Predicting the shift in viscoelastic response caused by physical aging of glassy polymers

1982 ◽  
Vol 15 (6) ◽  
pp. 1559-1561 ◽  
Author(s):  
R. R. Lagasse ◽  
J. G. Curro
2013 ◽  
Vol 46 (24) ◽  
pp. 9806-9817 ◽  
Author(s):  
Phillip M. Rauscher ◽  
Justin E. Pye ◽  
Roman R. Baglay ◽  
Connie B. Roth

2019 ◽  
Vol 57 (19) ◽  
pp. 1300-1314 ◽  
Author(s):  
Coen C. W. J. Clarijs ◽  
Marc J. W. Kanters ◽  
Marco J. Erp ◽  
Tom A. P. Engels ◽  
Leon E. Govaert

2011 ◽  
Vol 314-316 ◽  
pp. 914-917
Author(s):  
Wen Bo Luo ◽  
Chu Hong Wang ◽  
Xiu Liu ◽  
Qiang Shen

The influence of physical aging on mechanical properties of glassy polymers was investigated in this paper. After annealing above Tg to release the previous thermal and stress history, the polymethyl methacrylate (PMMA) samples were quenched to 27°C, aged for various times (ta), and were then stretched at the same temperature by two ways: (1) step stresses with four different magnitudes varying from 15MPa to 30MPa; (2) constant rate stretch up to fracture. The physical aging effect was monitored by measuring the initial instantaneous elastic modulus (E) and the fracture strength (σf) from the stress-strain curves as a function of ta up to 1368h. It is shown that both E and σf of the material increase with aging time and approach to their asymptotic values, which satisfy the KWW rule, while the isochronous creep compliance decreases with log ta in a linear manner within the aging time range considered in this paper.


Soft Matter ◽  
2018 ◽  
Vol 14 (42) ◽  
pp. 8475-8482 ◽  
Author(s):  
Vladimir V. Palyulin ◽  
Christopher Ness ◽  
Rico Milkus ◽  
Robert M. Elder ◽  
Timothy W. Sirk ◽  
...  

Parameter-free predictions of viscoelastic moduli at finite temperature are obtained by accounting for internal stresses and instantaneous normal modes within athermal non-affine theory.


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