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羧酸在弱酸性阳离子交换树脂上的空位离子排斥色谱法。

Vacancy ion-exclusion chromatography of carboxylic acids on a weakly acidic cation-exchange resin.

作者信息

Tanaka Kazuhiko, Ding Ming-Yu, Helaleh Murad I H, Taoda Hiroshi, Takahashi Hayato, Hu Wenzhi, Hasebe Kiyoshi, Haddad Paul R, Fritz James S, Sarzanini C

机构信息

National Institute of Advanced Industrial Science and Technology, and Graduate School of Engineering, Chubu University, Seto, Japan.

出版信息

J Chromatogr A. 2002 May 17;956(1-2):209-14. doi: 10.1016/s0021-9673(02)00393-x.

Abstract

In this preliminary study, a new approach to ion-exclusion chromatography is proposed to overcome the relatively poor conductivity detection response which occurs in ion-exclusion chromatography when acids are added to the eluent in order to improve peak shape. This approach, termed vacancy ion-exclusion chromatography, requires the sample to be used as eluent and a sample of water to be injected onto a weakly acidic cation-exchange column (TSKgel OApak-A). Vacancy peaks for each of the analytes appear at the retention times of these analytes. Highly sensitive conductivity detection is possible and sharp, well-shaped peaks are produced, leading to efficient separations. Retention times were found to be affected by the concentration of the analytes in the eluent, and also by the presence of an organic modifier such as methanol in the eluent. Detection limits for oxalic, formic, acetic, propionic, butyric and valeric acids were 0.1, 0.2, 0.3, 0.3, 0.4 and 0.5 microM, respectively, and linear ranges for some acids extended over two orders of magnitude. Precision values for retention times were 0.21% and for peak areas were <1.90%. The vacancy ion-exclusion chromatography method was found to give detection responses four to 10 times higher than conventional ion-exclusion chromatography using sulfuric acid eluent and two to five times higher than conventional ion-exclusion chromatography using benzoic acid eluent.

摘要

在这项初步研究中,提出了一种离子排斥色谱的新方法,以克服在离子排斥色谱中,为改善峰形而向洗脱液中添加酸时出现的相对较差的电导检测响应。这种方法称为空位离子排斥色谱,要求将样品用作洗脱液,并将一份水样注入弱酸性阳离子交换柱(TSKgel OApak - A)。每种分析物的空位峰出现在这些分析物的保留时间处。可以进行高灵敏度的电导检测,并产生尖锐、峰形良好的峰,从而实现高效分离。发现保留时间受洗脱液中分析物浓度的影响,也受洗脱液中甲醇等有机改性剂的存在的影响。草酸、甲酸、乙酸、丙酸、丁酸和戊酸的检测限分别为0.1、0.2、0.3、0.3、0.4和0.5 microM,一些酸的线性范围扩展了两个数量级。保留时间的精密度值为0.21%,峰面积的精密度值<1.90%。发现空位离子排斥色谱法的检测响应比使用硫酸洗脱液的传统离子排斥色谱法高4至10倍,比使用苯甲酸洗脱液的传统离子排斥色谱法高2至5倍。

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