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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Analysis of hydroxide, inorganic sulphur species and organic anions in kraft pulping liquors by capillary electrophoresis
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Analysis of hydroxide, inorganic sulphur species and organic anions in kraft pulping liquors by capillary electrophoresis

机译:毛细管电泳法分析牛皮纸制浆液中的氢氧根,无机硫和有机阴离子

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A new method has been developed for the determination of hydroxide, sulphide. thiosulphate, sulphate, sulphite, chloride. oxalate and formate in kraft green, white and black liquors by capillary electrophoresis. The method provides baseline resolution of all analytes of interest using an electrolyte composed of 10 mM sodium chromate and 2 nM tetradecyltrimethylammonium hydroxide. Separations are conducted under constant current conditions at 25 degreesC and analytes are quantified by indirect UV-detection at 275 nm. A brief. post run wash of the capillary with 0.5 M NaOH and water gave improved inter- and intra-run repeatability of both migration times and peak areas. Sulphide and other oxysulphur species were relatively stable in white and green liquors diluted in helium-sparged water. However, sulphide present in black liquor samples diluted in the same solvent underwent rapid oxidation to form sulphite and thiosulphate, thereby precluding the measurement of all three anions. We discovered that quinone-type compounds present in black liquor catalyze the oxidation of sulphide and that the addition of reduced glutathione at a concentration of 1 mg/mL during black liquor dilution completely stabilized sulphide, sulphite and thiosulphate for at least one hour, thus allowing for quantitative analysis of the analytes. A mechanism is proposed to explain the action of both quinones and that of glutathione. Results obtained by the new method compared well with those obtained by ion chromatography, titrimetry, and from spike-recovery experiments. (C) 2004 Elsevier B.V. All rights reserved.
机译:已经开发出一种测定氢氧化物,硫化物的新方法。硫代硫酸盐,硫酸盐,亚硫酸盐,氯化物。草酸和甲酸在牛皮纸绿,白和黑液中的毛细管电泳。该方法使用由10 mM铬酸钠和2 nM十四烷基三甲基氢氧化铵组成的电解质提供所有目标分析物的基线分辨率。分离是在25°C的恒定电流条件下进行的,分析物通过275 nm的间接UV检测进行定量。简要。用0.5 M NaOH和水对毛细管进行运行后清洗,可以改善迁移时间和峰面积的运行内和运行内重复性。在用氦气喷射的水稀释的白液和绿液中,硫化物和其他氧化硫物质相对稳定。但是,在用相同溶剂稀释的黑液样品中存在的硫化物会快速氧化形成亚硫酸盐和硫代硫酸盐,从而排除了对所有三种阴离子的测定。我们发现黑液中存在的醌型化合物可催化硫化物的氧化,并且在黑液稀释过程中以1 mg / mL的浓度添加还原型谷胱甘肽可完全稳定硫化物,亚硫酸盐和硫代硫酸盐至少一小时,从而使用于分析物的定量分析。提出了一种机制来解释醌和谷胱甘肽的作用。通过新方法获得的结果与通过离子色谱,滴定法和加标回收实验获得的结果进行了很好的比较。 (C)2004 Elsevier B.V.保留所有权利。

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