The response of Newtonian liquids to small perturbations is usually considered to be fully described by homogeneous transport coefficients like shear and dilatational viscosity. However, the presence of strong density gradients at the liquid/vapor boundary of fluids hints at the possible existence of an inhomogeneous viscosity. Here, we show that a surface viscosity emerges from the collective dynamics of interfacial layers in molecular simulations of simple liquids. We estimate the surface viscosity to be 8-16 times smaller than that of the bulk fluid at the thermodynamic point considered. This result can have important implications for reactions at liquid surfaces in atmospheric chemistry and catalysis.
We discuss hydrodynamic forces acting on a two-dimensional liquid domain that moves laterally within a supported fluid membrane in the presence of odd viscosity. Since active rotating proteins can accumulate inside the domain, we focus on the difference in odd viscosity between the inside and outside of the domain. Taking into account the momentum leakage from a two-dimensional incompressible fluid to the underlying substrate, we analytically obtain the fluid flow induced by the lateral domain motion, and calculate the drag and lift forces acting on the moving liquid domain. In contrast to the…
Spectral Decomposition of Liquid Viscosity into Instantaneous Normal Modes
Institute of Mechanics, Chinese Academy of Sciences（中国科学院力学研究所）；University of Chinese Academy of Sciences（中国科学院大学）；The Chinese University of Hong Kong, Shenzhen（香港中文大学（深圳））；Shanghai Jiao Tong University（上海交通大学）
If a liquid is cooled rapidly to form a glass, its structural relaxation becomes retarded, producing a drastic increase in viscosity. In two dimensions, strong long-wavelength fluctuations persist, even at low temperature, making it difficult to evaluate the microscopic structural relaxation time. This Letter shows that, in a 2D glass-forming liquid, relative displacement between neighbor particles yields a relaxation time that grows in proportion to the viscosity. In addition to thermal elastic vibrations, hydrodynamic fluctuations are found to affect the long-wavelength dynamics, yielding a …
Liquids realize a highly complex state of matter in which strong competing kinetic and interaction effects come to life. As such, liquids are more challenging to understand than either gases or solids generally. In weakly interacting gases, the kinetic effects dominate. By contrast, low temperature solids typically feature far smaller fluctuations about their ground state. Notwithstanding their complexity, with the exception of quantum fluids and supercooled liquids, various aspects of common liquid dynamics such as their dynamic viscosity are often assumed to be given by rather simple, Arrhen…
The aim of this paper is to present a modeling for the rheological behavior of simple liquids as a function of the amplitude of the imposed shear stress or strain. The elastic mode theory (Ref. 6) is first generalized to take into account the fact that during a flow experiment, mechanical energy is injected in a system initially at thermodynamic equilibrium. This generalized theory can be seen as a particular aspect of the general problem of perturbation by the measurement, associated with that of the coupling between fluctuation and dissipation. This generalization leads to a "finitary" chara…
Transport properties of dense fluids are fundamentally challenging, because the powerful approaches of equilibrium statistical physics cannot be applied. Polar fluids compound this problem, because the long-range interactions preclude the use of a simple effect-diameter approach based solely on hard spheres. Here, we develop a kinetic theory for dipolar hard-sphere fluids that is valid up to high density. We derive a mathematical approximation for the radial distribution function at contact directly from the equation of state, and use it to obtain the shear viscosity. We also perform molecular…
Nucleation kinetics of vapor bubbles in a liquid with arbitrary viscosity
在[J. Phys. Chem. B 116，9445（2012）]中针对高粘度的情况开发的单组分液体中的蒸汽气泡成核的理论（（V，/rho，T）-理论）被扩展到任意粘度的情况。为此目的，朗之万的方法在理论的布朗运动，或Kramers的模型的化学反应，被雇用。所得到的气泡成核速率的表达式是有效的任意之间的关系的动力学参数控制的成核过程：粘度，液体的惯性，蒸发成气泡的速度和气泡和周围液体之间的热交换速率。因此，所提出的理论与（V，/rho，T）-理论一起给出了单组分液体中汽泡成核动力学的完整描述。考虑了上述参数的极限情况，特别是低粘度极限。结果表明，低粘度和高粘度的成核速率在定性和定量上彼此不同。讨论了该理论应用于超流氦-4空化的可能性。
Recently, it has been found that the kinematic viscosity of liquids at the minimum, $ν_m$, can be expressed in terms of fundamental physical constants, giving $ν_m$ on the order of $10^{-7}~{\rm m^2/s}$. Here, we show that the kinematic viscosity of quark-gluon plasma (QGP) has a similar value and support this finding by experimental data and theoretical estimations. The similarity is striking, given that the dynamic viscosity and the density of QGP are about 16 orders of magnitude larger than in liquids and that the two systems have disparate interactions and fundamental theories. We discuss …
In the last few decades, theoretical and experimental studies of glass-forming liquids have revealed presence of universal regularities in the viscosity-temperature data. In the present work, we propose a viscosity model for scaling description of experimental viscosity data. A feature of this model is presence of only two adjustable parameters and high accuracy of experimental data approximation by this model for a wide temperature range. The basis of the scaling description is an original temperature scale. Within this scaling description we obtain the transformed Angell plot, in which the a…
Nanofluids; dispersions of nanometer-sized particles in a liquid medium; have been proposed for a wide variety of thermal management applications. It is known that a solid-like nanolayer of liquid of typical thickness 0.5-1 nm surrounding the colloidal nanoparticles can act as a thermal bridge between the nanoparticle and the bulk liquid. Yet, its effect on the nanofluid viscosity has not been elucidated so far. In this article, we compute the local viscosity of the nanolayer using equilibrium molecular dynamics based on the Green-Kubo formula. We first assess the validity of the method to pre…
Unlike crystalline solids or ideal gases, transport properties remain difficult to describe from a microscopic point of view in liquids, whose dynamics result from complex energetic and entropic contributions at the atomic scale. Two scenarios are generally proposed: one represents the dynamics in a fluid as a series of energy barrier crossings, leading to Arrhenius-like laws, while the other assumes that atoms rearrange themselves by collisions, as exemplified by the free volume model. To assess the validity of these two views, we computed, using molecular dynamics simulations, the transport …
The shear viscosity and thermal conductivity coefficients of various liquids exhibit minima along certain trajectories on the phase diagram. These minima arise due to the crossover between the momentum and energy transport mechanisms in gas-like and liquid-like regimes. We demonstrate that the magnitudes of the minima are quasi-universal in appropriately reduced units, especially for the viscosity coefficients. Results presented in support of this observation concern the transport properties of three simple model systems with different pairwise interaction potentials (hard spheres, Lennard-Jon…
We combine the shoving model of $T$-dependent viscosity of supercooled liquids with the Zwanzig-Mountain formula for the high-frequency shear modulus, using the $g(r)$ of MD simulations of metal alloys as the input. This scheme leads to a semi-analytical expression for the viscosity as a function of temperature, which provides a three-parameter model fitting of experimental data of viscosity for the same alloy for which $g(r)$ was calculated. The model provides direct access to the influence of atomic-scale physical quantities such as the interatomic potential $ϕ(r)$, on the viscosity and frag…
An alternative approach to the phonon theory of liquids: An analytical study of Frenkel frequency and heat capacity as a function of pressure and temperature
The term "fragility" describes the rate at which viscosity grows when a supercooled liquid approaches its putative glass transition temperature. The field of glassy materials is actively searching for a structural origin that governs this dynamical slowing down in the supercooled liquid, which occurs without any discernible change in structure. Our work shows clear evidence that growing many-body static amorphous order is intimately correlated with the kinetic fragility of glass-forming liquids. It confirms that the system's dynamical response to temperature is concealed in its micro-structure…
Theory and numerical simulations of the thinning of liquid threads at high superficial concentration of surfactants suggest the existence of an asymptotic regime where surface tension balances surface viscous stresses, leading to an exponential thinning with an $e$-fold time $F(Θ)\,(3μ_s + κ_s)/σ$, where $μ_s$ and $κ_s$ are the surface shear and dilatational viscosity coefficients, $σ$ is the interfacial tension, $Θ=κ_s/μ_s$, and $F(Θ)$ is a universal function. The potential use of this phenomenon to measure the surface viscosity coefficients is discussed.
Viscosity ($η$) is one of the most important properties of disordered matter. The temperature-dependence of viscosity is used to adjust process variables for glass-making, from melting to annealing. The aim of this work was to develop a physics-informed machine learning model capable of predicting $η(T)$ of oxide liquids. Instead of predicting the viscosity itself, the NN predicts the parameters of the MYEGA viscosity equation: the liquid's fragility index, the glass transition temperature, and the asymptotic viscosity. With these parameters, $η$ can be computed at any temperature of interest,…
In this work we present a simple qualitative model to describe shear rheological behavior of the twist-bend nematic liquid crystals. We find that at relatively low shear rate the effective viscosity decreases with the shear rate manifesting so-called shear-thinning phenomenon. At intermediate shear rate the stress is almost independent of the shear rate (a sort of plateau), and at large shear rate Newtonian rheology takes place. Within our theory we estimate the critical values of the shear rate in terms of coarse grained shear viscosity coefficients of the effective smectics equivalent to the…
Viscosity measurements in combination with pulsed magnetic fields are developed by use of a quartz-crystal microbalance (QCM). When the QCM is immersed in liquid, the resonant frequency, $f_0$, and the quality factor, $Q$, of the QCM change depending on $(ρη)^{0.5}$, where $ρ$ is the mass density and $η$ the viscosity. During the magnetic-field pulse, $f_0$ and $Q$ of the QCM are simultaneously measured by a ringdown technique. The typical resolution of $(ρη)^{0.5}$ is 0.5 %. As a benchmark, the viscosity of liquid oxygen is measured up to 55 T.
