Quantization and instability of the damped harmonic oscillator subject to a time-dependent force

We consider the one-dimensional motion of a particle immersed in a potential field U(x) under the influence of a frictional (dissipative) force linear in velocity () and a time-dependent external force (K(t)). The dissipative system subject to these forces is discussed by introducing the extended Bateman’s system, which is described by the Lagrangian: which leads to the familiar classical equations of motion for the dissipative (open) system. The equation for a variable y is the time-reversed of the x motion. We discuss the extended Bateman dual Lagrangian and Hamiltonian by setting specifically for a dual extended damped–amplified harmonic oscillator subject to the time-dependent external force. We show the method of quantizing such dissipative systems, namely the canonical quantization of the extended Bateman’s Hamiltonian ?. The Heisenberg equations of motion utilizing the quantized Hamiltonian surely lead to the equations of motion for the dissipative dynamical quantum systems, which are the quantum analog of the corresponding classical systems. To discuss the stability of the quantum dissipative system due to the influence of an external force K(t) and the dissipative force, we derived a formula for transition amplitudes of the dissipative system with the help of the perturbation analysis. The formula is specifically applied for a damped–amplified harmonic oscillator subject to the impulsive force. This formula is used to study the influence of dissipation such as the instability due to the dissipative force and/or the applied impulsive force.     

Active thermophoresis and diffusiophoresis

Thermophoresis and diffusiophoresis respectively refer to the directed drift of suspended particles in solutions with external thermal and chemical gradients, which have been widely used in the manipulation of mesoscopic particles. We here study a phoretic-like motion of a passive colloidal particle immersed in inhomogeneous active baths, where the thermal and chemical gradients are replaced separately by activity and concentration gradients of the active particles. By performing simulations, we show that the passive colloidal particle experiences phoretic-like forces that originate from its interactions with the inhomogeneous active fluid, and thus drifts along the gradient field, leading to an accumulation. The results are similar to the traditional phoretic effects occurring in passive colloidal suspensions, implying that the concepts of thermophoresis and diffusiophoresis could be generalized into active baths.     

Molecular-dynamics simulations with explicit hydrodynamics II: On the collision of polymers with molecular obstacles

We present a study of the dynamics of single polymers colliding with molecular obstacles using Molecular-dynamics simulations. In concert with these simulations we present a generalized polymer-obstacle collision model which is applicable to a number of collision scenarios. The work focusses on three specific problems: i) a polymer driven by an external force colliding with a fixed microscopic post; ii) a polymer driven by a (plug-like) fluid flow colliding with a fixed microscopic post; and iii) a polymer driven by an external force colliding with a free polymer. In all three cases, we present a study of the length-dependent dynamics of the polymers involved. The simulation results are compared with calculations based on our generalized collision model. The generalized model yields analytical results in the first two instances (cases i) and ii)), while in the polymer-polymer collision example (case iii)) we obtain a series solution for the system dynamics. For the case of a polymer-polymer collision we find that a distinct V-shaped state exists as seen in experimental systems, though normally associated with collisions with multiple polymers. We suggest that this V-shaped state occurs due to an effective hydrodynamic counter flow generated by a net translational motion of the two-chain system.     

Thermophoresis in colloidal suspensions driven by Marangoni forces

In a hydrodynamic approach to thermophoretic transport in colloidal suspensions, the solute velocity u and the solvent flow v(r) are derived from Stokes' equation, with slip boundary conditions imposed by thermal Marangoni forces. The resulting fluid velocity field v(r) significantly differs from that induced by an externally driven particle. We find, in particular, that thermophoresis due to surface forces is insensitive to hydrodynamic interactions. As a consequence, the thermal diffusion coefficient D(T) of polymer solutions is independent of molecular weight and concentration.     

Time-dependent effects in high viscosity fluid dynamics

Flows dominated by high viscosity are often described using the steady Stokes equation. We will discuss three situations where the limits that are needed in order to arrive at this representation are questionable, and will show that unexpected flow behaviour arises: (i) under the influence of a time-dependent force, flows need not be reversible and chaotic advection can arise; (ii) the flow field around an oscillating sphere becomes that of the steady flow only for slow motion and sufficiently close to the sphere; (iii) the time-dependence in the fluid motion modifies the response of a sphere to an oscillatory force; (iv) when these forces are taken into account, the limits of particle size to zero and observation time to infinity do not commute and small particles do not maintain a uniform distribution.     

Study of a generalized Langevin equation with nonlocal dissipative force,harmonic potential and a constant load force

We analyze the motion of a particle governed by a generalized Langevin equation with nonlocal dissipative force, linear external force and a constant load force. We consider the dissipative memory kernel consisting of two terms. One of them is described by the Dirac delta function which represents a local friction, whereas for the second one we consider two types: the exponential and power-law functions which represent nonlocal dissipative forces. For these cases, one can obtain exact results for the relaxation function. Then, we obtain the first moments and variances of the displacement and velocity. The long-time behaviors of these quantities are also investigated.     

Self-Interacting Gas in a Gravitational Wave Field

We investigate a relativistic self-interacting gas in the field of an external pp gravitational wave. Based on symmetry considerations we ask for those forces which are able to compensate the imprint of the gravitational wave on the macroscopic 4-acceleration of the gaseous fluid. We establish an exactly solvable toy model according to which the stationary states which characterize such a situation have negative entropy production and are accompanied by instabilities of the microscopic particle motion. These features are similar to those which one encounters in phenomena of self-organization in many-particle systems.     

The Colloidal Probe Technique and its Application to Adhesion Force Measurements

Knowledge of the interaction forces between colloidal particles and surfaces is a precondition for understanding the stability of dispersed systems and adhesion phenomena. One of the methods available for direct measurement of surface forces is the atomic force microscope (AFM). Based on this method the so called “colloidal probe technique” was developed more than 10 years ago. Using a micron‐sized particle glued to the end of an AFM cantilever as the force sensor, this technique is predestined for the study of colloidal interactions. In this review we describe the colloidal probe technique and give an overview of its application in the field of adhesion forces.     

Diffusion in flashing periodic potentials

The one-dimensional overdamped Brownian motion in a symmetric periodic potential modulated by external time-reversible noise is analyzed. The calculation of the effective diffusion coefficient is reduced to the mean first passage time problem. We derive general equations to calculate the effective diffusion coefficient of Brownian particles moving in arbitrary supersymmetric potential modulated by: (i) an external white Gaussian noise and (ii) a Markovian dichotomous noise. For both cases the exact expressions for the effective diffusion coefficient are derived. We obtain acceleration of diffusion in comparison with the free diffusion case for fast fluctuating potentials with arbitrary profile and for sawtooth potential in case (ii). In this case the parameter region where this effect can be observed is given. We obtain also a finite net diffusion in the absence of thermal noise. For rectangular potential the diffusion slows down, for all parameters of noise and of potential, in comparison with the case when particles diffuse freely.     

Single-particle thermal diffusion of charged colloids: Double-layer theory in a temperature gradient

The double-layer contribution to the single-particle thermal diffusion coefficient of charged, spherical colloids with arbitrary double-layer thickness is calculated and compared to experiments. The calculation is based on an extension of the Debye-Hückel theory for the double-layer structure that includes a small temperature gradient. There are three forces that constitute the total thermophoretic force on a charged colloidal sphere due to the presence of its double layer: i) the force F _W that results from the temperature dependence of the internal electrostatic energy W of the double layer, ii) the electric force F _el with which the temperature-induced non-spherically symmetric double-layer potential acts on the surface charges of the colloidal sphere and iii) the solvent-friction force F _sol on the surface of the colloidal sphere due to the solvent flow that is induced in the double layer because of its asymmetry. The force F _W will be shown to reproduce predictions based on irreversible-thermodynamics considerations. The other two forces F _el and F _sol depend on the details of the temperature-gradient-induced asymmetry of the double-layer structure which cannot be included in an irreversible-thermodynamics treatment. Explicit expressions for the thermal diffusion coefficient are derived for arbitrary double-layer thickness, which complement the irreversible-thermodynamics result through the inclusion of the thermophoretic velocity resulting from the electric- and solvent-friction force.     

Tunable-slip boundaries for coarse-grained simulations of fluid flow

On the micro- and nanoscale, classical hydrodynamic boundary conditions such as the no-slip condition no longer apply. Instead, the flow profiles exhibit "slip" at the surface, which is characterized by a finite slip length (partial slip). We present a new, systematic way of implementing partial-slip boundary conditions with arbitrary slip length in coarse-grained computer simulations. The main idea is to represent the complex microscopic interface structure by a spatially varying effective viscous force. An analytical equation for the resulting slip length can be derived for planar and for curved surfaces. The comparison with computer simulations of a DPD (dissipative particle dynamics) fluid shows that this expression is valid from full slip to no slip.     

Surface structuring of particle laden drops using electric fields

Emulsion drops readily adsorb particles at their surfaces, which may lead to a fluid or solid layer encapsulating the drop, known as an armored drop. In this review, we discuss how electric fields can be used to manipulate colloidal surface structures, by dielectrophoretic or electro-hydrodynamic mechanisms and we also compare this to related phenomena in lipid bilayer vesicles. The phenomena discussed are important for a wide range of uses of particle laden drops, including emulsion stabilization, Janus or patchy mesocapsule-, scaffold- or other materials-production.     

The physics of active membranes

We review recent work on the physical properties of model fluid membranes in nonequilibrium situations resembling those encountered in the living cell and contrast their properties with those of the more familiar membranes at thermal equilibrium. We survey models for the effect of (i) active pumps and (ii) active fission–fusion processes encountered in intracellular trafficking on the stability and fluctuations of fluid membranes. Our purpose is twofold: to highlight the exciting nonequilibrium phenomena that arise in biological systems, and to show how some crucial features of living systems, namely dissipative energy uptake and directed motion, can fruitfully be incorporated into physical models of biological interest.     

Low-energy excitations in the three-dimensional random-field Ising model

General conservation equations are derived for 2D dense granular flows from the Euler equation within the Boussinesq approximation. In steady flows, the 2D fields of granular temperature, vorticity and stream function are shown to be encoded in two scalar functions only. We checked such prediction on steady surface flows in a rotating drum simulated through the Non-Smooth Contact Dynamics method even though granular flows are dissipative and therefore not necessarily compatible with Euler equation. Finally, we briefly discuss some possible ways to predict theoretically these two functions using statistical mechanics.     

也谈带电粒子在电磁场中动态受力平衡条件

电磁场中相对论带电粒子的经典轨道运动受到洛伦兹力和辐射阻尼力的影响,在一定条件下会达到受力平衡状态．基于洛伦兹一狄拉克方程,本文介绍了计及辐射阻尼力后电磁场中带电单粒子(包括导体中的自由电子)受力平衡条件的一种可能的相对论协变形式．     

Influence of wall motion on particle sedimentation using hybrid LB-IBM scheme

We integrate the lattice Boltzmann method (LBM) and immersed boundary method (IBM) to capture the coupling between a rigid boundary surface and the hydrodynamic response of an enclosed particle laden fluid. We focus on a rigid box filled with a Newtonian fluid where the drag force based on the slip velocity at the wall and settling particles induces the interaction. We impose an external harmonic oscillation on the system boundary and found interesting results in the sedimentation behavior. Our results reveal that the sedimentation and particle locations are sensitive to the boundary walls oscillation amplitude and the subsequent changes on the enclosed flow field. Two different particle distribution analyses were performed and showed the presence of an agglomerate structure of particles. Despite the increase in the amplitude of wall motion, the turbulence level of the flow field and distribution of particles are found to be less in quantity compared to the stationary walls. The integrated LBM-IBM methodology promised the prospect of an efficient and accurate dynamic coupling between a non-compliant bounding surface and flow field in a wide-range of systems. Understanding the dynamics of the fluid-filled box can be particularly important in a simulation of particle deposition within biological systems and other engineering applications.     

Force-driven micro-rheology

Within a microscopic formalism for the nonequilibrium response of colloidal suspensions driven by an external force, we study the active micro-rheology of a glass-forming colloidal suspensions. In this technique, a probe particle is subject to an external force, and its nonequilibrium dynamics is monitored. Strong external forcing delocalizes the particle from its nearest-neighbor cage, resulting in a pronounced force-thinning behavior of the single-particle friction. We discuss the dynamics in the vicinity of this delocalization transition, and how long-range transport is induced for a particle that is localized in the quiescent case.     

粘滞性流体动力学

We briefly discuss the phenomenological theory of dissipative fluid. We also present some numerical results for hydrodynamic evolution of QGP fluid with dissipation due to shear viscosity only. Its effect on particle production is also studied.     

黏滞性流体动力学

We briefly discuss the phenomenological theory of dissipative fluid. We also present some numerical results for hydrodynamic evolution of QGP fluid with dissipation due to shear viscosity only. Its effect on particle production is also studied.