非惯性参考系中弹性壳的非线性振动分析

给出了弹性壳处于非惯性参系中的运动描述，基于Ｈａｍｉｌｔｏｎ原理建立了中厚壳在非惯性参考系中的非线性运动控制方程，应用多尺度法及谐波平衡法具体地分析了圆柱壳的非线性振动问题     

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.     

消减舰船变形的影响和为全舰提供高精度姿态基准

引用国内外一些文献列举的现代舰船船体变形的数据，论证了消减船体变形的影响和为全舰提供精确的姿态基准的重要意义。对舰载航向姿态基准的功能、性能与特点进行了综述。介绍了基于激光陀螺和光纤Bragg光栅传感器测量船体变形的新方法。最后，探讨了分布式姿态基准系统的技术方案。     

On Fractional Adaptive Control

Introducing fractional operators in the adaptive control loop, and especially in Model Reference Adaptive Control (MRAC), has proven to be a good mean for improving the plant dynamics with respect to response time and disturbance rejection. The idea of introducing fractional operators in adaptation algorithms is very recent and needs to be more established, that is why many research teams are working on the subject. Previously, some authors have introduced a fractional model reference in the adaptation scheme, and then fractional integration has been used to deal directly with the control rule. Our original contribution in this paper is the use of a fractional derivative feedback of the plant output, showing that this scheme is equivalent to the fractional integration, one with a certain benefit action on the system dynamical behaviour and a good robustness effect. Numerical simulations are presented to show the effectiveness of the proposed fractional adaptive schemes.     

特种合金钢系列标准物质研制

介绍了特种合金钢系列标准物质的研制过程。采用合理的冶炼锻轧工艺,选取不同部位的样品进行均匀性检验,确定了15种元素的认定值及扩展不确定度,并进行了线性、一致性考察以及与国内外同类标准物质的比对。结果表明,本套特种合金钢系列标准物质的均匀性良好,定值准确且有良好的梯度分布。     

Water PMF for predicting the properties of water molecules in protein binding site

Water is an important component in living systems and deserves better understanding in chemistry and biology. However, due to the difficulty of investigating the water functions in protein structures, it is usually ignored in computational modeling, especially in the field of computer‐aided drug design. Here, using the potential of mean forces (PMFs) approach, we constructed a water PMF (wPMF) based on 3946 non‐redundant high resolution crystal structures. The extracted wPMF potential was first used to investigate the structure pattern of water and analyze the residue hydrophilicity. Then, the relationship between wPMF score and the B factor value of crystal waters was studied. It was found that wPMF agrees well with some previously reported experimental observations. In addition, the wPMF score was also tested in parallel with 3D‐RISM to measure the ability of retrieving experimentally observed waters, and showed comparable performance but with much less computational cost. In the end, we proposed a grid‐based clustering scheme together with a distance weighted wPMF score to further extend wPMF to predict the potential hydration sites of protein structure. From the test, this approach can predict the hydration site at the accuracy about 80% when the calculated score lower than ?4.0. It also allows the assessment of whether or not a given water molecule should be targeted for displacement in ligand design. Overall, the wPMF presented here provides an optional solution to many water related computational modeling problems, some of which can be highly valuable as part of a rational drug design strategy. © 2012 Wiley Periodicals, Inc.     

Understanding the effect of inhomogeneous fuel–air mixing on knocking characteristics of various ethanol reference fuels with RON 100 using rapid compression machine

We investigated the effect of inhomogeneous mixing of a fuel–air mixture in a spark-ignition engine on knocking characteristics and the dependency of the effect on the fuel, especially for various ethanol reference fuels with a fixed RON of 100. We assumed that a locally lean spot and rich spots exist in the end gas owing to inhomogeneous mixing and calculated their thermodynamic states with a multizone spark-ignition engine simulation. Subsequently, the ignition delay around the state was measured using a rapid compression machine at varying temperatures and equivalence ratios. The obtained results were processed to calculate ξ, which is the ratio of sound speed to auto-ignition propagation speed, and $?$, defined as the time required for acoustic front to exit the hot spot divided by the excitation time. Then, we analyzed the knocking occurrence and intensity from the locally lean spot and rich spots based on Zel'dovich and Bradley's ξ–$?$ theory. Our results show that the lean spot has a shorter ignition delay than the stoichiometric mixture (ξ?>?0) regardless of the ethanol content, whereas the rich spot does not (ξ?<?0), implying that only the lean spot can initiate knocking. This is because the temperature of the lean spot is higher than the surrounding mixture owing to its higher specific heat ratio and less charge cooling effect. In addition, the knocking intensity from the lean spot is found to be maximized with ERF0, showing the largest ${\xi }^{?2}$ value. Further analysis was conducted by dividing ξ into the effect of the temperature gradient, ξ_T, and that of the equivalence ratio gradient, ξ_?. Consequently, we found that the magnitude of ξ_T is related to the activation energy of the fuel, while that of ξ_? is determined by the dependency of the pre-heat release characteristics of the fuel on the equivalence ratio.     

A dynamic process interpretation of the sparse ERGM reference model

Exponential family random graph models (ERGMs) can be understood in terms of a set of structural biases that act on an underlying reference distribution. This distribution determines many aspects of the behavior and interpretation of the ERGM families incorporating it. One important innovation in this area has been the development of an ERGM reference model that produces realistic behavior when generalized to sparse networks of varying sizes. Here, we show that this model can be derived from a latent dynamic process in which tie formation takes place within small local settings between which individuals move. This derivation provides one possible micro-process interpretation of the sparse ERGM reference model and sheds light on the conditions under which constant mean degree scaling can emerge.     

A comparison of quantitative nuclear magnetic resonance methods: internal,external, and electronic referencing

The performance of three quantitative NMR methods was compared in terms of short‐term and long‐term precision and accuracy, robustness, linear range, and general applicability. The Internal Reference method employs a reference material co‐dissolved with sample; the External Reference method employs a reference material contained in a separate solution; and the third method, known as Electronic REference To access In vivo Concentrations (ERETIC), employs an externally calibrated digital reference peak. The Internal Reference method results were the most precise and remained stable within 0.1% for at least 4 weeks. The results from the External Reference and ERETIC methods were practically equivalent to each other during this time. These methods exhibited small differences relative to the standard set by the Internal Reference method and slightly lower precision, establishing them as practical alternatives to the Internal Reference method. In contrast to the Internal Reference method, the External Reference and ERETIC methods possess several advantages that address peak overlap, flexibility of calibration, and duration of applicability. The study was designed such that each spectrum contained the information needed to compare the three methods while all other variables were kept constant. Applicability of pulse width compensation is addressed. ERETIC software compensation and minor adjustments to 90° pulse width were concluded to be unnecessary for this system. Although each of the methods was applied here to specifically calculate and compare chemical purity values, this evaluation applies generally to absolute quantitation by NMR. Copyright © 2013 John Wiley & Sons, Ltd.     

Trifluoroethylxanthate as an Analytical Reagent: AAS of Zinc,Antimony and Lead After Coprecipitation of Their Trifluoroethylxanthates onto Microcyrstalline Naphthalene

Abstract

A sensitive method has been developed for the direct atomic absorption spectrometric determination of zinc, antimony and lead after coprecipitation of their trifluoroethylxanthates onto microcrystalline naphthalene. The metal xanthates are quantitatively coprecipitated over the pH ranges: Zn, 5.9–8.4; Sb, 4.0–6.0 and Pb, 4.0–11.0. The solid mass consisting of the metal complex and naphthalene is dissolved in DMF. This solution is aspirated into an air-acetylene flame at 213.9, 217.6 and 217.0nm for Zn, Sb and Pb, respectively. Beer's law is obeyed in the concentration range 2–50, 3–90 and 5–60 μg of Zn, Sb and Pb, respectively in 10ml of the final DMF solution. RSDs are at the ± (0.5–0.6)% level (n=10). The concentration for 1% absorption is 0.019, 0.035 and 0.060μg/ml for Zn, Sb and Pb, respectively. The method is suitable for the preconcentration of the metals from a larger volume of the aqueous phase, and has been employed for their determination in standard reference materials. It may be employed for the simultaneous determination of Zn, Pb and Sb in a solution by pH control.