Abstract
A constitutive equation based on the generalized concept of thermally activated flow units is developed to describe the stress–strain behavior of polymers as a function of temperature, strain-rate, and superposed hydrostatic pressure under conditions in which creep and long-term relaxation effects are negligible. The equation is shown to describe the principal features of the dynamic stress–strain behavior of polytetrafluoroethylene and, also, the yield stress of polymethylmethacrylate as a function of temperature and strain rate. A key feature of the model, not utilized in previous constitutive equation descriptions, is an inverse shear stress dependence of the shear activation volume. In contrast to metal deformation behavior, an enhanced strain hardening with increasing strain at higher strain rates and pressures is accounted for by an additional rate for immobilization of flow units. The influence of hydrostatic pressure enters through a pressure activation volume and also through the flow unit immobilization term. The thermal activation model is combined with a temperature dependent Maxwell–Weichert linear viscoelastic model that describes the initial small strain part of the stress strain curve.
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References
Eyring H (1935) J Chem Phys 3:107
Eyring H (1936) J Chem Phys 4:283
Bauwens-Crowet C (1973) J Mater Sci 8:968
Fotheringham D, Cherry BW (1976) J Mater Sci 11:1368
Bauwens-Crowet C (1976) J Mater Sci 11:1370
Armstrong RW (1973) (Indian) J Sci Indust Res 32:591
Zerilli FJ, Armstrong RW (1992) Acta Metall Mater 40:1803
Li JCM (1982) In: Escaig B, G’Sell C (eds) Plastic deformation of amorphous and semicrystalline materials. Publ les Ulis, Les editions de physique, France, p 29
Rivier N, Gilchrist H (1985) J Non-Cryst Sol 75:259
Rivier N (1994) Sol State Phenom 35:107
Porter D (1995) Group interaction modeling of polymer properties. Marcel Dekker, New York
Porter D (1997) J Non-Newtonian Fluid Mech 68:141
Walley SM, Field JE (1994) DYMAT J 1:211
Briscoe BJ, Nosker RW (1985) Polymer Comm 26:307
Fleck NA, Stronge WJ, Liu JH (1990) Proc Roy Soc Lond A429:459
Tschoegl NW (1989) The phenomenological theory of linear viscoelastic behavior. Springer-Verlag, Berlin, p 158
Zener C (1948) Elasticity and anelasticity of metals. University of Chicago Press, Illinois, p 43
Johnston WG, Gilman JJ (1959) J Appl Phys 30:129
Krausz AS, Eyring H (1975) Deformation kinetics. Wiley, New York
Perzyna P (1966) Advances in applied mechanics, vol 9. Academic Press, New York
Bardenhagen SG, Stout MG, Gray GT III (1997) Mech Mater 25:235
Thomas DA (1969) Polymer Eng Sci 9:415
Sauer JA, Mears DR, Pae KD (1970) Euro Polymer J 6:1015
Christiansen AW, Baer E, Radcliffe SV (1971) Philos Mag 24:451
Joseph SH, Duckett RA (1978) Polymer 19:837
Davis LA, Pampillo CA (1971) J Appl Phys 42:4659
Pae KD (1977) J Mater Sci 12:1209
Hu LW, Pae KD (1963) J Franklin Inst 275:491
Escaig B (1978) Ann Phys France 3:207
Hasan OA, Boyce MC (1993) Polymer 34:5085
Kauzmann W (1941) Trans Am Inst Min Metall Eng 143:57
Gilman JJ (1973) J Appl Phys 44:675
Bergstrom Y (1970) Mater Sci Eng 5:193
Argon AS (1973) Philos Mag 28:839
Flack HD (1972) J Polymer Sci A-2 10:1799
Sperati CA, Starkweather HW Jr (1961) Fortschr Hochpolym-Forsch (Adv Polymer Sci) 2:465
Weeks JJ, Clark ES, Eby RK (1981) Polymer 22:1480
Pistorius CWFT (1964) Polymer 5:315
Rigby HA, Bunn CW (1949) Nature 164:583
Bunn CW, Howells ER (1954) Nature 174:549
McCrum NG (1959) Makromol Chem 34:50
McCrum NG, Read BE, Williams G (1967) Anelastic and dielelectric effects in polymeric solids. Wiley, New York
Lau S, Wesson JP, Wunderlich B (1984) Macromolecules 17:1102
Walley SM, Field JE (1994) DYMAT J 1:211, Fig. 20
Walley SM, Field JE, Pope PH, Safford NA (1991) J Phys III France 1:1889, Fig. 161
Gray GT III (1998) In: Khan AS (ed) Proceedings of plasticity ‘99, the seventh intern. symp. on plasticity and its current applications. Neat Press, Fulton, MD
Sauer JA, Pae KD (1974) Colloid Polymer Sci 252:680
McCrum NG (1959) J Polymer Sci 34:355
Engeln I, Hengl R, Hinrichsen G (1984) Colloid Polymer Sci 262:780
Hopkins IL, Hamming RW (1957) J Appl Phys 28:906
Nagamatsu K, Yoshitomi T, Takemoto T (1958) J Colloid Sci 13:257
Rae PJ, Dattelbaum DM (2004) Polymer 45:7615
Rae PJ, Brown EN, Clements BE, Dattelbaum DM (2005) J Appl Phys 98:063521
Rae PJ, Gray GT III, Dattelbaum DM, Bourne NK (2005) In: Furnish MD, Gupta YM, Forbes JW (eds) Shock compression of condensed matter – 2004. Amer Inst Phys, Melville NY, p 671
Gray GT III (1997) Methods in materials research. Wiley, New York
Zerilli FJ, Armstrong RW (2000) In: Furnish MD, Chhabildas LC, Hixon RS (eds) Shock compression of condensed matter – 1999. AIP Conf. Proc. CP505, Am Inst Phys, Melville, New York, p 531
Armstrong RW (1973) In: Kochendorfer A (ed) Third international conference on fracture. Verein Deutscher Eisenhuttenleute, Munich, Paper III-421
Bilby BA, Cottrell AH, Swinden KH (1963) Proc Roy Soc Lond A272:304
Berry JP (1964) In: Rosen B (ed) Fracture processes in polymeric solids. Interscience Wiley, New York, p 195
Acknowledgements
This work was principally supported by the NSWC Independent Research Program with partial support from the Office of Naval Research. Additional partial support was provided by NSWC for Ronald Armstrong. Appreciation is expressed to Stephen Mitchell and Wayne Reed for the NSWC IR support, Chester Clark for the NSWC support, and to Judah Goldwasser for the ONR support. Appreciation is also expressed to G. T. Gray, III for providing us his Hopkinson bar data on PTFE in advance of publication.
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Appendix A: obtaining parameters for the viscoplastic element
Appendix A: obtaining parameters for the viscoplastic element
Each stress–strain curve not already reported as true stress-true strain is transformed to true stress-true strain with the formulae
where S and e are load and elongation, respectively, and σ and ɛ are true stress and true strain, respectively. While this transformation applies only if the flow is volume conserving, the error in applying it to the entire stress–strain curve is generally small. Then, for each curve, a guess is made for the initial linear viscoelastic modulus, and the elastic strain is subtracted from the total strain to obtain the viscoplastic strain. Each true stress–viscoplastic strain curve is then fitted to an equation of the form
and σ0 is obtained from the intercept (or extrapolated intercept) with the σ-axis at zero viscoplastic strain. K and ω could be obtained with a non-linear least squares fit to the data, but a quicker and better result is obtained simply by solving for K and ω by taking two points on the curve, one near the end, at large strain, and one at half that strain.
To obtain B, β 0, and β 1, write
where \({\beta_0 = \beta_1 \ln {\dot {\varepsilon}}_{0\beta}}.\) Pick an \({{\dot {\varepsilon}}_{0\beta }},\) and plot \({\ln \sigma_0}\) against \({T \ln ({\dot {\varepsilon }}_{0\beta}/\dot{\varepsilon})}.\) With the best value of \({{\dot {\varepsilon }}_{0\beta}},\) all the data points will lie on or close to a single straight line whose slope is \({-\beta_1}\) and intercept is ln B. Similarly, to obtain B 0, α 0, and α 1, write
Finally, the dependence of ω on strain rate and pressure may be determined by a linear regression and the pressure dependence of B and B 0 may be determined by a series of linear regressions with differing trial exponents.
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Zerilli, F.J., Armstrong, R.W. A constitutive equation for the dynamic deformation behavior of polymers. J Mater Sci 42, 4562–4574 (2007). https://doi.org/10.1007/s10853-006-0550-5
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DOI: https://doi.org/10.1007/s10853-006-0550-5