旋涂速度对制备P3HT有机场效应晶体管性能的影响

采用溶液化的方法制备了以PMMA为绝缘层、P3HT为有源层的有机场效应晶体管.研究了P3HT有源层和PMMA绝缘层的旋涂速度对器件性能的影响.实验结果表明,当P3HT和PMMA的旋涂速度均为2 000 r/min时,器件的性能最佳.峰值场效应迁移率为6.84×10^-2 cm²·V^－1·s^－1.结果表明,选择适当的旋涂速度是一种有效提高溶液化制备有机场效应晶体管性能的方法.     

基于多导体传输线理论的差模激励新型线束串扰模型研究

传统的线束串扰模型只是在系统内共模激励的基础上建立的, 没有考虑系统间差模激励下线束串扰的情况. 针对差模激励下系统独立回路间线束串扰的物理问题, 提出了一种基于多导体传输线理论的差模激励新型线束串扰的计算方法.该方法根据差模激励下线间的耦合机理, 利用传输线传播横向电磁模式得到新型三导体传输线寄生参数电路及数学矩阵模型, 通过镜像法以及诺埃曼公式推导出寄生参数的计算公式, 并在频域内得到新型线束串扰的链参数矩阵方程, 根据新型差模串扰模型始端、终端边界条件最终得到串扰电压的频域解.以差模激励下平行双线回路对其他回路受扰线的串扰为例, 通过仿真受扰线不同布置情况下的串扰电压, 得到了差模激励源的线束间串扰的物理规律, 即受扰线位于差模回路之间时所受的串扰要远大于位于回路外时所受的串扰, 并验证所提出的模型及方法可以计算不同频率差模激励引起的干扰. 利用解析的方法解决了线束串扰中差模激励下的导线串扰问题, 为实际中如大量导线的捆扎以及导线干扰的预测等电磁兼容问题提供了理论依据, 具有指导意义, 完善了多导体传输线理论在线束串扰中的应用.     

基于单片机的电缆导通测试方法 

文章介绍了一种基于单片机的电缆导通测试方法。该方法以小型化、智能化为目标,采用了嵌入式设计,不仅使测试系统的体积大幅度降低,而且使操作界面更加简洁方便;系统采用C8051F120单片机做为核心控制器,以及技术成熟的万用表作为测量模块;通过设计接口电路,实现了单片机与液晶显示模块、微型打印机模块和键盘模块的互通;通过使用移位寄存器和继电器阵列,系统也实现了多个通道间的切换;系统用单片机驱动外部测量模块,完成了某型伺服系统电缆束的导通、不导通的测试;该测试方法改变了一直以来电缆导通测试需要依赖人工手动测试的现状,同时提高了测试的效率和准确性。     

Simultaneous determination of ascorbic acid,dopamine and uric acid based on tryptophan functionalized graphene

A new type of tryptophan-functionalized graphene nanocomposite (Trp-GR) was synthesized by utilizing a facile ultrasonic method via π–π conjugate action between graphene (GR) and tryptophan (Trp) molecule. The material as prepared had well dispersivity in water and better conductivity than pure GR. The surface morphology of Trp-GR was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Raman spectroscopy. The electrochemical behaviors of ascorbic acid (AA), dopamine (DA), and uric acid (UA) were investigated by cyclic voltammetry (CV) on the surface of Trp-GR. The separation of the oxidation peak potentials for AA–DA, DA–UA and UA–AA was about 182 mV, 125 mV and 307 mV, which allowed simultaneously determining AA, DA, and UA. Differential pulse voltammetery (DPV) was used for the determination of AA, DA, and UA in their mixture. Under optimum conditions, the linear response ranges for the determination of AA, DA, and UA were 0.2–12.9 mM, 0.5–110 μM, and 10–1000 μM, with the detection limits (S/N = 3) of 10.09 μM, 0.29 μM and 1.24 μM, respectively. Furthermore, the modified electrode was investigated for real sample analysis.     

Analysis of Cembranoids in Flue‐cured Tobacco by Accelerated Solvent Extraction and Gas Chromatography‐Mass Spectrometry‐Selected Ion Monitoring

An efficient and sensitive analytical method based on accelerated solvent extraction (ASE) and gas chromatography‐mass spectrometry‐selected ion monitoring (GC‐MS‐SIM) was developed and validated for analysis of cembranoids in flue‐cured tobacco leaves. Extraction efficiency of different pretreatment methods including liquid‐solid extraction (LSE), ultrasound‐assisted extraction (UAE), Soxlet extraction and accelerated solvent extraction (ASE) was compared and ASE was chosen as the optimal extraction method. During ASE procedure, effect of four parameters on extraction efficiency was considered and the experimental conditions were selected as follows: extraction solvent: dichloromethane; oven temperature: 50 °C; static time: 5 min and number of cycles: 2. Working standards of cembranoids were isolated by silica gel column chromatography and the identification was performed by mass spectrometry. Performance characteristics such as linearity, limit of detection (LOD), limit of quantitation (LOQ), precision and recovery were studied. The LOD and LOQ values were ranging from 5.0 × 10^?3 to 6.9 × 10^?3 μg/mL and 1.7 × 10^?2 to 2.3 × 10^?2 μg/mL for all analytes. At three different spiked levels, recoveries for CBT‐ol, α‐CBT‐diol and β‐CBT‐diol were 94.6%‐105.1%, 93.0%‐97.2% and 88.7%‐107.5% while the relative standard deviations (RSDs) were in the ranges of 3.9%‐6.2%, 1.8%‐8.7% and 1.7%‐6.0%, respectively. The proposed analytical methodology was successfully applied in the analysis of cembranoids in tobacco samples.     

LC–MS–MS Method to Simultaneously Determine Six Probe Drugs for CYP450 Isozymes in Human Liver Microsomes

Here, we report a rapid and specific method based on high-performance liquid chromatography coupled with tandem mass spectrometry (LC–MS–MS) capable of quantifying six CYP450-specific probe substrates in human liver microsomal incubation mixtures simultaneously. These analytes were prepared by single-step extraction and detected in one run by switching polarity of electrospray ionization mode three times. Following optimization of the chromatographic conditions, the peaks were well separated, and retention times ranged between 2.0 and 8.4 min. The total run time for a single injection was within 9 min. This method was fully validated over linear range of 18.8–3,000.0 ng mL^?1 for diclofenac, 0.8–3,000.0 ng mL^?1 for dapson, 1.5–3,000.0 ng mL^?1 for dextromethorphan, 2.0–4,000.0 ng mL^?1 for omeprazole, 75.0–3,000.0 ng mL^?1 for chlorzoxazone and 0.8–3,000.0 ng mL^?1 for phenacetin using diazepam as internal standard. Samples were prepared by protein precipitation and analyzed on the LC–MS–MS equipped with ESI interface. For each analyte, inter- and intra-day precision (RSD%) were <15 % and accuracy was within 85–115 %. The specificity, precision, accuracy, stabilities and matrix effect were evaluated.     

Quantification of Ocular Biologically Effective UV Exposure for Different Rotation Angle Ranges Based on Data from a Manikin

Human outdoor activities are randomly orientated at different angles to the sun. To quantify the ocular UV and biologically effective UV (UVBE; i.e. the ocular UV irradiance exposure for photokeratitis (UVpker), photoconjunctivitis (UVpcon), and cataract (UVcat)) exposure for different rotation angle ranges, a rotating manikin was used to monitor the ocular UV exposure at different rotation angles in clear skies during July 2010 in Sanya, China. As a result, the ocular UV and UVBE irradiance was directly influenced by the rotation angle variations, primarily for the 120° rotation angle ranges facing the morning and afternoon sun when the solar elevation was lower than 60°; during these times, the UV and UVBE spectral irradiance decreased as the rotation angle increased. When compared to the 360° rotation angle ranges (which were considered to be the average exposure situation), the cumulative ocular UVBE for 60°, 120° and 180° rotation angle ranges were maximally 91% (UVcat), 94% (UVpker) and 121% (UVpcon); 71% (UVcat), 74% (UVpker) and 95% (UVpcon); 42%(UVcat), 45%(UVpker) and 55% (UVpcon) higher respectively. Meanwhile, the cumulative ocular UVBE for the 180° rotation angle ranges facing away from the sun were 46% (UVpker), 59% (UVpcon) and 45% (UVcat) lower.     

Risk of Ocular Exposure to Biologically Effective UV Radiation in Different Geographical Directions

To quantify ocular exposure to solar ultraviolet radiation (UVR) and to assess the risk of eye damage in different geographical directions due to UVR exposure, we used a spectrometer and a manikin to measure horizontal ambient and ocular exposure UVR in different geographical directions at four different locations at the Northern Hemisphere. Describing the relationship of exposure to risk of eye damage requires the availability of UV hazard weighting function. So, we used the UV hazard weighting function (ICNIRP) proposed by International Commission on Non‐Ionizing Radiation Protection to determine the biologically effective UV irradiance (UVBE_eye) and then cumulative effective radiant exposure (H_eye) to shown the risk of eye. We found that in different geographical directions, distributions of ocular exposure to UVR were markedly different from those of horizontal ambient UVR. When the midday maximum SEA > 50°, eye received more UVR from the east and west directions during the morning and evening hours, respectively. However, when the midday maximum SEA < 50°, eye received more UVR from the south direction at noon. The results of this research indicate that the higher risk of eye caused by UVR varies according to the midday maximum SEA corresponding to different geographical direction.     

Investigation on “Excimer” Formation Mechanism of Linear Oligofluorenes‐Functionalized Anthracenes by Using Transient Absorption Spectroscopy

We study the photophysical characters of two oligofluorenes‐functionalized anthracenes molecules with different fluorine‐vinylene (FV) units, which exhibits that “excimer” state appears in the solution after photoexcitation. The dynamic data shows that two mechanisms are responsible for the generation of “excimer”. The fast one is controlled by the arene‐arene interaction between molecules and the slow one is influenced by the diffusion motion of molecules. Increasing the number of FV units may suppress the DM‐dependent “excimer” and enhance the yield of intrinsic fluorescence, which finally improves the fluorescence property of molecules in solution.     

Sinulariols A-S, 19-oxygenated cembranoids from the Chinese soft coral Sinularia rigida

Chemical examination of a Chinese soft coral Sinularia rigida resulted in the isolation and characterization of 19 new cembrane-type diterpenoids, designated as sinulariols A-S (1-19). Their structures were determined on the basis of extensive spectroscopic (2D NMR, IR, and MS) analysis in association with modified Mosher’s method. All compounds featured unusual 19-oxygenated functionalities, which are rarely found from cembranoid family. The biogenetic transformation of the isolated compounds is postulated. Part of the isolated cembranoids showed significant anti-fouling activity.