Polypyrrole Hollow Nanotubes Loaded with Au and Fe3O4 Nanoparticles for Simultaneous Determination of Ascorbic Acid,Dopamine, and Uric Acid

An ultrasensitive electrochemical biosensor was fabricated for electroanalytical determination of ascorbic acid(AA), dopamine(DA) and uric acid(UA) individually and simultaneously based on polypyrrole hollow nanotubes loaded with Au and Fe₃O₄ nanoparticles(NPs) uniformly(PPy@Au-Fe₃O₄). The PPy@Au-Fe₃O₄ nanotubes were synthesized in one-pot using MoO₃ nanorods as templates and the polymerization of Py, the formation of Au and Fe₃O₄ NPs and the removel of MoO₃ templates took place stimultaneously. Electrochemical studies reveal that PPy@Au-Fe₃O₄modified glassy carbon electrode(GCE) possesses excellent electro-catalytic activities toward the oxidation of AA, DA and UA. Their oxidation peak currents increase linearly in the concentration ranges of 1-2000 μmol/L for AA, 0.01-25 and 25-300 μmol/L for DA and 0.1-300 μmol/L for UA. Their detection limit values(S/N=3) were calculated as 0.45, 0.0049, and 0.051 μmol/L for AA, DA and UA in the individual detection. By changing the concentrations simultaneously, the calibration curves showed linearity to 1000, 200, and 200 μmol/L with detection limit of 0.39, 0.0060, and 0.060 μmol/L for AA, DA, and UA, respectively. Finally, the obtained biosensor was successfully applied to the detection of AA, DA, and UA with satisfactory results on actual samples.     

斜波压缩下HMX晶体的弹塑性行为

开展了（010）、（011）晶向HMX晶体的斜波压缩实验,获得了约15 GPa压力下的速度响应剖面。实验结果表明,HMX单晶存在明显弹塑性转变行为,且速度波形有下降趋势,这是材料的黏性效应导致,材料的弹性极限随着样品厚度增加而变化,不同晶向的材料动力学特性存在差异。结合Hobenemser-Prager黏弹塑性本构关系和三阶Birch-Murnaghan物态方程开展了HMX晶体斜波压缩物理过程的数值模拟,计算结果可以很好地描述HMX晶体的弹塑性转变这一物理过程。     

咪唑对碳酸钙晶型和形貌的调控研究

120 ℃下,分别在水、DMF/H2O(DMF:N, N-二甲基甲酰胺)、CH3CH2OH/H2O体系中,利用咪唑调控合成CaCO3,并采用XRD、FT-IR、SEM对反应产物进行了表征,研究了咪唑浓度、溶剂和阴离子对CaCO3晶型和形状的影响.研究表明:在水体系,CaAc2为钙源物,没有咪唑时,形成棒状的文石晶体;当咪唑的浓度分别是50;、60;、70;时,得到的产物分别是方解石和球霰石、文石和方解石的混合物、纯的方解石晶体;在120 ℃条件下,60;咪唑的DMF/H2O(v/v=3:2)、CH3CH2OH/H2O(v/v=3:2)体系中合成的CaCO3分别是球霰石和文石的混合物、纯的文石;同样在60;咪唑的水体系中,钙源物为CaCl2和Ca(NO3)2时,生成的晶体是文石和方解石的混合体,但粒子形状不同.实验结果表明,咪唑的浓度、溶剂和阴离子都对CaCO3的晶型和形貌都有影响.     

Fe掺杂Mn/TiO2低温脱硝催化剂的催化性能研究

采用氧化沉淀-浸渍法制备了不同含量Fe掺杂的Fe-Mn/TiO2低温脱硝催化剂,考察了催化剂在80~180 ℃范围内的脱硝能力并通过XRD、BET、TG、H2-TPR、NH3-TPD等测试手段,对催化剂的物理化学性质进行了表征.实验结果表明,Fe的加入并没有改变Mn/TiO2的主要晶相,仍是锐钛矿型的TiO2,MnOx和FeOx均以非晶态结构高度分散于载体表面,而且Fe的加入可以有效地改善催化剂的微观形貌、比表面积及表面酸性位点,从而提高其低温脱硝性能.Fe掺量在Fe/Ti为0.10时催化剂具有最佳性能,在120 ℃时脱硝率可达90;以上.     

用云纹干涉法测量带孔复合材料板应变系数

介绍云纹干涉法在复合材料中应用的一个例子，用云纹干涉法测量带孔复合材料板应变集中系数．     

高分子溶液壁湍流减阻机理的TRPIV实验研究

利用高时间分辨率粒子图像测速技术(TRPIV)对回流式水槽中低浓度高分子溶液壁湍流的减阻机理进行实验研究。通过对比分析高分子溶液和纯水平板湍流边界层在相同来流速度下的平均速度剖面、湍流强度和雷诺应力,发现高分子溶液的壁面摩擦阻力减小了21.77%,并且其缓冲层增厚,按对数律外移,雷诺应力减小;高分子聚合物主要在近壁区起到抑制湍流脉动的作用,而在主流区的作用不太明显。用流向局部平均多尺度速度结构函数和相干结构条件采样方法,检测并对比了高分子溶液和水的壁湍流相干结构“喷射”和“扫掠”事件中的脉动速度、展向涡量、雷诺应力等物理量的二维拓扑形态,发现高分子溶液近壁区相干结构在猝发时的脉动速度减小,涡量受到抑制,雷诺应力明显减小,说明高分子溶液湍流近壁区相干结构“喷射”和“扫掠”的强度变弱,猝发频率降低,动量和能量的输运减弱,揭示出高分子溶液减阻的重要机理。     

柔性壁面湍流边界层相干结构控制的实验研究

本文利用热膜测速技术对刚性壁面和柔性壁面湍流边界层的流向速度分量进行了实验测量,首先研究了柔性壁面对平均速度分布和湍流度分布的影响,结果表明:柔性壁面的边界层速度分布在对数律层向上有所平移,缓冲层加厚,具有一般的壁面减阻特征;而柔性壁的湍流度比刚性壁的湍流度要低,分布也更为平坦。然后综合运用自相关法和条件采样技术研究了湍流近壁区的相干结构,结果表明:刚性壁自相关曲线的第二峰值出现的时间比柔性壁的短,柔性壁的猝发频率比刚性壁的低许多。实验结果表明柔性壁面具有一定的减阻作用。     

卫星减振的试验研究

根据某卫星发射对减振性能的要求,本文提出在适配器与星箭界面之间安装整星隔振器并且在适配器表面粘贴约束阻尼层的减振方案。并且利用振动台分别对卫星减振系统施加垂向和横向的基础激励,测量卫星上关键位置处的加速度响应,比较减振前后其频率响应特性的变化,以验证卫星减振方案的减振性能。试验结果的对比分析验证了此卫星减振系统能够隔离卫星高频段的横向和垂向振动,降低卫星结构频率响应的幅值,能够减小运载火箭发射时传递给卫星的环境载荷,提高卫星发射的可靠性。本文对于相关的航天器的减振设计具有实用的参考价值。     

多参数二次特征值问题重特征值的灵敏度分析

本文研究解析依赖于多参数的二次特征值问题重特征值的灵敏度分析,得到了重特征值的方向导数,证明了相应的特征向量矩阵和特征值平均值的解析性,给出了其一阶偏导数的表达式．然后以这些结论为基础,定义了二次特征值问题重特征值及其不变子空间的灵敏度,并给出了确定二次特征值问题所含矩阵中敏感元素的方法．     

Rapid Screening of Lipase Inhibitors from Ophiopogonis Radix Using High-Performance Thin Layer Chromatography by Two Step Gradient Elution Combined with Bioautographic Method

In this study, a high-performance thin layer chromatography (HPTLC) method by two step gradient elution with two mobile phases was developed for the simultaneous analysis of seven constituents in Ophiopogonis Radix. The chromatography was performed on silica gel 60 F₂₅₄ plate with dichloromethane-methanol-ethyl acetate-water (70:25:12:3, v/v/v/v) and dichloromethane-methanol (300:1, v/v) as the mobile phase for two step gradient elution. Then, the HPTLC profiles were observed after derivatization with 10% sulfuric acid in ethanol solution. The obtained HPTLC images were further analyzed by chemometric approaches and the samples could be clustered based on regions and/or growth years, which were two important factors affecting the constituents in Ophiopogonis Radix. Furthermore, five compounds including ophiopogonin D, ophiopojaponin C, ophiopogonin D’, ophiopogonin C’ and methylophiopogonanone B were screened as potential lipase inhibitors from Ophiopogonis Radix by the HPTLC-bioautographic method. The binding modes and interactions between the five compounds and lipase were further explored by molecular docking analysis. The developed HPTLC method could be used for quality control of Ophiopogonis Radix and screening of the potential lipase inhibitors.