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Apparent exponents for the chain length dependence of the volume fraction in critical polymer solutions

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TLDR
In this article, the authors investigated the exponent of the power law with a constant exponent based on an equation of state model and experimental data for various chain-molecule solutions and showed that the exponent depends on the chain length of the dissolved chain molecules.
Abstract
The dependence of the critical volume fraction at constant pressure as a function of the chain length of a polymer/solvent system can be described by a power law. The exponent of this power law is investigated based on an equation of state model and experimental data for various chain-molecule solutions here. The results are compared to recent molecular simulation data taken from the literature and analytical models. The theoretical models, simulation, and experimental data show that the exponent depends on the chain length of the dissolved chain molecules. The power law with a constant exponent is therefore not a universal relationship for this dependence. Based on the investigation of the chain length dependence a correlation for the critical volume fraction is proposed here. This function generalizes the Flory and a renormalization group model and is applied to the correlation of the experimental data. This more general relationship includes the power law with the exponent obtained from the Flory theory as limiting behavior. Some additional experimental data for oligomer solutions which are necessary for an investigation of the short chain length limit have been measured.

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Citations
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Competition of mesoscales and crossover to theta-point tricriticality in near-critical polymer solutions.

TL;DR: A theory for crossover between two universal regimes: a regime with Ising (fluctuation-induced) asymptotic critical behavior, where the correlation length prevails, and a mean-field tricritical regime with theta-point behavior controlled by the mesoscopic polymer chain.
Journal ArticleDOI

Stability limits in binary fluids mixtures.

TL;DR: The stability limits in binary fluid mixtures are investigated on the basis of the global phase diagram approach employing a model for the attracting hard-sphere fluid and in addition to the diffusion spinodals the mechanicalspinodals are included.
Journal ArticleDOI

Heat capacity of the liquid-liquid mixture nitrobenzene and dodecane near the critical point.

TL;DR: The heat capacity of the liquid-liquid mixture nitrobenzene-dodecane has been measured for the first time near its upper critical consolute point using an adiabatic calorimeter and the two-scale-factor universality ratio X was violated when using a previously published value for the correlation length.
Journal ArticleDOI

Solution thermodynamics near the liquid–liquid critical point: I. First-order excess derivatives

TL;DR: In this article, a phenomenological approximation to the study of various non-universal features of liquid-liquid phase transitions in the framework of an approximate equation that relates the excess volume, the excess enthalpy, and the slope of the critical line is presented.
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Influence of polymer molecular weight and concentration on coexistence curve of isobutyric acid + water.

TL;DR: The experimental results explicitly elucidate that most of polymer chain entangles in water rich phase, thereby the polymer monomers strongly interact with neighbor solvent particles and also intra chain interaction between polymer monomer.
References
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Journal ArticleDOI

Critical Lines and Phase Equilibria in Binary Van Der Waals Mixtures

TL;DR: In this article, the locus of the critical line in pressure-temperature-composition space is determined exactly by solving a set of equations with the aid of a computer and nine characteristic types of critical lines are distinguished and these correspond to nine separate regions on a van der Waals equation-based phase diagram.
Journal ArticleDOI

Phase equilibria of associating fluids

TL;DR: In this article, the authors derived expressions for changes in the thermodynamic properties due to association in mixtures of molecules with multiple bonding sites, where the equations are written in terms of a hard-core reference whose pair distribution function is known.
Journal ArticleDOI

Thermodynamic perturbation theory of polymerization

TL;DR: In this paper, the authors derived several extensions of a previously given first-order perturbation theory (TPT 1) for fluids in which chain and ring polymers can be formed, due to the presence of two singly bondable molecular attraction sites.
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