Search results for "Mechanical equilibrium"
showing 3 items of 13 documents
Stability analysis of an electromagnetically levitated sphere
2006
We present a combined numerical and analytical approach to analyze the static and dynamic stabilities of an electromagnetically levitated spherical body depending on the ac frequency and the configuration of a three-dimensional (3D) coil made of thin winding which is modeled by linear current filaments. First, we calculate numerically the magnetic vector potential in grid points on the surface of the sphere and then use Legendre and fast Fourier transforms to find the expansion of the magnetic field in terms of spherical harmonics. Second, we employ a previously developed gauge transformation to solve analytically the 3D electromagnetic problem in terms of the numerically obtained expansion…
Dynamic coarse-graining of polymer systems using mobility functions.
2021
We propose a dynamic coarse-graining (CG) scheme for mapping heterogeneous polymer fluids onto extremely CG models in a dynamically consistent manner. The idea is to use as target function for the mapping a wave-vector dependent mobility function derived from the single-chain dynamic structure factor, which is calculated in the microscopic reference system. In previous work, we have shown that dynamic density functional calculations based on this mobility function can accurately reproduce the order/disorder kinetics in polymer melts, thus it is a suitable starting point for dynamic mapping. To enable the mapping over a range of relevant wave vectors, we propose to modify the CG dynamics by …
Comment on “Surface diffusion near the points corresponding to continuous phase transitions” [J. Chem. Phys. 109, 3197 (1998)]
1999
It is well known that unlike static equilibrium properties, kinetic quantities in Monte Carlo simulations are very sensitive to the details of the algorithm used for the microscopic transition rates. This is particularly true near the critical region where fluctuations are pronounced. We demonstrate that when diffusion of oxygen adatoms near the order–disorder transition of a lattice-gas model of the O/W(110) model system is studied, the transition rates must be chosen carefully. In particular, we show that the choice by Uebing and Zhdanov [J. Chem. Phys. 109, 3197 (1998)] is inappropriate for the study of critical effects in diffusion.