两参数轴向冲击载荷作用下圆柱壳弹塑性动力屈曲

研究圆柱壳在两参数轴向冲击载荷下的弹塑性动力屈曲问题，基本控制方程由弹塑性连续介质中关于加速度的最小原理获得，本构关系采用增量理论。研究表明：屈曲过程可划分为两相，两相之间由临界时间ｔ表征，并分别讨论了应力波对屈曲的影响，压缩波与弯曲波的相互作用及几何尺寸，材料参数，初始缺陷，载荷峰值及持续时间等诸多因素与动力屈曲的关系。     

圆柱壳轴向流固冲击屈曲与塑性失效的实验研究

通过对三种不同径厚比圆柱壳进行的流固冲击实验，分析了它们在流固冲击载荷下的动力响应特点，并与相应的高速撞击与静力屈曲实验作了简单的比较，分析了它们之间的异同点。同时文中对极值冲击倒塌特性进行了详细分析     

Surface‐Specific Functionalization of Nanoscale Metal–Organic Frameworks

A method for modifying the external surfaces of a series of nanoscale metal–organic frameworks (MOFs) with 1,2‐dioleoyl‐sn‐glycero‐3‐phosphate (DOPA) is presented. A series of zirconium‐based nanoMOFs of the same topology (UiO‐66, UiO‐67, and BUT‐30) were synthesized, isolated as aggregates, and then conjugated with DOPA to create stably dispersed colloids. BET surface area analysis revealed that these structures maintain their porosity after surface functionalization, providing evidence that DOPA functionalization only occurs on the external surface. Additionally, dye‐labeled ligand loading studies revealed that the density of DOPA on the surface of the nanoscale MOF correlates to the density of metal nodes on the surface of each MOF. Importantly, the surface modification strategy described will allow for the general and divergent synthesis and study of a wide variety of nanoscale MOFs as stable colloidal materials.     

Synthesis of Functional Poly(disubstituted acetylene)s through the Post‐Polymerization Modification Route

We report the recent progress in the preparation of functional poly(disubstituted acetylene)s (PDSAs) through post‐polymerization modification routes. The metathesis polymerization of disubstituted acetylene monomers activated by Mo/W–Sn complex catalysts, which do not tolerate highly polar functionalities, was assumed to be a key step in the polymer synthetic procedures. We and other groups have explored several approaches to prepare PDSAs with latent reactive functionalities, which are inactive to Mo/W–Sn complex catalysts but can be used as highly reactive sites for post‐polymerization modification. Click chemistry, Michael‐type addition reactions, the use of activated esters and other strategies are demonstrated by recently published examples. These works indicate that post‐polymerization modification is an efficient route to the synthesis of various functional PDSAs.     

Nanometrization of Lanthanide‐Based Coordination Polymers

Heteronuclear lanthanide‐based coordination polymers are microcrystalline powders, the luminescence properties of which can be precisely tuned by judicious choice of the rare‐earth ions. In this study, we demonstrate that such materials can also be obtained as stable solutions of nanoparticles in non‐toxic polyols. Bulk powders of the formula [Ln_2?2xLn′_2x(bdc)₃ ? 4 H₂O]_∞ (where H₂bdc denotes 1,4‐benzene‐dicarboxylic acid, 0≤x≤1, and Ln and Ln′ denote lanthanide ions of the series La to Tm plus Y) afford nanoparticles that have been characterized by dynamic light‐scattering (DLS) and transmission electron microscopy (TEM) measurements. Their luminescence properties are similar to those of the bulk materials. Stabilities versus time and versus dilution with another solvent have been studied. This study has revealed that it is possible to tune the size of the nanoparticles. This process offers a reliable means of synthesizing suspensions of nanoparticles with tunable luminescence properties and tunable size distributions in a green solvent (glycerol). The process is also extendable to other coordination polymers and other solvents (ethylene glycol, for example). It constitutes a new route for the facile solubilization of lanthanide‐based coordination polymers.     

Highly Isospecific Polymerization of Silyl‐Protected ω‐Alkenols Using an [OSSO]‐Type Bis(phenolato) Dichloro Zirconium(IV) Precatalyst

The coordination polymerization of silyl‐protected ω‐alkenols such as ω‐alken‐α‐oxytriisopropylsilanes 1 provides poly(ω‐alkenyl‐α‐oxytriisopropylsilalne)s with a highly isospecific microstructure ([mmmm] > 95%) when a combination of [OSSO]‐type bis(phenolato) dichloro zirconium(IV) complex 2 and dried methylaluminoxane is used as the precatalyst and activator, respectively. The resulting siloxy‐substituted polymers could be efficiently transformed into the corresponding functionalized polyolefins, which contained up to 90% acetyl groups and ≈7% hydroxy groups in the terminal side chains.

     

Dynamic Docking and Undocking Processes Addressing Selectively the Outside and Inside of Polymersomes

Increasing complexity and diversity of polymersomes and their compartments is a key issue for mimicking cellular functions and protocells. Thus, new challenges arise in terms of achieving tunable membrane permeability and combining it with control over the membrane diffusion process, and thus enabling a localized and dynamic control of functionality and docking possibilities within or on the surface of polymeric compartments. This study reports the concept of polymersomes with pH‐tunable membrane permeability for controlling sequential docking and undocking processes of small molecules and nanometer‐sized protein mimics selectively on the inside and outside of the polymersome membrane as a further step toward the design of intelligent multifunctional compartments for use in synthetic biology and as protocells. Host–guest interactions between adamantane and β‐cyclodextrin as well as noncovalent interactions between poly(ethylene glycol) tails and β‐cyclodextrin are used to achieve selective and dynamic functionalization of the inner and outer spheres of the polymersome membrane.     

工程结构静力分析和屈曲分析程序系统DDJTJQ及其应用

DDJTJQ是一个国内开发的组合结构静力分析和屈曲分析有限元程序系统,自1986年通过技术鉴定以来又有了许多发展。本文介绍该程序系统的功能和特点、求解能力以及在不同工程领域结构分析中的应用。     

盘绕式空间可展折叠无铰伸展臂的屈曲分析理论研究

首先介绍了无铰可展空间伸展臂(Hingeless Mast)构造特点、展开折叠机理和受力特点,然后根据弹性稳定理论和能量原理,分别推导出局部卷压屈曲和整体螺旋屈曲的临界压力表达式,并据此进行参数特性分析。本文分析理论对无铰空间伸展臂的设计具有重要指导意义。     

复杂载荷下复合材料对称层合板的椭圆形分层屈曲

应用Ｒａｙｌｅｉｇｈ－Ｒｉｔｚ法对含有单个椭圆形分层的复合材料对称层板在压剪载荷联合作用下的脱层屈曲问题进行了分析计算。给出相应于不同的椭圆长短半轴之比ａ／ｂ值下及不同椭回主轴的偏角时，脱层屈曲的临界应变值。此计算考虑了层板的拉伸剪切藕合刚度影响及子层本身弯曲－扭转耦合刚度，和拉伸－弯曲耦合刚度的影响，给出有工程参考价值的计算结果。