卤化银探测器及其某些特性

文中简述了卤化银(主要是溴化银)单晶片的某些特性,氯化银单晶片与此大致相似。作为低温晶体探测器,对~(241)Am-α放射源,分辨率为17%。卤化银晶片是固体电解质,只有Ag离子对输出电信号有贡献,有显著的极化现象。在液氮槽内溴化银晶片的电导率在几个数量级内成为可控的,由在室温下外加偏置电压大小所引起的分解状态下的初始电流决定。     

气体动压轴承动态参数测定原理

将气体动压轴压简化为转化气膜系统后，针对其动力特点，给出气膜在微幅振动下动压轴承的实用数学模型和测定动态参数的方法，并进行了测量误差的修正。     

Equations of state for hard-sphere fluids

Equations of state and contact values of hard-sphere radial distribution functions (rdf's) which are given by a linear combination of the Percus— Yevick and scaled-particle virial expressions are considered. In the one-component case the mixing coefficient() is, in general, a function of the volume fraction. In mixtures the coefficient( _i ,d _i ), in general, depends upon the volume fraction _i , and diameterd _i , of each species,i andj. For the contact valuesY _ij of the rdf's, the mixing coefficients _ij ( _k ) also depend on speciesi andj. Density expansions for the exact for the one-component hard-sphere fluid are obtained and compared with several approximations made in earlier works and in our own work, as well as with simulations. For a mixture, it turns out that one cannot obtain the exact fourth virial coefficient by using a linear combination of the Percus-Yevick and scaled-particle virial expressions forY _ij unless one allows _ij to depend on mole fractionsx _i even at the zeroth order of its density expansion. We also find that _ij must depend on particle speciesi andj in order to satisfy the exact limits obtained earlier by Sung and Stell. A new equation of state for the binary hard-sphere mixture which satisfies all the exact limits we have considered is suggested.Paper presented at the Tenth Symposium on Thermophysical Properties, June 20–23, 1988, Gaithersburg, Maryland, U.S.A.     

非相似度保持投影

由主成分分析(PCA)可知任何一幅人脸图像都可以通过一组特征脸的线性加权来重构,PCA是最小均方误差意义下图像的最优表示,但是传统的PCA最终只通过比较加权系数的欧氏距离来进行识别,没有考虑残差。因此,提出非相似尺度的概念,将两个样本同时投影到相同向量上,在确定它们关系时既考虑投影系数,也考虑重构所产生的残差。两者的投影系数和残差相差越大,说明这两个样本越不相似。和保局投影(LPP)有所不同,非相似度保持投影算法不必预先设定近邻个数,它是利用非相似度的概念,创建非相似度散布矩阵,最终通过最大化目标函数获取最优子空间。在AR库和Feret库上的实验结果证明了该方法的有效性。     

基于人类视觉模型的各向异性扩散滤波方法

针对各向异性扩散模型中扩散系数的梯度阈值确定问题进行了研究,提出了一种基于人类视觉模型的各向异性扩散滤波器。首先在PM方程的基础上研究了各向异性扩散系数中梯度阈值的取值问题。根据仿生学原理,分析了韦伯比曲线,将图像根据背景亮度划分为不同的区域,分别采用不同的公式计算梯度阈值。然后讨论了改进后算法在8邻域内的离散实现问题。仿真结果表明,与传统的恒常梯度阈值扩散模型相比,改进后的算法在有效保留图像重要信息的同时对噪声的抑制效果更为理想。     

基于RS的关键帧提取仿真研究

研究视频图像中关键图像提取问题,视频图像传输采集效率低,且易造成资源浪费。针对传统的视频图像关键帧技术,都是以图像中的关键特征为提取依据的。当关键图像中特征不明显或者与非关键图像特征重复时,由于特征的关键帧图像提取就会发生错误,导致算法错误率和漏检率高。为解决上述问题,提出一种基RS理论的关键帧提取算法,首先提取图像DCT系数,利用RS理论的属性约简产生信息系统的核,对应到视频即为关键帧,避免了传统方法对图像关键特征的依赖。实验结果表明,算法可以提高关键帧提取的准确性和提取效率,为快速提取提供了依据。     

Group contributions to activity coefficients from the hard sphere expansion corresponding states theory

A new method has been developed for predicting liquid activity coefficients in ternary mixtures from group contributions. In this method, activity coefficients are obtained from the excess Gibbs free energy of mixing at constant temperature and pressure. In calculating this excess function, the constituent and mixture Gibbs free energies are each represented by an expansion about a pure reference fluid in powers of ratios of hard-sphere diameters and molecular attraction parameters. When the pure component differs from the reference by a single structural group, these ratios represent, respectively, the size contribution and the attraction contribution of this group to the thermodynamic property of the pure fluid. Contributions of intermolecular repulsion to the excess Gibbs free energy are calculated directly from hard-sphere equations of state for the mixture and pure components. The effect of polar contributions calculated by a Padé approximant is also examined. Results indicate that the method developed from the hard-sphere expansion corresponding-states theory is useful for predicting activity coefficients in ternary mixtures when unlike-pair interaction parameters are fitted to binary activity coefficient data. Furthermore, the method shows promise in providing a theoretical basis for applying group contributions to activity coefficients.Nomenclature A Residual Helmholtz free energy - C _p Constant-pressure heat capacity - H _vap Heat of vaporization - P ^s Saturated vapor pressure - R Gas constant - T Temperature - U ^HS Hard-sphere internal energy - V _c Critical volume - V ^L Liquid volume - x Dimensionless residual thermodynamic property - Z Compressibility factor - d Center-to-center distance between two touching molecules - k Boltzmann constant - n Moles - x Liquid mole fraction - y Vapor mole fraction - Volume expansivity - Liquid activity coefficient - Minimum molecular attraction potential - Isothermal compressibility - Permanent dipole moment - 3.14159... - Density - Fugacity coefficient Paper presented at the Ninth Symposium on Thermophysical Properties, June 24–27, 1985, Boulder, Colorado, U.S.A.     

Influence of HDDR treatment on magnetic properties of TbFe2- and DyFe2-based intermetallics

Magnetic properties of TbFe₂, DyFe₂, Tb(Fe_0.8M_0.2)₂ and Dy(Fe_0.8M_0.2)₂ with M=Co, Al, Si, Ga alloys affected by the Hydrogenation-Decomposition-Desorption-Recombination processing have been studied. After hydrogen treatment the coercive force H_c grows sharply, so HDDR-powders can be used as isotropic permanent magnets with the energy product up to 26 MG Oe at T=77 K. In Dy(Fe_0.8Al_0.2)₂ at T<10 K the stepwise magnetic reversal has been observed. The HDDR-treatment increases the critical field of magnetic reversal from 11 up to 18.4 kOe at 4.2 K. It is shown that the effect of the stepwise magnetic reversal is caused by a heat release in a sample during an avalanche motion of narrow domain walls.     

预分离色谱法直接测定微量组份无限稀释活度系数

预分离色谱法可直接测定混合物中微量组份的无限稀释活度系数(γ~∞),而不必把此组份从混合物中分离出来。主要由四步组成:被测组份的预浓缩,被测组份的定性,选择预分离柱和γ~∞的测定。预浓缩样品经过预分离柱分出被测组份,然后进入测量柱测定γ~∞。此方法简捷、可靠与常规以纯溶质进样的色谱测y~∞的方法具有相同的测定精度,可广泛用于缺少纯样的场合。用此法测定了戊烯-1-炔-4、丁炔-2在若干酸醇中的γ~∞,分别求得了修正和未修正的UNlFAC参数,对kikic修正模型其值为ac=c,CooH=694.9(K)acooH,c=c=-99.08(K),ac=c,oH=812.99(K),aoH,c=c=143.36(K)     

Determination of the solubility parameter of poly(ethylene oxide) at 25°C by gas-liquid chromatography

The solubility parameter of poly(ethylene oxide) at 25°C has been determined using the method developed by DiPaola-Baranyi and Guillet, by the extrapolation of the values of the interaction parameter χ, at high temperatures, ranging from 70°–90°, 90°–110° and 110°–130°C down to 25°C. The values of the solubility parameter obtained, depending on the temperature ranges employed, are 9.8, 9.9 and 10.1, respectively.