主动控制压电旋转悬臂梁的参数振动稳定性分析

在工程实际中旋转机械由于制造和加工误差,装配的不均匀性等原因,往往会脉动运行,这将使得机械系统发生参数振动. 当脉动参数满足一定关系时,这种参数振动将会失稳,进而影响机械结构的正常运转. 本文针对这一问题,引入压电材料对 脉动旋转悬臂梁系统的振动进行控制,研究主动控制悬臂梁系统的参数振动优化设计问题,采用 Hamilton 变分原理与一阶 Galerkin 离散相结合的方法,建立了受速度反馈传感器主动控制的压电旋转悬臂梁的一阶近似线性控制方程. 运用多尺度方法,得到了压电旋转悬臂梁系统在发生1/2亚谐波参数共振时稳定性边界的控制方程,并利用直接分析方法验证了解析摄动解的正确性. 将摄动解中临界阻尼比和轮毂角速度脉动幅值的无量纲参数作为评价系统稳定性能的指标. 通过数值算例,分析了轮毂半径、轮毂角速度平均值和脉动幅值、梁长以及速度传感器的反馈增益系数对系统稳定性区域的影响. 研究结果表明,梁长、轮毂半径、脉动幅值会降低系统稳定性,反馈增益系数可以提高系统稳定性,而轮毂角速度平均值与系统稳定性之间有非单调的关系. 为进一步设计压电旋转机械结构提供了理论依据.      

时程稳定性系数确定的边坡逐孔起爆孔间微差降振时间

为了获得边坡逐孔爆破最佳降振微差时间,以某个实际边坡逐孔微差爆破施工现场为原型,先利用ANSYS建立二维静态模型,借助有限元折减法确定自然状态下的潜在滑动面和静态安全系数;基于已确定的二维潜在滑动面重新建立同尺寸同性质的三维逐孔微差爆破动态模型,利用LS-DYAN进行动力分析,整个过程分别设置同排3个炮孔0、17、25、42和65 ms等5种不同孔间微差起爆方式;同时,对该施工现场进行排、孔间(25 ms,17 ms)、(25 ms,25 ms)、(25 ms,42 ms)、(25 ms,65 ms)等4种微差时间控制的等比例相似小炮测振实验。提取模拟结果中3个炮孔同时起爆时滑面单元的应力数值代入极限平衡法计算公式,绘制了冲击载荷作用下边坡稳定性系数曲线,通过对曲线的理论分析发现,最佳降振微差时间约为48 ms;而三维数值模拟和测振实验结果均显示,孔间微差时间取42 ms时降振效果较佳。这说明,边坡稳定性系数曲线给出的微差时间与模拟和实验结果较为接近,可为今后边坡逐孔微差爆破降振研究提供参考。     

等热流密度加热垂直下降液膜的研究

利用等热流密度加热条件下降膜流动的三维模型方程进行线性稳定性分析和数值模拟。线性稳定性分析表明,模型方程在小到中等Reynolds数下都适用,并且流向不稳定性增长率随着Reynolds数和Marangoni数增加而增加,展向不稳定性增长率则随着Marangoni数增加而增加,随着Reynolds数增加而减小,流向和展向对扰动波数都存在一个不稳定区间。三维数值模拟表明,在等热流密度加热条件下,液膜在随机扰动的情况下最终会形成带孤立波的三维溪流状结构,液膜与气体的换热也因溪流状结构的出现而加强;在随机扰动的基础上引入占优势地位的展向最不稳定扰动会使得换热增强,液膜会提前破裂;在随机扰动的基础上引入占优势地位的流向最不稳定扰动时,液膜的换热会增强,但不会提前破裂;在随机扰动的基础上同时引入占优势地位的流向和展向最不稳定扰动时,换热会加强且液膜会提前破裂。     

Modification of an implicit approach based on nonstandard rules for structural dynamics analysis

The present study aims to modify a recently suggested implicit approach consisted of the approximate Euler method and closed-form exponential mapping (herein referred to as the Liu scheme) for the dynamic analysis of structures. Such modification has been developed based upon nonstandard rules. The equation of motion is formulated in the augmented dynamic space to apply the exponential mapping as a group preserving scheme. The formulation of the proposed method involves the hyperbolic sine and cosine functions. The method is therefore prone to divergence due to the behavior of the hyperbolic functions in structures with a high ratio of stiffness to mass. In the present study, to consider the properties of the structural equation into the formulation of the time step size and thereby avoid the divergence, a parameter, known as stability parameter, is thus derived from the exact solution of the equation of motion based on nonstandard rules. Embedding this parameter into the proposed method improves its stability. Afterward, for evaluating the performance of the proposed method, it is applied to several structures with different loading patterns while implemented in programing environment of the Matlab software. The results are compared to those of several commonly used numerical methods in structural applications. It is found that the proposed method has acceptable convergence and accuracy, and low time consumption compared to several commonly used methods. Furthermore, its stability is guaranteed by embedding the stability parameter into the proposed method.     

Electric Double Layer in Water-Organic Mixed Solvents: Titania in 50% Ethylene Glycol

Ethylene glycol (EG) and its mixtures with water are popular components of nanofluids used as heat transfer fluids. The stability of nanofluids against coagulation is correlated with their zeta potential. The electrophoretic mobility of titania nanoparticles in 50-50 w/w EG was studied as a function of the concentration of various solutes. HCl, NaOH, SDS and CTMABr at concentrations up to 0.01 M are strong electrolytes in 50% EG, that is, the conductance of their solutions is proportional to the concentration. HCl, NaOH and CTMABr were very efficient in inducing a high zeta potential for titania in 50% EG. NaOH induced a negative zeta potential in excess of 70 mV, and HCl and CTMABr induced a positive zeta potential in excess of 70 mV at concentrations below 10⁻⁴ M. Apparently, HCl, NaOH and CTMABr are also more efficient than SDS in terms of nanofluid stabilization against coagulation. An overdose of base (>1 mM) results in depression of the negative zeta potential. This result may be due to the specific adsorption of sodium on titania from 50% EG.     

Quantification of Structural Integrity and Stability Using Nanograms of Protein by Flow-Induced Dispersion Analysis

In the development of therapeutic proteins, analytical assessment of structural stability and integrity constitutes an important activity, as protein stability and integrity influence drug efficacy, and ultimately patient safety. Existing analytical methodologies solely rely on relative changes in optical properties such as fluorescence or scattering upon thermal or chemical perturbation. Here, we present an absolute analytical method for assessing protein stability, structure, and unfolding utilizing Taylor dispersion analysis (TDA) and LED-UV fluorescence detection. The developed TDA method measures the change in size (hydrodynamic radius) and intrinsic fluorescence of a protein during in-line denaturation with guanidinium hydrochloride (GuHCl). The conformational stability of the therapeutic antibody adalimumab and human serum albumin were characterized as a function of pH. The simple workflow and low sample consumption (40 ng protein per data point) of the methodology make it ideal for assessing protein characteristics related to stability in early drug development or when having a scarce amount of sample available.     

无焰燃烧烟密度标准物质的研制

介绍无焰燃烧烟密度标准物质的研制方法。选用合适的α-纤维素作为原材料,经打浆造纸后,作为标准物质候选物,经均匀性检验和稳定性考察合格后,对标准物质进行定值。在无焰燃烧条件下烟密度标准物质的标准值为175,扩展不确定度为8;校正烟密度标准物质的标准值为166,扩展不确定度为8。     

Revisiting the Synthesis of Functionally Substituted 1,4-Dihydrobenzo[e][1,2,4]triazines

A series of novel 1,4-dihydrobenzo[1,2,4][e]triazines bearing an acetyl or ester moiety as a functional group at the C(3) atom of the 1,2,4-triazine ring were synthesized. The synthetic protocol is based on an oxidative cyclization of functionally substituted amidrazones in the presence of DBU and Pd/C. It was found that the developed approach is suitable for the preparation of 1,4-dihydrobenzo[e][1,2,4]triazines, but the corresponding Blatter radicals were isolated only in few cases. In addition, a previously unknown dihydrobenzo[e][1,2,4]triazolo[3,4-c][1,2,4]triazine tricyclic open-shell derivative was prepared. Studies of thermal behavior of the synthesized 1,4-dihydrobenzo[1,2,4][e]triazines revealed their high thermal stability (up to 240–250 °C), which enables their application potential as components of functional organic materials.     

Metal Ion Recognition. Interaction of New Oxygen-Nitrogen Donor Macrocycles with Selected Transition and Post-Transition Metal Ions

As part of an ongoing investigation of the factors influencing metal ionrecognition, we have investigated structure/function relationships involvingthe metal-ion binding by three new N-benzyl-substituted, 15- and 16-membered,macrocyclic ligands incorporating N₂O ₃- and N ₃O ₃-donor sets (withthe N ₃O ₃-system consisting of a N ₂O ₃-macrocyclic ring with an attachedCH ₂CH ₂NCH ₂C ₆H ₅ pendant arm). Selected solid complexes of thelatter ligand were isolated and the X-ray structures of individual Ni(II) and Ag(I) complexeswere obtained.Where solubility permitted, potentiometric titration studies in 95% methanolwere employed to investigate the binding affinities of all three ligand derivativestowards Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Ag(I) and Pb(II). The 15-memberedN ₂O ₃-ring was found to be selective for Ag(I) over the other six metalsinvestigated, including Cu(II). However, the presence of a further nitrogen donorin the form of the pendant benzylamine functionality in the N ₃O ₃-donorsystem results in an increase in its binding affinity for Ag(I) but an even greaterincrease occurs for Cu(II). As a consequence, the latter ion is now more stronglybound than Ag(I). The factors influencing these respective selectivities are discussed.     

高岭石—金—硫系列的化学键与稳定性研究

用密度泛函离散变分计算方法（ＤＦＴ－ＤＶＭ）,研究了高岭石、高岭石－金和高岭石－金－硫系列,讨论了结构,化学键与稳定性之间的关系。选用了不含金及金或金－硫原子团位于不同方位的多个模型。计算结果表明,金位于层状高岭石侧面的模型比金位于上、下面更为稳定,在金位于层状高岭石侧面的情况下,金靠近铝的模型比金靠近铝空位更为稳定,高岭石－金－硫体系中的金－硫原子团比高岭石－金体系中的更容易被高岭石吸附。模型间