Evidence of Deformation-Dependent Heat Capacity and Energetic Elasticity in a Cross-Linked Elastomer Subjected to Uniaxial Elongation

• Published in: Macromolecules Vol. 51; no. 2; pp. 589 - 597
• Main Authors: Nieto Simavilla, David, Schieber, Jay D, Venerus, David C
• Format: Journal Article
• Language: English
• Published: American Chemical Society 23.01.2018
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/acs.macromol.7b02139

We present a novel infrared thermography technique to investigate the dependence of heat capacity on deformation in cross-linked polymers. This phenomenon is directly related with the longstanding question of whether or not there is an energetic contribution to the stress in deformed polymers and, in general, to the nonisothermal, viscoelastic behavior of polymer materials. By tracking the temperature evolution of samples heated by a laser, we are able to measure heat capacity changes relative to the equilibrium value in an elastomer subjected to uniaxial extension. We find that the heat capacity increases with elongation in lightly cross-linked cis-1,4-polyisoprene. Remarkably, the onset of heat capacity dependence on deformation is observed at strains similar to those required to achieve finite extensibility. The deviation from the equilibrium value of heat capacity is consistent with an independent set of experiments comparing anisotropy in thermal diffusivity from forced Rayleigh scattering and thermal conductivity from steady-state infrared thermography. Finally, we propose a straightforward thermodynamic analysis of the results based on classical rubber elasticity.