阶梯压电层合梁的波动动力学特性

采用行波理论系统地研究了压电阶梯梁的自由振动分析以及强迫响应的分析方法. 基于分布 参数理论研究了压电阶梯梁的波传播特性，忽略柔性梁横向剪切和转动惯量的影响，给出了 梁的轴向和横向的简谐波解. 将压电阶梯梁离散化为单元，考虑压电片的刚度和质量的影响， 建立了节点散射模型. 应用位移连续和力平衡条件，推导了节点的波反射和波传递矩阵，在 此基础上，引入波循环矩阵的概念，给出波循环矩阵、波传递系数矩阵的确定方法. 应用波 循环矩阵可以有效地计算结构的固有频率. 另外，应用波传递系数研究了压电陶瓷作动器位 置对其驱动能力的影响. 得出两个主要结论：1)作动器靠近悬臂梁固定端将有较强的驱动 能力，悬臂梁边界反射行波产生弯曲消失波有利于增大压电波的模态传递系数；2)模态传 递系数与固有频率的灵敏度密切相关，波传递系数越大, 对应该处固有频率变化灵敏度越大. 另外，数值算例表明了行波方法比有限元方法具有更高的计算精度.     

EFFECT OF POLYETHYLENEIMINE ON THE PROPERTIES OF CONCENTRATED SUSPENSIONS OF TITANIUM DIOXIDE MICROBEADS

The effect of polyethyleneimine (PEI) concentration on the properties of titanium dioxide (TiO2) suspensions is studied with or without the addition of an electrolyte (barium acetate). Measurements of the apparent viscosity and the stability of TiO2 suspensions showed that PEI is an effective dispersant for TiO2 particles in suspension in the absence of an electrolyte, not only reducing the viscosity of the suspension but also increasing its stability. In the presence of an electrolyte, however, small quantities of polyethyleneimine could neither disperse the TiO2 particles nor de-crease the viscosity of the TiO2 suspensions; only PEI concentrations beyond saturation adsorption could perceptively improve the stabilitv of TiO2 suspensions.     

狭窄流道中Fahraeus效应研究进展

本文详细论述了毛细管和二维狭缝中流过血液时的Fahraeus效应研究历史及现状,给出了迄今为止得到的全部结论,并报道了笔者对狭缝缝隙中Fahraeus效应研究的最新进展。本文所涉及的内容对于微循环的理论与应用以至有关流变学仪器的设计优化都有重要意义。     

Two new eudesmane derivatives from Verbesina virginica

<正>Two new eudesmane derivatives were isolated from the leaves and flowers of Verbesina virginica,along with the known 6-O-β-E -p-coumaroyl-4α-hydroxyeudesmane(1).Their structures were determined as 6-O-β-Z-p-coumaroyl-4α-hydroxyeudesmane(2) and 6-O-α-E-p-coumaroyl-1β-4α-dihydroxyeudesmane(3) by spectroscopic methods.     

Synthesis and characterization of six-arm star-shaped liquid crystalline cyclotriphosphazenes

<正>The synthesis and mesomorphic properties of a new class of liquid crystalline cyclotriphosphazenes with rigid cyanostilbene groups and flexible alkoxy groups are reported.The thermal behaviors of cyclotriphosphazene derivatives 5a-5d are studied by the means of differential scanning calorimetry,polarizing optical microscopy.Nematic phases were observed in compounds 5a-5d both on heating and cooling.The clear temperatures of compounds 5a-5d slightly increased with increasing length of terminal alkyl chain.Compounds 5a-5d showed different mesogenic region from minimum 5℃to maximum 142℃.     

A convenient synthesis of pyrroles catalyzed by acidic resin under solvent-free condition

<正>A convenient and effective Paal-Knorr condensations of 2,5-hexanedione with most amines have been carried out at room temperature under solvent-free condition.Macroporous strongly acidic styrol resin(D001) as a novel,efficient,cost-effective,and reusable solid acid catalyst for the synthesis of pyrroles under the same conditions.The pyrroles were obtained in high yields in short reaction times.     

Study on curing reaction of 4-aminophenoxyphthalonitrile/bisphthalonitrile

<正>A series of phthalonitrile blending resins were prepared from 4-aminophenoxyphthalonitrile(APN) and 4,4'-bis(3,4- dicyanophenoxy)biphenyl(BPH) by directly powder-mixing and copolymerization.Differential scanning calorimeter(DSC) and dynamic rheology were used to study the curing reaction behaviors of APN/BPH blends,and the results indicated that the introduction of APN accelerated the curing rate of BPH,and the existence of BPH decreased the curing temperature of APN/BPH systems.The thermal stability of postcured APN/BPH resins was investigated by thermogravimetric analysis(TGA),and the TGA results indicated that the crosslinked polymers of APN/BPH systems possessed good thermal stability.     

Electrochemical biosensing for dsDNA damage induced by PbSe quantum dots under UV irradiation

<正>An electrochemical sensor for the detection of the natural double-stranded DNA(dsDNA) damage induced by PbSe quantum dots(QDs) under UV irradiation was developed.The biosensing membranes were prepared by successively assembling 3- mercaptopropionic acid,polycationic poly(diallyldimethyl ammonium) and dsDNA on the surface of the gold electrode.Damage of dsDNA was fulfilled by immersing the sensing membrane electrode in PbSe QDs suspension and illuminating it with an UV lamp. Cyclic voltammetry was utilized to detect dsDNA damage with Co(phen)_3~(3+) as the electroactive probe.The UV irradiation,Pb~(2+) ions liberated from the PbSe QDs under the UV irradiation and the reactive oxygen species(ROS) generated in the presence of the PbSe QDs also under the UV irradiation were the three factors of inducing the dsDNA damage.The synergistic effect of the three factors might dramatically enhance the damage of dsDNA.This electrochemical sensor provided a simple method for detecting DNA damage,and may be used for investigating the DNA damage induced by other QDs.     

Facile synthesis of a melt-spinnable polyborazine from asymmetric alkylaminoborazine

<正>A novel asymmetric alkylaminoborazine monomer,2-propylamino-4,6-bis(methylamino)borazine,was synthesized for the first time,and directly polymerized to give a melt-spinnable polyborazine(PBN).This asymmetric alkylaminoborazine was synthesized by an aminolysis reaction of 2,4,6-trichloroborazine(TCB) with different amines under mild conditions.This route turns out to be much cheaper and simpler than the conventional routes.The chemical composition,structure,molecular weights and ceramic yield were investigated by EA,FTIR,NMR,GPC and TG analysis.The PBN exhibits suitable rheological property for melt-spinning, which suggests that it is a potential precursor for BN fibers.     

Investigation of the interaction of carbofuran and DNA by voltammetry and fluorescence with the aid of chemometrics

<正>The interactions of carbofuran and DNA were studied using voltammetry and fluorescence spectroscopy.The formation of carbofuran-DNA makes the current peak of DNA decreased by voltammetry method.The binding number(n) and constant(K_a) for complex carbofuran-DNA were calculated to be 1.06±0.04 and 0.11±0.03mol~(-1) L,respectively by fluorescence measurement.Chemometrics approach,such as singular value decomposition(SVD) was used to evaluate the number of spectral species in the drug-DNA binding process.And the pure spectra and concentration profiles in the kinetic system were clearly deduced by multivariate curve resolution alternating least squares(MCR-ALS) with the initial estimates by evolving factor analysis(EFA).