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由于兰姆波的多模和频散特性,实际检测时在同一激发频率下存在多种模式的混合信号,而各模式信号有不同的频散特性,使得在时频混叠的情况下兰姆波的检测变得十分复杂.本文在频散补偿的基础上,通过时延函数建模,依靠不同模式频散趋势的差异性,将时频混叠信号的分离问题转化为部分模式混叠信号的分离问题.基于分数阶微分的理论,用信号幅值谱分数阶微分极大值和对应频率分别与微分阶次拟合多项式实现特征参数的提取并依靠特征参数重建幅值谱.结合相位谱重构时域信号以实现部分混叠信号中频散补偿后的模式的分离.最后恢复频散获得分离后的兰姆波信号.仿真和实验结果表明,本文方法不仅可以实现时频混叠多模式兰姆波信号的分离,更能保证分离精度,有助于复杂多模式频散信号的分离与处理的进一步研究. 相似文献
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The methylation effects in the energy transfer between Kr atoms and highly vibrationally excited 2-methylnaphthalene in the triplet state were investigated using crossed-beam/time-sliced velocity-map ion imaging at a translational collision energy of approximately 520 cm(-1). Comparison of the energy transfer between naphthalene and 2-methylnaphthalene shows that the difference in total collisional cross section and the difference in energy transfer probability density functions are small. The ratio of the total cross sections is sigma(naphthalene): sigma(methylnaphthalene)=1.08+/-0.05:1. The energy transfer probability density function shows that naphthalene has a little larger probability at small T-->VR energy transfer, DeltaE(u)<300 cm(-1), and 2-methylnaphthalene has a little larger probability at large V-->T energy transfer, -800 cm(-1)相似文献
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A new phenolic derivative, 4-hydroxyphenol-1-O-[6-O-(E)-feruloyl-β-d-glucopyranosyl]-(1→6)-β-d-glucopyranoside (1), and a new terpenylated coumarin, named altissimacoumarin H (2) were identified from the fruit of Ailanthus altissima (Mill.) Swingle (Simaroubaceae), together with ten known compounds (3–12), including two coumarins and eight phenylpropanoids. Their structures were determined on the basis of chemical method and spectroscopic data. Antiviral effect against Tobacco mosaic virus (TMV) of all the compounds obtained were evaluated using leaf-disc method. 相似文献
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A rapid kinetic method for the simultaneous determination of levodopa, dopamine, and dobutamine was examined and developed.
It was based on a consecutive reaction of a reduction of Cu(II) to Cu(I) by catecholamines, followed by the complexation of
Cu(I) with neocuproine to form a yellow product in an acetic acid-acetate buffer. Spectrophotometric data were recorded at
453 nm (wavelength at the yellow complex absorption maximum) for 300 s. Linear calibrations were obtained in the concentration
ranges of (0.08–1.44) × 10−5 mol L−1, (0.08–1.44) × 10−5 mol L−1, and (0.16–1.44) × 10−5 mol L−1 for levodopa, dopamine, and dobutamine, respectively. A variety of multivariate calibration models was developed for simultaneous
analysis of the three analytes; while most models produced satisfactory prediction results for synthetic samples, the hybrid
linear analysis method was arguably the best-performing (relative prediction error, RPET = 6.6 %). The proposed method was
applied to an analysis of spiked rabbit serum samples and the results showed good agreement with the high performance liquid
chromatography measurements. 相似文献
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Pengjuan Ni Yujing Sun Haichao Dai Shu Jiang Wangdong Lu Yilin Wang Zhen Li Zhuang Li 《Mikrochimica acta》2016,183(9):2589-2595
We describe a sensitive and selective colorimetric method for the determination of the activity of the enzyme acetylcholinesterase (AChE) and its inhibitors. Detection is based on the fact that acetylthiocholine iodide (ATCI) catalyzes the oxidation of the substrate 3,3′,5,5′-tetramethylbenzidine (TMB) by H2O2 to form a blue product (ox-TMB) with an absorption peak at 652 nm, but that oxidation is suppressed if ACTI previously is hydrolyzed by AChE to form thiocholine which decolorizes ox-TMB. In the presence of inhibitor, the activity of AChE is inhibited, thereby inducing the recovery of the blue coloration. Based on these findings, a highly sensitive method is developed for the determination of AChE and its inhibitors. The assay only requires mixing of buffer, solutions of ATCI, TMB, H2O2 and a sample containing AChE and photometric measurement. It works in the 0.05 to 5 mU?mL?1 enzyme activity range and has a detection limit as low as 30 μU?mL?1. The inhibitor neostigmine causes 50 % enzyme inhibition in 14.5 nM concentration. This analytical system has a wide scope in that it may be applied to the determination of the activity of various other hydrolases with proper substrates. 相似文献
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