A SINGULAR VALUE DECOMPOSITION BASED TRUNCATION ALGORITHM IN SOLVING THE STRUCTURAL DAMAGE EQUATIONS

The structural damage identification through modal data often leads to solving a set of linear equations. Special numerical treatment is sometimes required for an accurate and stable solution owing to the ill conditioning of the equations. Based on the singular value decomposition (SVD) of the coefficient matrix, an error based truncation algorithm is proposed in this paper. By rejection of selected small singular values, the influence of noise can be reduced. A simply-supported beam is used as a simulation example to compare the results to other methods.Illustrative numerical examples demonstrate the good efficiency and stability of the algorithm in the nondestructive identification of structural damage through modal data.     

铝单晶体潜在硬化的指向性行为研究

应用高纯铝单晶体，采用偏离弹性线法定义其在潜在滑移系统在屈服应力，研究了潜在滑移系在正负两个滑移方向上的屈服及应变硬化行为。结果表明，潜在滑移系负行为的差异要远远小于动滑移系的Ｂａｕｓｃｈｉｎｇｅｒ效应，其正负方向的屈服应力一般均等于或略小于预应变时的最大分切应力，大大高于动滑移系的负向屈服应力，潜在滑移系和原始滑移系的相对取向及预应变的大小对单晶体潜在移系在潜在硬化的影响不大，但对其起始过渡区应     

透明导电薄膜ITO对浅面浮雕VCSEL的影响

对于顶面出光的浅面浮雕VCSEL结构,有源区的电流密度分布的不均性制约着单模稳定性的提高。为此,提出了一种新型结构:氧化铟锡透明导电薄膜(ITO)浅面浮雕VCSEL。该结构不仅能够增大高阶模式的阈值增益,还能够提高基模的增益,实现基模对高阶模式的稳定抑制。研究了ITO的厚度对阈值增益的影响及ITO对VCSEL有源区电流密度分布的影响。研究结果表明:在ITO的厚度为半波长的整数倍时,基模对高阶模式的限制作用最强;ITO通过改善VCSEL有源区的电流密度分布,达到了增大基模的增益和降低高阶模式增益的目的,同时还降低了串联电阻和外电压。     

基于单粒子模型与偏微分方程的锂离子电池建模与故障监测

锂离子电池内部结构是一种复杂的分布参数系统, 如果为了降低计算难度而使用常微分方程描述锂离子电池, 可能会引入系统误差, 降低系统模型的可信度, 需要使用偏微分方程建立分布参数系统的精确模型. 本文提出了一种基于单粒子模型和抛物型偏微分方程的锂离子电池系统建模与故障监测系统设计方法, 当锂离子浓度实测值与理想值的残差大于预设门槛时判定分布参数系统处于故障状态. 通过一个仿真实例进行了锂离子电池系统建模和故障诊断实验, 实验证明基于单粒子模型和偏微分方程的锂离子电池故障监测系统具有更高的精确度和可信度.     

FTIR spectroscopy of biodegraded historical textiles

Fungal attack is a common and severe problem in the storage rooms of museums. Fungi can damage different materials; organic materials are especially sensitive. In this work two different FTIR spectroscopy methods (micro-spectroscopy with diamond anvil cell and ATR) were used to investigate structural changes on biodeteriorated and non-affected textile fibres obtained from different Slovene museums and sacred objects. Several structural changes were observed in spectra of biodeteriorated as well as of non-affected cellulosic fibres, whereas no changes were observed in proteinaceous fibres. In the scope of spectral analysis crystallinity index has also been calculated by comparing two different band ratios. The research showed that the crystallinity index, calculated from the band intensity ratio I₁₃₇₂/I₂₉₀₀ groups fibres into two groups; biodeteriorated fibres predominantly have lower crystallinity index.     

New bicyclic phosphorous ligands: synthesis, structure and catalytic applications in ionic liquids

New azadioxaphosphabicyclo[3.3.0]octane ligands showing a trans arrangement with regard to the two five-membered heterocycles, were obtained as a mixture of three conformers, in agreement with molecular modelling studies. The stability of oxaphosphane ligands was studied under basic catalytic conditions, monitored by NMR spectroscopy. Palladium catalytic systems containing these ligands were active in Suzuki C-C cross-coupling reactions between phenylboronic acid and aryl halides (bromide and chloride derivatives) bearing electron-donor or electron-withdrawing substituents, in both organic and ionic liquid solvents. The catalytic systems showed a high stability even under the most severe reaction conditions used in this work. The ionic liquid catalytic phase could be recycled up to ten times without significant activity loss.     

Capping ligand perturbed slow magnetic relaxation in dysprosium single-ion magnets

Single-ion magnets 1 and 2 and their diamagnetic analogues 3 and 4 for magnetic-site dilution were obtained through substitution of the coordinated water molecules of [Ln(TTA)(3)(H(2)O)(2)] (Ln=Dy (1, 2), Y (3, 4); TTA=4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionate) by 2,2'-bipyridine (1, 3) and 1,10-phenanthroline (2, 4) capping ligands. Their structures and magnetic properties were investigated with the goal of identifying features relevant to modulating relaxation dynamics of single-ion magnets. The metal ions in all complexes adopt an approximately square-antiprismatic (SAP) O(6)N(2) coordination environment. The SAP polyhedrons for both 1 and 2 show slight longitudinal compression, while the coordination sphere of 1 deviates more from an ideal SAP than that of 2, as indicated by the skew angles of the SAP environment. The similar values of U(eff) for the two magnetically diluted samples imply nearly the same distribution of low-lying states for their Dy(III) centers, which is consistent with the slight axial contraction observed for 1 and 2 and further corroborated by ligand-field analysis. The fast quantum tunneling rate τ(QTM) of 1, which is about ten times faster than that of 2, can presumably be associated with the larger rotation of the SAP surroundings. This distortion may result in a significant transverse anisotropy terms, and thus strongly affect the dynamic behavior of the system.     

一种基于Q学习的单路口交通信号控制方法

利用Watkins(1989)提出的Q学习算法,基于不同相位的动态最小时间需求,并以相位通行需求时间为研究对象,以动态相位时间差为状态转换控制目标,建立了单路口交通信号控制的一种动态智能控制方法.计算机模拟仿真表明这种控制方法的好的控制效果.     

A novel single‐electron sodium bond system of H3C···Na?Y (YH,OH, F,CCH, CN,and NC)

A novel single‐electron sodium bond system of H₃C···Na? H (I), H₃C···Na? OH(II), H₃C···Na? F(III), H₃C···Na‐CCH(IV), H₃C···Na? CN (V) and H₃C···Na? NC (VI) complexes has been studied by using MP2/6‐311++G** and MP2/aug‐cc‐pVTZ methods for the first time. We demonstrated that the single‐electron sodium bond H₃C···Na? Y formed between H₃C and Na? Y (Y?H, OH, F, CCH, CN, and NC) could induce the Na? Y increased and stretching frequencies of I–IV and VI are red‐shifted, including the Na? N bond in complex V is blue‐shifted abnormally. The interaction energies are calculated at two levels of theory [MP2, CCSD(T)] with different basis. The results shows that the strength of binding bond in group 2 (IV–VI) with π electrons are stronger than that of group 1 (I–III) without π electrons. For all complexes, the main orbital interactions between moieties H₃C and Na? Y are LP₁(C)→LP*₁(Na). By comparisons with some related systems, it is concluded that the strength of single‐electron bond is increased in the order: hydrogen bond < bromine bond < sodium bond < lithium bond. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2011