组合曲线回归法计算螺旋扁管管内对流传热系数

针对螺旋扁管壁面温度难于准确测试的特点,提出采用线性曲线回归与非线性曲线回归相结合的方法进行管内传热系数计算.进行了光管与螺旋扁管管内对流传热实验,并用该方法计算管内对流传热系数.光管传热系数计算值与经典公式的大偏差小于6%.螺旋扁管管内传热系数的计算值略大于通过测量壁温获得的传热系数值,分析了二者存在差异的原因.组合...     

THE AREA INTEGRAL ON NEGATIVE CURVATURE SPACE FORM

In this note, we show that the area integral of positive harmonic functions on a constant negative curvature space form is almost everywhere finite with respect to a harmonic measure on S(∞).     

Spectroscopic and electrochemical studies on the interaction of an inclusion complex of β-cyclodextrin/fullerene with bovine serum albumin in aqueous solution

The potential effect of human exposure to carbonaceous nanomaterials (e.g., fullerenes or their derivatives) in the environment has become a concern. In the current study, we report the interaction of one water-soluble fullerene with bovine serum albumin using spectroscopic and electrochemical methods under aqueous solutions. The novel supramolecular inclusion complex of the water-soluble fullerene (β-CD)₂/C₆₀ was synthesized and characterized. In the mechanism discussed, the spectroscopic methods such as fluorescence quenching and ultraviolet-visible absorption, proved that the fluorescence quenching of BSA by (β-CD)₂/C₆₀ was the result of the formation of (β-CD)₂/C₆₀-BSA complex and that the mechanism of quenching might be a static quenching procedure. The binding constants K_a, the number of binding sites n, and the corresponding thermodynamic parameters ΔG, ΔH, and ΔS at different temperatures were calculated through fluorescence spectroscopy, then as an auxiliary method, the electrochemical impedance spectroscopy (EIS) experiments confirmed this conclusion. The results indicated that the electrostatic interactions play a major role in (β-CD)₂/C₆₀-BSA association. The circular dichroism spectra show the conformation change of the effect of (β-CD)₂/C₆₀ on the conformation of BSA, which was confirmed by the results of the three-dimensional fluorescence spectra. Site marker competitive experiments indicate that the binding of (β-CD)₂/C₆₀ to BSA primarily took place in site I. The distance r between donor (BSA) and acceptor ((β-CD)₂/C₆₀) was obtained according to fluorescence resonance energy transfer (FRET). This work aims to demonstrate the mechanisms of the formation of the complex between water-soluble fullerene and protein under physiological conditions, as well as the remediation for the possible unwarranted biological effects of water-soluble fullerene.     

Preparation of chitosan functionalized monolithic silica column for hydrophilic interaction liquid chromatography

A novel cationic hydrophilic interaction monolithic stationary phase based on the chemical modification of carboxymethyl chitosan (CMCH) to the monolithic silica skeleton using carbodiimide as an activation reagent was prepared for performing capillary liquid chromatography. The amino and hydroxy moieties of CMCH functioned as both the ion-exchange sites and polar providers. The performance of the column was studied by the separation of polar acidic compounds. The chitosan functionalized monolithic silica column showed good selectivity for nucleosides, nucleotides, aromatic acids and aliphatic acids. The mechanism for the separation of these compounds was also studied. The results showed that these compounds were separated primarily based on the hydrophilic interaction mechanism.     

Micro-punching process based on spallation delamination induced by laser driven-flyer

In this article, we proposed a micro-punching process for microstructure on films based on laser driven-flyer induced spallation delamination phenomenon at the interface between a film and its substrate. To validate such a micro-punching process, a series of experiments were carried out for fabrication of microstructures on Au films coated on K9 glass substrates and polyimide substrate. Results show that through such a punching process, the microstructure on Au films can be fabricated efficiently and the spatial resolution is able to reach micron level. Moreover, we found that this method was more suitable for films coated on soft substrates rather than that coated on brittle substrates due to the additional destruction of the brittle substrate. This micro-punching process has a wide range of potential application in microfluidic devices, biodevices and other MEMS devices.     

WnSi20,±（n=1-5）团簇结构与光谱的理论研究

利用密度泛函理论（DFT）在B3LYP/Lanl2dz水平上对WnSi20,±（n=1-5）团簇的各种可能构型进行了几何结构优化,预测了各团簇的基态结构。并对基态构型的平均结合能、能隙、红外光谱及拉曼光谱进行了系统的理论分析。结果表明：WnSi20,±（n=2-5）团簇的基态结构及亚稳态结构中的Si-Si原子不成键,W5Si20,±团簇的基态构型与W7团簇的基态构型相似,W3Si2＋团簇的基态构型与W50,±团簇的基态构型相似;W5Si2－团簇是比较理想的复合材料;WnSi20,±（n=1-5）团簇的所有IR吸收峰都属于红外光谱中的指纹区的特征吸收区域;除W4Si2－团簇外,其它团簇都具有非刚性特性。     

Longitudinal coupling effect in microfiber Bragg gratings

We theoretically present longitudinal coupling effect (LCE) in air-cladding microfiber Bragg gratings (MFBGs). Distinct from conventional weakly-guiding optical fibers, large longitudinal electric field (E_z) exists in wavelength-scale microfibers. Due to LCE, MFBG reflectivity can be reduced by more than 30% within the band-gap and the full width at half maximum (FWHM) is obviously narrowed. This theoretical analytical work is instructive to precisely design and fabricate MFBGs that are promising in the areas of optical sensing and nanophotonics.     

Synthesis and characterization of ferrocenylalkoxygermatranes and crystal structures of FcCH2OGe (OCH2CH2)3N and FcCH(CH3)OGe(OCH2CH2)3N1

Germatranes bearing a ferrocenylalkoxyl moiety have been obtained by the reaction of HOGe(OCH₂CH₂)₃N with various ferrocenyl alcohols. A convenient new synthesis method of FcCH₂OGe(OCH₂CH₂)₃N was reported. FcCH₂OGe(OCH₂CH₂)₃N was prepared in 93% yield when FcCH₂OH reacted with HOGe(OCH₂CH₂)₃N in chloroform at room temperature in the presence of molecular sieves (3 Å) as a dehydrating agent. All compounds were characterized by elemental analysis, ¹H NMR and IR spectroscopy. The molecular structures of FcCH₂OGe(OCH₂CH₂)₃N and FcCH(CH₃)OGe(OCH₂CH₂)₃N have been determined by X‐ray diffraction. The antitumor activities of FcCH₂OGe(OCH₂CH₂)₃N and p‐FcC₆H₄CH₂OGe(OCH₂CH₂)₃N were determined. Copyright © 2005 John Wiley & Sons, Ltd.