接触问题的非线性互补－接触柔度法

基于势能互补原理，不引入额外松弛变量，对库仑摩擦定律未做预先线性化近似，提出了三维弹性摩擦接触问题的非线性互补－接触柔度法，收敛性和收敛速率得到了严格理论保证。数值实验结果表明方法可靠、有效、低存储量、高精度     

中空纤维三相液相微萃取-高效液相色谱法测定水中的4种酚类化合物

建立了中空纤维液-液-液三相微萃取-高效液相色谱法测定水中4种酚类化合物的方法.实验系统地优化了影响萃取效率的因素(包括有机溶剂种类、接收相浓度、分散相pH值、加盐量、转速及萃取时间).得到的最佳萃取条件为:萃取剂为正辛醇,接收相NaOH溶液的浓度为0.09 mol/L,分散相的pH为4,萃取时间为40 min,搅拌速...     

区域低碳协同发展评价:京津冀、长三角和珠三角城市群的比较分析

京津冀、长三角和珠三角城市群是中国经济高度发达、最具发展潜力的区域,在低碳发展方面起到引领作用.从经济、资源、环境和绩效的角度构建区域低碳协同发展评价指标体系,采用结合逼近理想解的TOPSIS方法、灰色关联理论和距离协同模型,利用2005~2014年三大城市群50个城市数据实证分析了三大城市群的低碳协同发展程度.结果表明,三大城市群低碳协同发展度整体上呈现上升趋势,其低碳协同程度从高到底依次为长三角、珠三角和京津冀城市群.     

A three‐dimensional coordination polymer based on the Zn4(μ3‐OH)2 unit: poly[[(μ4‐benzene‐1,4‐dicarboxylato)bis(μ3‐benzene‐1,4‐dicarboxylato)bis(μ3‐hydroxido)bis(1,10‐phenanthroline‐5,6‐dione)tetrazinc] dihydrate]

The title compound, {[Zn₄(C₈H₄O₄)₃(OH)₂(C₁₂H₆N₂O₂)₂]·2H₂O}_n, has been prepared hydrothermally by the reaction of Zn(NO₃)₂·6H₂O with benzene‐1,4‐dicarboxylic acid (H₂bdc) and 1,10‐phenanthroline‐5,6‐dione (pdon) in H₂O. In the crystal structure, a tetranuclear Zn₄(OH)₂ fragment is located on a crystallographic inversion centre which relates two subunits, each containing a [ZnN₂O₄] octahedron and a [ZnO₄] tetrahedron bridged by a μ₃‐OH group. The pdon ligand chelates to zinc through its two N atoms to form part of the [ZnN₂O₄] octahedron. The two crystallographically independent bdc²⁻ ligands are fully deprotonated and adopt μ₃‐κO:κO′:κO′′ and μ₄‐κO:κO′:κO′′:κO′′′ coordination modes, bridging three or four Zn^II cations, respectively, from two Zn₄(OH)₂ units. The Zn₄(OH)₂ fragment connects six neighbouring tetranuclear units through four μ₃‐bdc²⁻ and two μ₄‐bdc²⁻ ligands, forming a three‐dimensional framework with uninodal 6‐connected α‐Po topology, in which the tetranuclear Zn₄(OH)₂ units are considered as 6‐connected nodes and the bdc²⁻ ligands act as linkers. The uncoordinated water molecules are located on opposite sides of the Zn₄(OH)₂ unit and are connected to it through hydrogen‐bonding interactions involving hydroxide and carboxylate groups. The structure is further stabilized by extensive π–π interactions between the pdon and μ₄‐bdc²⁻ ligands.     

三维电子散斑干涉技术及其应用研究

通过大错位剪切镜和一作为参考物的压电陶瓷相移器将三个电子散斑干涉系统组成一新的三维电子散斑干涉系统。利用该系统，结合相移技术和图像处理技术，可得到独立的位移场(u,v和w场)。该技术的特点是用三个激光器作为光源，一个压电陶瓷相移器产生参考光并实现相移，CCD摄像机前放置大错位剪切镜以使物光和参考光产生干涉。将该技术应用到柴油发动机零部件测量上，得到了主轴承孔周的三维位移场。     

侧柱对串列双柱脉动压力的干扰

研究了串列双圆柱旁加上一个等直径的圆柱，组成一个等边三角形排列的三圆柱的脉动压力分布．着重研究侧柱对串列双圆柱脉动压力分布的影响．研究的结果表明，绕流等边三角形排列的三圆柱，受影响最严重的是后柱．脉动压力分布出现了严重的不对称，外侧的压力脉动极其强烈，内侧的压力脉动较弱，与时均压力分布，很好的对应关系．另外，侧柱对于串列双圆柱是否达到超过临界间距的绕流流态，有很大的影响     

三维复杂流动的间断有限元方法模拟

本文基于三维可压缩Euler方程,采用基于Runge-Kutta时间离散的间断有限元方法(RKDG方法),对三维前台阶、三维Riemann问题和球Riemann等问题进行了模拟。结果表明,本文的RKDG方法能够在很少的网格内清晰地捕捉到三维复杂流场中的激波和接触间断;同时,将球Riemann问题中z=0.4平面压强沿到对称轴距离的分布与文献中的近似精确解相比,吻合较好,这也验证了本文的RKDG方法不仅能够进行三维复杂流场的定性描述,也能够应用于三维复杂流场的定量计算。     

用三维光弹法确定轴表面横向半椭圆裂纹应力强度因子及其修正系数

用三维光弹法测定了轴表面横向半椭圆裂纹的应力强度因子，并分析计算了应力强度因子修正系数，结果表明，应力强度因子的分布型式对加载条件和裂纹几何不敏感；修正系数对裂纹深度呈现对称分布趋势，仅取决于裂纹几何参数。     

A three‐dimensional cadmium coordination polymer based on 1,4‐bis(1,2,4‐triazol‐1‐yl)but‐2‐ene and benzene‐1,3,5‐tricarboxylic acid

The Cd^II three‐dimensional coordination poly[[[μ₄‐1,4‐bis(1,2,4‐triazol‐1‐yl)but‐2‐ene]bis(μ₃‐5‐carboxybenzene‐1,3‐dicarboxylato)dicadmium(II)] dihydrate], {[Cd₂(C₉H₄O₆)₂(C₈H₁₀N₆)]·2H₂O}_n , (I), has been synthesized by the hydrothermal reaction of Cd(NO₃)₂·4H₂O, benzene‐1,3,5‐tricarboxylic acid (1,3,5‐H₃BTC) and 1,4‐bis(1,2,4‐triazol‐1‐yl)but‐2‐ene (1,4‐btbe). The IR spectrum suggests the presence of protonated carboxylic acid, deprotonated carboxylate and triazolyl groups. The purity of the bulk sample was confirmed by elemental analysis and X‐ray powder diffraction. Single‐crystal X‐ray diffraction analysis reveals that the Cd^II ions adopt a five‐coordinated distorted trigonal–bipyramidal geometry, coordinated by three O atoms from three different 1,3,5‐HBTC²⁻ ligands and two N atoms from two different 1,4‐btbe ligands; the latter are situated on centres of inversion. The Cd^II centres are bridged by 1,3,5‐HBTC²⁻ and 1,4‐btbe ligands into an overall three‐dimensional framework. When the Cd^II centres and the tetradentate 1,4‐btbe ligands are regarded as nodes, the three‐dimensional topology can be simplified as a binodal 4,6‐connected network. Thermogravimetric analysis confirms the presence of lattice water in (I). Photoluminescence studies imply that the emission of (I) may be ascribed to intraligand fluorescence.     

Highly Efficient Three Primary Color Organic Single‐Crystal Light‐Emitting Devices with Balanced Carrier Injection and Transport

Organic single crystals have a great potential in the field of organic optoelectronics because of their advantages of high carrier mobility and high thermal stability. However, the application of the organic single crystals in light‐emitting devices (OLEDs) has been limited by single‐layered structure with unbalanced carrier injection and transport. Here, fabrication of a multilayered‐structure crystal‐based OLED constitutes a major step toward balanced carrier injection and transport by introducing an anodic buffer layer and electron transport layer into the device structure. Three primary color single‐crystal‐based OLEDs based on the multilayered structure and molecular doping exhibit a maximum luminance and current efficiency of 820 cd cm^?2 and 0.9 cd A^?1, respectively, which are the highest performance to date for organic single‐crystal‐based OLEDs. This work paves the way toward high‐performance organic optoelectronic devices based on the organic single crystals.