氘氚聚变中子发生器旋转氚靶传热特性研究

强流氘氚中子发生器可用于模拟聚变堆中子环境, 对于开展聚变堆包层材料相关实验研究具有重要意义. 本文提出了一种用于10¹² n·^-1量级氘氚中子发生器HINEG (high intensity neutron generator)的旋转氚靶系统设计方案, 并对其技术难点和强化传热方法进行了介绍. 为考查该氚靶系统的传热特性, 利用Computational Fluid Dynamics方法对冷却水层厚度、冷却水流速和氚靶系统旋转速度对靶面冷却的影响进行了分析, 并对不同热功率密度下靶面的传热过程进行了研究. 结果显示, 大的水层厚度、大的冷却水流速和高的靶系统旋转速度有利于靶面的冷却, 但水层厚度和水流速的变化对靶面传热影响较小. 一定条件下靶面所承受的热功率密度不能超过某个限值.     

低强度空心玻璃微球充氘氚气体工艺研究

 采用分步法对低强度空心玻璃微球充氘氚气体。为了充气,建立一套高压系统,在15MPa下漏率为3.7×10^-4 PaL/s。用铀床和LaNi₅床组合起来,作为充气的高压气源。室温和250℃时,玻璃微球的最大承受压力为1.0MPa,内外压之比约0.51。在250℃时,对微球进行充气,充进微球内的氘氚气体量为0.51～0.54Mpa,满足了物理实验的要求。     

低强度空心玻璃微球充氘氚气体工艺研究

采用分步法对低强度空心玻璃微球充氘氚气体。为了充气,建立一套高压系统,在15MPa下漏率为3.7×10-4 PaL/s。用铀床和LaNi5床组合起来,作为充气的高压气源。室温和250℃时,玻璃微球的最大承受压力为1.0MPa,内外压之比约0.51。在250℃时,对微球进行充气,充进微球内的氘氚气体量为0.51～0.54Mpa,满足了物理实验的要求。     

要认真探索异常核现象 含氘固体测氚实验的启示

 1989年3月Fleischmann和Pons报道了他们的“室温核聚变”实验以来已经快三年了.关心的人们都在探问:究竟现况如何?1991年12月6日Fleischmann主动到美国加州理工学院(C.I.T.)举行一场专题报告,接着又有人对当年C.I.T的Lewls等人所作的钯电极电解重水实验提出了新的解释.     

新型无油、小体积微球高压充氘氚系统的研制

根据国内激光惯性约束聚变研究对氘氚微球靶的更高要求，新研制了一套能制备15．0MPa氘氚玻璃微球靶系统，结构见图1。     

压缩氘氚球的热核燃烧特性研究

本文利用LARED-S程序模拟了等密度和等压力条件下压缩氘氚球的热核反应燃烧过程.对于等密度模型,模拟了两个具体算例,与国外计算结果进行了比较,验证了程序的可靠性.对于等压力模型,利用数值模拟给出了热核反应燃烧与压缩氘氚球初始状态之间的关系曲线,分析发现,氘氚装量、压力和主燃料密度的增加有利于提高热核反应放能和燃耗,中心热斑的温度和面密度分别达到70—80 MK和3—4 kg·m^-2时热核反应才有显著的放能,提高主燃料密度,可以适当放宽对中心热斑的点火要求.最后对实际点火靶进行了数值模拟并且与等压力模拟计算结果进行了比较分析.     

ICF靶丸氘氚总量非破坏性荧光测量法

 介绍了惯性约束聚变（ICF）研究中，氘氚（DT）气体燃料靶丸中的氚总量监测新方法—可见光荧光法。该方法是一种非破坏性测量技术，不但适用于直接驱动的内爆靶丸，而且也适用于间接驱动方式下的各种空腔靶现场监测。给出了1992年“神光”装置内爆靶丸的现场监测结果，并给出了该方法用于绝对测量时需考虑的因素以及刻度因子，特别是讨论了未来发展高灵敏度荧光底片或探测器的必要性。     

压缩氘氚球的热核燃烧特性研究

本文利用LARED-S程序模拟了等密度和等压力条件下压缩氘氚球的热核反应燃烧过程.对于等密度模型,模拟了两个具体算例,与国外计算结果进行了比较,验证了程序的可靠性.对于等压力模型,利用数值模拟给出了热核反应燃烧与压缩氘氚球初始状态之间的关系曲线,分析发现,氘氚装量、压力和主燃料密度的增加有利于提高热核反应放能和燃耗,中心热斑的温度和面密度分别达到70—80 MK和3—4 kg·m^-2时热核反应才有显著的放能,提高主燃料密度,可以适当放宽对中心热斑的点火要求.最后对实际点火靶进行了数值模拟并且与等压力模拟计算结果进行了比较分析. 关键词： 压缩氘氚球 等密度模型 等压力模型 热核反应聚变     

Suppression of ice nucleation in supercooled water under temperature gradients

Understanding the behaviours of ice nucleation in non-isothermal conditions is of great importance for the preparation and retention of supercooled water. Here ice nucleation in supercooled water under temperature gradients is analyzed thermodynamically based on classical nucleation theory (CNT). Given that the free energy barrier for nucleation is dependent on temperature, different from a uniform temperature usually used in CNT, an assumption of linear temperature distribution in the ice nucleus was made and taken into consideration in analysis. The critical radius of the ice nucleus for nucleation and the corresponding nucleation model in the presence of a temperature gradient were obtained. It is observed that the critical radius is determined not only by the degree of supercooling, the only dependence in CNT, but also by the temperature gradient and even the Young's contact angle. Effects of temperature gradient on the change in free energy, critical radius, nucleation barrier and nucleation rate with different contact angles and degrees of supercooling are illustrated successively. The results show that a temperature gradient will increase the nucleation barrier and decrease the nucleation rate, particularly in the cases of large contact angle and low degree of supercooling. In addition, there is a critical temperature gradient for a given degree of supercooling and contact angle, at the higher of which the nucleation can be suppressed completely.     

The nonlinear Cahn-Hilliard equation: Transition from spinodal decomposition to nucleation behavior

The behavior of the nonlinear Cahn-Hilliard equation for asymmetric systems,c _t =²(±c+Bc ²+c ³-² c) within the unstable subspinodal region is explored. Energy considerations and amplitude equation methods are employed. Evidence is given for a transition from periodically structuredspinodal behavior to nucleation behavior somewhere within the traditional spinodal. A mechanism for describing a time-dependent lengthening of the dominant wavelength is explored.     

Determination of the colloidal crystal nucleation rate density

Colloidal suspensions of charged latex microspheres in water exhibit liquid-like or crystalline ordering depending on particle interaction and concentration. By virtue of large particle spacing and slow dynamics, colloidal systems offer a unique opportunity to study interfacial structure and dynamics. This paper presents the first reported experimental study of the nucleation rate density, c, of an nonequilibrium (supercooled) colloidal liquid to colloidal crystal first order phase transition. Local and global observations of colloidal crystals growing from a metastable colloidal liquid were used to determine c. Microscopic local observations revealed homogeneous nucleation and constant interface velocity growth of quasispherical crystallites in the bulk and heterogeneous nucleation of a crystalline sheet with lower growth velocity at the cell wall. Complementary global observations of the recrystallization transition made by measuring the time dependence of the suspension transparency (the fraction of transmitted laser light) determined c by fitting this curve to a model based on an extension of Avrami's theory of crystallization.     

Generalized surface thermodynamics with application to nucleation

Gibbs formulated a complete and general thermodynamics for surfaces in multicomponent fluid systems. When considering solid–fluid surfaces, he restricted attention to single-component solids in contact with fluids that could contain multiple components. Attempts that have been offered to generalize Gibbs’ results for surfaces between multicomponent solids and fluid are problematic owing to the difficulty that the surface chemical potentials for components that also reside on substitutional lattice sites in the solids are not well defined. Therefore any expressions involving these surface chemical potentials, such as the conventional definition of the surface energy, will also not be well defined. In order to formulate a general thermodynamics of equilibrium that takes into account capillary effects in systems containing surfaces between a multicomponent solids and fluids, it is shown that the concept of thermodynamic availability (exergy) can be employed that, when applied to surfaces, depends on the extensive but not the intensive variables (such as the chemical potentials) of the surfaces. Using this approach, Gibbs–Thomson–Freundlich effects for finite-size solids, an adsorption equation for solid–fluid surfaces and the thermodynamics of nucleation during solidification can be treated in a straightforward manner without referring to the ill-defined surface chemical potentials. A derivation is given that appears to be the first one that properly generalizes Gibbs’ analysis for the reversible work to form a critical nucleus to the case of solidification.     

Characteristics of acoustic emissions during nucleation of superheated droplets

Superheated droplet nucleation and subsequent bubble oscillation produces an acoustic pressure pulse that contains valuable information about the nucleation process. Spectral analysis of the pressure pulse indicates excitation of different modes of bubble oscillations in the nucleation process. In the present study it is observed that gamma induced droplet nucleation excites higher modal oscillations and also emits higher intensity acoustic emission compared to that of spontaneous nucleations.     

The effect of the interaction between the minority phase droplets on the nucleation behavior during the liquid-liquid phase transformation

The microstructure evolution during the liquid-liquid phase transformation of Al-Pb alloy was calculated. The numerical results indicate that the interaction between the minority phase droplets has effect on the nucleation process of the droplets, and the effect increases with the cooling rate and the content of Pb. Supported by the National Natural Science Foundation of China (Grant Nos 50395104, 50671111 and 50620130095)     

Vibrational spectra of high- and low-density amorphous ice,ice Ic,and ice Ih by neutron scattering

Abstract

The vibrational spectra of high- and low-density amorphous ice made ice Ic and Ice Ih have been obtained at 15 K using inelastic incoherent neutron scattering     

The critical supersaturations predicted by nucleation theory

A general set of equations is derived for calculating the supersaturation required to obtain a given rate of nucleation. This set is general enough to encompass all the present theories, the classical theory, the Lothe-Pound theory, the Reiss-Katz-Cohen theory, a recent theory by H. Reiss, and any other theory which includes a size-dependent correction to the classical theory. Comparison of these predictions is made for various substances.