## Abstract For a binary mixture of polydisperse polymers with strong interactions, the free energy, the equation of state, the chemical potentials and the spinodal are formulated on the basis of the lattice fluid model. Further, the spinodal curves for the system with strong interactions are simul
Statistical thermodynamics in the framework of the lattice fluid model, 2. Binary mixture of polydisperse polymers of special distribution
✍ Scribed by Lijia An; Bingzheng Jiang; Zhenhua Jiang; Yuxin Hu; Xinyi Tang
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 792 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1022-1344
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✦ Synopsis
Abstract
In this paper, the Gibbs free energy, the equation of state and the chemical potentials of polydisperse multicomponent polymer mixtures are derived. For general binary mixtures of polydisperse polymers, we also give the Gibbs free energy, the equation of state and the chemical potentials and derive the stability criteria and spinodal. Furthermore, binary polydisperse polymer mixtures of special distribution, i.e., Flory distribution, uniform distribution and Schulz distribution, are discussed and the influence of polydispersity on the interaction energy parameter is considered. For these special‐distribution systems, the spinodal curves are simulated and the influence of chain length and polydispersity on the spinodal curves is discussed. The results suggest that the spinodal temperature of the mixture with a given volume fraction of one component decreases with increasing polydispersity and the extent of the shift decreases with increasing degree of polymerization when η = M̄~w~/M̄~n~ is given. In addition, the variations of the spinodal curves with polydispersity and chain length are shown and they are qualitatively compared with the experimental results.
📜 SIMILAR VOLUMES
## Abstract The Gibbs free energies and equations of state of polymers with special molar mass distributions, e.g., Flory distribution, uniform distribution and Schulz distribution, are derived based on a lattice fluid model. The influence of the polydispersity (or the chain length) on the close‐pa