基于临界状态的砂土本构模型研究

砂土孔隙比及所受压力是其力学特性的重要影响因素. 本文基于砂土临界状态线特性分析,采用以e-(p/p_a)ξ平面内的线性关系描述其等向压缩线. 通过对比分析两种不同压缩线函数 与临界状态线函数之间的关系提出更适合描述砂土在等向压缩下的参考压缩线,并给出了基于参考压缩线的等向硬化规律. 建议了适用于 描述砂土剪切特性的屈服面函数,并给出利用等向压缩和等p路径确定屈服面形状参数μ的方法. 将不同应力比对应的压缩线作为砂土状态参量参考线,以获取潜在强度M_f与特征状态应力比M_c,进而描述砂土压缩与剪切特性;基于等向压缩与等p路径建立了当前应力比与状态参量参考线之间的相关关系,从而实现了砂土状 态参量参考线由参考压缩线向临界状态线平稳过渡. 建立的砂土本构模型共11个参数,均能够通过常规土工试验或经验获取. 基于模型预测与Toyoura砂的等向压缩、三轴不排水剪切试验及排水剪切试验的对比结果,本文建立的砂土本构模型很好地描述了Toyoura 砂在不同孔隙比和不同压力下的压缩与剪切特性.      

Effect of nano-fillers on conductivity of polyethylene/low melting point metal alloy composites

A novel method for preparing conductive polyethylene(PE) composites has been developed. In the method, the powder of low melting point metal alloy(LMPA) is filled into the PE matrix by using twin screw extruder at a temperature below the melting point of the LMPA, and followed by a die drawing process at a temperature around the melting point of the metal alloy. It has been found that die drawing process, repeating the die drawing process and adding nano-fillers, such as montmorillonite(MMT) and multi-wall carbon nanotubes(MWCNTs), all help reduce the metal particle size in the PE matrix, thus improve the conductivity of the composite. The conductivity improvement is attributed to an increased number of the smaller metal particles. Therefore, conductive composites of polymer/metal alloy/nano-filler with high conductivity are possible to be prepared by using the new method.     

利用改进的胶束电动毛细管色谱法和液相色谱法测定6类重点食品中的脱氢乙酸

改进了实验室建立的测定脱氢乙酸的胶束电动毛细管色谱(MEKC)和国标的液相色谱(LC)的分离及样品前处理方法. 改进后的两种方法均能准确测定6类重点食品中的脱氢乙酸,为重新评估脱氢乙酸的风险、修订或制定其在不同食品中的限量标准提供依据. 改进后的MEKC和LC方法的检出限及定量限分别为0.2、0.5 mg/L和0.05、0.2 mg/L. 6类重点食品空白基质的加标回收率均在81.9%~116.0%之间,相对标准偏差在0.4%~7.3%之间. 测定了284件食品样品,结果均无超标. 使用改进的两种方法同时测定了45件样品,对其中20件阳性样品的结果进行了比较,结果吻合. 改进后的MEKC及LC方法样品前处理简单,非常适合大量样品检测.     

井下巷道围岩变形的散斑分析法

通过对散斑计量法原理分析、数学描述及观测实例的论述，证明激光散斑法是研究煤矿地下结构物相似模型变形状态的一种新的无损检测技术，若采用白光作为光源，该项技术可用于二维变形场的实地测试。     

CCQM-K74国际比对中二氧化氮浓度的测量

介绍了国际比对样品中10μmol/mol NO2气体浓度精确分析方法的建立过程。该方法的建立包括标准物质的制备、分析仪器的选择和测量结果的不确定度3个主要的方面。标准物质的制备及其量值的不确定度评价采用了气体标准物质定值的基准方法——称量法。对傅立叶变换红外光谱法(FTIR)和化学发光光谱法进行了比较研究。确定了更适合于本次国际比对样品的分析方法为化学发光光谱法,测量结果的相对扩展不确定度为1.0%(k=2)。本次比对的最终结果报告显示,所建立的分析方法准确可靠。     

ZnO纳米棒阵列到纳米管结构的自转化机制及其在相变封装材料中的应用

In the emerging field of nanoscience, tubular structures have been attracting remarkable interest due to their well-defined geometry, high specific area, and exceptional physical and chemical properties. Among them, oriented ZnO tubular arrays are regarded as promising candidates for various applications such as optoelectronics, solar cells, sensors, field emission, piezoelectrics, and catalysis. Although template-directed and selective dissolution synthesizing strategies are commonly used to prepare ZnO nanotubes, repeatability and large scale preparation are still challenging. In this study, ZnO nanotube arrays were controllably prepared by tuning the hydrothermal parameters, without the use of any additives. The mechanism underlying the self-conversion of ZnO nanorods to nanotubes was comprehensively studied based on the surface energy theory. It has been proved that the metastable top surface of the ZnO nanorods dissolves preferentially to reach a stable state during the hydrothermal growth. The specific surface energy of different crystal faces of ZnO nanorods was calculated using molecular dynamics simulation. The top surface of the ZnO nanorod, the Zn-terminated [0001] face, demonstrated much higher surface free energy than did the lateral faces, which indicated that the self-dissolution of top face (002) is energetically favorable. The self-conversion behavior of ZnO nanorod arrays with different diameters was specifically investigated by adjusting the initial precursor concentration, density of the crystal seed layers, and growth time. The dissolution-crystallization equilibrium concentration, determined by crystal surface energy, was found to be a key factor for the formation of the tubular structure. Notably, the critical equilibrium conditions for the self-conversion of ZnO nanorods to nanotubes, including zinc ion concentration and pH, have been identified by studying parameters corresponding to the dissolution-crystallization equilibrium for the metastable top surface of the ZnO nanorods. The preparation of the ZnO nanotube arrays was successfully accelerated and simplified via two-step procedure: (1) preparation of ZnO nanorod arrays and (2) self-conversion of ZnO nanorods to nanotubes. The preparation method based on the self-conversion mechanism from rods to tubes for polar oxides is simpler and more easily controllable as compared to the reported methods involving variety of additives. Because of the advantages of adaptability to a wide range of substrates, excellent conducting properties, and filling ability, the prepared ZnO nanotube array films were used in encapsulating phase-change materials. The encapsulated phase-change material exhibited excellent heat storage/release properties and heat conductivities. This indicates the potential application of precision devices for temperature control.     

应用理性优化蚁群算法提高激光三维复制的重现度

三维复制人工耳和打印手枪把激光三维复制技术推向新的一页。激光三维扫描是激光应用中一个新兴的重要领域,在三维复制中扮演着无可替代的角色,其复制精度在目前所有复制技术中是最高的。而重现度标志着复制结果与复制对象几何形状上的一致程度,是激光三维复制最重要的指标。分析了激光三维复制的误差,得出激光扫描的点云数据处理是减小误差、提高重现度的关键所在的结论。主要创新点在于,在传统蚁群算法的基础上,将提出理性优化蚁群算法应用于激光三维复制中的数据处理。经计算对比发现,有效减小了复制的误差,提高了复制的重现度。     

Getting to the bottom morphology of block copolymer thin films

We demonstrate a general approach for attaining the bottom morphology of block copolymer(BCP) thin films. In our former measurements on PS-b-PMMA films, surface morphology maps of the BCP films revealed distinct ordering regimes where the cylinders orient predominantly perpendicular or parallel to the interface and an ‘intermediate' regime where these morphologies coexist. However, this earlier work did not explore the bottom morphology of BCP thin films. In this study, we investigated the block copolymer morphology near the solid substrate in the cast block copolymer film having a perpendicular cylinder morphology on the surface.     

Blocking the defect sites on ultrathin Pt nanowires with Rh atoms to optimize the reaction path toward alcohol fuel oxidation

Anodic electrocatalyst plays the core role in direct alcohol fuel cells (DAFCs), while traditional Pt-catalysts suffer from limited catalytic activity, high over potential and severe CO poisoning. Herein, by selectively depositing Rh atoms on the defective-sites of Pt nanowires (NWs), we developed a new Pt@Rh NW electrocatalyst that exhibited enhanced electrocatalytic performance for both methanol oxidation (MOR) and ethanol oxidation (EOR). Both cyclic voltammetry (CV) and in-situ infrared spectroscopy revealed that the presence of Rh atoms suppressed the generation of poisonous intermediates and completely oxidized alcohols molecule into CO₂. Atomic resolusion spherical aberration corrected high-angle annular dark field scanning transmission electron microscopy (CS-HAADF-STEM) and energy-dispersive X-ray spectroscopy (EDS) mapping analysis revealed that Rh atoms were primarily deposited on the defective sites of Pt NWs. Meanwhile, the presence of Rh atoms also modified the electronic state of Pt atoms and therefore lowered the onset potential for alcohols oxidation potential. This work gives the first clear clue on the role of the defective sites of Pt nanocatalyst poisoning, and propose that selectively blocking these sites with trace amount of Rh is an effective strategy in designing advantageous electrocatalysts.