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41.
A titanium dioxide sol with narrow particle size distribution was synthesized using TiCl4 as the starting material. The sol was prepared by a process where HCl was added to a gel of hydrated titanium oxide to dissolve it. The resulting aqueous titanic acid solution was heated to form titanium dioxide sol. The effects of preparation parameters were investigated. TiCl4 was slowly added to distilled water at 5°C. Aqueous solution of sodium hydroxide was added to adjust the pH of the system to 8–12. After aging for a period of time, the peptized sol was filtered and sufficiently washed. The filtered cake was repulped in water. Hydrochloric acid was slowly added to the solution with stirring. After condensation reaction and crystallization, a transparent sol with suspended TiO2 was formed. XRD results show that the crystalline phase was anatase. The suspended TiO2 particles were rhombus primary particles with the major axis ca. 20 nm and the minor axis ca. 5 nm. The TiO2 particles prepared at pH 8 had the largest surface area of 141 cm3/g and it was microporous. The compositions of the solution which yielded the smallest suspended TiO2 particles were TiO2:HCl (35% HCl) = 1:1 (molar ratio), concentration of TiO2 = 10%. Hydroxypropyl cellulose with viscosity of 150–400 cps was added as a dispersant. The sol was excellent in dispersibility and long-term stability. Transparent thin films could be obtained through dip-coating glass substrate in the sol. The dip-coating on glass can be less than three times to have one monolayer TiO2. The transparent TiO2 thin film had strong hydrophilicity after being illuminated by UV light. 相似文献
42.
Ting-Fu Jiang 《Analytica chimica acta》2003,479(2):249-254
Ionic substances with melting points close to room temperature are referred to as ionic liquids. Because ionic liquids are environmentally benign and are good solvents for a wide range of both organic and inorganic materials, interest for their potential uses in different chemical processes is increasing. In this paper, a capillary electrophoretic method for the analysis of basic proteins including lysozyme, cytochrome c, trypsinoge, and α-chymotyypsinogen A is reported. The method, in which 1-alkyl-3-methylimidazolium-based ionic liquids are used as the running electrolytes, leads to a surface charge reversal on the capillary wall. The effects of the alkyl group, imidazolium counterion, and the concentration of the ionic liquids were discussed. The optimum buffer system was a 90 mM 1-ethyl-3-methylimidazolium tetrafluoroborate (1E-3MI-TFB) solution. The applied voltage was −15 kV and detection was performed by monitoring absorbance at 240 nm. Baseline separation, high efficiencies, and symmetrical peaks of four proteins were obtained. The R.S.D. values of migration times and peak areas were <0.68 and <3.0%, respectively. The separation mechanism seems to involve association between the imidazolium cations and the proteins. 相似文献
43.
Ostanina T. N. Rudoi V. M. Yaroslavtseva O. V. Solov'ev A. S. Subbotina O. Yu. Dokashenko S. I. 《Russian Journal of Electrochemistry》2004,40(10):1019-1023
The impedance of zinc-rich polymer coatings on steel in a 3-% NaCl solution is studied. The electrochemical behavior of the electrode is satisfactorily described by an equivalent circuit that contains a constant-phase element, which reflects fractal properties of the zinc surface in the binder. From the results of calculations of the circuit elements for metal-rich electrodes with different zinc contents computed are fractions of the active area of the surface of the coating and its fractal dimensionality. 相似文献
44.
Martin Gilges Heribert Husmann Maria-Helen Kleemiß Stephan R. Motsch Gerhard Schomburg 《Journal of separation science》1992,15(7):452-457
Mixtures of several basic proteins have been used to test CZE capillaries with surfaces modified by new pretreatment procedures; the performance obtained has been compared with that achieved using capillaries treated by procedures described in the literature. It has been shown that addition of non-ionic polyvinylalcohols (PVA) to CZE buffer solutions deactivates even bare, i.e. untreated, fused silica surfaces and renders them suitable for separations of basic proteins. The performance obtained from such surfaces was comparable with that of capillaries modified by the more elaborate procedures of etching, silanol derivatization, and/or adsorptive coating (again with polymers). A home-made device is described which enables derivatization and coating reactions to be performed on fused silica capillaries under an inert atmosphere, i.e. one free from oxygen and water. 相似文献
45.
环氧丙烯酸酯的紫外光固化 总被引:8,自引:0,他引:8
制备了适于配制紫外光固化涂料的环氧丙烯酸酯,研究了反应温度、阻聚剂、催化剂等因素对环氧树脂与丙烯酸反应的影响;讨论了反应机理和动力学;并利用红外光谱观察了产物的紫外光固化行为。季铵盐能有效地催化环氧树脂和丙烯酸的反应,当其用量为0.6%~1.2%时,在90~110℃反应4.5~8小时后,环氧基转化率大于97%。由此配制的光固化涂料经紫外光辐照能快速固化。 相似文献
46.
47.
《Surface and interface analysis : SIA》2005,37(3):310-315
Carbon film coatings have been produced by a hot‐wall chemical vapor deposition (CVD) method under moderate conditions from pyrolysis of a mixture of propane and argon on an Fe(110) substrate at temperatures of 800–900 °C for different deposition times. The effects of temperature and reaction time on the growth of the carbon films were studied. Field‐emission scanning electron microscopy (FESEM), Raman microscopy, Auger electron spectroscopy (AES) and x‐ray diffraction methods have been performed to study the surface morphologies, growth features and microstructures of the carbon film coatings. The FESEM analyses indicated that carbon films on an Fe substrate consisted of flat‐layer and filamentous morphologies. Raman and AES analyses showed that the carbon initially was crystalline but the degree of disorder in the top layer of the carbon film increased with increasing deposition temperature. High‐resolution transmission electron microscopy studies are also in agreement with Raman results. The same trend was observed when the deposition time was increased from 5 to 30 min. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
48.
Marina Lulla Jelena Asari Jaan Aarik Kaupo Kukli Raul Rammula Unto Tapper Eero Kauppinen Väino Sammelselg 《Mikrochimica acta》2006,155(1-2):195-198
Quantitative electron probe microanalysis of highly insulating materials is a complicated problem, partially solved by coating
samples with grounded thin conductive layers or using novel scanning electron microscopy (SEM) techniques, such as low-voltage
and/or variable pressure SEM. In this work, some problems of quantitative X-ray microanalysis of thin HfO2 films, in particular the possibility to determine mass thickness correlated to the density of the layer material, are discussed.
For comparison, Al2O3, Ta2O5 and TiO2 films grown onto both semiconductive Si and insulating quartz substrates were also analysed. All the films studied were synthesized
by atomic layer deposition method. 相似文献
49.
V. G. Nefedov O. A. Artyushenko E. V. Kashevarova 《Russian Journal of Electrochemistry》2006,42(6):638-642
Mass transfer to a horizontal electrode during electrolytic evolution of oxygen and hydrogen at current densities of 100 to 10 000 A/m2 is studied. The mass transfer intensity is evaluated from the diffusion layer thickness, which varies from 60 to 5 μm at such current densities. Calculations show that the decrease in the diffusion layer thickness is due to bubbles with a stationary interphase surface crossing the diffusion layer. During the hydrogen evolution, the diffusion layer thickness is nearly the same for vertical and horizontal electrodes. During the oxygen evolution, the diffusion layer is much thinner for a horizontal electrode. Additional decrease of the diffusion layer thickness during the evolution of oxygen is associated with the lesser solution density in the near-electrode layer and with its transport away by means of natural convection. 相似文献
50.
Pengchong Li Zhi Shang Kejian Cui Huan Zhang Zhi Qiao Caizhen Zhu Ning Zhao Jian Xu 《中国化学快报》2019,30(1):157-159
Polystyrene (PS) fibers with core-shell structure were prepared by coaxial electrostatic spinning using liquid epoxy or curing agent as the core and PS solution as the shell. Scratch self-healing coatings were realized by using the healant-loaded core-shell fibers in the matrix. 相似文献