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1.
分类时间序列在生物医学、社会学和遗传学等领域有着广泛的应用,累积Logistic回归模型是分类时间序列建模的一类重要模型.本文基于偏似然得分过程(Partial likelihood score process)提出一种变点序贯检验方法,监测累积Logistic回归模型的结构是否发生变化.原假设下推导检验统计量的极限分布,备择假设下证明其一致性.模拟试验和实例分析说明了方法的有效性.  相似文献   
2.
A CE instrument that can be assembled from commercially available components with minimal construction effort is described. Except for the electronic control circuitry no specially made parts are required. It is based on a flexible design of microfluidic, electropneumatic, and electronic sections and different configurations can easily be implemented. Automated injection into the capillary is performed hydrodynamically by the application of a pressure for a controlled length of time. The performance of the device was tested with a contactless conductivity detector by separating different metal ions. In addition, nine metal cations related to the quality of honey were separated in 2.3 min and four honey samples were analysed quantitatively to demonstrate the applicability of the method.  相似文献   
3.
Technical advances in the development of field-deployable capillary and microchip electrophoretic instruments and reports of their deployment between 2013 and 2017 were reviewed. Strategies and considerations in the design of the injection, separation and detection hardware, chemistry and associated infrastructure were discussed from an in-field perspective, with portability, robustness and automation/“ease of use” featuring as key requirements. Integration of functionality is important for adequate in-field performance. Progress was made towards the use of multiple channel devices for increased throughput and/or resolving power, mixing devices for on-line/in-line sample derivatization, battery operation and temperature control. The strengths and weaknesses of the various approaches described in the literature are discussed from the perspective of in-field operation. An overview of the applications of the field electrophoretic instruments is provided, including environmental science and planetary investigation.  相似文献   
4.
In this paper, we use character-theoretic techniques to give new nonexistence results for (n,m,k,λ)-strong external difference families (SEDFs). We also use cyclotomic classes to give two new classes of SEDFs with m=2.  相似文献   
5.
A method using high-performance liquid chromatography with diode array detection (HPLC-DAD) as a powerful separation technique has been developed for the simultaneous determination of the four flavonols rutin, quercetin, kaempferol and isorhamnetin in food supplements and pharmaceutical formulations. The chromatographic separation was achieved in 36?min using a Symmetry C18 column (250?×?3?mm; 5?µm) as the stationary phase and a mixture of methanol, acetonitrile, and pH 2.5 aqueous acetic acid as the mobile phase in gradient elution mode. The analytical wavelengths were 256?nm for rutin, quercetin and isorhamnetin, and 368?nm for kaempferol. An ultrasound-assisted extraction protocol was performed using methanol as solvent. The detection and quantification limits were lower than 0.03?µg mL?1 and 0.08?µg mL?1, respectively. The inter-day and intra-day precisions were less than 4.8 and 5.1%, respectively, and the average recoveries were in the range from 96 to 107%. The method was applied for the determination of the studied flavonols in food supplements and pharmaceutical preparations. The satisfactory recovery values demonstrate the potential of the developed method for the determination of the analytes in these samples. In addition, the method is suitable for routine quality control due its ease of operation.  相似文献   
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7.
吴晓甫  童辉  王利祥 《化学进展》2019,31(11):1509-1527
作为荧光传感材料,荧光聚合物不仅具有传感单元多、荧光亮度高、光稳定性好等特点,而且方便制备荧光传感薄膜,易于实现器件化,在爆炸物荧光检测中得到了广泛的研究与应用。近年来,随着荧光聚合物从传统的线型结构向支化和多孔网络结构的拓展,以及各种功能单元的引入,大量的新型荧光聚合物有效地提升了爆炸物检测的灵敏度、选择性和响应速度等性能。本综述从线型聚合物、支化聚合物、多孔聚合物三类体系出发,总结和评述了用于爆炸物荧光检测的线型共轭与非共轭聚合物、树枝状分子与超支化聚合物、无定形与结晶型多孔聚合物等典型体系的分子结构设计策略、功能特点以及传感性能,并展望了荧光聚合物未来在爆炸物检测应用中所面临的机遇和挑战。  相似文献   
8.
Flow injection analysis with amperometric detection (FIA‐AD) at screen‐printed carbon electrodes (SPCEs) in optimum medium of Britton‐Robinson buffer (0.04 mol ? L?1, pH 2.0) was used for the determination of three tumor biomarkers (homovanillic acid (HVA), vanillylmandelic acid (VMA), and 5‐hydroxyindole‐3‐acetic acid (5‐HIAA)). Dependences of the peak current on the concentration of biomarkers were linear in the whole tested concentration range from 0.05 to 100 μmol ? L?1, with limits of detection (LODs) of 0.065 μmol ? L?1 for HVA, 0.053 μmol ? L?1 for VMA, and 0.033 μmol ? L?1 for 5‐HIAA (calculated from peak heights), and 0.024 μmol ? L?1 for HVA, 0.020 μmol ? L?1 for VMA, and 0.012 μmol ? L?1 for 5‐HIAA (calculated from peak areas), respectively.  相似文献   
9.
The composite of carbon nanotube (CNT) and phenolic resin was prepared in a piece of fused silica capillary based on the far infrared‐assisted crosslinking of phenolic novolac resin in the presence of CNTs and hexamethylenetetramine for electrochemical sensing. The surface morphology and structure of the prepared materials were investigated by scanning electron microscopy, energy dispersive X‐ray spectroscopy and Fourier transform infrared spectroscopy. The results indicated that CNTs in the composite was adhered by the crosslinked phenolic resin to form an electrically conductive network. Many broken ends of CNTs appeared on the surface of the composite electrode in the form of a nanoelectrode array. The novel electrode was employed in the amperometric detection of synephrine and hesperidin in Citri Reticulatae Pericarpium in combination with capillary zone electrophoresis. The novel CNT‐based electrode owned the advantages of high sensitivity, low fabrication expense and excellent electrocatalytic performances, indicating great promise for the electrochemical detection in other analysis systems.  相似文献   
10.
Bidentate ureido-dihomooxacalix[4]arene based supramolecular hosts (n-propyl 1 and tert-butyl 2) were processed into organic nanoparticles via a bottom up approach in which a single step of re-precipitation was employed. These organic nanoparticles were then coupled with gold nanoparticles on the surface, resulting in an organic – inorganic hybrid framework (n-propyl H1 and tert-butyl H2). Photophysical studies of the organic nanoparticles and of the hybrid material were performed. The size and morphology were determined by TEM and DLS analysis. Moreover, the prepared hybrid frameworks were screened against various anions using UV-Visible absorption and fluorescence spectrophotometry. H1 exhibited ratiometric response towards iodide ion in aqueous medium, and colour change of the solution from pink to light blue was observed. This hybrid material selectively and sensitively detected iodide ion with detection limit of 8.3 nM and with almost no interference from other anions. H1 sensor ability was also tested with artificial and real urine samples. H2 showed different responses and no selectivity to any anion.  相似文献   
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