Heat Transfer Problems Induced By Multi-shocks Interaction

Numerical simulations of the multi-shock interactions observable around hypersonic vehicles were carried out by solving Navier-Stokes equations with the AUSMPW scheme and the new type of the IV interaction created by two incident shock waves was investigated in detail. Numerical results show that the intersection point of the second incident shock with the bow shock plays important role on the flow pattern, peak pressures and heat fluxes. In the case of two incident shocks interacting with the bow shock at the same position, the much higher peak pressure and more severe heat transfer rate are induced than the classical IV interaction. The phenomenon is referred to as the multi-shock interaction and higher requirements will be imposed on thermal protection systems.

用双流体模型模拟超声速气固两相流动

采用了双流体模型对JPL(Jet Propulsion Laboratory)喷管中气固两相流动以及超声速射流两相流动进行了数值模拟,并研究了可压缩两相流动中气相与颗粒的相互作用规律.自主开发的一般曲线坐标系下二维轴对称可压缩双流体程序Solve2D,对气相求解Navier-Stokes(N-S)方程组,采用k-ε湍流模型,颗粒相求解Euler方程组.对JPL喷管内的两相流场和湍流两相射流流场进行了数值模拟,研究了不同颗粒质量百分数以及不同颗粒直径时的气固两相流场的流动规律.

气泡/液滴运动的Level Set方法模拟研究

利用Level Set方法，结合投影法求解了描述气泡/液滴运动的Navier-Stokes方程。对地面常重力场中不同大小的空气泡在高黏度糖浆溶液中的自由上升运动现象，数值模拟结果与实验观测结果符合甚好，表明该方法能够计算大密度比和黏度比$(>1000:1)$情况下的气液两相流动。而对等密度液滴的热毛细迁移现象的数值模拟结果同样能够与实验结果相一致，表明该方法同样适于研究具有Marangoni效应的两相流动现象，特别是在空间微重力环境中的气液两相传热现象中的局部流动与传热问题。

三维波流数值水槽的构建方法

为了模拟波浪与水流的联合作用,基于Reynolds平均的Navier-Stokes方法,构建了一个三维波流数值水槽. 使用该模型对不同出流边界条件进行了对比分析. 结果表明:引入合理的入流和出流边界条件,可以保证在计算稳定后,水槽平均水面基本保持不变. 垂向时均流速分布的计算结果与实验数据吻合良好. 这表明:该波流数值水槽具有较好的波流特性,可用于计算波浪与水流、以及与三维固定结构之间相互作用.

可压缩湍流直接数值模拟

der="0" alt="" width="300" height="300" align="left" />本书是以作者及其研究小组多年来的研究工作为基础撰写的，主要是可压缩湍流的直接数值模拟。全书共分两部分。第一部分为数值模拟方法：针对可压缩湍流的多尺度非定常非稳定流动特征，所构造的高精度差分格式（高于三阶精度），分析了各种高精度差分格式的数值行为特征和模拟小尺度物理结构、分辨非定常间断面的能力，重点分析了正确模拟多尺度物理结构及其非线性干扰对数值方法的要求。第二部分是物理问题的直接数值模拟：根据可压缩湍流的流动物理特征，所建立的求解可压缩Navier-Stokes方程的高精度数值模拟方法，详细描述了不稳定流和可压缩湍流的直接数值模拟，以及在此基础上所发现的一些新的物理现象。直接数值模拟主要针对典型可压缩湍流，包括均匀各向同性湍流、槽道湍流、平面混合流、射流、平板边界层湍流和钝楔、钝锥边界层湍流等，重点是可压缩湍流从层流转捩到湍流的直接数值模拟及其流动机理的研究。书中还介绍了我课组所研制的高精度、高效并行算法的软件。

Enhancements of the simulation method on the edge effect in resin transfer molding processes

In resin transfer molding processes, small clearances exist between the fiber preform and the mold edges, which result in a preferential resin flow in the edge channel and then disrupt the flow patterns during the mold filling stage. A mathematical model including the effect of cavity thickness on resin flow was developed for flow behavior involving the interface between an edge channel and a porous medium. According to the mathematical analysis of momentum equations in a fully developed rectangular duct and formulations of the equivalent edge permeability, comparing with three-dimensional Navier-Stokes equations, the governing equations were modified in the edge channel. The volume of fluid (VOF) method was applied to track the flow front. A simple case is numerically simulated using the modified governing equations. The effects of edge channel width and cavity thickness on flow front and inlet pressure are analyzed, and the evolution characteristics of simulated results are in agreement with the experimental results. (c) 2007 Elsevier B.V. All rights reserved

Reactive Mold Filling in Resin Transfer Molding Processes with Edge Effects

Reactive mold filling is one of the important stages in resin transfer molding processes, in which resin curing and edge effects are important characteristics. On the basis of previous work, volume-averaging momentum equations involving viscous and inertia terms were adopted to describe the resin flow in fiber preform, and modified governing equations derived from the Navier-Stokes equations are introduced to describe the resin flow in the edge channel. A dual-Arrhenius viscosity model is newly introduced to describe the chemorheological behavior of a modified bismaleimide resin. The influence of the curing reaction and processing parameters on the resin flow patterns was investigated.

Rational Design, Synthesis, and Optical Properties of Film-Forming, Near-Infrared Absorbing, and Fluorescent Chiromophores with Multidonors and Large Heterocyclic Acceptors

A new series of film-forming, low-bandgap chromophores (1a,b and 2a,b) were rationally designed with aid of a computational study., and then synthesized and characterized. To realize absorption and emission above the 1000 nm wavelength, the molecular design focuses on lowering the LUMO level by fusing common heterocyclic units into a large conjugated core that acts an electron acceptor and increasing the charge transfer by attaching the multiple electron-donating groups at the appropriate positions of the acceptor core. The chromophores have bandgap levels of 1.27-0.71 eV, and accordingly absorb at 746-1003 nm and emit at 1035-1290 nm in solution. By design, the relatively high molecular weight (up to 2400 g mol(-1)) and non-coplanar structure allow these near-infrared (NIR) chromophores to be readily spin-coated as uniform thin films and doped with other organic semiconductors for potential device applications. Doping with [6,6]-phenyl-C-61 butyric acid methyl ester leads to a red shift in the absorption on]), for la and 2a. An interesting NIR electrochromism was found for 2a, with absorption being turned on at 1034 nm when electrochemically switched (at 1000 mV) from its neutral state to a radical cation state. Furthermore, a large Stokes shift (256-318 nm) is also unique for this multidonor-acceptor type of chromophore.

N-Methyl-N-Allylpyrrolidinium Based Ionic Liquids for Solvent-Free Dye-Sensitized Solar Cells

We prepared four new ionic liquids consisting of N-methyl-N-allylpyrrolidinium cation in conjunction with anions including iodide, nitrate, thiocyanate, and dicyanamide, respectively, and measured their physical properties of density, viscosity, and conductivity. Owing to the relatively lower melting point of electroactive N-methyl-N-allylpyrrolidinium iodide, in combination with three other nonelectroactive ionic liquids, we could construct solvent-free electrolytes possessing high iodide concentrations for dye-sensitized solar cells. We correlated temperature-dependent electrolyte viscosity with molar conductivity and triiodide mobility through applying an empirical Walden's rule and a modified Stokes-Einstein equation, respectively. We have further found that these anions (nitrate, thiocyanate, and dicyanamide) have different influences on surface states and electron transport in the mesoporous titania film, resulting in different photovoltages and photocurrents of dye-sensitized solar cells.

Syntheses of Ag, PbSe, and PbTe nanocrystals and their binary self-assembly exploration at low size-ratio

Nanocrystals of Ag, PbSe, and PbTe were prepared via a high-temperature organic solution approach, respectively. Using a size-selection technique, the size-distribution of each set of nanocrystals could be fine-tuned and finally monodisperse products were achieved. Superlattice structure of binary self-assemblies in low size-ratio were also explored and characterized by transmission electron microscopy. It is realized that a success of achieving binary self-assembly pattern is greatly dependent on several key factors including particle size-distributions, relative concentrations of both components, as well as the size-ratios between Ag and PbSe (or PbTe) nanocrystals.

Mesoscopic simulation of the impregnating process of unidirectional fibrous preform in resin transfer molding

The resin transfer molding has gained popularity in the preparation of fiber-reinforced polymer-matrix composites because of its high efficiency and low pollution. The non-uniform inter-tow and intra-tow flows are regarded as the reason of void formation in RTM. According to the process characteristics, the axisymmetric model was developed to study the interaction between the flow in the inter-tow space and that in the intra-tow space. The flow behavior inside the fiber tows was formulated using Brinkman's equation, while that in the open space around the fiber tows was formulated by Stokes' equation. The volume of fluid (VOF) method was applied to track the flow front, and the effects of filling velocity, resin viscosity, inter-tow dimension and intra-tow permeability on fluid pressure and flow front were analyzed. The results show that the flow front difference between the inter-tow and intra-tow becomes larger with the decrease of intra-tow permeability, as well as the increase of filling velocity and inter-tow dimension.

A new luminescent material: Li2CaSiO4 : Eu2+

In our study, the Eu2+ doped Li2CaSiO4 phosphors were initially synthesized by high temperature solid state method, and their luminescent properties were also investigated. Eu2+ ions occupied 8-coordinatid distorted dodecahedral Ca sites, leading to strong crystal field splitting. The strong crystal field splitting made the broad excitation band extending from UV to visible region. In addition, the high concentration of Li+ ions in the structure constrained the distortion of the emission centers, then resulted in a small stokes shift, similar to 1100 cm(-1). Under excitation, the Li2CaSiO4:Eu2+ phosphors emitted bluish green light with peak of 480 nm, FWHM of 31 nm and color coordination of (0.06, 0.44). The Eu2+ doped Li2CaSiO4 phosphor would be suitable for bluish green phosphor of white LEDs due to its excellent excitation profile and chromaticity.

Tunable photoluminescence in sol-gel derived silica xerogels

Silica xerogels prepared by sol-gel method show blue emission under UV excitation with a smaller Stokes shift. The luminescent properties have been investigated under various preparation conditions and compositions. The silica xerogels show similar luminescent properties when using C2H5OH and N,N-dimethylformamide (DMF) as solvents, which are very different from those when using dimethylsulfoxide (DMSO) as solvent, i.e., a red shift of excitation and emission has been observed in the latter case. The emission intensity of the silica xerogels also depends on the water content and pH of the starting reaction solution. The introduction of organic group (-CH3) in the silica xerogel modifies the network structure and further changes their luminescence properties. Heat treatment results in the decomposition of the organic (-SiCH3) groups, which eliminates the old luminescent centers and produces new luminescent centers in longer wavelength simultaneously. (C) 2000 Elsevier Science B.V. All rights reserved.

Encapsulation of Eu(TTA)(3) into MCM-41 mesoporous molecular sieve by sol-gel method

The rare earth complex Eu(TTA)(3) was successfully encapsulated into MCM-41 mesoporous molecular sieve by the addition of the complex into the sol-gel mixture for the synthesis of MCM-41 mesoporous material under microwave radiation. The as-synthesized MCM-41-hosted Eu(TTA)(3) mesophase was confirmed to possess hexagonally ordered mesostructure and a uniform crystal. size of about 30 nm with XRD and HRTEM techniques. Moreover, the IR spectrum, photoluminescence effect and fluorescence lifetime of the Eu(TTA)(3)/MCM-41 hybrid were also studied. An increase in Stokes' shift and no change in luminescence lifetime were observed to the resultant mesophase in comparison with Eu(TTA)(3) in ethanol solution.