结构损伤识别的周期小波方法

通过对结构损伤前后模态特征的变化进行分析,利用损伤结构的位移振型函数构造出曲率振型函数γi(x),然后再在曲率振型函数的基础上提出一个用于探测和评定损伤程度的新指标———损伤因子r(x)=∑i∈Idγi2(x);基于小波分析的方法,对损伤因子进行周期小波变换,通过小波系数的取值范围提出了一种结构损伤定位和损伤程度的评估方法.数值仿真表明,这是一种行之有效的损伤识别方法.     

二次概周期系数微分方程的概周期解

利用指数二分性,Schauder不动点定理和Grownwall不等式证明了一类概周期系数微分方程的概周期解、有界解的存在唯一性及概周期解的全局吸引性.     

周期函数Fourier级数展开式唯一性的简单证明与推广

对于周期函数f(x)按不同的周期展开对应不同的Fourier级数,这些表面上不同的式子是否一致引起了人们的注意[1],[2].本文应用Parseval等式给出一个关于这种唯一性的简单证明,并把这一种性质推广到高维情况的多重Fourier级数.     

Boussinesq方程行波解的存在性

利用平面动力系统方法的分支理论,研究了Boussinesq方程,通过对Boussinesq方程进行行波变换,得到了相应行波系统的首次积分和平衡点,给出了不同参数条件下的相图,证实了Boussinesq方程存在孤立波解和周期波解。     

Beddington-DeAngelis型捕食-食饵动力系统的正平衡点及其稳定性

A class of Beddington-DeAngelis' type predator-prey dynamic system with prey and predator both having linear density restriction is considered. By using the qualitative methods of ODE, the existence and uniqueness of positive equilibrium and its global asymptotic stability are analyzed. The direct criterions for local stability of positive equilibrium and existence of limit cycle are also established when inference parameter of predator is small.     

具有反馈控制的非自治Logistic模型的正周期解

A nonautonomous delayed logistic model with linear feedback regulation is pro- posed in this paper.Sufficient conditions are derived for the existence,uniqueness and global asymptotic stability of positive periodic solution of the model.     

(2+1)维色散长波方程的双周期解

借助计算机代数操作系统,引入Jacob ian椭圆函数负幂次展开的方法,求解(2+1)维色散长波方程,得到一系列新的双周期解。     

具有Holling Ⅲ类功能反应捕食者食脉冲系统正周期解的存在性

利用重合度理论中的连续性定理研究一类具有Holling Ⅲ类功能反应捕食者食脉冲系统正周期解的存在性, 建立了存在正周期解的充分条件, 推广 并改进了已有的相关结果.     

非对称损失下正态均值的区间估计

考虑非对称损失下正态均值的区间估计, 在位置变换群下给出容许的最优同变置信区间, 其为通常置信区间的推广. 同时, 利用估计问题中对序限制下参数估计量的改进方法, 结合分布参数之间的序限制改进了所得的最优同变置信区间, 构造了一族改进置信区间.     

Comparison of Proton Acceptor and Proton Donor Properties of H2O and H2O2 in Organic Crystals of Drug-like Compounds: Peroxosolvates vs. Crystallohydrates

Two new peroxosolvates of drug-like compounds were synthesized and studied by a combination of X-ray crystallographic, Raman spectroscopic methods, and periodic DFT computations. The enthalpies of H-bonds formed by hydrogen peroxide (H₂O₂) as a donor and an acceptor of protons were compared with the enthalpies of analogous H-bonds formed by water (H₂O) in isomorphic (isostructural) hydrates. The enthalpies of H-bonds formed by H₂O₂ as a proton donor turned out to be higher than the values of the corresponding H-bonds formed by H₂O. In the case of H₂O₂ as a proton acceptor in H-bonds, the ratio appeared reversed. The neutral O∙∙∙H-O/O∙∙∙H-N bonds formed by the lone electron pair of the oxygen atom of water were the strongest H-bonds in the considered crystals. In the paper, it was found out that the low-frequency Raman spectra of isomorphous crystalline hydrate and peroxosolvate of N-(5-Nitro-2-furfurylidene)-1-aminohydantoin are similar. As for the isostructural hydrate and peroxosolvate of the salt of protonated 2-amino-nicotinic acid and maleic acid monoanion, the Raman spectra are different.