The rapid uncertainty prediction of the ocean-acoustic coupled model

Focusing on the rapid prediction of acoustic field uncertainty in environment with temporal and spatial sound speed perturbation, evolvement of sound speed structure over time is predicted based on the ocean-acoustic coupled model to obtain the uncertainty distribution of the vertical structure of sound speed. Further, a method combining the arbitrary polynomial chaos expansion with the empirical orthogonal function is proposed to reduce the dimensionality of uncertain parameters and to obtain the uncertainty distribution of the acoustic field. Simulations have shown that the computational complexity can be reduced by 2 orders of magnitude compared to the conventional polynomial chaos expansion while ensures the same precision.Moreover, the computational complexity is not influenced by the complexity of the sound speed profile. The acoustic field and uncertainty predicted in uncertain environment by proposed method also have been tested with the experimental data.     

分光光度法测定蒙药中痕量铅

采用双硫腙显色分光光度法测定蒙药中痕量铅,该方法具有简单、快速、灵敏等特点,用以测定蒙药中的痕量铅,获得了满意的结果.该方法线性范围为0.00-0.40μg/mL Pb2 ,相关系数0.9993.回收率95%-ll0%.     

航空胶片冲洗机直流电机调速控制系统设计

针对航空胶片冲洗机控制困难表现其电机负载不均匀，低速运行情况下电机震动剧烈．研制了专用的反馈控制系统．以双89C51单片机为核心组成控制电路，编写了系统操作程序和数字PID控制程序．对PID参量对控制系统稳定性的影响进行了分析，得出适应于本系统的PID控制规律，并经过大量的试验，获得了能使各档速度稳定运行下的PID控制参量．实践表明，该控制系统运行稳定可靠，低速控制准确度在3％以内，中高速准确度达到1％．     

Photooxidation of lens proteins with xanthurenic acid: a putative chromophore for cataractogenesis.

The tryptophan metabolite, xanthurenic acid (Xan), is produced through a transamination reaction in high concentrations in human lenses with age and has been isolated from aged human cataractous lenses. It has appreciable absorption between 300 and 400 nm (lambda max = 334 nm), the range absorbed by the human lens. Our recent studies have shown that unlike most tryptophan metabolites in the eye, Xan is photochemically active, producing both superoxide and singlet oxygen. To determine if Xan could act as a photosensitizer and photooxidize cytosolic lens proteins, alpha-, beta- and gamma-crystallins were irradiated (lambda > 300 nm, 12 mW/cm2) in the presence and absence of Xan. Upon irradiation and in the presence of Xan, lens proteins polymerized in the order alpha > beta > gamma as assessed by sodium dodecyl sulfate polyacrylamide gel electrophoresis. Further analysis of the photolyzed alpha-crystallin by mass spectrometry indicated that histidine, tryptophan and methionine residues were oxidized at specific positions in a dose-dependent (irradiation time) manner. In alpha A-crystallin two forms of oxidized histidine 154 were observed, 2-imidazolone and 2-oxohistidine. Our results suggest that naturally occurring Xan is a chromophore capable of photosensitization and photooxidation of lens proteins. Furthermore, this compound could play a role in age-related cataractogenesis.     

非线性抛物型偏积分微分方程的H1-Galerkin 混合有限元方法

收稿给出一类非线性抛物型偏积分微分方程的H1-Galerkin混合有限元方法.给出了一维空间的半离散、全离散格式及最优阶误差估计,并将该方法推广到二维和三维空间.     

Strong Photoluminescence Enhancement from Colloidal Quantum Dot Near Silver Nano-Island Films

We present the fabrication and optical investigation of highly random self-assembled, nano-scale films, probing their influence on the luminescence properties of near surface CdSe/ZnS colloidal quantum dots. When compared to quantum dots distributed on unstructured quartz substrates, the average luminescence intensity is found to be enhanced by a factor of 160×. The silver nanoparticles are prepared using slow thermal evaporation on quartz substrates and post-deposition annealing to produce a randomly-arranged layer of smooth nano-islands. Clear polarization dependent hot spots are observed. Such hot spots deliver a maximal enhancement of the emission intensity of 240× and have a spatial density of (0.050±0.002) μm^− 2. The results show that silver nano-island films strongly enhance the optical efficiency of near quantum dots emitters.     

Sparse asymptotic minimum variance based bearing estimation algorithm for a single vector hydrophone

For underwater target detection using a single vector hydrophone, sparse asymptotic minimum variance(SAMV) method is used to estimate the target bearing. The SAMV discretizes the entire scanning space and the target bearing is located at the position of the discrete direction. The SAMV algorithm utilizes the sparsity of the spatial signal to improve the estimation performance of the target bearing. Background noise level(BNL) of the bearing estimation of SAMV algorithm is lower than those of the conventional beam forming(CBF)method and minimum variance distortionless response(MVDR) method for different signal noise ratios(SNRs). When the SNR is higher than 0 d B, the direction-finding error of this algorithm is less than 2°. Moreover, the SAMV algorithm has a better dimensional orientation resolution capability. The experimental results show that the SAMV algorithm gives a bearing and time recording map with a lower BNL, which effectively verifies the effectiveness of SAMV algorithm in terms of underwater target detection.     

离子交换色谱法分离测定磷霉素的研究

分别采用全多孔型硅胶基键合强阴离子交换柱与氨丙基键合硅胶柱，在低波长 ２００ ｎｍ 处检测，分离测定了磷霉素 探讨了流动相条件，如ｐ Ｈ 值、离子强度等对磷霉素保留及分离选择性的影响，优化分离条件，建立了一种测定磷霉素的高效液相色谱新方法方法简便、快速     

Laser Machined Plastic Laminates: Towards Portable Diagnostic Devices for Use in Low Resource Environments

Despite significant progress in development of bioanalytical devices cost, complexity, access to reagents and lack of infrastructure have prevented use of these technologies in resource‐limited regions. To provide a sustainable tool in the global effort to combat infectious diseases the diagnostic device must be low cost, simple to operate and read, robust, and have sensitivity and specificity comparable to laboratory analysis. In this mini‐review we describe recent work using laser machined plastic laminates to produce diagnostic devices that are capable of a wide variety of bioanalytical measurements and show great promise towards future use in low‐resource environments.     

N‐Alkoxyheterocycles As Irreversible Photooxidants

Irreversible photooxidation based on N–O bond fragmentation is demonstrated for N‐methoxyheterocycles in both the singlet and triplet excited state manifolds. The energetic requirements for bond fragmentation are studied in detail. Bond fragmentation in the excited singlet manifold is possible for ππ* singlet states with energies significantly larger than the N–O bond dissociation energy of ca 55 kcal mol^?1. For the nπ* triplet states, N–O bond fragmentation does not occur in the excited state for orbital overlap and energetic reasons. Irreversible photooxidation occurs in the singlet states by bond fragmentation followed by electron transfer. Irreversible photooxidation occurs in the triplet states via bimolecular electron transfer to the donor followed by bond fragmentation. Using these two sensitization schemes, donors can be irreversibly oxidized with oxidation potentials ranging from ca 1.6–2.2 V vs SCE. The corresponding N‐ethylheterocycles are characterized as conventional reversible photooxidants in their triplet states. The utility of these sensitizers is demonstrated by irreversibly generating the guanosine radical cation in buffered aqueous solution.