高分辨率多光谱数字相机电子学系统的设计

设计了一种基于多光谱技术的机载数字相机电子学系统。它包括时序产生单元、信号处理单元、信号控制单元、数据输出接口单元和数据采集存储单元等几部分。系统具有调光和行频调节功能,用以满足在不同能量状态和不同飞行高度下的成像质量。考虑到机载设备的特殊要求,对其进行了轻量化设计和机载稳定平台设计。它具有实时高速存储和实时采集数据的功能。结果表明,机载数字相机电子学系统的各种功能完全满足设计要求,为实现高分辨率探测提供了保证。     

Fluorocarbon- containing hydrophobically modified poly(N-isopropylacrylamide)

A fluorocarbon-modified poly(N-isopropylacrylamide) has been synthesized by copolymerization of N-isopropyl acrylamide with a small amount of acrylate or methacrylate containing a perfluoroalkyl group. It was found that the hydrophilicity of macromolecular backbone is an important factor to the solution properties of the copolymers and that hydrophobic association between fluorocarbon groups is stronger than that between the corresponding hydrocarbon analogies. The viscosity of some of the copolymer solutions was very sensitive to temperature. It was dilatant at higher fluorocarbon comonomer content ( > 0.20-1.0 mol%) and was Newtonian at very low fluorocarbon comonomer content (0.03-0.2 mol% ) . Evidence for hydrophobic association of the fluorocarbon groups was obtained from the effects of adding Nad and surfactants on the solution viscosity. The LC-ST properties of these copolymers were studied by DSC method and this was also found to be consistent with hydrophobic association between the fluorocarbo     

A new method for the numerical solution of time dependent viscous flow

A new method of solving numerically the Navier-Stokes equations for time dependent flow is presented. The velocity components and pressure are used as the main variables, but in order to ensure continuity on a global scale, the Stokes stream function is also employed. The solution process is formulated in cylindrical polar co-ordinates and both implicit and explicit versions are discussed. Time dependent development in the entrance region of a cylindrical pipe is investigated using the method and several interesting flow features are predicted.     

固相微萃取与高效液相色谱联用技术的进展

 较全面地评述了固相微萃取与高效液相色谱联用技术的发展与应用 ,包括该技术的原理、接口装置、涂层材料等。     

Preparation and Characterization of Zirconia-Magnesia Support Modified by Alkylphosphonic Acid for Liquid Chromatography

Interest in zirconia as a chromatography support has increased considerably recently because of its chemical inertness and its promise as a useful support. We have reported the preparation of spherical zirconia and characterization of its chromatographic behavior. However, the zirconia was found unsatisfactory for its chromatographic efficiency, probably owing to the poor pore structure of it. In this paper, we for the first time report the preparation of alkylphosphonic acid modified zirconia-magnesia stationary phase, and characterization of its structure and chromatographic behavior.     

On-line determination of sulphite in brine by flow-injection analysis

A spectrophotometric flow-injection procedure for the determination of sulphite in aqueous media over the range 0.5–20 mg 1^?1 is described. The reagent used was the organic disulphide 5,5′-dithiobis(2-nitrobenzoic acid). Results are presented for a laboratory-based method for sulphite in water and a potential on-line method for sulphite in high ionic strength potassium chloride brine. The general attractions of flow-injection-based monitors for the on-line analysis of liquid process streams are also discussed.     

碱基在十二胺-N,N-二亚甲基膦酸改性氧化锆固定相上色谱行为的研究

研究了碱基在十二胺-N,N-二亚甲基膦酸(DDPA)改性氧化锆固定相（DPZ）上的色谱保留行为,考察了流动相中甲醇含量、流动相pH值、缓冲溶液中离子类型和离子强度对碱基保留的影响,对DDPA在氧化锆表面的吸附方式进行了研究。研究结果表明,DDPA仅以一个膦酸基与氧化锆结合,因而DPZ固定相表面上除了有长链的疏水烷基外,还有酸性的膦酸基和碱性的氨基。碱基分子中也存在氨基和酰胺基等极性基团,因此碱基在DPZ固定相上除了有疏水作用外,还具有电荷排斥作用、离子交换作用等多种保留机理。由于多种保留机理的存在,使得碱基在DPZ固定相上具有较好的分离选择性,在酸性条件下对碱基混合样品的分离取得了满意的结果。     

[5-(芳亚甲基氨基)-1,3,4-噻二唑-2-基]硫乙酰芳胺的合成及 生物活性研究

在K2CO3存在下利用聚乙二醇-400 (PEG-400)作相转移催化剂, 于固-液相转移催化条件下, 通过5-芳亚甲基氨 基-2-巯基-1,3,4-噻二唑与氯乙酰芳胺的硫烷基化反应, 合成了16个未见文献报道的[5-(芳亚甲基氨基)-1,3,4-噻二唑-2-基]硫乙酰芳胺衍生物. 经元素分析, FT-IR,1H NMR和13C NMR确证了其结构. 生物活性实验结果表明, 部分化合物对小麦幼苗的生长具有明显的植物生长调节活性, 并对枯草杆菌具有一定的抑制活性.     

Highly Catalytic Enantioselective Addition of Diethyl Zinc to Aldehydes and Chalcone in the Presence of Chiral Ligands

Catalytic asymmetric carbon-carbon bond formation is one of the most important reactions and have attracted much attention to develop more efficient enantioselective C-C formation methods in organic synthesis. In this field, asymmetric addition of diethylzinc to aldehydes[1] and conjugate addition to enones[2] have drawn special interests and have been greatly developed. Regardless of it, much spaces in these areas still exist, so it needs more extensive and intensive researches for the purpose of as follows: (1) attaching ligands to a polymer for the easy separation of the catalysts so as to be able to allow very efficient recovery and reuse of the catalysts, and the possibility of carrying out the desired transfomation in continuous mode in a flow reactor, etc., (2) searching for novel chiral catalysts with such features as more suitable for more extensive substrates varieties, and more convenient and economical as well as possessing applicable prospect, and so on. Here we report some works in these areas done in our laboratory.