双路激光混沌复用系统的混沌同步及安全性能研究

针对一种新型的双路激光混沌复用系统, 建立相应的速率方程模型, 详细分析了两个主激光器的单个参数失配、多个参数同时失配、反馈强度差异以及频率失谐对混沌同步性能的影响, 并对此复用系统的安全性能和频谱性能进行了研究. 研究结果表明: 采用参数失配方案, 通过合理选择两个主激光器的参数, 可以保证两个主激光器之间的同步性能较差而两对主从激光器间实现高品质的混沌同步, 因此满足双路激光混沌复用的条件; 两个主激光器之间的参数失配对它们之间的同步性能影响较大, 然而对配对主从激光器间同步性能的影响并不明显, 进一步说明参数失配方案的有效性和可行性. 另外, 通过自相关函数和频谱分别分析混沌复用信号的时域和频域特征, 发现双路激光混沌复用系统可提供更高的安全性.     

铽掺杂羟基磷灰石的制备及其荧光特性

在室温下采用化学沉淀法制备了铽掺杂的羟基磷灰石(Tb-HAP),通过X射线衍射分析(XRD)、傅里叶变换红外光谱(FT-IR)和荧光光谱(PL)等对其结构和荧光性能进行了表征分析。XRD和FT-IR测试表明,Tb³⁺的掺杂对羟基磷灰石的结构没有显著影响。荧光光谱分析表明:在545 nm波长监测下,测得的最佳激发波长为378 nm。样品的发光强度随Tb³⁺在样品中的掺杂摩尔分数先增大后减小,在8%时发光最强。此外,Tb-HAP样品的荧光寿命随着Tb³⁺掺杂摩尔分数的增加呈现减小的趋势。     

路径约束条件下车辆行为的时空演化模型

复杂地理环境下车辆运行线路具有空间三维特征, 它对车辆行为的约束是显然的, 非一维空间和二维空间所能描述. 将复杂地理环境下车辆运行线路抽象为空间曲线, 引入微分几何理论, 利用弧长、曲率和挠率等几何不变量参数建立沿空间曲线运动的Serret-Frenet活动标架; 然后, 对空间曲线上任意一点处Serret-Frenet标架具有时变属性的动态行为进行数学描述, 进而建立路径约束条件下车辆行为的时空演化模型, 并在数学上严格证明了所建时空演化模型适用于车辆(Serret-Frenet标架)直线运行和做匀速圆周运动的特殊情形. 为后续复杂地理环境中交通线路上的车辆跟驰、变道等微观行为和交通流宏观行为研究, 奠定了理论基础.     

非均匀光纤中暗孤子传输特性研究

由于变系数非线性Schrödinger方程的增益、色散和非线性项都是变化的, 根据方程这一特点可以研究光脉冲在非均匀光纤中的传输特性. 本文利用Hirota方法, 得到非线性Schrödinger方程的解析暗孤子解. 然后根据暗孤子解对暗孤子的传输特性进行讨论, 并且分析各个物理参量对暗孤子传输的影响. 经研究发现, 通过调节光纤的损耗、色散和非线性效应都能有效的控制暗孤子的传输, 从而提高非均匀光纤中的光脉冲传输质量. 此外, 本文还得到了所求解方程的解析双暗孤子解, 最后对两个暗孤子相互作用进行了探讨. 本文得到的结论有利于研究非均匀光纤中的孤子控制技术.     

基于多摄像机的航空器滑行冲突检测研究

对机场场面航空器滑行冲突检测进行了研究,分析了基于多摄像机的航空器滑行冲突检测流程,基于图像识别和目标跟踪技术,提取航空器的滑行轨迹,提出了基于DCPA(distance of closest point of approach)和TCPA(time of closet point of approach)的滑行冲突检测模型,开发了基于多摄像机的航空器滑行冲突检测原型系统并应用于西南某通航机场;实验结果表明,基于多摄像机视频目标跟踪和冲突检测模型可有效地检测机场场面航空器的滑行冲突,可作为中小机场主要监视手段以及大型机场场监雷达系统的辅助,防止航空器机场滑行冲突,提高机场场面运行安全和效率。     

砷化镓光阴极直流高压注入器研究进展

主要介绍自由电子激光相干强太赫兹源(FEL-THz)装置上的砷化镓光阴极直流高压注入器的研究进展,并讨论其驱动未来高重复频率短波长自由电子激光器的差距。通过综合砷化镓阴极寿命的三大影响因素,提出了其工作寿命的定性物理模型;通过该模型对阴极和注入器进行优化,在直流高压电子枪上得到了5mA,32min的连续稳定输出;测量了电子束在4.8mA下归一化发射度约为4.0πmm·mrad,阴极热发射度约为0.6πmm·mrad,电子束本征横向能量约为92meV,250keV电子束在距离阴极90.6cm处纵向均方根长度约为11.5ps。这一束流状态已经基本满足FEL-THz需求。     

Direct on-strip analysis of size- and time-resolved aerosol impactor samples using laser induced fluorescence spectra excited at 263 and 351 nm

We report a novel atmospheric aerosol characterization technique, in which dual wavelength UV laser induced fluorescence (LIF) spectrometry marries an eight-stage rotating drum impactor (RDI), namely UV-LIF-RDI, to achieve size- and time-resolved analysis of aerosol particles on-strip. The UV-LIF-RDI technique measured LIF spectra via direct laser beam illumination onto the particles that were impacted on a RDI strip with a spatial resolution of 1.2 mm, equivalent to an averaged time resolution in the aerosol sampling of 3.6 h. Excited by a 263 nm or 351 nm laser, more than 2000 LIF spectra within a 3-week aerosol collection time period were obtained from the eight individual RDI strips that collected particles in eight different sizes ranging from 0.09 to 10 μm in Djibouti. Based on the known fluorescence database from atmospheric aerosols in the US, the LIF spectra obtained from the Djibouti aerosol samples were found to be dominated by fluorescence clusters 2, 5, and 8 (peaked at 330, 370, and 475 nm) when excited at 263 nm and by fluorescence clusters 1, 2, 5, and 6 (peaked at 390 and 460 nm) when excited at 351 nm. Size- and time-dependent variations of the fluorescence spectra revealed some size and time evolution behavior of organic and biological aerosols from the atmosphere in Djibouti. Moreover, this analytical technique could locate the possible sources and chemical compositions contributing to these fluorescence clusters. Advantages, limitations, and future developments of this new aerosol analysis technique are also discussed.     

Use of a porous silicon–gold plasmonic nanostructure to enhance serum peptide signals in MALDI-TOF analysis

Small peptides in serum are potential biomarkers for the diagnosis of cancer and other diseases. The identification of peptide biomarkers in human plasma/serum has become an area of high interest in medical research. However, the direct analysis of peptides in serum samples using mass spectrometry is challenging due to the low concentration of peptides and the high abundance of high-molecular-weight proteins in serum, the latter of which causes severe signal suppression. Herein, we reported that porous semiconductor-noble metal hybrid nanostructures can both eliminate the interference from large proteins in serum samples and significantly enhance the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) yields of peptides captured on the nanostructure. Serum peptide fingerprints with high fidelity can be acquired rapidly, and successful discrimination of colorectal cancer patients based on peptide fingerprints is demonstrated.     

Pesticide Multi-Residue Analysis in Tea Using d-SPE Sample Cleanup with Graphene Mixed with Primary Secondary Amine and Graphitized Carbon Black Prior to LC–MS/MS

Graphene is a novel class of carbon nanostructures with ultrahigh specific surface area. Graphene has already been used in many fields and has great promise for use in sorbent materials. In this study, we used graphene mixed with primary secondary amine (PSA) and graphitized carbon black (GCB) as dispersive solid-phase extraction materials for the cleanup of tea for the first time. Compared to the literature, the amount of PSA and GCB was greatly reduced. A multi-residue method combined with liquid chromatography–tandem mass spectrometry was validated for rapid determination of 25 pesticide residues in tea. Green tea, black tea, and white tea were selected as matrixes, representing the majority of tea types. Recoveries ranged from 71.1 to 108.3 % and consistent relative standard deviations <13.6 % for all 25 pesticides. Graphene has significant potential as a promising new adsorbent for pesticide residue analysis of teas. This method can be used to analyze tea samples with different degrees of fermentation.     

Native Protein Separation by Isoelectric Focusing and Blue Gel Electrophoresis-Coupled Two-Dimensional Microfluidic Chip Electrophoresis

The use of microfluidic chip-based two-dimensional separation holds great promise in the proteomics field, given its portability, simplicity, speed, efficiency, and throughput. However, inclusion of sodium dodecyl sulfate, reported to be necessary for increasing protein-resolving capability, was also accompanied by the loss of both protein conformation and biological function. Here, we describe separation of native proteins by introducing blue native gel electrophoresis into isoelectric focusing and gel electrophoresis (IEF/CGE)-coupled protein two-dimensional microfluidic chip electrophoresis. After assessing the influence of various experimental conditions, the best separation ability and reproducibility of blue native IEF/CGE (IEF/BN-CGE) chip electrophoresis achieved until now were demonstrated no matter whether with a simple simulated mixture or with a complex mixture of total Escherichia coli proteins. Finally, instead of theoretical calculations, the image analysis technique was also used for the first time to quantitatively evaluate the actual peak capacities of chip electrophoresis. According to the number of features abstracted in the electrophoresis patterns, the superiority of the IEF/BN-CGE two-dimensional microfluidic chip electrophoresis was then exhibited quantitatively. The high native protein separation performance makes this established chip electrophoresis method possible for further application in widely needed drug screening, analysis of bio-molecular function, and assays of protein–protein interactions.