Energy of formation for and liquid binary alloys

We have investigated the free energy of formation for Ag_xIn_1-x and Ag_xSn_1-x liquid binary alloys at temperatures 1173 and 1250 K, respectively. A microscopic theory based on the first order perturbation has been applied. The interionic interaction and a reference liquid are the fundamental components of the theory. The interionic interaction is described by a local pseudopotential. A liquid of hard spheres (HS) of two different effective diametres and charges is used to describe the reference system. The results of the calculations for energy of formation agree very well with the available experimental data. Our calculations also reveal that a simple perturbative approach along with appropriate effective pair potentials can produce nearly quantitative results for the concerned alloys.     

Elasticity in nanocrystalline Nd2Fe14B+αFe magnetic composites

The dynamic Young modulus (E) of magnetic Nd₂Fe₁₄B+αFe nanocomposites is investigated with mechanical spectroscopy techniques (vibrating reed configuration, f≈1.5 kHz <10⁻⁶). Reduced values of E are obtained (88–152 GPa) as compared with that predicted by the rule of mixtures for the composite (164 GPa). Three contributions to this reduction are briefly discussed: a large volume fraction of the specimen with grain boundary like structure; internal pores, resulting from the high cooling rate during processing (10⁶ K/min) and magneto-mechanical effects. Even when porosity is identified as the principal cause of modulus reduction, magnetic effects are also detected.     

New results for virial coefficients of hard spheres inD dimensions

We present new results for the virial coefficientsB _k for κ<- 10 for hard spheres in dimensionsD = 2,..., 8.     

Effects of pH and citric acid contents on characteristics of ester-derived BaFe12O19 powder

The single domain size of BaFe₁₂O₁₉ powder with crystallite sizes less than 200 nm was produced using a citric acid precursor method. Fe³⁺ and Ba²⁺, in a molar ratio of 12, were chelated by COOH⁻ in an aqueous solution. After ethylene glycol additions, esterification, dehydration, and calcination led to the formation of ester-derived BaFe₁₂O₁₉ powder. High pH and/or high citric acid contents in the starting solution are required to complete chelate metallic ions in the solution and to form pure barium ferrite powder at 1073 K. Pure single magnetic domain BaFe₁₂O₁₉ particles of M(30 kOe)≈54 emu/g, M_r≈28 emu/g, and H_c≈3.7 kOe were produced using [citric acid]/[metallic ions]=1.5 and pH7.     

荧光钙探针试剂及其在生物分析中的应用

本文评论了荧光钙探针试剂合成、性质、结构和生物分析应用方面的进展。各种典型的荧光钙探针试剂均已分别加以讨论。     

Modification of the GV-MSA model in obtaining the activity and osmotic coefficients of aqueous electrolyte solutions

In this work a modified form of the Ghotbi–Vera Mean Spherical Approximation model (MGV-MSA) has been used to correlate the mean ionic activity coefficients (MIAC) for a number of symmetric and asymmetric aqueous electrolyte solutions at 25 °C. In the proposed model the hard sphere as well as the electrostatic contributions to the MIAC and the osmotic coefficient of the previously GV-MSA model has been modified. The results of the proposed model for the MIAC of the electrolyte solutions studied in this work are used to directly calculate the values of the osmotic coefficients without introducing any new adjustable parameter. In the MGV-MSA model the cation diameter as well as the relative permittivity of water depends on the electrolyte concentration. Having considered such dependency for both cation and relative permittivity for water in an electrolyte solution the modification of the GV-MSA has been made. It should be stated that in the MGV-MSA model the anion diameter in the solution similar to that in the GV-MSA model remains constant and independent of the electrolyte concentration. The results obtained from the proposed model have been favorably compared with those of the GV-MSA model. The results showed that the MGV-MSA model can more accurately correlate the MIAC of the single electrolyte solutions than those of the GV-MSA model. The same comparison has been observed in case of the osmotic coefficients for the electrolyte solutions studied in this work. It should be noted that in order to do an unequivocal comparison between the results obtained from the models used in this work the same minimization procedure and the same experimental data for the MIAC and the osmotic coefficients have been used. Also it should be mentioned that in the MGV-MSA model the conversion from the McMillan–Mayer (MM) framework to that of the Lewis–Randall (LR) has been performed. It has been concluded that such transformation can affect the results in particular at higher electrolyte concentrations.     

流体熵相关性质的Monte Carlo模拟新方法

提出了用于计算实际体系熵相关性质的Monte Carlo多级取样分子模拟方法. 应用这一方法, 对硬球流体的化学势及Helmholtz自由能进行了估算, 得到了满意的结果. 计算化学势时, 不存在通常试验粒子方法所遇到的高密度问题. 该方法特别适合规律性的系统研究, 较之普通模拟方法要有效得多. 模拟得到的硬球体系无限稀释组份的超额化学势与对比直径的关系, 在相变区域为一条双凹曲线; 无论是在相变区还是在单相区, Carnahan-Starling公式对这一关系的描述均有较大偏差.     

多支链烷基苯磺酸钠水溶液的表面性质

用自制的四种高纯度多支链烷基苯磺酸钠,研究了支链结构对其表面性质的影响.结果表明,随支链烷基碳数增加,临界胶束浓度降低,标准吸附自由能DGadӨ更负;但是,饱和吸附量Γmax却随支链烷基碳数增加而减小,且临界胶束浓度时的表面张力γcmc随吸附量减小而降低,表现出与一般表面活性剂不同的变化趋势.从多支链烷基苯磺酸钠的分子结构特点,解释了随支链烷基碳数增加Γmax和γcmc的变化规律,探讨了分子的独占面积(as)对Γmax及γcmc的影响.     

High-density properties of hard spheres within a modified Percus-Yevick theory: The role of thermodynamic consistency

Using an integral-equation approach based upon an approximation for the tail function, the equilibrium properties of a system of hard spheres are studied with special concern for the behavior in the region of close packing. The closure adopted is such that full, internal consistency is ensured in the thermodynamics of the model with respect to both the two zero-separation theorems as well as to the more standard virial and fluctuation routes to the equation of state. The scheme also makes use of the continuity properties of the tail function and of the cavity distribution function at contact. These properties are explictly tested in the low-density limit up to the fourth derivative. The theory generates an equilibrium branch bounded on the high-density side by a point corresponding to a packing fraction0.78, a value which closely matches Rogers' least upper bound for the densest packing of spheres. The pair structure of the fluid in the state of random close packing is also compared to the type of local order predicted by the theory at similar densities.     

Quantitative measurement of hard X-ray spectra from laser-driven fast ignition plasma

Absolute Kα line spectroscopy is proposed for studying laser–plasma interactions taking place in the Au cone-guided fast ignition targets. X-ray spectra ranging from 20 to 100 keV were quantitatively measured with a Laue spectrometer composed of a cylindrically curved crystal and a filter-absorption method for Bremsstrahlung continuum emission. The absolute sensitivities of the Laue spectrometer systems were calibrated using pre-characterized laser-produced X-ray sources and radioisotopes. The integrated reflectivity for the crystal is in good agreement with predictions by an X-ray diffraction code. The energy transfer efficiency from incident laser beams to hot electrons, as the energy transfer mechanism, is derived from this work. The absolute yield of Au and Ta Kα lines were measured in the fast ignition experimental campaign performed at Institute of Laser Engineering, Osaka University. Applying the hot electron spectrum information from electron spectrometer and scaling laws, the energy transfer efficiency from the incident LFEX, a kJ-class PW laser, to hot electrons was derived for the first time.