scholarly journals Spatially heterogeneous dynamics during physical aging far below the glass transition temperature

2002 ◽  
Vol 40 (21) ◽  
pp. 2463-2472 ◽  
Author(s):  
Courtney T. Thurau ◽  
M. D. Ediger
Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 954
Author(s):  
Xavier Monnier ◽  
Sara Marina ◽  
Xabier Lopez de Pariza ◽  
Haritz Sardón ◽  
Jaime Martin ◽  
...  

The present work aims to provide insights on recent findings indicating the presence of multiple equilibration mechanisms in physical aging of glasses. To this aim, we have investigated a glass forming polyether, poly(1-4 cyclohexane di-methanol) (PCDM), by following the evolution of the enthalpic state during physical aging by fast scanning calorimetry (FSC). The main results of our study indicate that physical aging persists at temperatures way below the glass transition temperature and, in a narrow temperature range, is characterized by a two steps evolution of the enthalpic state. Altogether, our results indicate that the simple old-standing view of physical aging as triggered by the α relaxation does not hold true when aging is carried out deep in the glassy state.


2004 ◽  
Vol 70 (22) ◽  
Author(s):  
D. Cangialosi ◽  
M. Wübbenhorst ◽  
J. Groenewold ◽  
E. Mendes ◽  
H. Schut ◽  
...  

2011 ◽  
Vol 287-290 ◽  
pp. 2234-2239 ◽  
Author(s):  
Sil Ro Jin ◽  
Jong Keun Lee

The effects of the polyhedral oligomeric silsequioxanes (POSS) in stacked poly(methyl methacrylate) (PMMA) film samples were investigated in two different film thicknesses, ~50 and ~660 nm. The types of the POSS include methacryl-, octaisobutyl-, and octasilane-POSS. The glass transition temperature (Tg) and isothermal physical aging was depressed by the reduction of film thickness. Among POSS molecules used in this work, methacryl-POSS was the greatest effect in both Tgand relaxation enthalpy (DHRelax) due to the physical aging. The Kohlrausch-Williams-Watts (KWW) relaxation function was used to further understand the effect of POSS and film thickness on the physical aging.


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