Kochmann Sven, Matysik Frank-Michael
Institute of Analytical Chemistry, University of Regensburg, Universitätsstr. 31, D-93053, Regensburg, Germany.
Rapid Commun Mass Spectrom. 2014 Dec 15;28(23):2670-80. doi: 10.1002/rcm.7056.
Mass spectrometry (MS) is an attractive method for extending capillary-size ion chromatography (cHPIC) to create a valuable technique for speciation analysis. For hyphenation, the aqueous effluent of cHPIC has to be transformed into a volatile mixture for MS while preserving analytical concentrations as well as peak shapes during transfer from cHPIC to MS. Finally, the approach should technically be flexible and easy-to-use. A combination of cHPIC and sheath-flow electrospray ionization (ESI)-MS offers to solve all these challenges.
cHPIC/sheath-flow-ESI-TOFMS was used in this study for the speciation analysis of various arsenic model compounds. These model compounds were analyzed with different hyphenation setups and configurations of cHPIC/MS and their respective assets and drawbacks were examined and discussed. The parameters (flow rate and composition of sheath liquid) of sheath-flow ESI and their influence on the performance of the spray and the sensitivity of the detector were investigated and compared with those of sheathless ESI.
Using an injection valve to couple cHPIC and MS was found to be the best method for hyphenation, since it constitutes a flexible and dead-volume-free approach. The investigation of sheath-flow ESI revealed that the flow rate of the sheath liquid has to resemble the flow rate of the IC effluent to ensure a stable spray and that a composition of 2-propanol/water/ammonia at 50:50:0.2 (v/v/v) suits most applications without unilaterally promoting the sensitivity for either organic or inorganic compounds. The optimized setup and conditions were successfully applied to the analysis of a mixture of important arsenic species and used to determine limits of detection of organic and inorganic arsenic species (3.7 µg L(-1) elemental arsenic).
A method for cHPIC/sheath-flow-ESI-MS was developed. The method was shown to be a valuable tool for speciation and trace analysis. It features no dead volume, fast transfer from IC to MS, only minimal peak-widening, high reproducibility, and the ability to fine-tune the ESI spray for higher sensitivity and stability by adjusting the composition of the sheath-liquid.
质谱法(MS)是一种很有吸引力的方法,可用于扩展毛细管尺寸离子色谱法(cHPIC),从而创建一种用于形态分析的有价值技术。对于联用技术,cHPIC的水性流出物必须转化为用于质谱分析的挥发性混合物,同时在从cHPIC转移到MS的过程中保持分析浓度和峰形。最后,该方法在技术上应灵活且易于使用。cHPIC与鞘流电喷雾电离(ESI)-MS的结合提供了解决所有这些挑战的方法。
本研究使用cHPIC/鞘流-ESI-TOFMS对各种砷模型化合物进行形态分析。这些模型化合物采用不同的cHPIC/MS联用设置和配置进行分析,并对其各自的优缺点进行了研究和讨论。研究了鞘流ESI的参数(鞘液流速和组成)及其对喷雾性能和检测器灵敏度的影响,并与无鞘ESI的参数进行了比较。
发现使用进样阀连接cHPIC和MS是联用的最佳方法,因为它构成了一种灵活且无死体积的方法。对鞘流ESI的研究表明,鞘液流速必须与离子色谱流出物的流速相似,以确保稳定的喷雾,并且50:50:0.2(v/v/v)的2-丙醇/水/氨组成适合大多数应用,而不会单方面提高对有机或无机化合物的灵敏度。优化后的设置和条件成功应用于重要砷形态混合物的分析,并用于确定有机和无机砷形态的检测限(3.7 µg L⁻¹元素砷)。
开发了一种cHPIC/鞘流-ESI-MS方法。该方法被证明是形态分析和痕量分析的有价值工具。它具有无死体积、从离子色谱快速转移到质谱、峰展宽最小、重现性高以及能够通过调整鞘液组成来微调ESI喷雾以提高灵敏度和稳定性的能力。