An embedding domain approach for a class of 2-d shape optimization problems: mathematical analysis

This contribution combines a shape optimization approach to free boundary value problems of Bernoulli type with an embedding domain technique. A theoretical framework is developed which allows to prove continuous dependence of the primal and dual variables in the resulting saddle point problems with respect to the domain. This ensures the existence of a solution of a related shape optimization problem in a sufficiently large class of admissible domains.     

Coercive boundary value problems for regular degenerate differential-operator equations

This study focuses on nonlocal boundary value problems (BVP) for degenerate elliptic differential-operator equations (DOE), that are defined in Banach-valued function spaces, where boundary conditions contain a degenerate function and a principal part of the equation possess varying coefficients. Several conditions obtained, that guarantee the maximal L_p regularity and Fredholmness. These results are also applied to nonlocal BVP for regular degenerate partial differential equations on cylindrical domain to obtain the algebraic conditions that ensure the same properties.     

The spectrum of cyclic BSA(ν, 3, λ; α) with α = 2, 3

Balanced sampling plans excluding contiguous units (or BSEC) were first introduced by Hedayat, Rao, and Stufken in 1988. In this paper, we generalize the concept of a cyclic BSEC to a cyclic balanced sampling plan to avoid the selection of adjacent units (or CBSA for short) and use Langford and extended Langford sequences to construct a cyclic BSA(ν, 3, λ; α) with α = 2, 3. We finally establish the necessary and sufficient conditions for the existence of a cyclic BSA(ν, 3, λ; α) where α = 2, 3. © 2005 Wiley Periodicals, Inc. J Combin Designs.     

60keV质子辐照对TiNi记忆合金薄膜马氏体相变的影响

 利用磁控溅射的方法在氧化后的单晶Si基片上制备了TiNi形状记忆合金薄膜，利用示差扫描量热法和原位X射线衍射研究了薄膜的马氏体相变特征。通过60keV质子注入（辐照）薄膜样品研究了H+离子对合金薄膜马氏体相变特征的影响，结果表明氢离子注入后引起了马氏体相变开始Ms和结束点Mf以及逆马氏体相变开始As和结束温度Af的下降，而对R相变开始Rs和结束温度Rf影响不大。掠入射X射线衍射表明H+离子注入后有氢化物形成。H⁺离子注入形成的氢化物是引起相变点的变化的主要因素。     

会聚厄米-双曲余弦高斯光束的光强分布和焦移

 基于厄米-双曲余弦高斯光束通过无光阑限制薄透镜聚焦的解析传输公式，研究了厄米-双曲余弦高斯光束聚焦区域的光强分布，并对光束的焦移进行了分析，讨论了偏心参数对光强主极大位置的影响。结果表明：TEM₁₁模厄米-双曲余弦高斯光束的相对焦移（绝对值）随偏心参数和菲涅尔数的减小而增大，菲涅尔数较大时相对焦移趋于零。TEM₂₂模光束在偏心参数小于0.54时，轴外与轴上光强极大值的比值大于1，此时光强主极大在轴外，偏心参数大于0.54时则相反；在偏心参数等于0.54时比值为1，此时光束有两个主极大，偏心参数愈大光强愈集中于轴上。使用LW法和GH法得到的TEM₂₂模光束的相对焦移（绝对值）随偏心参数和菲涅尔数的变化规律与TEM₁₁模光束一致，但相同参数下使用这两种方法得出的具体结果不同。     

CCD相机调制传递函数测试软件的研制

数学傅立叶分析法是测量调制传递函数常用的一种方法，为了迅速地给出采用该方法进行调制传递函数测试的结果，针对刀口扫描测试CCD相机调制传递函数的测试系统研制了测试软件。软件可读入CCD相机摄取的数字图像文件，对数据进行消噪声处理，并自动识别刀口位置，选择合适区域计算出相机的调制传递函数。软件采用VC语言编制，结果以列表和曲线两种形式输出，用户界面良好，使用方便。利用该软件得到的测试结果与俄罗斯软件的计算结果吻合较好。     

Synthesis of 4,6-disubstituted pyrimidines via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine

A series of 4,6-disubstituted pyrimidines were synthesized via Suzuki and Kumada coupling reaction of 4,6-dichloropyrimidine.     

Rod–coil block copolymers: An iterative synthetic approach via living free-radical procedures

A modular approach has been developed for the synthesis of rod–coil block copolymers involving the initial preparation of a macroinitiator based on the rod block followed by the growth of the coil segment with living free-radical procedures. The key feature of this strategy is the utilization of an alkoxyamine group from the beginning of the synthesis, which serves as a solubilizing group and ensures that each rod block contains a single initiating fragment. Using this approach permits block copolymers based on insoluble biphenyl ester oligomers to be conveniently prepared with coil segments that range from styrenes to acrylates to 1,3-dienes. The tendency of the rod segments to crystallize is strongly dependent on the weight fraction of the rod segment and the chemical nature of the coil segment. Rod–coil molecules containing at least 25–35 wt % polystyrene or poly(n-butyl acrylate) coil segments show a two-dimensional hexagonal arrangement of rod aggregates, as characterized by transmission electron microscopy and small-angle X-ray scattering. Polyisoprene block copolymers exhibit a lamellar microstructure with short rigid domains in which the rod units lie in an interdigitated smectic C arrangement. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3640–3656, 2003     

Synthesis of side‐chain liquid‐crystalline homopolymers and triblock copolymers with p‐methoxyazobenzene moieties and poly(ethylene glycol) as coil segments by atom transfer radical polymerization and their thermotropic phase behavior

A series of side‐chain liquid‐crystalline (LC) homopolymers of poly[6‐(4‐methoxy‐4′‐oxy‐azobenzene) hexyl methacrylate] with different degrees of polymerization were synthesized by atom transfer radical polymerization (ATRP), which were prepared with a wide range of number‐average molecular weights from 5.1 × 10³ to 20.6 × 10³ with narrow polydispersities of around 1.17. Thermal investigation showed that the homopolymers exhibit two mesophases, a smectic phase, and a nematic phase, and the phase‐transition temperatures of the homopolymers increase clearly with increasing molecular weights. A series of novel LC coil triblock copolymers with narrow polydispersities was synthesized by ATRP, and their thermotropic phase behavior was investigated with differential scanning calorimetry and polarized optical microscopy. The LC coil triblocks were designed to have an LC conformation of poly[6‐(4‐methoxy‐4′‐oxy‐azobenzene) hexyl methacrylate] with a wide range of molecular weights from 3.5 × 10³ to 1.7 × 10⁴ and the coil conformation of poly(ethylene glycol) (PEG) (number‐average molecular weight: 6000 or 12,000) segment. Their characterization was investigated with ¹H NMR, Fourier transform infrared spectra, and gel permeation chromatography. Triblock copolymers exhibited a crystalline phase, a smectic phase, and a nematic phase. The phase‐transition temperatures from the smectic to nematic phase and from the nematic to isotropic phase increased, and the crystallization of PEG depressed with increasing molecular weight of the LC block. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2854–2864, 2003