Aggregation of theta-polymers in spherical confinement
arXiv:1412.1322 · doi:10.1063/1.4893307
Abstract
We investigate the aggregation transition of theta polymers in spherical confinement with multicanonical simulations. This allows for a systematic study of the effect of density on the aggregation transition temperature for up to 24 monodisperse polymers. Our results for solutions in the dilute regime show that polymers can be considered isolated for all temperatures larger than the aggregation temperature, which is shown to be a function of the density. The resulting competition between single-polymer collapse and aggregation yields the lower temperature bound of the isolated chain approximation. We provide entropic and energetic arguments to describe the density dependence and finite-size effects of the aggregation transition for monodisperse solutions in finite systems. This allows us to estimate the aggregation transition temperature of dilute systems in a spherical cavity, using a few simulations of small, sufficiently dilute polymer systems.
10 pages, 9 figures
References in corpus (7)
- Accurate estimate of the critical exponent for self-avoiding walks via a fast implementation of the pivot algorithm
- Microcanonical Analyses of Peptide Aggregation Processes
- Elastic Lennard-Jones Polymers Meet Clusters -- Differences and Similarities
- Thermodynamics of Peptide Aggregation Processes. An Analysis from Perspectives of Three Statistical Ensembles
- Advanced multicanonical Monte Carlo methods for efficient simulations of nucleation processes of polymers
- Monte Carlo study of the evaporation/condensation transition on different Ising lattices
- Simple flexible polymers in a spherical cage