Equation of State and Entropy Theory Approach to Thermodynamic Scaling in Polymeric Glass-Forming Liquids
arXiv:2103.09415 · doi:10.1021/acs.macromol.1c00075
Abstract
We show that thermodynamic scaling can be derived by combining the Murnaghan equation of state (EOS) with the generalized entropy theory (GET) of glass formation. In our theory, thermodynamic scaling arises in the non-Arrhenius relaxation regime as a scaling property of the fluid configurational entropy density , normalized by its value at the onset temperature of glass formation, , so that a constant value of corresponds to a \textit{reduced isoentropic} fluid condition. Molecular dynamics simulations on a coarse-grained polymer melt are utilized to confirm that the predicted thermodynamic scaling of by the GET holds both above and below and to test whether the extent of stringlike collective motion, normalized its value at , also obeys thermodynamic scaling, as required for consistency with thermodynamic scaling. While the predicted thermodynamic scaling of both and is confirmed by simulation, we find that the isothermal compressibility and the long wavelength limit of the static structure factor do not exhibit thermodynamic scaling, an observation that would appear to eliminate some proposed models of glass formation emphasizing fluid `structure' over configurational entropy. It is found, however, that by defining a low temperature hyperuniform reference state, we may define a compressibility relative to this condition, , a transformed dimensionless variable that exhibits thermodynamic scaling and which can be directly related to . Further, the Murnaghan EOS allows us to interpret as a measure of intrinsic anharmonicity of intermolecular interactions that may be directly determined from the pressure derivative of the material bulk modulus.
77 pages, 14 figures
References in corpus (14)
- Strong scaling of general-purpose molecular dynamics simulations on GPUs
- Thermodynamic interpretation of the scaling of the dynamics of supercooled liquids
- Strong pressure-energy correlations in van der Waals liquids
- A critical test of the mode-coupling theory of the glass transition
- The instantaneous shear modulus in the shoving model
- Polymer Glass Formation: Role of Activation Free Energy, Configurational Entropy, and Collective Motion
- An equation for the description of volume and temperature dependences of the dynamics of supercooled liquids and polymer melts
- Influence of Cohesive Energy and Chain Stiffness on Polymer Glass Formation
- Large-scale structure and hyperuniformity of amorphous ices
- Determination of the Thermodynamic Scaling Exponent from Static, Ambient-Pressure Quantities
- Lattice cluster theory for polymer melts with specific interactions
- Thermodynamic scaling of vibrational dynamics and relaxation
- Effect of entropy on the dynamics of supercooled liquids: New results from high pressure data
- Density scaling of the diffusion coefficient at various pressures in viscous liquids
Cited by in corpus (5)
- Thermodynamic-Dynamic Interrelations in Glass-Forming Polymer Fluids
- Combined Description of Pressure-Volume-Temperature and Dielectric Relaxation of Several Polymeric and Low-Molecular-Weight Organic Glass-Formers using 'SL-TS2' Mean-Field Approach
- Anharmonic theory of superconductivity and its applications to emerging quantum materials
- General Two-Parameter Model of Alpha-Relaxation in Glasses
- Positional information as a universal predictor of freezing