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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Vacancy ion-exclusion chromatography of inorganic acids on a weakly acidic cation-exchange resin column
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Vacancy ion-exclusion chromatography of inorganic acids on a weakly acidic cation-exchange resin column

机译:弱酸阳离子交换树脂柱上无机酸的空位离子排斥色谱

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Vacancy ion-exclusion chromatography (VIEC) for inorganic acids such as H2SO4, HCl, H3PO4, HNO3, HI and HF is tested on a polymethacrylate-based weakly acidic cation-exchange resin column in the H+-form. That is, mixture of inorganic acids in the mobile phase is adsorbed to the resin phase passing through the separation column. and each vacant peak induced by injecting water is determined. Retention times are dependent on the degrees of retention for each analyte in the resin phase. In VIEC, well-shaped peaks of inorganic acids are produced, leading to efficient separations. However, retention behaviors of inorganic acids were strongly affected by the concentrations of the acids in the mobile phase. Sulfosalicylic acid was mixed with inorganic acids in the mobile phase prior to the introduction of a separation column in order to obtain the well-resolutions in the lower concentrations of the acids. By using this method, the separations of inorganic acids could be achieved in the range of 0.01-1 mM, and the linear ranges could be extended over two-orders of magnitude. This is considered since the protonated carboxylic groups fixed on the resin phase were increased with increasing the acid concentrations in the mobile phase, and the penetration effects for the acids to the resin phase were thus enhanced. The detection limits (S/N = 3) were below 1.0 mu M for all analyte acids. Precision values for retention times were below 0.32% and for peak area were below 0.91%. (c) 2006 Elsevier B.V. All rights reserved.
机译:无机酸(如H2SO4,HCl,H3PO4,HNO3,HI和HF)的空位离子排斥色谱(VIEC)在H +型的基于聚甲基丙烯酸酯的弱酸性阳离子交换树脂柱上进行测试。即,流动相中的无机酸的混合物被吸附到通过分离柱的树脂相上。确定注入水引起的每个空峰。保留时间取决于树脂相中每种分析物的保留程度。在VIEC中,会生成形状良好的无机酸峰,从而实现了有效的分离。但是,无机酸的保留行为受到流动相中酸浓度的强烈影响。在引入分离柱之前,将磺基水杨酸与无机酸在流动相中混合,以便在较低浓度的酸中获得良好的分离度。通过使用这种方法,可以在0.01-1 mM的范围内实现无机酸的分离,并且线性范围可以扩展两个数量级。考虑到这是因为固定在树脂相上的质子化的羧基随流动相中酸浓度的增加而增加,因此酸对树脂相的渗透作用得以增强。所有分析物酸的检出限(S / N = 3)均低于1.0μM。保留时间的精度值低于0.32%,峰面积的精度值低于0.91%。 (c)2006 Elsevier B.V.保留所有权利。

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