Non-chromatographic speciation analysis of mercury by flow injection on-line preconcentration in combination with chemical vapor generation atomic fluorescence spectrometry |
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Affiliation: | 1. School of Chemistry and Chemical Engineering, State Key Laboratory of Coordination Chemistry and Key Laboratory of MOE for Life Science, Nanjing University, Nanjing 210093, China;2. Department of Chemistry, Xuzhou Normal University, Xuzhou 221116, China;1. Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, Republic of Korea;2. Department of Chemistry, Soongsil University, Seoul, Republic of Korea;3. Laboratory of Veterinary Pharmacology, Seoul National University, Seoul, Republic of Korea;4. National Cancer Center, Goyang, Gyeonggi, Republic of Korea;1. Research Institute for Applied Physics, University of Tabriz, Tabriz 51665-163, Iran;2. Laser-Plasma Research Institute, Shahid Beheshti University, G.C., Evin, Tehran 19839-63113, Iran;1. Anadolu University, Faculty of Sciences, Department of Biology, 26470 Eskişehir, Turkey;2. Anadolu University, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, 26470 Eskisehir, Turkey |
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Abstract: | A novel non-chromatographic approach for direct speciation of mercury, based on the selective retention inorganic mercury and methylmercury on the inner wall of a knotted reactor by using ammonium diethyl dithiophosphate and dithizone as complexing agents respectively, was developed for flow injection on-line sorption preconcentration coupled with chemical vapor generation non-dispersive atomic fluorescence spectrometry. With the sample pH kept at 2.0, the preconcentration of inorganic mercury on the inner walls of the knotted reactor was carried out based on the exclusive retention of Hg–DDP complex in the presence of methylmercury via on-line merging the sample solution with ammonium diethyl dithiophosphate solution, and selective preconcentration methylmercury was achieved with dithizone instead of ammonium diethyl dithiophosphate. A 15% (v/v) HCl was introduced to elute the retained mercury species and merge with KBH4 solution for atomic fluorescence spectrometry detection. Under the optimal experimental conditions, the sample throughputs of inorganic mercury and methylmercury were 30 and 20 h− 1 with the enhancement factors of 13 and 24. The detection limits were found to be 3.6 ng l− 1 for Hg2+ and 2.0 ng l− 1 for CH3Hg+. The precisions (RSD) for the 11 replicate measurements of each 0.2 μg l− 1 of Hg2+ and CH3Hg+ were 2.2% and 2.8%, respectively. The developed method was validated by the analysis of certified reference materials (simulated natural water, rice flour and pork) and by recovery measurements on spiked samples, and was applied to the determination of inorganic mercury and methylmercury in biological and environmental water samples. |
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