阵列像素器件投影显示系统中自动对焦评价函数研究

数字投影显示已成为现代数字显示领域的主流,阵列像素器件投影成像的的精确会聚,直接决定了显示的效果。阵列像素器件的自动对焦,是实现生产自动化的关键技术。以CCD(电荷耦合器件)采集阵列像素器件的局部投影图像为基础,试验和分析了梯度算子、拉普拉斯算子、Sobel算子、Prewitt算子、方差函数和熵函数评价方法在阵列像素器件大屏幕投影显示系统中自动对焦的作用及性能。实验表明,方差算子具有良好的稳定性和对噪声的不敏感性,调节效果较好,可以作为这一特殊系统中的评价方法。     

电磁力作用下发电机定子端部绕组的两自由度主共振

对压板松动时大型汽轮发电机定子端部单根绕组的两自由度主共振问题进行了研究．在给出定子端部绕组区域磁感应强度表达式、绕组所受电磁力以及与松动压板间摩擦力计算式的基础上,建立了研究绕组非线性电磁振动的力学分析模型．采用多尺度法对两自由度主、内共振问题进行求解,得到了稳态运动下的幅频响应方程和解的稳定性判定条件．通过算例,得到了反应系统跳跃现象和软硬特性的幅频响应曲线图,以及响应图、相图、Poincare映射图和频谱图,并阐述了系统可能存在的周期运动和锁模现象。     

消化-石油醚提取氢化物-原子荧光光谱法测定食用油中砷

采用消化 -石油醚提取方法处理食用调味油样品 ,以氢化物 -原子荧光光谱法测定砷 ,研究了样品的处理方法、线性关系及检出限 ,建立了快速测定食用调味油中砷含量的原子荧光光谱法。相对标准偏差小于1.79% ,加标回收率 96 .7%— 10 3.8%。     

基于Willgerodt-Kindler反应的两种二茂铁羧酸的合成及机理研究

以Na2S•9H2O为催化剂, 通过Willgerodt-Kindler反应分别合成了二茂铁乙酸和1,1’-二茂铁二乙酸, 用IR, 1H NMR, MS和元素分析对产物分别进行了结构表征, 并利用GC-MS研究了该反应机理, 推测反应是由多硫阴离子进攻羰基α碳所引发, 同时讨论了影响反应的各种因素.     

Effects of synthesis parameters on the microstructure and phase structure of porous 316L stainless steel supported TiO2 membranes

Porous stainless steel (PSS) supported TiO₂ membrane was synthesized from colloidal TiO₂ sol by the sol–gel technique. Morphology and phase structure of the obtained membranes were regulated through optimizing the synthesis parameters including organic binders, aging periods of the parent sol and concentrations of the casting solutions as well as the sintering temperatures. Polyvinyl alcohol (PVA) 1750 was found to be feasible to fabricate TiO₂ membrane with relatively flat surface and homogeneous morphology without crack. The aging period of the parent sol, which was revealed to be very important to the morphology of the particles deposited in the membranes on PSS, was decided to be 24 h. The concentration, under which the membranes could avoid macro-pores and have a uniform thickness of approximately 8 μm, was regulated to 0.0036 mol/l. Besides, a homogeneous microstructure with grain sizes of 0.08–0.2 μm was obtained in the membrane with a pure rutile phase when sintered at 850 °C. The obtained PSS supported TiO₂ membrane with homogeneous microstructure and rutile phase may be very promising for practical applications.     

A DFT Study on the Selective Extraction of Metallic Ions by 12-Crown-4

In order to predict the extraction ability of 12-crown-4 for different metallic ions, the complexes [M(12-crown-4)] and [M(H₂O)₄] (where M=Li⁺, Na⁺, K⁺, Be²⁺, Mg²⁺, Ca²⁺, Cu²⁺ and Zn²⁺) were investigated by the density functional theory without restrictions for their geometry. The metal binding capability was evaluated using the binding energy, and the effect of nature of the metal on the binding properties was also studied. The results of the calculations showed that the coordination ability of a donor molecule towards different metal ions increased in proportion to their ionization potential. In addition, based on the extraction distribution coefficient, we found that 12-crown-4 can selectively extract Cu²⁺ and Be²⁺ ions from aqueous solutions of mixed cations. Obviously, the stability of complexes and the extraction power of extractants depend greatly on the nature of the metal ions. Calculation results from our study could be used to predict the extraction power of this crown ether and could play a guiding role in planning experiments.     

Using support vector machines for prediction of protein structural classes based on discrete wavelet transform

The prediction of secondary structure is a fundamental and important component in the analytical study of protein structure and functions. How to improve the predictive accuracy of protein structural classification by effectively incorporating the sequence‐order effects is an important and challenging problem. In this study, a new method, in which the support vector machine combines with discrete wavelet transform, is developed to predict the protein structural classes. Its performance is assessed by cross‐validation tests. The predicted results show that the proposed approach can remarkably improve the success rates, and might become a useful tool for predicting the other attributes of proteins as well. © 2008 Wiley Periodicals, Inc. J Comput Chem 2009     

Morphological Transformation of Co(OH)2 Microspheres from Solid to Flowerlike Hollow Core–Shell Structures

Co(OH) ₂ that blooms : Flowerlike hollow spherical architectures of cobalt hydroxide obtained through a facile solvothermal process are reported for the first time (see picture). Their growth process involves aggregation of cobalt hydroxide nanoparticles into solid spheres and a hollowing effect through subsequent dissolution‐diffusion‐redeposition of the smaller crystallites under the surface layer.

     

Effect of organic and inorganic acids on chitosan/glycerophosphate thermosensitive hydrogel

The influence of organic and inorganic acids on chitosan/glycerophosphate (CS/GP) hydrogel has been investigated by dissolving chitosan in different acids. The results of gelation showed that all of the chitosan dissolved in monovalent acid solutions (i.e., formic, acetic, propionic, butyric, isobutyric, lactic, nitric, hydrochloric, and chloroacetic acid), when neutralized by GP solution, could transform into hydrogel after 2–5 min at 37 °C, while those dissolved in multivalent acids failed in gel formation. The inner structures of CS/GP hydrogels prepared with monovalent acids depended on the ionic strength and chain length of acids. Morphological examination by scanning electron microphotography demonstrated that large pores occurred during the gel-forming process, and the aperture size was also related to different acids. The cytotoxicity studies indicated that CS/GP systems prepared by dissolving chitosan in tested acids except chloroacetic acid were nontoxic to mouse embryonic fibroblasts and Hela cells.     

Palladium‐Catalyzed Intramolecular Hydroamination of Allenes Coupled to Aerobic Alcohol Oxidation

Taking the air! A Pd^II‐catalyzed intramolecular hydroamination of allenes coupled to alcohol oxidation has been developed. This reaction is performed by using a nitrogen‐based ligand under aerobic conditions, under which the molecular oxygen is used as the terminal oxidant for the reoxidation of Pd⁰ species to complete the catalytic cycle.