Twohill Eadaoin, Paull Brett
National Centre for Sensor Research, School of Chemical Sciences, Dublin City University, Ireland.
J Chromatogr A. 2002 Oct 11;973(1-2):103-13. doi: 10.1016/s0021-9673(02)01193-7.
An investigation into the use of zwitterionic ion chromatography for the determination of inorganic anions in water samples was carried out. When using an ODS stationary phase precoated with Zwittergent 3-14 and a pure water mobile phase, the stability of the adsorbed coating was insufficient for quantitative work. Recycling of the water mobile phase was used to stabilise the zwitterionic coating, and resulted in improved retention time precision (15.2% RSD down to 2.4% RSD for nitrate). Post-detection cation- and anion-exchange columns in acid and hydroxide form removed sample ions from the recycling mobile phase, with the desorbed Zwittergent 3-14 passing through unretained and passing back through the pump to the analytical column. A 200-ml volume of mobile phase was recycled over a 3-week period with retention times for sulphate, chloride and nitrate standards injected at the start and end of the period varying less than 2.5%. The same system was then used with a mobile phase containing 2 mM Zwittergent 3-14. This resulted in further improvements in retention time (0.2-0.5% RSD, n = 10) and peak area precision (2.6-6.0% RSD, 1 mM standards) and improved peak efficiencies (2421-4047 N). The developed method was applied to water samples, and results compared to those obtained using anion-exchange chromatography. All sample cations were exchanged to sodium using an off-line cation-exchange procedure prior to injection.
开展了一项关于使用两性离子离子色谱法测定水样中无机阴离子的研究。当使用预涂有两性离子表面活性剂Zwittergent 3 - 14的ODS固定相和纯水流动相时,吸附涂层的稳定性不足以用于定量分析。采用水流动相循环来稳定两性离子涂层,这使得保留时间精密度得到改善(硝酸盐的相对标准偏差从15.2%降至2.4%)。检测后,处于酸和氢氧化物形式的阳离子和阴离子交换柱从循环流动相中去除样品离子,解吸的Zwittergent 3 - 14未被保留,直接通过泵返回分析柱。在3周的时间内循环使用200毫升流动相,在此期间开始和结束时注入的硫酸盐、氯化物和硝酸盐标准品的保留时间变化小于2.5%。然后使用相同的系统,流动相中含有2 mM的Zwittergent 3 - 14。这进一步改善了保留时间(相对标准偏差为0.2 - 0.5%,n = 10)和峰面积精密度(相对标准偏差为2.6 - 6.0%,1 mM标准品),并提高了峰效率(2421 - 4047理论塔板数)。将所开发的方法应用于水样,并将结果与使用阴离子交换色谱法获得的结果进行比较。在进样前,使用离线阳离子交换程序将所有样品阳离子交换为钠离子。