the configurational entropy ΔSconf, and such behavior was explained by the stronger temperature dependence of the excess vibrational entropy of the liquid, ΔSvib, than that of the corresponding glass, . A relationship between the fragility index m, reduced excess heat capacity ΔCp(Tg)/Sm, and reduced glass transition temperature, Trg, was identified using the found correlation between the characteristic temperatures.


2002 ◽  
Vol 307-310 ◽  
pp. 154-160 ◽  
Author(s):  
Jae-Hyeon Ko ◽  
Seiji Kojima

2002 ◽  
Vol 82 (3) ◽  
pp. 263-271 ◽  
Author(s):  
C. dreyfus ◽  
S. Murugavel ◽  
R. Gupta ◽  
M. Massot ◽  
R. M. Pick ◽  
...  

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