相对论电子束真实发射度在线磁扫描测量系统

介绍了清华大学研制的相对论电子束（４～１０ＭｅＶ）真实发射度的测量系统，利用该系统测量了４ＭｅＶ驻波电子直线加速器的真实发射度，并且研究了该系统的测量误差和测量范围，实践表明。     

闪光X射线高速摄影荧光转换屏的设计和性质研究

本文描述了用于中间弹道高速摄影荧光转换屏的设计特点、性能测试和实验结果。文中讨论了Gd2O2S:Tb和(Zn,Cd)S对X射线的吸收系数、发光效率以及荧光光谱与变象管S-20阴极光谱灵敏度曲线相匹配的相关曲线;测试了转换屏的相对发光强度、分辨率及其余辉。实验证明本屏发光亮度比钨酸钙屏高60倍左右,屏分辩率达51p/mm,余辉时间为8μs,多幅摄影结果证明第一幅的图象对第二幅照片无“拖尾”现象,本屏已达到了中间弹道高速摄影转换屏的实用水平。     

10m×10m大靶面激光立靶设计

针对10m×10m大靶面、高精度立靶坐标测量的要求,提出了一种激光阵列式光电立靶坐标测量系统,该立靶采用半导体激光平行光管形成平行光光源,高灵敏度光电二极管及相应信号放大、转换电路组成接收阵列,光源和接收器件相距10m,当飞行弹丸穿越激光形成的光幕时,分别在X和Y方向上挡住了投射在某一个或几个光电二极管上的光线,该光电二极管对应的信号放大、转换电路将二极管产生的微弱电信号放大、整形,最后输出脉冲信号,后续信号编码识别电路将判断出被挡住光线的光电二极管的编号,进而得出弹丸穿越该光幕的X坐标和Y坐标。经实弹试验证明,系统具有测量靶面大,精度高的优点。     

高斯型弱散射屏产生的像面散斑场的分布特性研究

弱散射屏产生的远场散斑由一个中央亮斑和一个分布于亮斑周围而与正态散斑类似的散斑结构, 根据弱散射屏远场的散斑图样, 人们假设弱散射屏产生的像面散斑为均匀背景与正态散斑两者相干叠加的结果, 但这种假设与实际像面散斑存在歧异, 基于上述情况, 本文利用4f高通滤波光学成像系统, 研究了高斯型弱散射屏产生的像面散斑场的统计特性, 得出只有表面均方根粗糙度与入射光波的波长相差不多时上述假设才是可行的结论. 关键词： 弱散射屏 f光学成像系统')" href="#">4f光学成像系统 像面散斑     

The electrochemistry of arylated anthraquinones in room temperature ionic liquids

Arylated anthraquinone derivatives of different sizes and different π‐basicities have been prepared, and the electrochemical behaviour of these substances has been studied on screen printed graphite electrodes in the three room temperature ionic liquids (RTILs), 1‐butyl‐3‐methylimidazolium hexafluorophosphate ([C₄MIM][PF₆]), 1‐hexyl‐3‐methylimidazolium hexafluorophosphate ([C₆MIM][PF₆]) and 1‐octyl‐3‐methylimidazolium hexafluorophosphate ([C₈MIM][PF₆]). Half redox potentials for the first and second one electron reduction waves were identified, and the diffusion coefficient values were estimated from cyclic voltammetry measurements. The influence of the nature of the RTIL and of the substitution pattern of the anthraquinone on the solvodynamic radii were studied. A correlation of the reductive potentials with the corresponding Hammett constants of the substituents was tested. Copyright © 2013 John Wiley & Sons, Ltd.     

Practical High-Throughput Method to Screen Compounds for Anthelmintic Activity against Caenorhabditis elegans

In the present study, we established a practical and cost-effective high throughput screening assay, which relies on the measurement of the motility of Caenorhabditis elegans by infrared light-interference. Using this assay, we screened 14,400 small molecules from the “HitFinder” library (Maybridge), achieving a hit rate of 0.3%. We identified small molecules that reproducibly inhibited the motility of C. elegans (young adults) and assessed dose relationships for a subset of compounds. Future work will critically evaluate the potential of some of these hits as candidates for subsequent optimisation or repurposing as nematocides or nematostats. This high throughput screening assay has the advantage over many previous assays in that it is cost- and time-effective to carry out and achieves a markedly higher throughput (~10,000 compounds per week); therefore, it is suited to the screening of libraries of tens to hundreds of thousands of compounds for subsequent evaluation and development. The present phenotypic whole-worm assay should be readily adaptable to a range of socioeconomically important parasitic nematodes of humans and animals, depending on their dimensions and motility characteristics in vitro, for the discovery of new anthelmintic candidates. This focus is particularly important, given the widespread problems associated with drug resistance in many parasitic worms of livestock animals globally.     

Rapid Determination of Phenolic Compounds in Water Samples: Development of a Paper‐based Nanobiosensor Modified with Functionalized Silica Nanoparticles and Potato Tissue

In this study, we present a fast, simple, low‐cost and disposable method for determination of phenolic content in water samples, using a paper based polyphenol oxidase biosensor. The propylamine functionalized silica nanoparticles was dropped onto a paper sheet. After drying at room temperature, the potato tissue extract including polyphenol oxidase was immobilized on the paper via physical and chemical adsorption. The modified paper was placed on the top of the graphite screen printed electrode. To construct of an electrochemical nanobiosensor, the electrochemical behavior of the modified electrode in different steps was investigated by cyclic voltammetry and electrochemical impedance spectroscopy methods. After being optimized the effective parameters, the changes in the biosensor electrochemical response vs. to the different concentrations of the substrate (phenol solution) were monitored by differential pulse voltammetry and amperometry methods. The linear relationships for phenol detection were obtained in the concentration ranges of 0.01–160 μM and 0.1–300 μM with a detection limit of 0.007 μM and 0.042 μM with DPV and amperometry methods, respectively. This method was successfully used in the voltammetric determination of the phenol content in the real samples, like the river water and the wastewater of wood factory.     

基于对氨基苯硼酸修饰磁性纳米粒子及丝网印刷技术测定糖化血红蛋白

制备了对氨基苯硼酸修饰的磁性纳米粒子,其与血液中的糖化血红蛋白(Hb A1c)结合,通过网状玻璃态碳(RVC)电极的磁性区域后,可实现与未糖基化的血红蛋白分离。通过壳聚糖(CS)、正硅酸乙酯(TEOS)和碳纳米管构成的溶胶-凝胶膜修饰丝网印刷电极对血红蛋白进行电化学检测,从而建立了一种用于检测糖化血红蛋白的新方法。在0.10 V电位下,丝网印刷电极的电量与Hb A1c和Hb的浓度有较好的线性关系,检出限分别为6 mg/m L和0.05 mg/m L。该方法电极制作简单,有较好的重现性和稳定性,且能有效排除抗坏血酸(AA)、尿酸(UA)等的干扰,已成功应用于实际样品中Hb A1c的检测。     

Cobalt nanoparticles anchored to porous silicon as a novel modifier for the construction of enzyme‐free hydrogen peroxide screen‐printed sensor

In this work, a screen‐printed carbon electrode (SPCE) was modified with a cobalt/porous silicon (Co@PSi) nanocomposite powder to develop a nonenzymatic sensor for the detection of hydrogen peroxide. The Co@PSi nanocomposite was synthesized through the chemical reaction between silicon powder in a HF/HNO₃ solution and cobalt cations. In this process, cobalt nanoparticles were anchored on the porous silicon. The structure and morphology of the synthesized nanocomposite were investigated by X‐ray diffraction, Fourier transform infrared spectroscopy, X‐ray photoemission spectroscopy, energy dispersive X‐ray spectroscopy, and field‐emission scanning electron microscopy. The constructed nonenzymatic, screen‐printed sensors based on the Co@PSi nanocomposite showed perfect electrocatalytic oxidation response to hydrogen peroxide over the range 1–170 and 170–3,770 μmol/L with the limit of detection of 0.8 μmol/L. In addition, the Co@PSi‐SPCE sensor exhibited good selectivity for the determination of H₂O₂ in the presence of common interfering species including glucose, ascorbic acid, uric acid, dopamine, nitrate, and nitrite ions. The constructed electrochemical sensor was successfully used for the determination of H₂O₂ in real samples.     

An electrochemical sensor based on TiO2/activated carbon nanocomposite modified screen printed electrode and its performance for phenolic compounds detection in water samples

Herein, we reported a titanium oxide (TiO₂) modified activated carbon nanocomposite that showed advantageous characteristics in terms of electro-conductivity, catalytic activity and surface area. The designed nanocomposite was employed to modify the screen printed carbon electrode transducer surface in the construction of an electrochemical sensor. The electrode surface modification was characterised by cyclic voltammetry and impedimetric studies. The modified transducer surface was subsequently used for the detection of four phenolic endocrine disruptors, p-nitrophenol, hydroquinone, catechol and 1-naphtol. Under optimal conditions, TiO₂ modified activated carbon sensor was evaluated by differential pulse voltammetry showing a good linearity with correlation coefficients higher than 0.99. It showed, in parallel, a high sensitivity where the detection limits were 348 ng/L, 110.1 ng/L, 3.3 ng/L and 7.2 µg/L for the respective studied compounds (S/N = 3). Finally, we validated the method with river water samples, and good recovery values were obtained showing the potential application of the reported biosensor.