加速牛顿迭代收敛的新方法

提出了加速牛顿迭代收敛的新思想，构造出一类加权牛顿迭代格式，通过选取最优加权因子，使得该格式具有高阶收敛性和较小的渐近误差常数。     

一类非线性退化方程混合问题解的渐进性态

本文利用比较原理以及一种特殊变换研究了一类非线性退化方程的混合问题，得到了这类复杂问题解的渐进性质。     

单粒子势模型下价核子的密度分布

依据实验事实，利用单粒子势模型，计算了一些核态外层价核子的密度分布.计算给出了价核子在核外部分布的概率和贡献，以此作为晕核态的判断标准.通过研究均方根半径随结合能变化的规律，指出了晕核态存在的条件，尤其是质子晕核态存在的条件.这些对判断和寻找晕核态有现实的指导意义. 关键词： 单粒子势模型 价核子 密度分布 中子晕核态 质子晕核态     

高阶非线性时滞差分方程解的渐近性

研究如下的具强迫项的高阶非线性时滞差分方程△^my(n) u(n)l↑∑i=1 gi(y(n-τ))=v(n)其中，m≥1，u,v：N→R，gi：R→R且τ∈{0，1，2，3，…)，i=1，2，…，l，得到了使该方程的解具有某种渐近性态的充分条件。     

On Quasiclassical Field Theories Invariant with Respect to a Lie Group

Mathematical Notes -     

三阶非线性时滞差分方程解的渐近性

研究了一类三阶非线性变滞量差分方程解的渐近性,给出了该类方程的非振动解当n→+∞时渐近趋于零或趋于某有限数值的几个充分条件.     

Structural optimization design for large mirror

The system design must be started from the concept with low cost and high performance. In this point, the topological shape of the structure is very important in the view of the structural rigidities and light-weight design.In this paper, the optimization methodology is presented in the design stage of the large optical mirror. We obtain the optimal layout through the topology optimization and then design the details through the size or shape optimization for structural rigidity.     

Asymptotic Correction of More Sturm–Liouville Eigenvalue Estimates

The asymptotic correction technique of Paine, de Hoog and Anderssen can dramatically improve the accuracy of finite difference or finite element eigenvalues at negligible extra cost if closed form expressions are available for the errors in a simpler related problem. This paper gives closed form expressions for the errors in the eigenvalues of certain Sturm–Liouville problems obtained by various methods, thereby increasing the range of problems for which asymptotic correction can achieve maximum efficiency. It also investigates implementation of the method for more general problems.     

Asymptotic Methods Applied to Contact Problems

Asymptotic methods for contact problems are expounded. Some typical integral equations are considered     

A Generalized Unpaired Electron Spin Density Equation and Organic Hyperconjugation Mechanism

A large class of stereochemcial and related interactions in organic chemistry are repulsive and others are attractive, but the relative orientation of two methyl groups and the amount of energy required to twist one relative to the other (the hindered rotation energy barriers), or the alignment of such a group with respect to a conjugated ring to which it is attached (widely attributed to a mechanism called “hyperconjugation”) are estimated to be small in compared with the total energy of the molecule. We used theories of both isotropic and anisotropic proton hyperfine interactions in the π‐electron systems developed in the early sixties. They are approximated by the magnetic dipole nteractions between each proton and an electron spin magnetization that is distributed in 2s and 2p Slater atomic orbitals center on carbon atoms. We have extended these theories to the non‐planar olefinic cation radicals, which are very important in biochemistry as well as in petroleum catalysis. A three dimensional electron spin density equation has been developed in this paper to handle some Jahn‐Teller vibronic molecules. The new electron spin density equation related the observed proton hyperfine splittings to the non‐planar structures of the open‐chain alkene cation radicals generated by radiolysis and various chemical oxidation methods. The spin densities and the conformational calculations based on valence bond theory and symmetry principles are compared with some more elaborated molecular orbital calculations in the literature. The localized valence bond approaches are better in accord with our experimental results. The anomalous line‐width effect of the four methyl groups observed in the 2,3‐dimethyl‐2‐butene cation radicals also confirmed the positive sign of the electron‐proton hyperfine constant of hyper‐conjugation mechanism. A methyl substituent attached to a conjugated molecule often behaves as if it formed part of the region of conjugation; the charge appears to flow from the methyl group into the π electron system and it may also give rise to an appreciable dipole moment. Methylation also gives rise to an appreciable dipole moment, and the resultant red shift of electronic absorption bands is of some importance in the design of dye molecules.