{"title":"Separation of inorganic anions for analysis of sea-water by capillary zone electrophoresis","authors":"A. Timerbaev, T. Takayanagi, S. Motomizu","doi":"10.1039/A900323A","DOIUrl":null,"url":null,"abstract":"A number of trace-level inorganic anions in sea-water have been separated efficiently by capillary zone electrophoresis using direct UV detection. The carrier electrolyte contained 100 mM KCl at pH 4.0, which offered the possibility of preventing interference from high matrix salinity and avoided the use of an additional flow modifier. As a result, no impact of the chloride ion on the migration of high-mobility anions was observed and short migration times (within 8 min) were obtained by operating at a relatively low applied voltage (–10 kV). Modifications to the carrier electrolyte composition by incorporating 18-crown-6 or tetrabutylammonium chloride were found essential for furnishing the appropriate resolution. The role of ion-association and ion-inclusion interactions, taking place in the electrophoretic system and resulting in variations of the separation selectivity, are discussed. The problem of improving the detection sensitivity for quantification of inorganic anions in sea-water is also briefly addressed.","PeriodicalId":7814,"journal":{"name":"Analytical Communications","volume":"31 1","pages":"139-141"},"PeriodicalIF":0.0000,"publicationDate":"1999-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/A900323A","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15
Abstract
A number of trace-level inorganic anions in sea-water have been separated efficiently by capillary zone electrophoresis using direct UV detection. The carrier electrolyte contained 100 mM KCl at pH 4.0, which offered the possibility of preventing interference from high matrix salinity and avoided the use of an additional flow modifier. As a result, no impact of the chloride ion on the migration of high-mobility anions was observed and short migration times (within 8 min) were obtained by operating at a relatively low applied voltage (–10 kV). Modifications to the carrier electrolyte composition by incorporating 18-crown-6 or tetrabutylammonium chloride were found essential for furnishing the appropriate resolution. The role of ion-association and ion-inclusion interactions, taking place in the electrophoretic system and resulting in variations of the separation selectivity, are discussed. The problem of improving the detection sensitivity for quantification of inorganic anions in sea-water is also briefly addressed.
采用毛细管区带电泳直接紫外检测法对海水中多种微量无机阴离子进行了高效分离。载体电解质在pH 4.0下含有100 mM KCl,这提供了防止高基质盐度干扰的可能性,并且避免了使用额外的流动调节剂。因此,氯离子对高迁移率阴离子的迁移没有影响,并且在相对较低的施加电压(-10 kV)下操作,可以获得较短的迁移时间(在8分钟内)。通过加入18-冠-6或四丁基氯化铵对载体电解质组成进行修饰,可以获得适当的分辨率。离子结合和离子包涵相互作用的作用,发生在电泳系统和导致分离选择性的变化,进行了讨论。本文还简要讨论了提高海水中无机阴离子定量检测灵敏度的问题。