EVISA Print | Glossary on | Contact EVISA | Sitemap | Home   
 Advanced search
The establishment of EVISA is funded by the EU through the Fifth Framework Programme (G7RT- CT- 2002- 05112).

Supporters of EVISA includes:

Determination of arsenic species in water by means of capillary electrophoresis coupled to electrospray mass spectrometry


While arsenic often is considered a synonym for poison, the toxicity of different arsenic compounds varies from harmless to cancerogen.  Inorganic arsenic is very toxic and often present in groundwater resources depending on the geochemistry of the aquifer.  This has led the European Union and other global organizations to reduce the maximum residue limit for the total arsenic up to 10 μg L−1 in water for human consumption. In order to perform a meaningful risk assessment but also to reduce arsenic contamination levels by adequate water processing, information about the arsenic speciation is mandatory.  Most methods for such speciation analysis are based on the use of a senstive element detection system coupled with a separation  technique, with HPLC-ICP-MS being the most often used. Since the ICP-MS does not provide any molecular information, the different arsenic species are only identified by their chromatographic retention time by comparison with standards. On the other hand, the ICP-MS often provides compound-idependent element sensitivity, so that quantification of different species is possible with a single standard.

Molecular mass spectrometry such as electrospray mass spectrometry has often been used for the identification of unknown arsenic species but seldom for the quantification of arsenic species. The reason for its limited use is the fact, that the ionization efficiency of different species depends not only on the species but also the matrix, making quantification in complex samples difficult. Also most often ESI-MS cannot compete with ICP-MS for its detection power, calling for a preconcentration procedure, when ultimate detection limits are required.

The new study:
Considering these limitations, a spanish researcher from the University of Salamanca has developed a method for the determination of the four main toxic arsenic compounds (iAs(III), i-As(V), MMa and DMA) in water samples by capilarry electrophoresis (CE) coupled to ESI-MS. Separation of the four arsenic species is achieved by CE employing a basic electrophoretic separation medium containing a mixture of hexafluoro-2-propanol (HFIP) and ammonia. Sensitive detection is performed by ESI in negative mode.

Under optimized conditions, the analysis time was less than 6.5 min. Detection limits obtained were below 2 µg/l  and the quantification limits were below 6.5 µg/l for all four species. In case that the detection power of the CE-ESI-MS is not sufficient, the water volume of the sample is reduced 50:1 in a rotovap. These conditions are adequate for the arsenic speciation in weakly mineralized water samples.

Thirteen water samples from different locations in the province of Salamanca (W Spain) were analysed. The results obtained showed that CE-ESI(−)-MS could be use as another sensitive approach for the determination of As toxic species, both organic and inorganic.

The original study

Javier Domínguez-Álvarez, Capillary electrophoresis coupled to electrospray mass spectrometry for the determination of organic and inorganic arsenic compounds in water samples, Talanta, 212 (2020) 120803. DOI: 10.1016/j.talanta.2020.120803

Related studies (newest first)

H.G. Lee, J.Y. Kwon, D.S. Chung, Sensitive arsenic speciation by capillary electrophoresis using UV absorbance detection with on-line sample preconcentration techniques, Talanta 181 (2018) 366–372. DOI: 10.1016/j.talanta.2018.01.034

Pei-Yu Shuai, Xiao-Jun Yang, Zong-Qing Qiu, Xiao-Hui Wu, Xi Zhu, Ganga Raj Pokhrel, Yu-Ying Fu, Hui-Min Ye, Wen-Xiong Lin, Gui-Di Yang, Determination of arsenic species in Solanum Lyratum Thunb using capillary electrophoresis with inductively coupled plasma mass spectrometry, J. Sep. Sci., 39 (2016) 3239–3245. DOI: 10.1002/jssc.201600415

Na Jia, Mei Han, Guoxing Zhao, Lin Zhang, Bing-Bing Liu, Yi Li, Determination of Arsenic Species in Underground Water by CapillaryElectrophoresis-Inductively Coupled Plasma Mass Spectrometry, Asian J. Chem., 26/16 (2014) 5271-5274. DOI: 10.14233/ajchem.2014.17043

Lihong Liu, Zhaojun Yun, Bin He, Guibin Jiang, Efficient Interface for Online Coupling of Capillary Electrophoresiswith Inductively Coupled Plasma−Mass Spectrometry and Its
Application in Simultaneous Speciation Analysis of Arsenic and Selenium, Anal. Chem., 86 (2014) 8167−8175. DOI: 10.1021/ac501347d

Lihong Liu, Bin He, Zhaojun Yun, Jing Sun, Guibin Jiang, Speciation analysis of arsenic compounds by capillary electrophoresison-line coupled with inductively coupled plasma mass spectrometryusing a novel interface, J. Chromatogr. A, 1304 (2013) 227– 233. DOI: 10.1016/j.chroma.2013.07.034
Claudia Niegel, Simon A. Pfeiffer, Marco Grundmann, Uriel Arroyo-Abad, Jürgen Mattusch, Frank-Michael Matysik, Fast separations by capillary electrophoresis hyphenated to electrospray ionization time-of-flight mass spectrometry as a tool for arsenic speciation analysis,  Analyst, 137 (2012) 1956-1962. DOI: 10.1039/c2an15944a

Meng-Wei Hsieh, Chen-Ling Liu, Jing-Huan Chen, Shiuh-Jen Jiang, Speciation analysis of arsenic and selenium compounds by CE-dynamic reaction cell-ICP-MS, Electrophoresis, 31 (2010) 2272–2278. DOI: 10.1002/elps.200900632

J. Jaafar, K. Konishi, S. Terabe, T. Ikegami, N. Tanaka, Field enhanced sample injection for the CE determination of arsenic compounds using successive multiple ionic polymer layers coated capillaries, Chromatographia 69 (2009) 1437–1441. DOI: 10.1365/s10337-009-1063-60009-5893/09/06

last time modified: May 13, 2020


Imprint     Disclaimer

© 2003 - 2010 by European Virtual Institute for Speciation Analysis ( EVISA )