超细粉体微胶囊红磷阻燃剂的研制

红磷经湿法研磨预处理，在一定pH值（9．0－9．5），表面活性剂用量为0．8％－1．0％，2200Hz超声波振荡15min后，采用蜜胺树脂预聚体原位法包覆，制得了微胶囊红磷阻燃剂的超细粉体，其平均粒径为2．186um，并探讨了预处理，PH值，表面活性剂及超声波对粒度的影响。     

Catalysis of gasification of coal-derived cokes and chars

Calcium is the most important in-situ catalyst for gasification of US coal chars in O₂, CO₂ and H₂O. It is a poor catalyst for gasification of chars by H₂. Potassium and sodium added to low-rank coals by ion exchange and high-rank coals by impregnation are excellent catalysts for char gasification in O₂, CO₂ and H₂O. Carbon monoxide inhibits catalysis of the CH₂O reaction by calcium, potassium and sodium; H₂ inhibits catalysis by calcium. Thus injection of synthesis gas into the gasifier will inhibit the CH₂O reaction. Iron is not an important catalyst for the gasification of chars in O₂, CO₂ and H₂O, because it is invariably in the oxidized state. Carbon monoxide disproportionates to deposit carbon from a dry synthesis gas mixture (3 vol H₂ + 1 vol CO) over potassium-, sodium- and iron-loaded lignite char and a raw bituminous coal char, high in pyrite, at 1123 K and 0.1 MPa pressure. The carbon is highly reactive, with the injection of 2.7 kPa H₂O to the synthesis gas resulting in net carbon gasification. The effect of traces of sulphur in the gas stream on catalysis of gasification or carbon-forming reactions by calcium, potassium, or sodium is not well understood at present. Traces of sulphur do, however, inhibit catalysis by iron.     

多流形判别分析在人脸识别中的研究

局部保持投影LPP(Locality Preserving Projection)是一种有效的非线性降维方法,能够使投影降维后的数据与原输入空间中的相似局部结构保持一致,但是该方法没有充分利用类间样本点的权重等重要信息。为了解决这个问题,提出基于Fisher准则的多流形判别分析FMMDA(Fisher Multi-Manifold Discriminant Analysis)方法。结合Fisher准则训练样本类内拉普拉斯图和样本均值类间拉普拉斯图,既保持了原样本的相似局部结构,又充分地利用了不同类别之间的权重。在ORL及Yale人脸库上验证了该方法的有效性。与其他几种最先进的方法相比,FMMDA方法取得了更好的识别效果。     

心内膜三维几何模型交互式网格切割算法研究

针对心内膜三维标测系统中心内膜模型网格切割模块,提出一种新的交互式网格切割算法。系统在载入心内膜三维几何模型后初始化切割平板模型,由用户交互移动切割平板和旋转切割平板的法线。借助矩阵变换,针对心内膜三维几何模型实现能反映用户切割意图和保持网格细节特征的网格切割,而且切割平板可以消除锯齿效应。实验对比结果证明,该算法对于心内膜三维几何模型可以实现令用户满意的实时无锯齿交互式网格切割。     

Crystalline morphology and isothermal crystallization kinetics of poly(ethylene terephthalate)/clay nanocomposites

A poly(ethylene terephthalate) (PET)/montmorillonite clay nanocomposite was synthesized via in situ polymerization. Microscopic studies revealed that in an isothermal crystallization process, some crystallites in the nanocomposite initially were rod‐shaped and later exhibited three‐dimensional growth. The crystallites in the nanocomposite were irregularly shaped, rather than spherulitic, being interlocked together without clear boundaries, and they were much smaller than those of neat PET. With Avrami analysis, the isothermal crystallization kinetic parameters (the Avrami exponent and constant) were obtained. The rate constants for the nanocomposite demonstrated that clay could greatly increase the crystallization rate of PET. The results for the Avrami exponent were consistent with the observation of the rodlike crystallites in the PET/clay nanocomposite during the initial stage. Wide‐angle X‐ray scattering and Fourier transform infrared studies showed that, in comparison with neat PET, the crystal lattice parameters and crystallinity of the nanocomposite did not change significantly, whereas more defects may have been present in the crystalline regions of the nanocomposite because of the presence of the clay. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1381–1388, 2004     

磁盘阵列环境下的取证目标系统重构

封存原始硬盘与业务系统服务的连续性是计算机取证中面临的一对矛盾。在独立硬盘环境中,问题的解决并不困难,但在磁盘阵列(RAID)环境下,目前还缺乏有效的解决办法。为此,为RAID环境下的取证目标系统的重构提出一套解决方案,并设计实现其中关键任务的处理软件。实验表明,该方法可适用于不同RAID等级、不同操作系统下的系统重构,使得用户感受不到重构得到的系统与原系统有任何差异。与数据同步方法相比,该方法可以有效地减少重构的时间开销,且不会破坏原始证据硬盘上的数据。     

Interactions between Cytochrome c and DNA Strands Self-Assembled at Gold Electrode

In this work, we reported the investigation on the interaction between DNA strands self-assembled at gold electrodes and an electron transfer protein, cytochrome c. We observed that cytochrome c exhibited well-defined electrochemistry in both double-stranded and single-stranded DNA films. This suggested that the electron transfer reaction of cytochrome c arose possibly due to the electron hopping along DNA strands rather than wiring along the double helix. We also compared the heterogeneous electron transfer rate of cytochrome c with that of a ruthenium complex, which further confirmed this mechanism.     

Integrated UV-based photo microreactor-distillation technology toward process intensification of continuous ultra-high-purity electronic-grade silicon tetrachloride manufacture

Ultra-high-purity silicon tetrachloride (SiCl₄) is demanded as an electronic-grade chemical to meet the stringent requirements of the rapidly developing semiconductor industry. The high requirement for ultra-high-purity SiCl₄ has created the need for a high-efficient process for reducing energy consumption as well as satisfying product quality. In this paper, a mass of production technology of ultra-high-purity SiCl₄ was successfully developed through chlorination reaction in the ultraviolet (UV)-based photo microreactor coupled with the distillation process. The influences of key operational parameters, including temperature, pressure, UV wavelength and light intensity on the product quality, especially for hydrogen-containing impurities, were quantified by the infrared transmittance of Fourier transform infrared spectroscopy (FT-IR) at 2185 cm^-1 and 2160 cm^-1 indicating that characteristic vibrational modes of Si—H bonds, as well as the operating conditions of distillation were also investigated as key factors for metal impurities removing. The advanced intensification of SiCl₄ manufactured by the integration of photo microreactor and distillation achieves the products with superior specifications higher than the standard commercial products.     

Integrated UV-based photo microreactor-distillation technology toward process intensification of continuous ultra-high-purity electronic-grade silicon tetrachloride manufacture

Ultra-high-purity silicon tetrachloride (SiCl₄) is demanded as an electronic-grade chemical to meet the stringent requirements of the rapidly developing semiconductor industry. The high requirement for ultra-high-purity SiCl₄ has created the need for a high-efficient process for reducing energy consumption as well as satisfying product quality. In this paper, a mass of production technology of ultra-high-purity SiCl₄ was successfully developed through chlorination reaction in the ultraviolet (UV)-based photo microreactor coupled with the distillation process. The influences of key operational parameters, including temperature, pressure, UV wavelength and light intensity on the product quality, especially for hydrogen-containing impurities, were quantified by the infrared transmittance of Fourier transform infrared spectroscopy (FT-IR) at 2185 cm⁻¹ and 2160 cm⁻¹ indicating that characteristic vibrational modes of SiH bonds, as well as the operating conditions of distillation were also investigated as key factors for metal impurities removing. The advanced intensification of SiCl₄ manufactured by the integration of photo microreactor and distillation achieves the products with superior specifications higher than the standard commercial products.     

Preparation of NaBiO3 and the electrochemical characteristic of manganese dioxide doped with NaBiO3

NaBiO₃ crystal of high purity has been synthesized through chemical oxidization. The morphology and thermal stability of NaBiO₃ were examined with scanning electron microscope (SEM) and thermogravimetry-differential scanning calorimetry (TG-DSC). The electrochemical properties of MnO₂ electrodes with and without doping NaBiO₃ were studied through galvanostatic charge/discharge and cyclic voltammetry. The results indicate that the MnO₂ electrode doped with NaBiO₃ possesses remarkably higher discharge voltage and capacity and better reversibility than the pure MnO₂ electrode and Bi₂O₃ doping MnO₂ electrode.