On the nonequilibrium statistical mechanics of a binary mixture. II. The transport coefficients

This paper is devoted to the study of the hydrodynamic stage of a two-component dense fluid. Starting from the BBGKY hierarchy obtained earlier, we first derive the expressions for the generalized fluxes. We proceed to set up the generalized kinetic equations, using Bogoliubov's functional assumption. Then we solve these equations by means of a Chapman-Enskog method. The generalized expressions for the transport coefficients are thus obtained. All our results are independent of the existence of density expansions of the relevant quantities.     

Phase behaviors in binary mixture of diblock copolymers confined between two parallel walls

The phase behaviors in binary mixture of diblock copolymers confined between two parallel walls are investigated by using cell dynamics simulation of the time-dependent Ginzburg-Landau theory. The morphological dependence of the wall-block interaction and the distance between walls (confinement degree) has been systematically studied, and the effect of repulsive interactions between different monomers is also discussed. It is interesting that multiple novel morphological transitions are observed by changing these factors, and various multilayered sandwich structures are formed in the mixture. Furthermore, the parametric dependence and physical reasons for the microdomain growth and orientational order transitions are discussed. From the simulation, we find that much richer morphologies can form in binary mixture of diblock copolymers than those in pure diblock copolymer. Our results provide an insight into the phase behaviors under parallel walls confinement and may provide guidance for experimentalists. This model system can also give a simple way to realize orientational order transition in soft materials through confinement.     

Phase behaviors in a binary mixture of diblock copolymers confined between two parallel walls

The phase behaviors in a binary mixture of diblock copolymers confined between two parallel walls are investigated by using a cell dynamics simulation of the time-dependent Ginzburg-Landau theory.The morphological dependence of the wall-block interaction and the distance between walls(confinement degree) has been systematically studied,and the effect of repulsive interactions between different monomers is also discussed.It is interesting that multiple novel morphological transitions are observed by changing these factors,and various multilayered sandwich structures are formed in the mixture.Furthermore,the parametric dependence and physical reasons for the microdomain growth and orientational order transitions are discussed.From the simulation,we find that much richer morphologies can form in a binary mixture of diblock copolymers than those in a pure diblock copolymer.Our results provide an insight into the phase behaviors under parallel wall confinement and may provide guidance for experimentalists.This model system can also give a simple way to realize orientational order transition in soft materials through confinement.     

Perturbation theory for equilibrium properties of a binary mixture of hard discs

The radial distribution function (RDF) and thermodynamic properties of a two-dimensional hard-disc mixture are calculated by using the perturbation theory. Numerical results are given for theRDF, pressure and excess-free energy of the binary mixture of both additive and non-additive hard discs. It is found that the thermodynamic properties of the binary mixture of non-additive hard discs increase with Δ, the non-additive parameter.     

NaCl structure in a mixture of silica and gold sols

The formation of an NaCl structure in a mixture of a monodisperse silica sol with particle diameter of 5300 A and a gold sol with average particle size of 800 A is described. The mixture was left still for a month, and the particles settled to form a dense layer at the bottom, where phase separation appeared. In the ordered phase only gold particles were observed microscopically as bright spots at their individual lattice points, being arranged in hexagonal or in square pattern. From the distance between the particles in the square pattern and hexagonal pattern, the lattice type for gold particles was concluded to be fcc. Further, it was known that four gold particles forming a square hold one silica particle in its center. On these grounds, the entire lattice was concluded to be of the NaCl-type.     

Regular Binary Thermal Lattice-Gases

We analyze the power spectrum of a regular binary thermal lattice gas in two dimensions and derive a Landau–Placzek formula, describing the power spectrum in the long-wavelength, low frequency domain, for both the full mixture and a single component in the binary mixture. The theoretical results are compared with simulations performed on this model and show a perfect agreement. The power spectrums are found to be similar in structure as the ones obtained for the continuous theory, in which the central peak is a complicated superposition of entropy and concentration contributions, due to the coupling of the fluctuations in these quantities. Spectra based on the relative difference between both components have in general additional Brillouin peaks as a consequence of the equipartition failure.     

Binary nonadditive hard-sphere mixtures at high dimension

At high spatial dimension, a suitably scaled classical system of interacting particles truncates at second virial terms. A binary mixture of nonadditive hard spheres with sufficiently repulsive interaction between unlike particles decomposes at sufficiently high density into two coexisting phases. The region around the critical density behaves classically.     

Soret效应对具有自由表面的圆柱形浅池内双组分溶液热对流影响的实验研究

为了探究Soret效应对具有自由表面的圆柱形浅液池内双组分溶液热对流过程的影响, 通过实验观察了质量分数为50%的正癸烷/正己烷混合溶液在不同深宽比的液池内流动失稳后的自由表面耗散结构及液池内的温度波动. 结果表明, 双组分溶液流动失稳的临界热毛细Reynolds数小于纯工质的值, 且其随液层深宽比的变化规律与纯工质相同. 当深宽比小于0.0848时, 流动失稳后在自由表面观察到热流体波, 监测点处温度波动主频随热毛细Reynolds数增大而增加; 当深宽比大于0.0848时, 随热毛细Reynolds数的增大, 流动失稳后自由表面依次呈现轮辐状、花苞状、分离-合并-分离交替变化的条纹状结构.     

The formation of biaxial nematic phases in binary mixtures of thermotropic liquid-crystals composed of uniaxial molecules

ABSTRACT

Monte Carlo simulations in the isothermal-isobaric ensemble are used to investigate the formation of an ordered, biaxial nematic phase in a binary mixture of thermotropic liquid crystals. The orientational dependence of the interaction between molecules of each pure component is the same as in the well-known Maier-Saupe model; each pure component of the mixture is therefore capable of forming a uniaxial nematic phase. For the interaction between molecules of different components, we use the same Maier-Saupe model but change the sign of the coupling constant. As a consequence a T-shaped arrangement of these molecules is energetically favoured. The formation of the biaxial phase occurs in two steps. At higher temperatures T, one of the components forms a uniaxial nematic phase whereas the other is in a quasi two-dimensional restricted isotropic liquid state. We develop a simple theoretical model to understand the high degree of (ostensible) nematic order in the latter. At lower T, the second component becomes nematic and then the entire mixture of the two compounds has biaxial symmetry. The biaxial nematic phase does not demix into domains rich in molecules of one or the other species.     

Optical Transfer Function of a Binary Markovian Mixture

A system of differential equations describing the optical transfer function (OTF) of a binary Markovian mixture is considered in a small-angle approximation. Its analytical solution has been found for the case where the mixture components have different extinction and scattering coefficients but identical scattering indicatrixes. The results of investigation show that the optical transfer function of the binary Markovian mixture depends strongly on the dimensions of nonuniformities and on the difference between the optical parameters of the mixture components, but it always markedly exceeds the optical transfer function of a uniform medium.     

分离比对混合流体Rayleigh-Bénard对流解的影响

混合流体Rayleigh-Bénard对流是研究非平衡对流的非线性动力学特性的典型模型之一.基于流体力学方程组的数值模拟,首先探讨了矩形腔体中具有强Soret效应(分离比Ψ=-0.60)的混合流体行波对流的分叉特性及斑图演化,沿着分叉曲线的上部分支,随着相对瑞利数的增加,此系统依次出现了局部行波对流、具有缺陷的行波对流、行波对流、摆动行波对流及定常对流5种行波对流解.然后,研究了分离比Ψ对对流解的影响,与弱Soret效应(Ψ=-0.11)时的对流解相比较,强Soret效应(Ψ=-0.60)时出现的对流解更丰富.由于有强Soret效应的对流的复杂性,Ψ=-0.60时的对流解与Ψ=-0.20,-0.4时的对流解不同.     

Dynamical instability of the dark state in the conversion of Bose-Fermi mixtures into stable molecules

In this paper,we investigate the dynamical instability of the dark state in the conversion of Bose-Fermi mixtures into stable molecules through a stimulated Raman adiabatic passage aided by Feshbach resonance.We analytically obtain the regions where the dynamical instability appears and find that such instability in the Bose-Fermi mixture system is caused not only by bosonic interparticle interactions but also by Pauli blocking terms,which is different from the scenario of a pure bosonic system where instability is induced by nonlinear interparticle collisions.Taking a 40 K-87 Rb mixture as an example,we give the unstable regions numerically.     

Optical and thermal studies on viscous lamellar smectic phases in binary mixture of DTAC and ortho-phosphoric acid

The binary mixture of two non-mesogenic compounds, namely, dodecyl trimethylammonium chloride (DTAC) and ortho-phosphoric acid (H₃PO₄) exhibits very interesting liquid crystalline smectic phases at large range of concentrations and temperature. The mixture with lower and higher concentrations of DTAC exhibits SmA, SmD, SmB and SmE phases, sequentially when the specimen is cooled from its isotropic phase. Different liquid crystalline phases observed in the mixture were studied using optical microscopic techniques. The temperature variations of optical anisotropy and electrical conductivity have also been discussed. Helfrich potential and elastic moduli have also been estimated in the smectic phase using the Helfrich model.     

Localization and Screening Enhancement in Asymmetric Binary Ionic Mixtures

The equation of state of binary ionic mixtures of similar ions, such as nitrogen, oxygen and carbon, has been extensively studied. The study of dense asymmetric mixtures, where Z₂ >> Z₁, has primarily focused on mixtures of hydrogen and iron at solar conditions. Using molecular dynamics simulations, we examine the behavior of highly asymmetric binary ionic mixtures, where the coupling of the high‐Z species may be orders of magnitude higher than the coupling of the low‐Z species. For the conditions we have studied, we find that strong correlations and signatures of solidification occur in the high‐Z species, while the low‐Z species exists as a freely flowing fluid within the high‐Z solid matrix. Solidification of the low‐Z species is correlated with the coupling between the two components. Using the Widom expansion method, we compute the plasma screening enhancement of the nuclear reaction rates for Z = 1 in a high‐Z matrix. We also provide some estimates of the coefficient of binary diffusion in the mixture. (© 2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

New integrable lattice hierarchies

In this Letter we give a new integrable four-field lattice hierarchy, associated to a new discrete spectral problem. We obtain our hierarchy as the compatibility condition of this spectral problem and an associated equation, constructed herein, for the time-evolution of eigenfunctions. We consider reductions of our hierarchy, which also of course admit discrete zero curvature representations, in detail. We find that our hierarchy includes many well-known integrable hierarchies as special cases, including the Toda lattice hierarchy, the modified Toda lattice hierarchy, the relativistic Toda lattice hierarchy, and the Volterra lattice hierarchy. We also obtain here a new integrable two-field lattice hierarchy, to which we give the name of Suris lattice hierarchy, since the first equation of this hierarchy has previously been given by Suris. The Hamiltonian structure of the Suris lattice hierarchy is obtained by means of a trace identity formula.     

Different localized states of travelling-wave convection in a rectangular container

We have performed numerical simulations of localized travelling-wave convection in a binary fluid mixture heated from below in a long rectangular container. Calculations are carried out in a vertical cross section of the rolls perpendicular to their axes. For a negative enough separation ratio, two types of quite different confined states were documented by applying different control processes. One branch of localized travelling waves survives only in a very narrow band within subcritical regime, while another branch straddles the onset of convection existing both in subcritical and supercritical regions. We elucidated that concentration field and its current are key to understand how confined convection is sustained when conductive state is absolutely unstable. The weak structures in the conducting region are demonstrated too.     

双组分混合流体中Eckhaus不稳定调谐的行波对流

在双组分混合流体的Rayleigh-Bénard对流系统中，数值模拟获得了周期性时空位错缺陷调谐的扩展行进波对流状态.研究了该状态的时空演化特性.结果表明，Eckhaus不稳定触发的对流涡卷对的产生是调谐的起源，对流涡卷在边界处生成与湮没频率的不同，又使系统返回不稳定区域，系统在稳定与不稳定的波数之间振荡.还探讨了一个周期内传热与混合特性的改变及其控制参数的变化规律. 关键词： 双组分混合流体 行波对流 时空位错缺陷 Eckhaus不稳定调谐     

On the critical non-additivity driving segregation of asymmetric binary hard sphere fluids

A previously proposed version of thermodynamic perturbation theory, appropriate for singular pair interactions between particles, is applied to binary mixtures of hard spheres with non-additive diameters. The critical non-additivity Δ_C required to drive fluid–fluid phase separation is determined as a function of the ratio ξ ≤ 1 of the diameters of the two species. Δ_C(ξ) is found to decrease with ξ and to go through a minimum for ξ ? 0.015 before increasing sharply as ξ → 0, irrespective of the total packing-fraction η of the mixture. These results are the basis of an estimate of the range of size ratios for which a binary mixture of additive hard spheres exhibit a fluid–fluid miscibility gap. This range is conjectured to be 0.01 ? ξ ? 0.1.     

乙醇-水溶液中团簇分子的基元荧光光谱研究

采用高斯分解法对236 nm的紫外光激发乙醇体积浓度为10%～95%的乙醇-水二元混合物产生的荧光光谱进行分解,得到了荧光谱线里面所包含的基元峰,发现每种浓度溶液的谱线都是由8个基元高斯峰组成的,并获得了每个基元谱线的相对强度、峰值位置数据。对这些高斯峰及相应参数进行分析,并结合乙醇-水混合物的荧光发射机理得到了各种发光团簇的相对大小以及构象信息,进一步计算了它们各自的荧光主发射跃迁能。另外,还对高斯峰半高宽与溶液中分子间缔合形态之间的联系做了初步探讨。研究结果可为进一步研究乙醇-水二元混合物的微观结构和特性提供理论和实验依据。