Why Is Seldom Zero for Polymer-Solvent Mixtures

نویسندگان

  • Scott T. Milner
  • William W. Graessley
چکیده

Typical good nonpolar solvents for nonpolar polymers have values of the Flory interaction parameter of 0.3 or higher. This is striking since miscible nonpolar polymer blends exist with well-matched solubility parameters and resulting very small values of 10-2 or less. Using a cell model, it has been previously argued that there is a generic contribution to in polymer-solvent systems of about 0.3, which ultimately arises from the difference in affinity for free volume of bonded chain mers and otherwise identical solvent mers. We explore this result with off-lattice MC simulations of hard-sphere freely jointed chains in identical hard-sphere solvent. We observe reductions in chain radii of gyration and of virial coefficients for dimers among hard-sphere solvents versus in vacuum, consistent with the cell model results. Finally, we extract free volume distributions and observe reduced free volume of chain mers compared to solvent. With a model of a single mer in a fluctuating cell surrounded by hard-sphere fluid, we construct free volume distributions in good agreement with our MC results and previous work of Sastry et al. on hard-sphere liquids.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Phase behavior of monomeric mixtures and polymer solutions with soft interaction potentials

We present Gibbs ensemble Monte Carlo simulations of monomer–solvent and polymer–solvent mixtures with soft interaction potentials, that are used in dissipative particle dynamics simulations. From the simulated phase behavior of the monomer–solvent mixtures one can derive an effective Flory–Huggins x-parameter as a function of the particle interaction potential. We show that this x-parameter ag...

متن کامل

Spinodal decomposition of asymmetric binary fluids in a micro-Couette geometry simulated with molecular dynamics.

The spinodal decomposition of quenched polymer/solvent and liquid-crystal/solvent mixtures in a miniature Taylor-Couette cell has been simulated by molecular dynamics. Three stacking motifs, each reflecting the geometry and symmetry of the cell, are most abundant among the fully phase separated stationary states. At zero or low angular velocity of the inner cylindrical drum, the two segregated ...

متن کامل

A new theory for polymer/solvent mixtures based on hard-sphere limit

Based on hard-sphere limit of binary mixtures with different molecular size of components a theory has been developed for calculating activities of solvents in polymer/solvent mixtures. The theory considers various chain configurations for polymer molecules, varying from extended chain to the coiled chain. According to this theory the activity of solvent can be calculated from molecular weights...

متن کامل

Colloid-polymer mixtures in the protein limit.

We computed the phase-separation behavior and effective interactions of colloid-polymer mixtures in the "protein limit," where the polymer radius of gyration is much larger than the colloid radius. For ideal polymers, the critical colloidal packing fraction tends to zero, whereas for interacting polymers in a good solvent the behavior is governed by a universal binodal, implying a constant crit...

متن کامل

Two-chamber lattice model for thermodiffusion in polymer solutions

When a temperature gradient is applied to a polymer solution, the polymer typically migrates to the colder regions of the fluid as a result of thermal diffusion ~Soret effect!. However, in recent thermodiffusion experiments on poly~ethylene-oxide! ~PEO! in a mixed ethanol/water solvent it is observed that for some solvent compositions the polymer migrates to the cold side, while for other compo...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2009