10MW串级脉冲发电机的理论、设计、实验及应用研究

 脉冲发电机具有小型、机动、灵活、可靠、寿命长等特点, 作为高功率固体激光器和加速器电源是一新的技术路线。比较了各种类型脉冲电源的性能指标,解释了旋转磁通压缩和串级原理,提出串级脉冲发电机的自激、偏极与双机同壳概念,给出电机的设计公式,10MW串级脉冲发电机的设计、实验及在强激光与粒子束领域中的潜在应用。     

光阴极注入器型能量回收射频加速器

光阴极注入器型能量回收射频加速器（PERL）是新一代加速器,在高平均功率自由电子激光和下一代高亮度光源等研究中有很好的应用前景。分析了PERL的强流与高平均功率特性,对注入器输出束流品质的要求及光阴极注入器、超导加速腔等关键技术进行了研究,设计分析了一种特殊结构的高压DC Gun光阴极注入器,能有效地提高DC加速腔中的加速场强,当高压为1MV和加速场达到10MV/m时,产生的电子束流能够基本满足PERL应用要求。同一超导加速段中的束流加速和能量回收的数值模拟计算结果表明,能获得高效率电子束流能量回收效果。     

利用“神光-Ⅱ”激光装置多路光束叠加直接驱动下的冲击波平面性及稳定性

利用“神光-Ⅱ”的3路基频光输出及小透镜列阵束匀滑技术,通过优化设计和合理地选择光路组合,实现了多路叠加斜入射的驱动激光, 在靶材料中产生一个650~750μm范围内平面性良好的冲击波,有效地提高了“神光-Ⅱ”输出光束的利用率。同时,利用斜面靶进行的冲击稳定性实验表明,在靶面功率密度分别为3.26×1014及2.56×1014W/cm2时,冲击波至少在28.38~55.82和22.13~35.07μm的Al样品厚度内是稳定传播的。     

电子束泵浦氩中高能电子分布的理论计算

改进了文献中报导的Boltzmann基本方程。与Boltzmann基本方程相比,改进后的Boltzmann方程更全面地描述了电子与基态氩原子碰撞的物理过程,并能计算出整个能量区间的电子分布。利用Boltzmann基本方程和改进的Boltzmann方程,对电子束泵浦氩中能量大于氩原子第一激发态能量(11.56eV)的高能电子分布函数进行了理论计算。计算中,选取了电子碰撞氩的微分电离截面和激发截面的解析表达式。对计算所得的稳态电子分布函数以及达到稳态分布所需的特征时间进行了分析和讨论。     

通过有光阑近轴ABCD光学系统激光束的近似解析传输公式

用傅立叶级数展开法研究光束通过有光阑限制的近轴ABCD光学系统的传输特性,导出了光阑透射率函数不同时的传输公式。硬边光阑的情况可作为其它光阑的特例得到,其它光阑也可视作硬边光阑来处理。数值计算表明了该方法快速的优点,并得到与用Collins公式直接积分一致结果。     

A model of melting of rare gases within bubbles of crystalline metal matrix

Abstract

On the basis of experimental results obtained in the present and some other works a model of melting of rare gas solids within bubbles formed in a crystalline metal matrix as a result of ion implantation is proposed. Rare gas solid is supposed to melt on heating at the expense of the bubble volume expansion by emission of a dislocation loop. On this basis the melting temperature can be estimated as one which is enough to provide for a pressure inside a bubble sufficient for the initiation of the dislocation loop punching. Values of melting temperatures obtained in this way are in good agreement with available experimental data.     

Contiguity relations for linearisable systems of Gambier type

We introduce the Schlesinger transformations for the Gambier, linearisable, equation and by combining the former construct the contiguity relations of the solutions of the latter. We extend the approach to the discrete domain obtaining thus the Schlesinger transformations and the contiguity relations of the solutions of the Gambier mapping. In all cases the resulting contiguity relation is a linearisable equation, involving free functions, and which can be related to the generic Gambier mapping.     

ON THE NONLOCAL SYMMETRIES OF THE μ-CAMASSA–HOLM EQUATION

The μ-Camassa–Holm (μCH) equation is a nonlinear integrable partial differential equation closely related to the Camassa–Holm and the Hunter–Saxton equations. This equation admits quadratic pseudo-potentials which allow us to compute some first-order nonlocal symmetries. The found symmetries preserve the mean of solutions. Finally, we discuss also the associated μCH equation.     

Densities and viscosities of propylene carbonate with aromatic hydrocarbons (benzene, 1,4-dimethylbenzene and ethylbenzene) at 288.15, 298.15 and 308.15 K

Densities and viscosities of the binary mixtures of propylene carbonate with benzene, 1,4-dimethylbenzene and ethylbenzene were measured over the entire mole fraction range at 288.15, 298.15 and 308.15?K. Using the experimental values of densities and viscosities the excess molar volumes and viscosity deviations were calculated. The results were fitted by Redlich–Kister equation. The results were discussed in terms of intermolecular interactions.     

The solubility of bosentan in aqueous-2-propanol mixtures at several temperatures,measurement and data correlation

ABSTRACT

The solubilities of bosentan (BST) in binary aqueous mixtures of 2-propanol at temperatures ranging from 293.15 to 313.15 K were determined using a shake-flask method. The produced data were modelled with the Jouyban-Acree-van’t Hoff model and difference between the predicted data and experimental ones were illustrated by percent average relative deviations (%ARD). Moreover, the thermodynamic functions of dissolution for BST in the aqueous 2-propanol solutions were computed which suggest that the dissolution process is endothermic and not spontaneous.