Ozonation of Two Acidic Azo Dyes with Different Substituents

The ozonation of two differently substituted azo dyes (Schwarz GRS and Orange Acid 8) in water media is studied. The influence of pH on the effectiveness of the ozonation at various initial concentrations of each dye is explored. It was found out that the rates of decolorization for amino-group substituted dyes reflect the considerable influence by the widely varying initial pH from 4.5 to 10. Specifically, the highest effect of decolorization of this dye was obtained at the highest pH studied (pH 10) for all initial concentrations of the solutions. Considering the dye without an amino-group substitute, the rates of color disappearance in ozonation reflected to a lower degree the variations of the initial pH. Pseudo-first-order trends of decolorization were observed in all the experimental runs. Regarding the kinetic results obtained, an attempt to explain the different dyes reactivity was made based on the absolute electronegativity (E_lumo + E_homo) of both dyes. The COD/BOD analysis shows that the ozonation of both azo dyes can reduce the sample COD but it could not improve the biodegradability ratio (BOD₅/COD). BOD decrease with ozonation time indicates that the intermediates of the ozonation are of lower biodegradability. Oxalic acid was found as the final product of ozonation of both dyes.     

Dye adsorption characteristics of alginate/polyaspartate hydrogels

This study examined the removal of some basic dyes, such as Methylene Blue, Malachite Green and Methyl Orange, using alginate or alginate/polyaspartate composite gel beads. The adsorption of dyes from aqueous solutions at 25 °C was examined using a batch sorption technique. The effects of CaCl₂ and the dye concentration on the adsorption were examined. Type-S adsorption isotherms were obtained, which is characteristic of a weak solute–solid interaction. The ionic interaction between the dye molecule and gel matrix appears to be responsible for the efficient adsorption of cationic dyes in this system. These results suggest that an alginate/polyaspartate gel can be used as an effective sorbent for water pollutants such as dyes, and the immobilization of these organic contaminants in the hydrogels from wastewater can solve one of the most important environmental problems in the related industry.     

涤棉府绸染色条花疵病的产生和控制

本文分析了T/C府绸集色条花产生的原因。通过工艺条件和操作方法,染色条花疵病得到明显改善。     

均三甲苯胺的合成及其应用

介绍了均三甲苯胺的合成工艺、反应机理、国内外产品的质量指标、提高质量与收率的途径,并对产品的应用作了讨论。     

人造参考星系统设计

简述了人造参考星系统，并用该系统作为大型望远镜主动光学和自适应光学的Ｓｈａｃｋ－Ｈａｒｔｍａｎ波面探测系统的光源。     

纺织品印染后整理剂Fs的研制

纺织品印染后整理剂Fs系多羟基多胺的阳离子树脂型缩合物,不含游离甲醛。本文介绍了纺织品印染后整理剂Fs的合成方法和应用条件。     

火焰原子吸收光谱法测定高纯石英粉中痕量钙

系统地研究了用空气——乙炔火焰原子吸收光谱分析法测定高纯石英粉中钙的最佳条件，建立了14％的乙醇作为增感剂，在2％盐酸介质中，0．4％ LaCl3溶液作为释放剂，用塞曼火焰原子吸收法测定的可行性方案，探讨了共存元素对钙的干扰及其消除。方法操作简便快速，干扰少，方法相对标准偏差小于3％，适用于日常分析石英粉中的杂质。     

发色团含有乙撑基或乙烯撑桥基的碳菁合成及其光谱和增感性能

本文研究发色团α,α′ 位上具有乙撑基和乙烯撑桥基的碳菁合成通法 ,染料的立体结构、质子化倾向和萤光特性。探讨了多甲川发色团的α,α′ 位桥基和中位取代基对硫碳菁在长波区域的电子吸收光谱的影响。研究结果指出 :多甲川链上含有乙撑桥的硫碳菁有可能使照相卤化银乳剂在远红区和近红外光谱区产生高效的光谱增感作用。     

TiO2 films prepared by micro-plasma oxidation method for dye-sensitized solar cell

Nanocrystalline TiO₂ films are widely investigated as the electrodes of dye-sensitized solar cell(s) with different preparation methods. In this paper, thin titanium dioxide films have been prepared on titanium plates by the micro-plasma oxidation method in the sulfuric acid solution. The thin TiO₂ films were sensitized with a cis-RuL₂(SCN)₂·2H₂O (L = cis-2,2′-bipyridine-4,4′-dicarboxylic acid) ruthenium complex and implemented into a dye-sensitized solar cell configuration. The influence of reaction current density (10, 15, 20, 25 and 30 A dm⁻²) on the structural and the surface morphology of the films was investigated by X-ray diffraction, scanning electron microscopy, atom force microscopy and X-ray photoelectricity spectroscopy. Impedance analysis for dye-sensitized solar cells was carried out by electrochemical impedance spectroscopy. The results show that the rise of current density leads to the increase in the amount of rutile and the thickness of the TiO₂ film, which makes the TiO₂ films have different photovoltages and photocurrents. The relatively higher photoelectricity properties were obtained in the TiO₂ films prepared at a current density of 20 A dm⁻². The open-circuit voltage and the short-circuit current are 605 mV and 165 μA cm⁻², respectively.