Determination of chloroacetic acids using ion chromatography with liquid-phase microextraction preconcentration

Q4 Chemistry Analitika i Kontrol Pub Date : 2020-03-20 DOI:10.15826/analitika.2020.24.1.004
R. Sirotkin, V. Krylov, E. V. Elipasheva, R. E. Grubov, K. A. Lutoshkina
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Abstract

In order to increase the sensitivity of the ion chromatographic determination of chlorinated acetic acids ( CAAs ) in water, an emulsion microextraction preconcentration was proposed. The emulsification of extractants was performed by the ultrasonic irradiation. Diethyl and methyl tert-butyl ethers were used as extractants. The comparison of extractants showed the advantages of methyl tert-butyl ether: stable aggregation into a separate phase after the dispersion, no loss of extractant at the analysis stages due to volatility. To reduce the detection limits and improve the chromatographic separation of analytes, the organic matrix of the extract was replaced by water. It was achieved by evaporating the extractant at room temperature and dissolving the dry residue in the eluent. Also, this operation eliminated the difficulties associated with the analysis of organic extracts using the ion chromatography with conductivity detector. The absence of loss of the analytes at this stage was experimentally proven. The dependences of the efficiency of microextraction preconcentration on the various process parameters (ultrasonic exposure time, centrifugation time, volume of extractant, salt additive concentration) were established. The detection limits reached were 1∙10 -3 ‒ 8∙10 -3 mg/l, which are 20-600 times lower than the maximum permissible values for CAAs. In addition, the advantages of this preconcentration technique over the published works were the simultaneous removal of interfering impurities, small volume of water samples (4.1 ml) and chromatograph injected volume (50 μl). The relative standard deviation did not exceed 25%. The proposed method was tested by analyzing the samples of tap water. Mono- and dichloroacetic acids were detected, their content did not exceed the MAC values.  Keywords : chlorinated acetic acids, ion chromatography, microextraction preconcentration DOI: http://dx.doi.org/10.15826/analitika.2020.24.1.004 R.G. Sirotkin, E.V. Elipasheva, V.A. Krylov, R.E. Grubov, K.A. Lutoshkina National Research Lobachevsky State University of Nizhny Novgorod (UNN) Gagarin pr., 23, Nizhny Novgorod, 603950, Russian Federation
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液相微萃取富集离子色谱法测定氯乙酸
为了提高离子色谱法测定水中氯化乙酸(CAAs)的灵敏度,提出了乳状液微萃取预富集方法。采用超声辐照对萃取剂进行乳化。采用二乙基和甲基叔丁基醚作为萃取剂。萃取剂的比较表明,甲基叔丁基醚的优点是:在分散后稳定地聚集成一个单独的相,在分析阶段不会因挥发性而损失萃取剂。为了降低检出限,提高分析物的色谱分离,将萃取物的有机基质用水代替。它是通过在室温下蒸发萃取剂并将干燥残留物溶解在洗脱液中来实现的。此外,该操作还消除了使用离子色谱电导率检测器分析有机提取物的困难。实验证明,在这一阶段分析物没有损失。建立了超声暴露时间、离心时间、萃取剂体积、盐添加剂浓度等工艺参数对微萃取预富集效率的影响规律。检出限为1∙10 -3 ~ 8∙10 -3 mg/l,低于CAAs最大允许值的20 ~ 600倍。与已发表的文献相比,该预富集技术具有同时去除干扰杂质、水样体积小(4.1 ml)、进样体积小(50 μl)等优点。相对标准偏差不超过25%。通过对自来水样品的分析,验证了该方法的有效性。单氯乙酸和二氯乙酸均未超过MAC值。关键词:氯化乙酸,离子色谱,微萃取预富集DOI: http://dx.doi.org/10.15826/analitika.2020.24.1.004 R.G. Sirotkin, E.V. Elipasheva, V.A. Krylov, R.E. Grubov, K.A. Lutoshkina下诺夫哥罗德国立大学国家研究中心(UNN) Gagarin出版社,23,下诺夫哥罗德,603950,俄罗斯联邦
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来源期刊
Analitika i Kontrol
Analitika i Kontrol Chemistry-Analytical Chemistry
CiteScore
0.90
自引率
0.00%
发文量
15
期刊介绍: Analitika i Kontrol is a scientific journal covering theoretical and applied aspects of analytical chemistry and analytical control, published since autumn 1997. Founder and publisher of the journal is the Ural Federal University named after the first President of Russia Boris Yeltsin (UrFU, Ekaterinburg).
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