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中空纤维基液-液-液微萃取结合高效液相色谱法用于有机汞形态分析

Hollow fiber-based liquid-liquid-liquid microextraction combined with high-performance liquid chromatography for the speciation of organomercury.

作者信息

Xia Linbo, Hu Bin, Wu Yunli

机构信息

Department of Chemistry, Wuhan University, Wuhan 430072, China.

出版信息

J Chromatogr A. 2007 Nov 30;1173(1-2):44-51. doi: 10.1016/j.chroma.2007.09.089. Epub 2007 Oct 13.

Abstract

A novel and extremely highly sensitive method for the speciation of organomercury in sea food and environmental water samples was developed by hollow fiber liquid-liquid-liquid microextraction (LLLME) coupled to high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection at 254 nm. By the use of toluene filled the pores of the hollow fiber wall as the organic phase and Na(2)S(2)O(3) aqueous solution in the lumen of hollow fiber as acceptor phase, the simultaneous preconcentration of methylmercury (MeHg), ethylmercury (EtHg), and phenylmercury (PhHg) could be realized, and the target mercury species in the post-extraction acceptor phase were directly injected into HPLC for their separation. The factors affecting on the liquid-liquid-liquid microextraction of three organomercury species, including organic solvent, the pH of donor phase, the concentration of complexing agent, extraction time and stirring rate were investigated and the optimal extraction conditions were established. With the consumption of 3.8 mL of sample solution, the enrichment factors were about 120, 215 and 350 for MeHg, EtHg, and PhHg, respectively. The limits of detection were in the range of 0.3-3.8 ng mL(-1) (as Hg) with precisions (RSDs (%), c=30 ng mL(-1) (as Hg), n=7) ranging from 6.4 to 8.9%. The developed technique was validated by analyzing a certified reference material (DORM-2, dogfish-muscle, NRCC) and an environmental water sample, and the analytical results were satisfactory.

摘要

通过中空纤维液-液-液微萃取(LLLME)与高效液相色谱(HPLC)联用,并在254 nm处进行紫外(UV)检测,开发了一种新颖且极其灵敏的方法,用于测定海鲜和环境水样中的有机汞形态。以填充在中空纤维壁孔中的甲苯为有机相,以中空纤维内腔中的硫代硫酸钠水溶液为接受相,可同时对甲基汞(MeHg)、乙基汞(EtHg)和苯基汞(PhHg)进行预富集,萃取后接受相中的目标汞形态直接注入HPLC进行分离。研究了影响三种有机汞形态液-液-液微萃取的因素,包括有机溶剂、供体相的pH值、络合剂浓度、萃取时间和搅拌速率,并确定了最佳萃取条件。在消耗3.8 mL样品溶液的情况下,MeHg、EtHg和PhHg的富集因子分别约为120、215和350。检测限在0.3 - 3.8 ng mL⁻¹(以Hg计)范围内,精密度(相对标准偏差,RSD(%),c = 30 ng mL⁻¹(以Hg计),n = 7)为6.4%至8.9%。通过分析有证标准物质(DORM - 2,鲨鱼肌肉,NRCC)和环境水样对所开发的技术进行了验证,分析结果令人满意。

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