动态空域扇区划分管制员指派优化方法

以训练成本最小化为目标,构建了动态扇区划分管制员指派数学模型,通过引入虚拟扇区将模型设计成标准指派问题,为采用LINGO或MATLAB等工具求解奠定了基础.用空间集合抽象了管制员所管控扇区在扇区变动前后的位置关系,根据位置关系用代数式量化了指派成本.根据计算分析结果,提出了减少训练成本,缩短动态扇、区前置准备时间的建议措施.     

Highly directional spaser array for the red wavelength region

The spaser offers an opportunity to achieve coherent optical sources at nanometer scales due to the extreme confinement of optical fields. However, achievement of spasers with directional propagation in the visible wavelength region remains a challenge thus far, owing to the unique optical feedback mechanism and large dissipative losses of the metal cavity. Here, we experimentally demonstrate for the first time a spaser showing highly directional emission in the visible by using a periodic subwavelength hole array perforated in a metal film, which function as plasmonic nanocavities, along with an organic laser dye to supply gain. The lasing occurs in the red wavelength region and shows a single mode. It is suggested that the optical feedback for spasing is provided by the SPP–Bloch wave, which is supported by the fact that no spasing was attained in aperiodic holes as well as in periodic holes that do not support the SPP–Bloch wave at the spasing wavelength.     

Assessing dynamic inefficiency of the Spanish construction sector pre- and post-financial crisis

This paper undertakes the full decomposition of dynamic cost inefficiency into technical, scale and allocative inefficiency based on the dynamic directional distance function. The empirical application estimates dynamic inefficiency in the Spanish construction industry before and during the current financial crisis over the period 2001–2009. Static inefficiency measures are biased in a context of a significant economic crisis with large investments and disinvestments as they do not account for costs in the adjustment of quasi-fixed factors. Allocative inefficiency is smaller, while technical inefficiency is larger when using the dynamic compared to the static framework. Results further indicate that overall dynamic cost inefficiency is very high with technical inefficiency being the largest component, followed by allocative and scale inefficiency. Moreover, overall dynamic cost inefficiency is significantly larger before the beginning of the financial crisis than during the financial crisis. Larger firms are less technically and scale inefficient than smaller firms on average, but have more problems in choosing the mix of inputs that minimizes their long-term costs. Firms that went bankrupt, on average, have a higher overall dynamic cost inefficiency and scale inefficiency than continuing firms.     

Orthogonal array design for the optimization of hollow fiber protected liquid-phase microextraction of salicylates from environmental waters

In the present study, a three phase-based hollow fiber protected liquid-phase microextraction (HF-LPME) method combined with high-performance liquid chromatography (HPLC) for the determination of salicylates in environmental waters was developed. The HF-LPME procedure was optimized by an L₁₆(4⁵) orthogonal array experimental design (OAD) with five factors at four levels. Under the optimal extraction condition (pHs of donor and receiving phases of 3.0 and 6.2, respectively, extraction time of 45 min, stirring speed of 1000 rpm, and salt addition of 20% (w/v)), salicylates could be determined in a linear range from 0.025 to 1.0 μg mL⁻¹ with a good correlation (r² > 0.9930). The limits of detection (LODs) ranged between 0.6 ng mL⁻¹ and 1.2 ng mL⁻¹ for the target analytes. The relative standard deviations (RSDs) of intra-day and inter-day were in the range of 0.64–14.58% and 0.16–15.45%, respectively. This procedure afforded a convenient, sensitive, accurate and cost-saving operation with high extraction efficiency for the model analytes. The method was applied satisfactorily to the determination of salicylates in two environmental waters.     

Investigation into the voltammetric behaviour and detection of selenium(IV) at metal electrodes in diverse electrolyte media

The voltammetric behaviour of selenium(IV) was studied at platinum and gold electrodes in sulphuric acid, perchloric acid and potassium chloride media as a basis for its voltammetric detection. The best voltammetric behaviour was recorded at gold electrodes with perchloric acid as the supporting electrolyte. The concomitant presence of metals, such as copper or lead, and of model biomolecules, such as bovine serum albumin, in the solution resulted in a deterioration of the electrochemical response for selenium(IV). Quantitative detection of selenium(IV) by square wave anodic stripping voltammetry at both a millimetre-sized gold disc electrode and a microband electrode array revealed linear responses to selenium concentration in the ranges 5–15 μM and 0.1–10 μM, respectively, with 60 s preconcentration. The sensitivities were 6.4 μA μM⁻¹ cm⁻² and 100 μA μM⁻¹ cm⁻² at the disc and the microband array, respectively. The detection limit at the microband electrode array was 25 nM, illustrating the potentiality of such microelectrodes for the development of mercury-free analytical methods for the trace detection of selenium(IV).     

Detection of LAMP Products Using CNT Array Electrode

We described here a novel strategy for discriminating target gene by integrating loop‐mediated isothermal amplification (LAMP) and differential pulse voltammetry (DPV). After a successful LAMP reaction, the anodic peak current (i_pa) of the free 2′‐deoxyguanosine 5′‐triphosphate (dGTP) decreased remarkably at a carbon nanotubes array working electrode, owing to the consumption of free dGTP as one of reactive substrates. Thus, the change of current response was used to characterize the result of LAMP reaction. And hence the presence of the target gene in template DNA could be discriminated easily. The malB gene extracted from Escherichia coli cells was tested as a model. After the reaction for 30 min, the LAMP mix was scanned directly. Then the information of the target gene in 0.8 picogram template DNA was obtained accurately. The result was in good accordance with that obtained with optical‐based methods (gel electrophoresis and fluorescent dye). The new strategy has the advantages of being very simple to perform, rapid response, elimination of post‐amplification processing, avoidance of auxiliary reagents and low cost (there was almost no cost for the detection step). Therefore, it was quite promising for use in miniaturized devices and in the development of point‐of‐care applications.     

光诱导约束刻蚀体系中羟基自由基生成的影响因素

采用荧光分析,暂态光电流响应分析,电化学交流阻抗谱(EIS)和Mott-Schottky响应分析考察了外加电位,光照时间,溶液pH等几个关键因素对光诱导约束刻蚀体系中TiO2纳米管阵列表面游离OH生成的影响.结果表明:当外加电位为1.0 V时,光电协同产生游离OH效率最高;OH的光催化生成与消耗能很快达到稳态,形成稳定的约束刻蚀剂层,有利于保持刻蚀过程中的精度;当pH为10时,TiO2纳米管光催化产生游离OH效率最高.研究结果对于调控和优化光诱导约束刻蚀平坦化铜的溶液体系,提高铜的刻蚀速度或平坦化精度有重要的指导意义.     

A facile high‐performance SERS substrate based on broadband near‐perfect optical absorption

Plasmonic systems based on metal nanoparticles on a metal film with high optical absorption have generated great interests for surface‐enhanced Raman scattering (SERS). In this study, we prepare a broadband‐visible light absorber consisting Au nanotriangles on the surface of a continuous optically opaque gold film separated with a dielectric SiO₂ layer, which is a typical metal‐insulator‐metal (MIM) system, and demonstrate it as an efficient SERS substrate. The MIM nanostructure, prepared using nanosphere lithography with a very large area, shows a broadband with absorption exceeding 90% in the wavelength regime of 630–920 nm. We observe an average SERS enhancement factor (EF) as large as 4.9 × 10⁶ with a 22‐fold increase compared to a single layer of Au nanotriangles directly on a quartz substrate. A maximum SERS EF can be achieved by optimizing the thicknesses of the dielectric layer to control the optical absorption. Owing to the simple, productive, and inexpensive fabrication technique, our MIM nanostructure could be a potential candidate for SERS applications. Copyright © 2015 John Wiley & Sons, Ltd.     

Multi-detection method for five common microalgal toxins based on the use of microspheres coupled to a flow-cytometry system

Freshwater and brackish microalgal toxins, such as microcystins, cylindrospermopsins, paralytic toxins, anatoxins or other neurotoxins are produced during the overgrowth of certain phytoplankton and benthic cyanobacteria, which includes either prokaryotic or eukaryotic microalgae. Although, further studies are necessary to define the biological role of these toxins, at least some of them are known to be poisonous to humans and wildlife due to their occurrence in these aquatic systems. The World Health Organization (WHO) has established as provisional recommended limit 1 μg of microcystin-LR per liter of drinking water. In this work we present a microsphere-based multi-detection method for five classes of freshwater and brackish toxins: microcystin-LR (MC-LR), cylindrospermopsin (CYN), anatoxin-a (ANA-a), saxitoxin (STX) and domoic acid (DA). Five inhibition assays were developed using different binding proteins and microsphere classes coupled to a flow-cytometry Luminex system. Then, assays were combined in one method for the simultaneous detection of the toxins. The IC₅₀'s using this method were 1.9 ± 0.1 μg L⁻¹ MC-LR, 1.3 ± 0.1 μg L⁻¹ CYN, 61 ± 4 μg L⁻¹ ANA-a, 5.4 ± 0.4 μg L⁻¹ STX and 4.9 ± 0.9 μg L⁻¹ DA. Lyophilized cyanobacterial culture samples were extracted using a simple procedure and analyzed by the Luminex method and by UPLC–IT-TOF-MS. Similar quantification was obtained by both methods for all toxins except for ANA-a, whereby the estimated content was lower when using UPLC–IT-TOF-MS. Therefore, this newly developed multiplexed detection method provides a rapid, simple, semi-quantitative screening tool for the simultaneous detection of five environmentally important freshwater and brackish toxins, in buffer and cyanobacterial extracts.     

Liquid chromatography with diode array detection and multivariate curve resolution for the selective and sensitive quantification of estrogens in natural waters

Following the green analytical chemistry principles, an efficient strategy involving second-order data provided by liquid chromatography (LC) with diode array detection (DAD) was applied for the simultaneous determination of estriol, 17β-estradiol, 17α-ethinylestradiol and estrone in natural water samples. After a simple pre-concentration step, LC–DAD matrix data were rapidly obtained (in less than 5 min) with a chromatographic system operating isocratically. Applying a second-order calibration algorithm based on multivariate curve resolution with alternating least-squares (MCR-ALS), successful resolution was achieved in the presence of sample constituents that strongly coelute with the analytes. The flexibility of this multivariate model allowed the quantification of the four estrogens in tap, mineral, underground and river water samples. Limits of detection in the range between 3 and 13 ng L⁻¹, and relative prediction errors from 2 to 11% were achieved.