Calibration Curve with Improved Limit of Detection for Cadmium in Soil: An Approach to Minimize the Matrix Effect in Laser-Induced Breakdown Spectroscopic Analysis

The present article describes a working or combined calibration curve in laser-induced breakdown spectroscopic analysis, which is the cumulative result of the calibration curves obtained from neutral and singly ionized atomic emission spectral lines. This working calibration curve reduces the effect of change in matrix between different zone soils and certified soil samples because it includes both the species' (neutral and singly ionized) concentration of the element of interest. The limit of detection using a working calibration curve is found better as compared to its constituent calibration curves (i.e., individual calibration curves). The quantitative results obtained using the working calibration curve is in better agreement with the result of inductively coupled plasma–atomic emission spectroscopy as compared to the result obtained using its constituent calibration curves.     

平板折叠桌的设计模型

根据折叠桌的运动特征,选取折叠桌的四分之一为研究对象,建立任意角度下桌脚点的运动变化模型。考虑到产品稳固性、加工便利性和节约用材三方面对加工参数的影响,对折叠桌进行受力分析,得到多目标组合优化模型,用以确定出折叠桌的最优设计参数。针对用户提出的桌面形状要求,建立桌脚曲线的参数方程。作为模型推广,以椭圆状折叠桌为例,运用Matlab画出了桌脚边缘线在折叠过程中的动态变化示意图。同时,又深入研究Robert van Embricqs的滑动折叠桌,建立了新的桌脚曲线参数方程。最后,运用Matlab对多种形状折叠桌进行仿真,编写多目标优化算法,得出了最优加工参数,并进行了算法描述。     

基于普侨直流自动功率曲线软件功能优化

本文以南方电网公司承建的±800KV特高压普侨直流输电线路自动功率曲线软件优化为例,对自动功率软件的具体优化进行了阐述分析,以此为广大的电力部门提供可借鉴的理论参考。     

SILAR次数对In掺杂CdS量子点敏化太阳电池的影响

以In掺杂CdS量子点太阳能电池为例,讨论了SILAR次数对In掺杂CdS量子点敏化太阳能电池性能的影响。通过SEM、EDS、IPCE、紫外吸收光谱、J-V曲线、EIS等实验测试结果表明,当In掺杂CdS的摩尔比固定在1:5时,随着SILAR次数的增加,电池的短路电流密度、开路电压和光电转换效率都随着增加,当SILAR次数为6次时,In掺杂CdS的QDSCs光电转化效率达到了最大值(η=0.76%)。随着SILAR次数的继续增加,其光电转换效率将会下降。     

基于伏安曲线的熔断器熔断电流的无损检测

调节熔断器电流的同时测量熔断器两端的电压,获得待测熔断器的U-I曲线并计算出U-R曲线,对比两种曲线分析了熔断机理和规律,发现当熔断器的U-I曲线开始偏离直线时表示其即将熔断,此时所对应的电流可以较准确地表征待测熔断器的实际熔断电流。U-I曲线检测方法简便并且对待测样品几乎无损,实验表明经过该法检测合格的熔断器可以更安全可靠地工作。     

Simultaneous Anodic Stripping Voltammetric Determination of Pb and Cd,Using a Vibrating Gold Microwire Electrode,Assisted by Chemometric Techniques

Simultaneous anodic stripping voltammetric determination of Pb and Cd is restricted on gold electrodes as a result of the overlapping of these two peaks. This work describes the quantitative determination of a binary mixture system of Pb and Cd, at low concentration levels (up to 15.0 and 10.0 µg L^?1 for Pb and Cd, respectively) by differential pulse anodic stripping voltammetry (DPASV; deposition time of 30 s), using a green electrode (vibrating gold microwire electrode) without purging in a chloride medium (0.5 M NaCl) under moderate acidic conditions (HCl 1.0 mM), assisted by chemometric tools. The application of multivariate curve resolution alternating least squares (MCR‐ALS) for the resolution and quantification of both metals is shown. The optimized MCR‐ALS models showed good prediction ability with concentration prediction errors of 12.4 and 11.4 % for Pb and Cd, respectively. The quantitative results obtained by MCR‐ALS were compared to those obtained with partial least squares (PLS) and classical least squares (CLS) regression methods. For both metals, PLS and MCR‐ALS results are comparable and superior to CLS. For Cd, as a result of the peak shift problem, the application of CLS was unsuitable. MCR‐ALS provides additional advantage compared to PLS since it estimates the pure response of the analytes signal. Finally, the built up multivariate calibration models, based either in MCR‐ALS or PLS regression, allowed to quantify concentrations of Pb and Cd in surface river water samples, with satisfactory results.     

Determination of phenolic compounds and authentication of PDO Lambrusco wines by HPLC-DAD and chemometric techniques

This work proposes a fast and simple method for detection and quantification of phenolic compounds in PDO Lambrusco wines using HPLC-DAD and chemometric techniques. Samples belonging to three different varieties of Lambrusco (Grasparossa, Salamino and Sorbara) were analyzed to provide a methodology appropriate for routine analysis. Given the high complexity of the sample and the coelution among chromatographic peaks, the use of chemometric techniques to extract the information of the individual eluting compounds was needed. Multivariate curve resolution-alternating least squares (MCR-ALS) allowed the resolution of the chromatographic peaks obtained and the use of this information for the quantification of the phenolic analytes in the presence of interferences. Use of multiset analysis and local rank/selectivity information was proven to be crucial for the correct resolution and quantification of compounds. The quantitative data provided by MCR-ALS about the phenolic targets and additional compounds present in the samples analyzed provided wine composition profiles, which were afterwards used to distinguish among wine varieties. Principal component analysis applied to the wine profiles allowed characterizing the wines according to their varieties.     

ClF-分子离子的结构与势能函数

采用单、双取代包括三重激发的二次组态相互作用[QCISD(T)]方法和单、双取代包括非迭代三重激发的耦合簇理论[CCSD(T)]方法, 结合相关一致基组aug-cc-pVXZ (X=D, T, Q, 5)对基态³⁵ClF^-和³⁷ClF^- (X²Σ⁺)分子离子进行了结构优化计算. 对CCSD(T)方法的计算结果用四种方法分别外推至基组极限, 得到了体系在基组极限的平衡结构常数. 在CCSD(T)/aug-cc-pVXZ (X=D, T, Q, 5)理论水平进行了单点能扫描. 对扫描计算结果进行基组外推并用Murrell-Sorbie 势能函数拟合得到了体系的解析势能函数表达式, 并进一步得到了³⁵ClF^-和³⁷ClF^-的光谱常数. 拟合所得势能曲线准确地再现了其离解能和平衡结构特征. 对ClF 中性自由基采用完全相同的理论方法进行了计算. 所得结果与有关文献中的实验结果符合得很好, 而且在一定程度上证明了将该理论方法应用于ClF^-分子离子的计算是合适而可靠的. ClF 自由基的优化计算结果还被用于计算其电子亲和能.ClF^-的垂直解离能也同时计算得出. 基于ClF^-的结构优化和单点能扫描计算结果, 通过求解核运动的径向薛定谔方程, 得到了无转动³⁵ClF^-和³⁷ClF^-(X²Σ⁺)的全部振动态及相应的分子常数.     

LABVIEW下冲击试验测试信号分析模块的设计

根据GJB冲击环境试验测试要求,介绍LABVIEW平台下两类典型冲击信号分析模块的设计方法,主要讲述利用多图层叠加编程技术实现GJB150.18-1986标准规定的半正弦波与后峰锯齿波动态套容差曲线分析模块的设计以及利用递归算法实现冲击响应谱分析模块的设计。其次,采用资源DLL封装技术对LABVIEW编程实现的冲击信号分析模块进行封装,在其他编程语言中调用DLL实现冲击信号分析模块在其他编程语言中的功能链接。实践表明,LABVIEW图形化编程技术可快速实现两类冲击信号分析模块的设计,将高速数据采集模块与冲击信号分析模块集成,可有效完成冲击试验测试与信号分析处理任务。