静态傅里叶变换超光谱全偏振成像技术

光谱偏振成像技术是成像光谱技术与偏振成像技术的有机融合, 是当前空间光学遥感技术研究的热点和前沿. 针对目前光谱偏振成像技术受测量原理、探测模式的限制, 普遍需要运动、电控调制等部件, 导致体积大, 结构复杂, 加工装调困难, 抗振能力差等问题, 我们于2010年在国际上首先提出了一种多信息融合的静态傅里叶变换超光谱全偏振成像方法. 本文在此基础上, 阐述了新方法的基本原理, 给出了具体实现方案. 新方案无需运动、电控调制部件, 可实现目标图像、光谱、全偏振信息的一体获取. 推导出了新方案的调制干涉强度数据表达式及Stokes矢量解调公式, 分析了新方法实现光谱、全偏振探测的物理过程. 对新方案进行了计算机数值模拟验证, 研制了原理验证样机开展了室内、室外验证实验, 首次获得了室外推扫光谱图像数据立方体和全色全偏振度图像, 模拟及实验结果均表明新方案原理正确, 技术可行. 上述研究为新型空间遥感器的开发提供了基础理论及实践支持. 关键词： 成像光谱 偏振成像 Stokes矢量     

基于复杂度分析logistic映射和Lorenz模型的研究

采用三次粗粒化方法得到了logistic映射和Lorenz模型的符号序列，运用动态非线性时间序 列分析方法——Lemper-Ziv复杂度，分别对两组符号序列进行了对比分析.对于logistic映 射，其复杂度反映了时间序列的演化；Lorenz模型三个分量的复杂度序列都具有混沌性质， 即由许多振幅非常接近而长度完全不同的循环所组成，反映了Lorenz模型内在的准周期特性 .进一步研究发现，当取不同的窗口长度时，复杂度序列的特征基本相同，并且复杂度反映 了时间序列的时空特性.因此，可以借助复杂度的计算来反演观测资料的动力学结构. 关键词： 三次粗粒化 Lemper-Ziv复杂度 logistic映射 Lorenz模型     

129I加速器质谱分析研究

通过对129I加速器质谱(AMS)分析中影响敏度和准确度各种参数的研究,如靶电极制备、压样、靶样中辅助介质（Matrix）的选择及使用比例等,优化了用于3 MV加速器质谱仪的SO-110型离子源的条件参数,确定129I-AMS测量的最佳靶电极材料为Cu,最佳的辅助介质为Nb粉末,Nb与AgI样品的最佳体积比为3∶1。在此条件下可以获得稳定且持续的I-束流进行测量129I/127I原子比值,实验测得西安加速器质谱仪的129I/127I本底值为1.5210-14。     

Intermolecular Domino Reaction of Two Aryl Iodides Involving Two C?H Functionalizations

A palladium‐catalyzed intermolecular cross‐coupling of two aryl iodides is reported, giving polycyclic ring systems with a high level of convergence and efficiency.     

Enhanced slow light propagation in photonic crystal waveguides using angular properties of scatter elements

Applicability of the angular properties of scatter elements as a tool to achieve improved slow light performance with small group velocity dispersion and large bandwidth in photonic crystal waveguides is investigated. A polyatomic photonic crystal waveguide, including two scatter elements with different geometrical shapes in each primitive cell, is proposed to investigate the feasibility of our method. Numerical results show that a versatile control of the dispersion relation of slow light modes, with large normalized delay-bandwidth products ranging from 0.2085 to 0.3394, can be obtained using a unique geometrical parameter.     

MIXED-CONVECTION HEAT AND MASS TRANSFER IN A FULLY DEVELOPED HORIZONTAL CHANNEL FLOW

An experimental study of mixed-convection heat and mass transfer flow of a CuS0₄ + H₂S0₄ + H₂O solution in a horizontal channel is performed by using an electrochemical system. Unstable temperature and concentration gradients imposed by a heated cathodic bottom initiate an ascending (secondary) flow of light boundary-layer fluid into the freestream. To visualize the flow, the shadowgraph technique is used. Electrical measurements are used to obtain mass transfer rates and to infer a Sherwood number. The ranges of the parameters studied in the present work for the square channel are Pr = 5-7, Sc = 1,700-2,300, Re = 100-1,000, Gr_m= 1.27 X 10⁶ and Gr_ab = 4.06 × 10⁶-2.4S × 10⁷.     

Electrochemical behavior of organosoluble gold nanoclusters and its application

Journal of Solid State Electrochemistry - This contribution described the electrochemical study of organosoluble gold nanoclusters (AuNCs).The AuNCs were characterized with UV-vis absorption...     

Polymeric ytterbium(ii) complex with pyridyl amido ligands

The reaction of potassium pyridyl amido ligand {L = [N(R)(2-C5H3N-6-Me)]–, R = CH2But} with YbI2(thf)2 afforded the linear polymeric complex [K0.5(L)3YbiiK0.5]n, which was characterized by X-ray structure analysis.     

Role of Tryptophan in the Active Site of Plant Esterase: Chemical Modification and Fluorometric Studies

Plant esterase extracted from wheat flour play key roles in the spectrophotometric detection of organophosphorus compounds (OPs) for food safety and human health. The purpose of the present study was to investigate the role of tryptophan residues in the activity and structure of plant esterase by chemical modification and fluorometric studies. Active site characterization of purified plant esterase showed the involvement of tryptophan in the catalytic activity. Only one was essential for the enzyme activity by the Tsou’s analysis. Substrate protection experiments further confirmed that the tryptophan residue was located at the substrate-binding site. Fluorescence quenching studies elucidated that the tryptophan residues were largely exposed to the solvent, and a smaller fraction of the surface tryptophan residues had electropositively charged amino acids around them. Experimental results obtained here are expected to promote the applications of plant esterase in OPs detection. Further confirmation of the existence of other critical residues and detailed explanation of their functions were also required for the elucidation of the mechanism involved in the detection of OPs.