渗透剂对小鼠皮肤光学特性影响的实时动态监测

自行研制了一套双积分球系统,应用该系统对离体小鼠皮肤在渗透剂无水甘油作用下,光学特性参量的变化进行了实时监测。实验结果表明：在无水甘油作用下,随着时间的延长,小鼠皮肤的约化散射系数明显减小,吸收系数略有增加,并最终导致了有效衰减系数的减小;但当作用时间超过25min后,样品的光学特性参量会趋于恒定。为生物组织光学特性控制作用提供了新的方法,这对组织光学成像研究是非常重要的。     

人膀胱癌组织对不同波长的激光及其线偏振激光的衰减特性比较研究

采用双积分球系统和光辐射测量技术的基本原理以及运用生物组织的光学模型,研究了4765,488,4965,5145,532nm激光及其线偏振激光辐照人膀胱癌组织的光衰减特性。结果表明在5个不同的激光波长范围内,KubelkaMunktwoflux模型下的人膀胱癌组织对不同波长的激光及线偏振激光的衰减特性是不同的,人膀胱癌组织对4765,4965,532nm激光及其线偏振激光的总衰减系数或有效衰减系数均具有显著性差异(P<005),而对488,5145nm波长的激光及其线偏振激光的总衰减系数或有效衰减系数则均没有显著性差异(P>005),人膀胱癌组织对532nm激光及其线偏振激光的总衰减系数或有效衰减系数均明显大于其他4个波长的Ar 激光及其线偏振激光的总衰减系数或有效衰减系数。在传输理论下人膀胱癌组织对5个不同波长的激光及其线偏振激光的总衰减系数均随着波长的增大而减小,人膀胱癌组织对4765,4965,5145nm波长的激光及其线偏振激光的总衰减系数均有显著性差异(P<005),其对488,532nm波长的激光及其线偏振激光的总衰减系数均没有显著性差异(P>005)。     

Mechanism of defect formation and polyanion transport in solid scandium tungstate type oxides

Abstract  The unique diffusion mechanism in the novel polyatomic anion conductor scandium tungstate is studied by molecular dynamics simulations of systems with artificially induced WO₄ ²⁻ defects and compared to our previous simulations of defect-free structure models. The diffusion activation energy obtained from structures with built-in defects is smaller than for the defect-free models and in the case of tungstate vacancies close to the experimental value, suggesting that extrinsic tungstate vacancies due to the volatility of WO₃ are important for the experimental conductivity. The validity of the force field used for the molecular dynamics simulations is further verified by investigating the orthorhombic to monoclinic phase transition of Sc₂(WO₄)₃ under compression. The lattice compressibility in both phases and the phase transition is qualitatively reproduced, though the simulated phase transition pressure occurred is about 0.55 GPa higher than the experimental one. Graphical abstract        

The Production and Characterisation of Novel Conducting Redox‐Active Oligomeric Thin Films From Electrooxidised Indolo[3,2,1‐jk]carbazole

Novel thin‐film materials have been produced from indolo[3,2,1‐jk]carbazole (see picture). These are conducting and redox‐active and, unusually, consist of three distinct covalently coupled luminescent dimer species, consistent with a specific radical‐cation coupling mechanism.

     

Preparation and Characterization of Cu3V2O7(OH)2·2H2O Hollow Spheres from NazV6O16·3HzO Nanobelts

Monoclinic Cu3V2O7(OH)2·2H2O(copper polyvanadate) hollow spheres were prepared with Na2V6O16·3H2O nanobelts as V-precursor by hydrothermal method.The purity and structure of the products were characterized by X-ray powder diffraction(XRD),Fourier transform infrared(FTIR) spectroscopy,Raman spectroscopy,thermogravimetric analysis(TGA) and X-ray photoelecton spectroscopy(XPS).The morphology and size were observed by scanning electron microscopy(SEM).We found that the Kagomé staircase-structural copper polyvanadate hollow spheres with an average diameter of 7 μm could be easily synthesized via the reaction of Na2V6O16·3H2O nanobelts with sufficient copper sulfate.The dielectric property of the copper polyvanadate demonstrates that dielectric loss hardly changes when the frequency of applied electric field is higher than 100 kHz.The formation process of the hollow spheres is discussed in detail by the observation of a series of products prepared for different reaction time.     

A simple method to prepare titania nanomaterials of core-shell structure, hollow nanospheres and mesoporous nanoparticles

A simple method to prepare titania nanomaterials of core-shell structure, hollow nanospheres and mesoporous nanoparticles has been developed. The core-shell nanostructures with NH4Cl as core and TiO2·xH2O-NH4Cl as shell were prepared in nonaqueous system by the deposition on the surface of the aggregated NH4Cl crystals, which could be transformed into mesoporous anatase nanoparticles or hollow nanospheres by calcination at 500℃ or extraction with methanol, respectively. The hierarchical mesoporous nanostruc...     

Wave motions in a stratified electrically conducting rotating fluid

The 3D dynamics equations for the stratified superconducting rotating fluid are studied. These equations are reduced to a scalar equation by representing the magnetic and density fields by a superposition of the unperturbed fields corresponding to the steady state of the fluid and the induced fields appearing due to the wave motion; the reduction also uses two auxiliary functions. The analysis of the scalar equation enables us to prove the solvability of the initial-boundary value problems of the wave theory for electrically conducting rotating fluids with nonhomogeneous density.     

Ternary composites of multi-wall carbon nanotubes,polyaniline, and noble-metal nanoparticles for potential applications in electrocatalysis

Multi-wall carbon nanotubes were coated with a conducting polymer, polyaniline phosphotungstate. Such composite structures have mixed electronic and proton conductivity, high surface area and porosity. These materials were decorated with catalytically-active noble metals — Pt, Pd, and Rh. Metal nanoparticles were uniformly distributed in the polymer matrix. Such ternary composites can be considered as electrode materials in sensors, electrolysers, supercapacitors, and especially in low-temperature fuel cells with a proton-conducting polymer membrane.     

Liquid crystalline conjugated polymers and their applications in organic electronics

This article describes the syntheses and electro‐optical applications of liquid crystalline (LC) conjugated polymers, for example, poly(p‐phenylenevinylene), polyfluorene, polythiophene, and other conjugated polymers. The polymerization involves several mechanisms: the Gilch route, Heck coupling, or Knoevenagel condensation for poly(p‐phenylenevinylene)s, the Suzuki‐ or Yamamoto‐coupling reaction for polyfluorenes, and miscellaneous coupling reactions for other conjugated polymers. These LC conjugated polymers are classified into two types: conjugated main chain polymers with long alkyl side chains, namely main‐chain type LC polymers, and conjugated polymers grafting with mesogenic side groups, namely side‐chain type LC conjugated polymers. In general, the former shows higher transition temperature and only nematic phase; the latter possesses lower transition temperature and more mesophases, for example, smectic and nematic phases, depending on the structure of mesogenic side chains. The fully conjugated main chain promises them as good candidates for polarized electroluminescent or field‐effect devices. The polarized emission can be obtained by surface rubbing or thermal annealing in liquid crystalline phase, with maximum dichroic ratio more than 20. In addition, conjugated oligomers with LC properties are also included and discussed in this article. Several oligo‐fluorene derivatives show outstanding polarized emission properties and potential use in LCD backlight application. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2713–2733, 2009     

Chelating Properties of Salicylhydroxamic Acid-functionalized Polystyrene Resins and Its Application to Efficient Removal of Heavy Metal Ions from Aqueous Solutions

Salicylhydroxamic acid(SHA) was covalently bound onto crosslinked polystyrene spheres(CPSs) via the Friedel-Crafts alkylation reaction between chloromethylated CPSs and SHA in the presence of SnCl4 as the Lewis acid catalyst. The resulted SHA-CPSs possessed very strong chelating ability for heavy metal ions. In particular, the saturated adsorption amount of SHA-CPSs for Cu²⁺ ions could reach as high as 34.2 mg/g at 318 K. The chelating capability of SHA-CPSs towards heavy metal ions was pH and temperature dependent. SHA-CPSs also showed selective metal coordination with the chelating capacity decreasing in the order of Cu²⁺>Zn²⁺>>Pb²⁺. The adsorption isotherms conformed well to the Langmuir model, and the adsorption process was found to be entropy-driven and endothermic. Besides, SHA-CPSs possessed the excellent reusability.