DYNAMICAL MONTE-CARLO STUDY OF EQUILIBRIUM POLYMERS - STATIC PROPERTIES

Citation
Jp. Wittmer et al., DYNAMICAL MONTE-CARLO STUDY OF EQUILIBRIUM POLYMERS - STATIC PROPERTIES, The Journal of chemical physics, 109(2), 1998, pp. 834-845
Citations number
45
Categorie Soggetti
Physics, Atomic, Molecular & Chemical
ISSN journal
00219606
Volume
109
Issue
2
Year of publication
1998
Pages
834 - 845
Database
ISI
SICI code
0021-9606(1998)109:2<834:DMSOEP>2.0.ZU;2-0
Abstract
We report results of extensive dynamical Monte Carlo investigations on self-assembled equilibrium polymers (EP) without loops in good solven t. (This is thought to provide a good model of giant surfactant micell es.) Using a novel algorithm we are able to describe efficiently both static and dynamic properties of systems in which the mean chain lengt h [L] is effectively comparable to that of laboratory experiments (up to 5000 monomers, even at high polymer densities). We sample up to sci ssion energies of E/k(B)T= 15 over nearly three orders of magnitude in monomer density phi, and present a detailed crossover study ranging f rom swollen EP chains in the dilute regime up to dense molten systems. Confirming recent theoretical predictions, the mean-chain length is f ound to scale as [L]proportional to phi(alpha)exp(delta E) where the e xponents approach alpha(d) = delta(d) = 1/(1 + gamma) approximate to 0 .46 and alpha(s) = 1/2[1 + (gamma - 1)/(vd - 1)] approximate to 0.6, d elta(s) = 1/2 in the dilute and semidilute limits respectively. The ch ain length distribution is qualitatively well described in the dilute limit by the Schulz-Zimm distribution p(s) approximate to s(gamma-1) e xp(-s) where the scaling variable is s = gamma L/[L]. The very large s ize of these simulations allows also an accurate determination of the self-avoiding walk susceptibility exponent y approximate to 1.165 +/- 0.01. As chains overlap they enter the semidilute regime where the dis tribution becomes a pure exponential p(s) = exp( -s) with the scaling variable now s = LI(L). In addition to the above results we measure th e specific heat per monomer c(v). We show that the average size of the micelles, as measured by the end-to-end distance and the radius of gy ration, follows a crossover scaling that is, within numerical accuracy , identical to that of conventional monodisperse quenched polymers. Fi nite-size effects are discussed in detail. (C) 1998 American Institute of Physics.