Cluster description of water-in-oil microemulsions near the critical and percolation points

The three-component ionic microemulsion system consisting of AOT/water/decane shows an unusual phase behavior in the vicinity of room temperature. The phase diagram in the temperature-volume fraction (of the dispersed phase) plane exhibits a lower consolute critical point at about 40 degrees centigrades and 10% volume fraction. A percolation line, starting from the vicinity of the critical point, cuts across the plane, extending to high volume fraction side at progressively lower temperatures. In this paper we review the evidence that allows to interpret the phase behavior of our system in terms of interacting spherical droplets. We also investigate the dynamics of droplets, below and approaching the critical point by dynamic light scattering. The first cumulant and time evolution of the droplet density correlation function can be quantitatively calculated by assuming the existence of polydispersed fractal clusters formed by the microemulsion droplets due to attraction. The relaxation phenomena observed in an extensive set of measurements of electrical conductivity and permittivity close to percolation is also reviewed and interpreted through the same cluster-forming mechanism, which reproduces the most relevant features of the frequency-dependent complex dielectric constant of this system. Paper presented at the I International Conference on Scaling Concepts and Complex Fluids, Copanello, Italy, July 4–8, 1994.     

电动汽车新技术双语课程教学方法研究

电动汽车新技术是电气工程专业一门新开课程,该门课程与当前市场发展联系紧密,知识更新快,科技水平高,行业术语多,包含多门电气工程专业课知识,对于培养学生综合运用电气工程专业的主干课程技能具有重要作用。本文从电气工程专业的实际培养需求出发,研究了该门课程的教学方法,从兴趣引导、课程思政、双语教学、自主学习四个角度进行了阐述,并总结了相关经验和方法。     

基于V-视差法的道路区域检测算法研究

针对当前基于双目视觉的道路环境分析实时性差、检测不准确等问题,提出了一种改进V视差法的道路区域检测算法。该算法首先对原始图片进行车道线检测确定道路消失点,从而确定图像的感兴趣区域。然后,使用极大最小值约束获取V视差图中的斜线,从而提取道路区域。实验结果表明,由于该方法在确定感兴趣区域后计算原始视差图,因此,速度提高了29.71%,且相对于传统V视差法,算法更好地实现了路面分割;同时,障碍物检测的精确率和召回率两个指标分别提高了2.165%和4.837%。基于该算法具有良好的准确性和实时性,能有效识别道路中的障碍物,因此,可以为车辆提供可行驶区域以及为驾驶员提供辅助作用。     

Conjugate points in

An example of a geodesic in with conjugate points is given, thus providing an affirmative answer to a question of V.I. Arnold.

     

Equivalent conditions involving common fixed points for maps on the unit interval

Let be a continuous self-map of the unit interval . Equivalent conditions are given to ensure that has a common fixed point with every continuous map that commutes with on a suitable subset of . This extends a recent result of Gerald Jungck.

     

Realization of fixed point sets

Letf:XX be a selfmap of a compact connected polyhedron, andA a nonempty closed subset ofX. In this paper, we shall deal with the question whether or not there is a mapg:XX homotopic tof such that the fixed point set Fixg ofg equalsA. We introduce a necessary condition for the existence of such a mapg. It is shown that this condition is easy to check, and hence some sufficient conditions are obtained.Partially supported by the Natural Science Foundation of Liaoning University.     

Freezing points,osmotic coefficients,and activity coefficients of some salts in ethylene carbonate: A high dielectric constant solvent without hydrogen bonding

The freezing points, conductivities, and densities of NaI, KI, CsI, Bu₄NCl, Bu₄NBr, Bu₄NI, Et₄NBr, and Pr₄NBr (where Et = ethyl, Pr = propyl, and Bu =n-butyl) in ethylene carbonate have been measured. Osmotic and activity coefficients were calculated from the results. All of the salts studied are strong electrolytes. The trends in the osmotic coefficients of the alkali metal iodides are NaI>KI>CsI, showing that Na⁺ is more solvated by ethylene carbonate than Cs⁺. For the tetraalkylammonium halides, the order of osmotic coefficients are Et₄NBrPr₄NBrBu₄NCl>Bu₄NBr>Bu₄NI. This is the same order as observed in two other high-dielectric-constant solvents, water andN-methylacetamide. The results indicate that the smaller anions are more solvated than the larger anions in ethylene carbonate in contrast to the usual behavior of dipolar aprotic (basic) solvents, such as dimethyl sulfoxide.     

Location of saddle points and minimum energy paths by a constrained simplex optimization procedure

Two methods are proposed, one for the location of saddle points and one for the calculation of steepest-descent paths on multidimensional surfaces. Both methods are based on a constrained simplex optimization technique that avoids the evaluation of gradients or second derivative matrices. Three chemical reactions of increasing structural complexity are studied within the PRDDO SCF approximation. Predicted properties of reaction hypersurfaces are in good overall agreement with those determined by gradient minimization and gradient following algorithms in connection with various ab initio SCF methods. Computational efforts required by the new procedures are discussed.     

Intrinsic Surface Reaction Constant in 1-pK Model of Mg-Fe Hydrotalcite-like Compounds

The relationship among intrinsic surface reaction constant (K) in 1-pK model, point of zero net charge (PZNC) and structural charge density (σst) for amphoteric solid with structural charges was established in order to investigate the effect of σst on pK. The theoretical analysis based on 1-pK model indicates that the independent PZNC of electrolyte concentration (c) exists for amphoteric solid with structural charges. A common intersection point (CIP) should appear on the acid-base titration curves at different c, and the pH at the CIP is pHPZNC. The pK can be expressed as pK=-pHPZNC log[(1 2αPZNC)/(1-2αPZNC)], where αPZNC≡σst/eNANs, in which e is the elementary charge, NA the Avogadro‘s constant and Ns the total density of surface sites. For solids without structural charges, pK=-pHPZNC. The pK values of hydrotalcite-like compounds (HTlc) with general formula of [Mg1-xFex(OH)2](Cl,OH)x were evaluated. With increasing x, the pK increases, which can be explained based on the affinity of metal cations for H^- or OH^- and the electrostatic interaction between charging surface and H^- or OH^-.     

Mixed strategy solutions forN-person quadratic games

Mixed strategy -equilibrium points are given forN-person games with cost functions consisting of quadratic, bilinear, and linear terms and strategy spaces consisting of closed balls in Hilbert spaces. The results are applied to linear-quadratic differential games with no information and quadratic integral constraints on the control functions.This work was supported by a Commonwealth of Australia, Postgraduate Research Award.