拓扑绝缘体(Bi0.5Sb0.5)2Te3薄膜中的线性磁阻

本文报道了拓扑绝缘体(Bi_0.5Sb_0.5)₂Te₃薄膜中线性磁阻问题的系统性研究工作. 此体系中, 线性磁阻在很宽的温度和磁场范围内出现: 磁场高达18 T时磁阻仍没有饱和趋势, 并且当温度不高于50 K时, 线性磁阻的大小对温度的变化不敏感. 栅压调控化学势可明显改变线性磁阻的大小. 当化学势接近狄拉克点时, 线性磁阻最为显著. 这些结果说明电荷分布的不均匀性是引起该材料线性磁阻的根源.     

高聚物减阻溶液对壁湍流输运过程的影响

基于相同雷诺数下清水和高分子聚合物溶液壁湍流的高时间分辨率粒子图像测速技术(time-resolved particle image velocimetry, TRPIV)的对比实验, 从高聚物溶液对湍流边界层动量能量输运影响的角度分析其减阻的机理. 对比两者的雷诺应力发现高聚物的存在抑制了湍流输运过程. 这一影响与高聚物对壁湍流中占主导地位的涡旋运动和低速条带等相干结构的作用密切相关. 运用条件相位平均、相关函数和线性随机估计(linear stochastic estimation, LSE)等方法, 分析提取了高聚物溶液流场中的发卡涡和发卡涡包等典型相干结构的空间拓扑形态. 相比于清水, 高聚物溶液中相干结构的流向尺度增大, 涡旋运动的发展及低速流体喷射的强度受到削弱, 表明了添加的高聚物阻碍了湍流原有的能量传递和自维持的机理. 正是通过影响相干结构, 高聚物抑制了湍流边界层中近壁区与外区之间的动量和能量输运, 使得湍流的无序性降低, 从而减小了湍流流动的阻力.     

不同滤波方法对揭示全球海洋条带结构的比较

海洋条带结构是近年物理海洋学研究的一个新热点. 在海洋中, 条带结构往往被大尺度环流过程所掩盖. 把这种隐蔽的海水运动现象显现出来的办法是对时间平均的速度场进行空间滤波. 利用全球简单海洋资料同化分析系统资料和中国科学院大气物理研究所大气科学和地球流体力学数值模拟国家重点实验室的气候系统海洋模式模拟数据对三种一维滤波方法进行了比较, 分别是常用的高斯和汉宁滤波方法, 以及本文引入的切比雪夫滤波方法. 结果表明, 尽管三种方法均可获得条带结构, 但以切比雪夫方法为最佳; 另外, 设计高通滤波器时需设定截断频率, 而它的选定取决于对具体数据的频谱分析, 当选取的归一化的截断频率值在0.1和0.4之间时, 可以有效地揭示出条带结构在全球海域内的分布. 因此本文的研究方法为海洋条带结构的深入研究提供了一个有力工具.     

多横模垂直腔面发射激光器及其波长特性

基于氧化限制型内腔接触垂直腔面发射激光器(VCSEL) 结构设计, 研究了VCSEL的多横模分布及其模式波长分裂特性与氧化孔径尺寸、形状的关系. 在实验基础上, 通过建立有效折射率模型, 并利用标量亥姆霍兹方程的迭代算法理论, 分别对椭圆形氧化孔径和圆形氧化孔径VCSEL的横向模式特性进行模拟研究, 计算得到不同形状孔径的多横模光场分布情况, 同时测量得到高阶横模多频输出光谱. 研究发现, 椭圆氧化孔形状不仅影响横模分布特性, 还会导致每个模式的波长产生分裂, 分裂值可达0.037 nm. 同时, 随着氧化孔径的增大, 波长分裂影响会逐渐减小, 直至趋近于圆形氧化孔径的分布特性. 研究结果为进一步实现氧化限制型VCSEL的多横模锁定提供了有益参考和借鉴.     

基于GPRS的输油管道阴极保护远程监测系统设计

为实现输油管道阴极保护系统的远程自动化监测与参数集中管理,开发了一种基于GPRS的分布式管道阴极保护参数远程监测系统;设计监测终端检测现场保护点的阴极电位、恒电位仪电压和阴极保护电流,采用GPRS无线网络以TCP/IP方式远传数据至监测中心工控机,实现了分布式多监测点阴极保护状态的在线监测与参数管理;运行测试结果表明,该系统稳定可靠,实现了对多站点、多通道数据的远程集中监测,阴极电位的检测精度达到了0.5%,可满足输油管线阴极保护的远程自动化监测需求。     

Simultaneous determination of the repertoire of classical neurotransmitters released from embryonal carcinoma stem cells using online microdialysis coupled with hydrophilic interaction chromatography–tandem mass spectrometry

Dynamic, continuous, and simultaneous multi-analysis of transmitters is important for the delineation of the complex interactions between the neuronal and intercellular communications. But the analysis of the whole repertoire of classical transmitters of diverse structure is challenging due to their different physico-chemical properties and to their high polarity feature which leads to poor retention in traditional reversed-phase columns during LC–MS analysis. Here, an online microdialysis coupled with hydrophilic interaction chromatography–tandem mass spectrometry (online MD-HILIC–MS/MS) detection method was developed for the simultaneous measurement of the repertoire of classical transmitters (acetylcholine, serotonin, dopamine, norepinephrine, glutamate, GABA, and glycine). Stable isotope labeled internal standards and authentic matrix have been applied to guarantee reliable results. The method was successfully employed to reveal the characteristics of transmitter release from embryonal carcinoma stem cells. The method features simple procedure (no sample preparation), high recovery (≥73%), high accuracy (89.36% ≤ RE ≤ 116.89%), good reproducibility (2.18% ≤ RSD ≤ 14.56%), and sensitive limits of detection (2 pg for acetylcholine, serotonin, and glutamate, 10 pg for dopamine, norepinephrine, GABA, and glycine). It can be flexibly applied to determine the contents of the classical transmitters in other biological matrix samples with minor changes.     

IR,Raman, and Surface‐enhanced Raman Spectroscopic Study on Triruthenium Dipyridylamide Diruthenium Nickel Dipyridylamide Family: Metal‐metal Bonding and Structures

We report the infrared, Raman, and surface‐enhanced Raman scattering (SERS) spectra of triruthenium dipyridylamido complexes and of diruthenium mixed nickel metal‐string complexes. From the results of analysis on the vibrational modes, we assigned their vibrational frequencies and structures. The infrared band at 323–326 cm^?1 is assigned to the Ru₃ asymmetric stretching mode for [Ru₃(dpa)₄Cl₂]^0–2+. In these complexes we observed no Raman band corresponding to the Ru₃ symmetric stretching mode although this mode is expected to have substantial Raman intensity. There is no frequency shift in the Ru₃ asymmetric stretching modes for the complexes with varied oxidational states. No splitting in Raman spectra for the pyridyl breathing line indicates similar bonding environment for both pyridyls in dpa^– , thus a delocalized structure in the [Ru₃]^6–8+ unit is proposed. For Ru₃(dpa)₄(CN)₂ complex series, we assign the infrared band at 302 cm^?1 to the Ru₃ asymmetric stretching mode and the weak Raman line at 285 cm^?1 to the Ru₃ symmetric stretching. Coordination to the strong axial ligand CN^– weakens the Ru‐Ru bonding. For the diruthenium nickel complex [Ru₂Ni(dpa)₄Cl₂]^0–1+, the diruthenium stretching mode ν_Ru‐Ru is assigned to the intense band at 327 and 333 cm^?1 in the Raman spectra for the neutral and oxidized forms, respectively. This implies a strong Ru‐Ru metal‐metal bonding.     

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.     

Fast Quantification of Salivary 8-Hydroxy-2′-deoxyguanosine as DNA Damage Biomarker Using CE with Electrochemical Detection

The aim of this study was to investigate the correlation between levels of a marker of oxidative DNA damage, 8-hydroxy-2′-deoxyguanosine (8-OHdG), in human saliva and urine, and to explore its potential application in fast diagnosis of many diseases (especially cancer) associated with oxidative damage. A simple and time-efficient method, based on capillary electrophoresis with electrochemical detection, was developed for the determination of salivary and urinary 8-OHdG. Under the optimum conditions, 8-OHdG and its coexisting analytes could be well separated within 16 min at a voltage of 14 kV in 60 mmol L^?1 borax running buffer (pH 8.2). A good linear relationship was established between peak current and concentration of analytes over three orders of magnitude with detection limits (S/N = 3) ranging from 0.41 × 10^?7 to 2.50 × 10^?7 mol L^?1 for all analytes.     

Diterpenoids from Aerial Parts of Clerodendranthus spicatus and Their Cytotoxic Activity

A chemical investigation of AcOEt‐soluble portion of the 95% EtOH extract of the aerial parts of Clerodendranthus spicatus led to the isolation and characterization of a new diterpenoid, named clerospicasin J ( 1 ). Structure elucidation of 1 was achieved by spectroscopic analyses, including 2D‐NMR. The diterpenoid 1 exhibited significant inhibitory activity on the proliferation of the SKOV3 cell lines. Moreover, the cytotoxicity of 1 against SKOV3 cells was related to apoptotis as confirmed by DAPI (=2‐(4‐amidinophenyl)‐1H‐indole‐6‐carboxamidine) nuclear staining and flow cytometry.