| Literature DB >> 32290482 |
A Álvarez-Vázquez1, A Fernández-Canteli1, Enrique Castillo2,3, F Pelayo1, M Muñiz-Calvente1, M J Lamela1.
Abstract
Time and temperature, besides pressure in a lesser extent, represent the most significant variables influencing the rheological behavior of viscoelastic materials. These magnitudes are each other related through the well-known Time-Temperature Superposition (TTS) principle, which allows the master curve referred to relaxation (or creep) behavior to be derived as a material characteristic. In this work, a novel conversion law to interrelate relaxation curves at different temperatures is proposed by assuming they to be represented by statistical cumulative distribution functions of the normal or Gumbel family. The first alternative responds to physical considerations while the latter implies the fulfillment of extreme value conditions. Both distributions are used to illustrate the suitability of the model when applied to reliable derivation of the master curve of Polyvinil-Butyral (PVB) from data of experimental programs. The new approach allows not only the TTS shift factors to be estimated by a unique step, but the whole family of viscoelastic master curves to be determined for the material at any temperature. This represents a significant advance in the characterization of viscoelastic materials and, consequently, in the application of the TTS principle to practical design of viscoelastic components.Entities:
Keywords: master curve; relaxation curves; shift factors; time–temperature superposition principle; viscoelastic behavior
Year: 2020 PMID: 32290482 PMCID: PMC7215287 DOI: 10.3390/ma13081809
Source DB: PubMed Journal: Materials (Basel) ISSN: 1996-1944 Impact factor: 3.623
Figure 1Scheme of the Time–Temperature Superposition (TTS) principle for the building master curve from short-time tests at different temperatures.
Figure 2Schematic illustration of a specimen of length L subject to a constant stress , subdivided in n elements of equal length .
Figure 3Viscoelastic moduli identified as survival functions for different values of the scale parameter associated with changes of temperature in the Gumbel model, within the experimental window and extrapolated along the time.
Figure 4Experimental relaxation curves at different temperatures for the Polyvinil–Butyral (PVB) (left), and experimental master curve for 20 °C (right).
Figure 5Theoretical predictions and experimental data for relaxation tests on PVB at different temperatures (−25 to 40 °C) using the normal model (left) and Q factors with 95% confidence intervals (right).
Estimates of dimensionless parameters and the absolute errors for the two proposed models in fitting short-term curves for PVB data.
| Model |
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| Error |
|---|---|---|---|---|---|---|---|---|
| Normal | 20.99 | 13.69 | −1.37 | 10.54 | 11.54 | −1.86 | 1.52 | 104.08 |
| Gumbel | 21.44 | 13.69 | −1.37 | 6.97 | — | −0.77 | 2.59 | 159.95 |
Figure 6Experimental data for short-term relaxation curves and corresponding master curves provided by the normal model or Gumbel model or using the Williams–Landel–Ferry model.