Effect of shear on nanoparticle dispersion in polymer melts: A coarse-grained molecular dynamics study.
نویسندگان
چکیده
Coarse-grained, molecular dynamics (MD) simulations have been conducted to study the effect of shear flow on polymer nanocomposite systems. In particular, the interactions between different components have been tuned such that the nanoparticle-nanoparticle attraction is stronger than nanoparticle-polymer interaction, and therefore, the final equilibrium state for such systems is one with clustered nanoparticles. In the current study, we focus on how shear flow affects the kinetics of particle aggregation at the very initial stages in systems with polymers of different chain lengths. The particle volume fraction and size are kept fixed at 0.1 and 1.7 MD units, respectively. Through this work, shear has been shown to significantly slow down nanoparticle aggregation, an effect that was found to be a strong function of both polymer chain length and shear rate. To understand our findings, a systematic study on effect of shear on particle diffusion and an analysis of relative time scales of different mechanisms causing particle aggregation have been conducted. The aggregation rate obtained from the time scale analysis is in good agreement with that determined from the aggregation time derived from the pair correlation function monitored during simulations.
منابع مشابه
A First Principle Approach to Rescale the Dynamics of Simu - lated Coarse -
Submitted for the MAR11 Meeting of The American Physical Society A First Principle Approach to Rescale the Dynamics of Simulated Coarse-Grained Macromolecular Liquids IVAN LYUBIMOV, MARINA GUENZA, University of Oregon — A first-principle approach has been developed to rescale dynamical data from mesoscopic molecular dynamics simulations of polymer liquids. We derive rescaling factors from Gener...
متن کاملCoarse-grain molecular dynamics simulations of nanoparticle-polymer melt: dispersion vs. agglomeration.
In this work, we study the influence of polymer chain length (m), based on Lennard-Jones potential, and nanoparticle (NP)-polymer interaction strength (ɛnp) on aggregation and dispersion of soft repulsive spherically structured NPs in polymer melt using coarse-grain molecular dynamics simulations. A phase diagram is proposed where transitions between different structures in the NP-polymer syste...
متن کاملStructural properties of hyperbranched polymers in the melt under shear via nonequilibrium molecular dynamics simulation.
Hyperbranched polymer melts have been simulated using a coarse-grained model and nonequilibrium molecular dynamics (NEMD) techniques. In order to determine the shear-induced changes in the structural properties of hyperbranched polymers, various parameters were calculated at different strain rates. The radii of gyration which characterize the size of the polymer were evaluated. The tensor of gy...
متن کاملCoarse-grained molecular dynamics study of block copolymer/nanoparticle composites under elongational flow.
Symmetric diblock copolymer/nanoparticle (NP) systems under planar elongational flow have been modeled and simulated using coarse-grained nonequilibrium molecular dynamics. The aim of our present study is to understand how the dispersion of NPs in a block copolymer system is influenced by elongational flow and how the presence of NPs changes the rheology and flow-induced morphology transition i...
متن کاملEntanglements in polymer nanocomposites containing spherical nanoparticles.
We investigate the polymer packing around nanoparticles and polymer/nanoparticle topological constraints (entanglements) in nanocomposites containing spherical nanoparticles in comparison to pure polymer melts using molecular dynamics (MD) simulations. The polymer-nanoparticle attraction leads to good dispersion of nanoparticles. We observe an increase in the number of topological constraints (...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of chemical physics
دوره 132 2 شماره
صفحات -
تاریخ انتشار 2010