Application of a master curve and the modified superposition principle for modeling creep and loading rate effects at small strains in high-density polyethylene

Author(s):  
A. Kühl ◽  
P. A. Muñoz-Rojas
Author(s):  
Hans-Werner Viehrig ◽  
Enrico Lucon ◽  
William L. Server

The Master Curve (MC) approach procedure standardized in ASTM E1921 is defined for quasi-static loading conditions. However, the extension of the MC method to dynamic testing is still under discussion. The effect of loading rate can be broken down into two distinct aspects: 1) the effect of loading rate on Master Curve To values for loading rates within the loading rate range specified in ASTM E1921 for quasi-static loading, and 2) the effect of loading rate on Master Curve To values for higher loading rates. The IAEA CRP8 includes both aspects, but primarily focuses on the second element of loading rate effects, i.e. loading rate ranges above the upper limit of the E1921 standard and it comprises: - results of a round-robin exercise to validate the application of the Master Curve approach to precracked Charpy (PCC) specimens tested in the ductile-to-brittle transition region using an instrumented pendulum, - Master Curve data obtained at different loading rates on various RPV steels, in order to assess the loading rate dependence of To and compare it with an empirical model proposed by Wallin, and - the comparison of results from unloading compliance and monotonic loading in the quasi-static range.


2003 ◽  
Vol 774 ◽  
Author(s):  
Susan M. Rea ◽  
Serena M. Best ◽  
William Bonfield

AbstractHAPEXTM (40 vol% hydroxyapatite in a high-density polyethylene matrix) and AWPEX (40 vol% apatite-wollastonite glass ceramic in a high density polyethylene matrix) are composites designed to provide bioactivity and to match the mechanical properties of human cortical bone. HAPEXTM has had clinical success in middle ear and orbital implants, and there is great potential for further orthopaedic applications of these materials. However, more detailed in vitro investigations must be performed to better understand the biological interactions of the composites and so the bioactivity of each material was assessed in this study. Specifically, the effects of controlled surface topography and ceramic filler composition on apatite layer formation in acellular simulated body fluid (SBF) with ion concentration similar to those of human blood plasma were examined. Samples were prepared as 1 cm × 1 cm × 1 mm tiles with polished, roughened, or parallel-grooved surface finishes, and were incubated in 20 ml of SBF at 36.5 °C for 1, 3, 7, or 14 days. The formation of a biologically active apatite layer on the composite surface after immersion was demonstrated by thin-film x-ray diffraction (TF-XRD), environmental scanning electron microscopy (ESEM) imaging and energy dispersive x-ray (EDX) analysis. Variations in sample weight and solution pH over the period of incubation were also recorded. Significant differences were found between the two materials tested, with greater bioactivity in AWPEX than HAPEXTM overall. Results also indicate that within each material the surface topography is highly important, with rougher samples correlated to earlier apatite formation.


2019 ◽  
Author(s):  
Ketan Khare ◽  
Frederick R. Phelan Jr.

<a></a><a>Quantitative comparison of atomistic simulations with experiment for glass-forming materials is made difficult by the vast mismatch between computationally and experimentally accessible timescales. Recently, we presented results for an epoxy network showing that the computation of specific volume vs. temperature as a function of cooling rate in conjunction with the time–temperature superposition principle (TTSP) enables direct quantitative comparison of simulation with experiment. Here, we follow-up and present results for the translational dynamics of the same material over a temperature range from the rubbery to the glassy state. Using TTSP, we obtain results for translational dynamics out to 10<sup>9</sup> s in TTSP reduced time – a macroscopic timescale. Further, we show that the mean squared displacement (MSD) trends of the network atoms can be collapsed onto a master curve at a reference temperature. The computational master curve is compared with the experimental master curve of the creep compliance for the same network using literature data. We find that the temporal features of the two data sets can be quantitatively compared providing an integrated view relating molecular level dynamics to the macroscopic thermophysical measurement. The time-shift factors needed for the superposition also show excellent agreement with experiment further establishing the veracity of the approach</a>.


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