Mean field calculations of the dynamic mechanical properties of two-phase elastomer blends: Included particles in a matrix phase

1989 ◽  
Vol 37 (7) ◽  
pp. 1877-1888 ◽  
Author(s):  
K. A. Mazich ◽  
H. K. Plummer ◽  
M. A. Samus ◽  
P. C. Killgoar
1989 ◽  
Vol 62 (2) ◽  
pp. 305-314 ◽  
Author(s):  
K. A. Mazich ◽  
P. C. Killgoar ◽  
J. A. Ingram

Abstract A method for calculating the dynamic mechanical properties of elastomer blends with co-continuous structures has been presented. The calculations are based on Kerner's packed-grain model for composite media. Comparisons of theoretical calculations with experimental data show that this model closely approximates the viscoelastic properties of blends with a co-continuous structure, at least in the glass-transition regions of the respective blend components. We have also shown that the storage modulus of co-continuous blends may be well-represented by a discrete-particle model. This result can be misleading, however, if the storage modulus alone is calculated and compared with experimental data. A comparison of viscoelastic data (log E′ and tan δ) with calculation clearly distinguishes the models and indicates that the packed-grain model is the correct representation of the structure of co-continuous blends. The agreement between theory and experiment reported above was principally found in the glass-transition regions of the respective components in the elastomer blend. We extended the comparison well into the rubbery region and found that the agreement between Kerner's mean-field theory and the experimental data was poor, particularly for the loss tangent. Different relaxation mechanisms (relaxations over greater periods of time) are available to the blend in the rubbery region of viscoelastic response, and these mechanisms are apparently not accounted for in the mean-field calculations.


Author(s):  
Rodrigue Matadi Boumbimba ◽  
Said Ahzi ◽  
Nadia Bahlouli ◽  
David Ruch ◽  
José Gracio

Similarly to unfilled polymers, the dynamic mechanical properties of polymer/organoclay nanocomposites are sensitive to frequency and temperature, as well as to clay concentration. Richeton et al. (2005, “A Unified Model for Stiffness Modulus of Amorphous Polymers Across Transition Temperatures and Strain Rates,” Polymer, 46, pp. 8194–8201) has recently proposed a statistical model to describe the storage modulus variation of glassy polymers over a wide range of temperature and frequency. In the present work, we propose to extend this approach for the prediction of the stiffness of polymer composites by using two-phase composite homogenization methods. The phenomenological law developed by Takayanagi et al., 1966, J. Polym. Sci., 15, pp. 263–281 and the classical bounds proposed by Voigt, 1928, Wied. Ann., 33, pp. 573–587 and Reuss and Angew, 1929, Math. Mech., 29, pp. 9–49 models are used to compute the effective instantaneous moduli, which is then implemented in the Richeton model (Richeton et al., 2005, “A Unified Model for Stiffness Modulus of Amorphous Polymers Across Transition Temperatures and Strain Rates,” Polymer, 46, pp. 8194–8201). This adapted formulation has been successfully validated for PMMA/cloisites 20A and 30B nanocomposites. Indeed, good agreement has been obtained between the dynamic mechanical analysis data and the model predictions of poly(methyl-methacrylate)/organoclay nanocomposites.


2015 ◽  
Vol 37 (2) ◽  
pp. 162-167
Author(s):  
V.A. Vilensky ◽  
◽  
L.V. Kobrina ◽  
S.V. Riabov ◽  
Y.Y. Kercha ◽  
...  

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