101 research outputs found
Domains in Melts of Comb-Coil Diblock Copolymers: Superstrong Segregation Regime
Conditions for the crossover from the strong to the superstrong segregation regime are analyzed for the case of comb-coil diblock copolymers. It is shown that the critical interaction energy between the components required to induce the crossover to the superstrong segregation regime is inversely proportional to mb = 1 + n/m, where n is the degree of polymerization of the side chain and m is the distance between successive grafting points. As a result, the superstrong segregation regime, being rather rare in the case of ordinary block copolymers, has a much better chance to be realized in the case of diblock copolymers with combs grafted to one of the blocks.
Structure of Colloid-Polymer Suspensions
We discuss structural correlations in mixtures of free polymer and colloidal
particles based on a microscopic, 2-component liquid state integral equation
theory. Whereas in the case of polymers much smaller than the spherical
particles the relevant polymer degree of freedom is the center of mass, for
polymers larger than the (nano-) particles conformational rearrangements need
to be considered. They have the important consequence that the polymer
depletion layer exhibits two widely different length scales, one of the order
of the particle radius, the other of the order of the polymer radius or the
polymer density screening length in dilute or semidilute concentrations,
respectively. Their consequences on phase stability and structural correlations
are discussed extensively.Comment: 37 pages, 17 figures; topical feature articl
Scale-free static and dynamical correlations in melts of monodisperse and Flory-distributed homopolymers: A review of recent bond-fluctuation model studies
It has been assumed until very recently that all long-range correlations are
screened in three-dimensional melts of linear homopolymers on distances beyond
the correlation length characterizing the decay of the density
fluctuations. Summarizing simulation results obtained by means of a variant of
the bond-fluctuation model with finite monomer excluded volume interactions and
topology violating local and global Monte Carlo moves, we show that due to an
interplay of the chain connectivity and the incompressibility constraint, both
static and dynamical correlations arise on distances . These
correlations are scale-free and, surprisingly, do not depend explicitly on the
compressibility of the solution. Both monodisperse and (essentially)
Flory-distributed equilibrium polymers are considered.Comment: 60 pages, 49 figure
Entropy-driven polymer collapse: Application of the hybrid MC/RISM method to the study of conformational transitions in macromolecules interacting with hard colloidal particles
Self-consistent hybrid MC/RISM method is used for calculating
properties of a linear polymer
surrounded by colloidal particles with purely repulsive, hard-core,
interactions between the
particles and chain beads. Our approach combines the traditional
atomistic Monte-Carlo (MC)
simulation of flexible polymer chains with the numerical solution
of the site-site Ornstein-Zernike-like
(RISM) integral equations. Since the condensed-phase environment of
a flexible macromolecule
affects the equilibrium configuration probability distribution of the
macromolecule, the site-site
intramolecular correlation function and the intramolecular potential
field are treated in a self-consistent manner. It is shown that in
such an athermal system the medium-induced collapse of a
polymer (similar to polymer collapse in a poor solvent) may occur.
Our analysis yields a simple
"entropic" interpretation of this transition. We present the detailed
study of the dependence of
conformational properties of the chains on the degree of polymerization,
density and size of colloidal particles
Conformation-dependent sequence design: evolutionary approach
A new modification of evolutionary approach to sequence design of copolymers has been proposed. A model of step-by-step evolution of a two-letter (HP) copolymer sequence has been studied by means of a coarse-grained Monte Carlo algorithm. The conditions for accepting a change in the primary sequence depend on the spatial conformation of HP-copolymer chain. This leads to a coupling between sequence and conformation and to formation of protein-like conformations and primary sequences (for some values of parameters of the model) independently of initial sequence and/or conformation. Simple theory describing these computer simulation observations is developed
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