Absorption/Expulsion of Oligomers and Linear Macromolecules in a Polymer Brush

Abstract

The absorption of free linear chains in a polymer brush was studied with respect to chain size L and compatibility with the brush by means of Monte Carlo (MC) simulations and Density Functional Theory (DFT) / Self-Consistent Field Theory (SCFT) at both moderate, σg = 0.25, and high, σg = 1.00, grafting densities using a bead-spring model. Different concentrations of the free chains 0.0625 φo 0.375 are examined. Contrary to the case of = 0 when all species are almost completely ejected by the polymer brush irrespective of their length L, for < 0 we find that the degree of absorption (absorbed amount) (L) undergoes a sharp crossover from weak to strong (≈ 100%) absorption, discriminating between oligomers, 1 L 8, and longer chains. For a moderately dense brush, σg = 0.25, the longer species, L > 8, populate predominantly the deep inner part of the brush whereas in a dense brush σg = 1.00 they penetrate into the "fluffy" tail of the dense brush only. Gyration radius Rg and end-to-end distance Re of absorbed chains thereby scale with length L as free polymers in the bulk. Using both MC and DFT/SCFT methods for brushes of different chain length 32 N 256, we demonstrate the existence of unique critical value of compatibility = c<0. For c(φo) the energy of free chains attains the same value, irrespective of length L whereas the entropy of free chain displays a pronounced minimum. At c all density profiles of absorbing chains with different L intersect at the same distance from the grafting plane. The penetration/expulsion kinetics of free chains into the polymer brush after an instantaneous change in their compatibility displays a rather rich behavior. We find three distinct regimes of penetration kinetics of free chains regarding the length L: I (1 L 8), II (8 L N), and III (L > N), in which the time of absorption τ grows with L at a different rate. During the initial stages of penetration into the brush one observes a power-law increase of tα with power α - φo whereby penetration of the free chains into the brush gets slower as their concentration rises.

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