Dynamic Buckling of Autonomous Systems Having Potential Energy Universal Unfoldings of Cuspoid Catastrophe

This work deals with dynamic buckling universal solutions of discrete nondissipative systems under step loading of infinite duration. Attention is focused on total potential energy functions associated with universal unfoldings of cuspoid type catastrophes with one active coordinate. The fold, dual cusp and tilted cusp catastrophes under statically applied loading occurring via limit points, asymmetric/symmetric bifurcations and nondegenerate hysteresis points are extended to the case of dynamic loading. Catastrophe manifolds of these types showing imperfection sensitivity under both types of loading are fully assessed. Important findings regarding dynamic buckling of imperfect systems generated by perfect systems associated with imperfect bifurcations are explored. The analysis is supplemented by a numerical application of a system exhibiting imperfect bifurcation when it is perfect as well as a hysteresis point associated with a tilted cusp catastrophe, when it becomes imperfect.     

缓变主流中三维气泡的非线性振动

空化现象和水下噪声机制与液体中气泡的动力学行为密切相关．在无粘势流的假定下，采用多参数摄动分析，研究了缓变主流中三维气泡的非线性体积模态振动．推导了关于缓变泡形展开的各阶扰动方程，获得了一阶振动的演化方程和一些特殊情况下的解析解；并采用高阶有限元离散的边界积分方程方法，对平面固壁和自由面附近三维气泡的固有频率进行了数值计算     

An atomistic-based continuum theory for carbon nanotubes: analysis of fracture nucleation

Carbon nanotubes (CNTs) display unique properties and have many potential applications. Prior theoretical studies on CNTs are based on atomistic models such as empirical potential molecular dynamics (MD), tight-binding methods, or first-principles calculations. Here we develop an atomistic-based continuum theory for CNTs. The interatomic potential is directly incorporated into the continuum analysis through constitutive models. Such an approach involves no additional parameter fitting beyond those introduced in the interatomic potential. The atomistic-based continuum theory is then applied to study fracture nucleation in CNTs by modelling it as a bifurcation problem. The results agree well with the MD simulations.     

Adaptive Control of Nonlinear Dynamical Systems Using a Model Reference Approach

In this paper we consider using a model reference adaptive control approach to control nonlinear systems. We consider the controller design and stability analysis associated with these type of adaptive systems. Then we discuss the use of model reference adaptive control algorithms to control systems which exhibit nonlinear dynamical behaviour using the example of a Duffing oscillator being controlled to follow a linear reference model. For this system we show that if the nonlinearity is small then standard linear model reference control can be applied. A second example, which is often found in synchronization applications, is when the nonlinearities in the plant and reference model are identical. Again we show that linear model reference adaptive control is sufficient to control the system. Finally we consider controlling more general nonlinear systems using adaptive feedback linearization to control scalar nonlinear systems. As an example we use the Lorenz and Chua systems with parameter values such that they both have chaotic dynamics. The Lorenz system is used as a reference model and a single coordinate from the Chua system is controlled to follow one of the Lorenz system coordinates.     

Fluid Simulation of a Cusped Field Thruster

The cusped field thruster is a kind of newly developed electric propulsion device. The electric field at the channel exit and the low frequency oscillation were measured by former experiments. While the formation mechanism of them have not been fully interpreted yet. Through studying two distinguishing typical electron paths in the thrusters, a fluid model is built up along two electron paths, and then the model is completed by synthetically analyzing the effect of two electron paths. Time‐averaged electric potential distribution, anode current oscillation curve and time‐synchronized atom density and ion density distribution are obtained by simulation. (© 2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

悬链曲面上的点粒子动力学及扩展空间约束系统量子化

扩张型正则量子化方案的核心内容是位置、动量以及哈密顿量同时量子化. 通过分析悬链面上粒子的扩张型正则量子化方案, 并且与薛定谔理论进行比较, 发现内禀几何中二维悬链面给不出与薛定谔理论相一致的结果, 而考虑将二维悬链面嵌入在三维欧氏空间之后, 还需要将正则量子化方案进行扩张, 可以得到体系的几何势能和几何动量, 并与薛定谔理论相一致.     

高能电子辐照绝缘厚样品的表面电位动态特性

采用数值计算和实验测量相结合的方法, 阐明了高能电子束照射下绝缘厚样品的表面电位和电子产额动态特性. 结果表明: 由于电子在样品内部的散射和输运, 沿着深度方向, 空间电位先缓慢下降到最小值, 然后逐渐升高并趋近于零; 随着电子束照射, 样品的表面电位逐渐下降, 可至负千伏量级, 电子总产额逐渐增大至一个接近于1的稳定值; 电子束停止照射后, 长时间放置下, 表面电位将逐渐升高, 但带电并不会消除; 表面电位随电子束能量的升高近似线性下降, 随入射角的增大而升高, 而随样品厚度的增大仅略有下降.     

Electrophoresis and stability of nano-colloids: History,theory and experimental examples

The paper contains an extended historical overview of research activities focused on determining interfacial potential and charge of dispersed particles from electrophoretic and coagulation dynamic measurements. Particular attention is paid to nano-suspensions for which application of Standard Electrokinetic Model (SEM) to analysis of experimental data encounters difficulties, especially, when the solutions contain more than two ions, the particle charge depends on the solution composition and zeta-potentials are high. Detailed statements of Standard Electrokinetic and DLVO Models are given in the forms that are capable of addressing electrophoresis and interaction of particles for arbitrary ratios of the particle to Debye radius, interfacial potentials and electrolyte compositions. The experimental part of the study consists of two groups of measurements conducted for Pt/C nano-suspensions, namely, the electrophoretic and coagulation dynamic studies, with various electrolyte compositions. The obtained experimental data are processed by using numerical algorithms based on the formulated models for obtaining interfacial potential and charge. While analyzing the dependencies of interfacial potential and charge on the electrolyte compositions, conclusions are made regarding the mechanisms of charge formation. It is established that the behavior of system stability is in a qualitative agreement with the results computed from the electrophoretic data. The verification of quantitative applicability of the employed models is conducted by calculating the Hamaker constant from experimental data. It is proposed how to explain the observed variations of predicted Hamaker constant and its unusually high value.     

Electrochemical assessment of water|ionic liquid biphasic systems towards cesium extraction from nuclear waste

A room temperature ionic liquid (IL) composed of a quaternary alkylphosphonium (trihexyltetradecylphosphonium, P₆₆₆₁₄⁺) and tetrakis(pentafluorophenyl)borate anion (TB⁻) was employed within a water|P₆₆₆₁₄TB (w|P₆₆₆₁₄TB or w|IL) biphasic system to evaluate cesium ion extraction in comparison to that with a traditional water|organic solvent (w|o) combination. ¹³⁷Cs is a major contributor to the radioactivity of spent nuclear fuel as it leaves the reactor, and its extraction efficiency is therefore of considerable importance. The extraction was facilitated by the ligand octyl(phenyl)-N,N′-diisobutylcarbamoylphosphine oxide (CMPO) used in TRans-Uranium EXtraction processes and investigated through well established liquid|liquid electrochemistry. This study gave access to the metal ion to ligand (1:n) stoichiometry and overall complexation constant, β, of the interfacial complexation reaction which were determined to be 1:3 and 1.6 × 10¹¹ at the w|P₆₆₆₁₄TB interface while the study at w|o elicited an n equal to 1 with β equal to 86.5. Through a straightforward relationship, these complexation constant values were converted to distribution coefficients, δ_α, with the ligand concentrations studied for comparison to other studies present in the literature; the w|o and w|IL systems gave δ_α of 2 and 8.2 × 10⁷, respectively, indicating a higher overall extraction efficiency for the latter. For the w|o system, the metal ion-ligand stoichiometries were confirmed through isotopic distribution analysis of mass spectra obtained by the direct injection of an emulsified water–organic solvent mixture into an electron spray ionization mass spectrometer.     

Ab initio spectroscopic study for the NaRb molecule in ground and excited states

A wide adiabatic study is performed for NaRb molecule, involving 15¹Σ⁺ electronic states including the ionic state Na^?Rb⁺, as well as 14³Σ⁺, 1–9^1,3Π, and 1–5^1,3Δ states. This investigation is performed using an ab initio approach which involves the effective core potential, the core polarization potential with l‐dependent cut‐off functions. The NaRb system has been treated as a two‐electron system and the full valence configuration interaction is easily achieved. The spectroscopic constants R_e, D_e, T_e, ω_e, ω_ex_e, B_e, and D₀ for all these states are derived. We have also computed the vibrational levels as well their spacing for different values of J. In addition, permanent and transition dipole moments are determined and analyzed. The Dunham coefficients have been used to perform experimental spacing to compare directly with our results. The present calculations on NaRb extend previous theoretical works to numerous electronic excited states in the various symmetries. © 2014 Wiley Periodicals, Inc.