冲击加载下Zr51Ti5Ni10Cu25Al9金属玻璃的塑性行为

进行了10—27 GPa应力范围内Zr₅₁Ti₅Ni₁₀Cu₂₅Al₉金属玻璃的平面冲击实验以研究其高压-高应变率加载下的塑性行为.由样品自由面粒子速度剖面的分析获得了冲击加载过程的轴向应力,并通过轴向应力与静水压线的比较获得剪应力.实验结果表明,尽管存在明显的松弛效应,但Zr基金属玻璃的Hugoniot弹性极限随着冲击应力的增加而增加.然而,塑性波阵面上的剪应力则显示先硬化而后软化现象,而且软化的幅度随冲击应力的增加而增加.冲击加载下Zr基金属玻璃的上述剪应力变化特征与分子动力学模拟结果比较一致,但与压剪实验结果和一维应力冲击实验结果明显不同.     

Vanishing viscosity limit of Navier–Stokes Equations in Gevrey class

In this paper, we consider the inviscid limit for the periodic solutions to Navier–Stokes equation in the framework of Gevrey class. It is shown that the lifespan for the solutions to Navier–Stokes equation is independent of viscosity, and that the solutions of the Navier–Stokes equation converge to that of Euler equation in Gevrey class as the viscosity tends to zero. Moreover, the convergence rate in Gevrey class is presented. Copyright © 2017 John Wiley & Sons, Ltd.     

基于单次旋转的旋转非对称面形误差绝对检测技术研究

绝对检测技术是剔除干涉仪系统误差进而提高面形检测精度的有效手段。基于单次旋转的绝对检测技术由被测球面绕光轴旋转前后的检测数据,采用基于最小二乘法的Zernike多项式拟合,剔除系统误差,获得被测面的旋转非对称面形误差。详细推导了理论计算公式,分析了单次旋转角度对算法检测精度的影响,并和多次旋转法作了对比,其残差均方根(RMS)值约为1.5nm。该方法只需一次旋转两次检测,在保证检测精度的同时简化了检测过程。     

1064nm纳秒激光脉冲激发的外腔式PbWO4拉曼激光器

研究了外腔式PbWO4拉曼激光器在纳秒脉冲抽运下的输出特性。利用主动调Q的Nd:YAG激光器产生的脉冲宽度为31.4ns,最大输出能量为200mJ的1064nm激光作为抽运源。拉曼激光谐振腔采用的是平凹腔设计。测量了输出的拉曼光脉宽与抽运能量的关系,分析了输出的拉曼光脉冲波形图和光谱图,测量了输出的拉曼光脉冲能量与抽运能量的关系,计算了转换效率与抽运能量的关系。当注入抽运光能量达到42mJ时,得到了一阶斯托克斯光脉冲的最大能量和转换效率分别为10mJ和24%,获得外腔式PbWO4拉曼激光器的一阶斯托克斯光脉冲波长为1177.6nm,典型的一阶斯托克斯光脉冲脉宽为20ns。     

HPLC测定注射用复方头孢西丁钠

建立注射用复方头孢西丁钠中两种有效成分的定量分析方法.采用Kromasil C18色谱柱(250mm×4.6mm,5μm),以乙腈-磷酸二氢钾(0.03mol·L-1)-10％四丁基氢氧化铵(35∶63.5∶1.5,V/V/V),用85％的磷酸调pH=4为流动相,流速1.0mL·min-1,进样量10μL,柱温30℃,在230nm的波长下进行他唑巴坦、头孢西丁两种物质的定量分析.他唑巴坦、头孢西丁浓度分别在0.125-0.50mg·mL-1(r=0.9998)、0.5-2.0mg·mL-1(r=0.9999)范围内与峰面积呈良好线性关系;方法的回收率(n=9)分别为99.7％、100.2％;样品相对标准偏差分别为1.5％、0.2％;稳定性实验表明上述两种成分在室温条件下8h内稳定.本法首次建立了注射用复方头孢西丁钠的含量测定方法,该法快速、简便、准确,重复性好,适用于该药物的含量测定.     

关于Finsler几何中的Hadamard定理

本文利用陈省身最近在Ｆｉｎｓｌｅｒ几何中引进的一个特殊仿射联络，把Ｒｉｅｍａｎｎ几何中关于非正曲率流形的Ｈａｄａｍａｒｄ定理推广到Ｆｉｎｓｌｅｒ几何中．     

In Silico Structure-Guided Optimization and Molecular Simulation Studies of 3-Phenoxy-4-(3-trifluoromethylphenyl)pyridazines as Potent Phytoene Desaturase Inhibitors

A series of novel 3-phenoxy-4-(3-trifluoromethylphenyl)pyridazines 2–5 were designed, based on the structure of our previous lead compound 1 through the in silico structure-guided optimization approach. The results showed that some of these new compounds showed a good herbicidal activity at the rate of 750 g ai/ha by both pre- and post-emergence applications, especially compound 2a, which displayed a comparable pre-emergence herbicidal activity to diflufenican at 300–750 g ai/ha, and a higher post-emergence herbicidal activity than diflufenican at the rates of 300–750 g ai/ha. Additionally, 2a was safe to wheat by both pre- and post-emergence applications at 300 g ai/ha, showing the compound’s potential for weed control in wheat fields. Our molecular simulation studies revealed the important factors involved in the interaction between 2a and Synechococcus PDS. This work provided a lead compound for weed control in wheat fields.     

Optical Properties of Fullerenated Poly(epoxy propyl carbazole)

Sincethedevelopmentofmethodslformassproductionoffullerenes,therehasbeengTeatinterestinit-Manyresearchgroups'havepaidgreatattentiontothefiJllerene-dopedpolymersinceWang'discoveredinl992thatfullerene-dopedPVKhasanapparentlyincreasingphotoconductivity.WehavereportedthechendcalattachmentofCcocagestothecarbazolegroupsonpoly(epoxypropylcarbazole)(PEPC)chainsbyFriedel-Craftstypereaction'.Here,theopticalpropertiesoffullerenatedPEPCwereinvestigated,whichwillshowitsgoodphotoconductivepropeFtiesbe…     

A Supramolecularly Activated Radical Cation for Accelerated Catalytic Oxidation

Tuning the activity of radicals is crucial for radical reactions and radical‐based materials. Herein, we report a supramolecular strategy to accelerate the Fenton reaction through the construction of supramolecularly activated radical cations. As a proof of the concept, cucurbit[7]uril (CB[7]) was introduced, through host–guest interactions, onto each side of a derivative of 1,4‐diketopyrrolo[3,4‐c]pyrrole (DPP), a model dye for Fenton oxidation. The DPP radical cation, the key intermediate in the oxidation process, was activated by the electrostatically negative carbonyl groups of CB[7]. The activation induced a drastic decrease in the apparent activation energy and greatly increased the reaction rate. This facile supramolecular strategy is a promising method for promoting radical reactions. It may also open up a new route for the catalytic oxidation of organic pollutants for water purification and widen the realm of supramolecular catalysis.     

Synthesis and structural characterization of a novel dimolybdenum(I) compound with mixed‐tribridging ligands: [Bu4N][Mo2(μ‐SPh)2(μ‐Cl(CO6]

A novel mixed‐tribridged dimolybdenum(I) compound [Bn₄N][Mo₂(μ‐SPh)₂(μ‐Cl)(CO)₆] (1) has been synthesized from the reaction of Mo₂(CO)₃(SPh)₂ with BU₄NCl. Compound 1 was characterized by IR, UV‐Vis and ¹H, ¹³C, ⁹⁵Mo NMR spectroscopic analyses. The electrochemical behavior was measured by cyclic voltammetry, indicating a quasi‐reversible two‐electron transfer in one step. The crystal structure determined by X‐ray crystallography shows that 1 contains a [Mo₂(μ‐S)₂(μ‐Cl)]^? core with a planar Mo₂S₂unit and a Cl bridge. The Mo? Mo distance is 0.28709(7) nm, and the Mo‐Cl‐Mo angle is 66.44(4)°. A newface‐sharing bioctahedral structure is discussed.