scholarly journals Total Arsenic and Arsenic Species Determination in Freshwater Fish by ICP-DRC-MS and HPLC/ICP-DRC-MS Techniques

Molecules ◽  
2019 ◽  
Vol 24 (3) ◽  
pp. 607 ◽  
Author(s):  
Izabela Komorowicz ◽  
Adam Sajnóg ◽  
Danuta Barałkiewicz

Analytical methods for the determination of total arsenic (TAs) and arsenic species (arsenite—As(III), arsenate—As(V), monomethylarsenic acid—MMA, dimethylarsenic acid—DMA and arsenobetaine—AsB) in freshwater fish samples were developed. Inductively coupled plasma mass spectrometry with dynamic reaction cell (ICP-DRC-MS) and high-performance liquid chromatography hyphenated to ICP-DRC-MS were used for TAs and arsenic species determination, respectively. The DRC with oxygen as a reaction gas was used. Sample preparation, digestion, and extraction were optimized. Microwave assisted digestion and extraction provided good recovery and extraction efficiency. Arsenic species were fully separated in 8 min using 10 mmol L−1 of ammonium dihydrogen phosphate and 10 mmol L−1 of ammonium nitrate. Overlapping of AsB and As(III) of arsenic species in the presence of a high concentration of AsB and trace amounts of As(III) were studied. Detailed validation of analytical procedures proved the reliability of analytical measurements. Both procedures were characterized by short-term and long-term precision: 2.2% (TAs) up to 4.2% (AsB), and 3.6% (TAs) up to 7.2% (DMA), respectively. Limits of detection (LD) were in the range from 0.056 µg L−1 for TAs to 0.15 µg L−1 for As(V). Obtained recoveries were in the range of 85%–116%. Developed methods were applied to freshwater fish samples analysis.

Author(s):  
Yung-Chun Chen ◽  
Shiuh-Jen Jiang

Liquid chromatography and dynamic reaction cell inductively coupled plasma mass spectrometry are used in tandem for the simultaneous speciation of arsenic and mercury in fish.


2006 ◽  
Vol 3 (2) ◽  
pp. 149 ◽  
Author(s):  
Suk Fun Kan ◽  
Peter A. Tanner

Environmental Context.Sulfate in particulate matter is usually collected by a high-volume air sampler and analysed as a soluble extract by ion chromatography. The use of an inductively coupled plasma mass spectrometer fitted with a dynamic reaction cell enables not only the water-soluble, but also the total sulfate to be determined at the same time as the analyses of metal ions. Results from Hong Kong show that sulfate is strongly correlated with crustal species in particulate matter. Abstract.An instrumental method has been developed for the determination of sulfur in particulate matter using inductively coupled plasma dynamic reaction cell mass spectrometry. The reaction gas O2 was employed to convert S+ into the diatomic species SO+, and analysed at two different mass-to-charge ratios. The limit of detection for the 32S16O+ determination is ~1 ng S m–3. The method has the advantages that not only soluble sulfur (as commonly analysed by ion chromatography) but also total sulfur can be determined on the same instrument as many metal species. The mean values (± standard deviations) for a spring sampling program of particulate matter of diameter less than 10 μm (PM10) in Hong Kong (n = 13) for soluble and total S were 5.2 ± 1.2 μg m–3 and 5.5 ± 1.3 μg m–3 respectively. These values are quite low owing to a predominantly easterly airstream. Sulfur in PM10 is strongly correlated with the crustal species Ca, Al and Mn.


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