4.3 Article

Determination of zinc in marine/lacustrine sediments by graphite furnace atomic absorption spectrometry using Pd/Mg chemical modifier and slurry sampling

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TAYLOR & FRANCIS LTD
DOI: 10.1080/03067310903254610

关键词

graphite furnace atomic absorption spectrometry (GF-AAS); slurry sampling; marine and lacustrine sediments; zinc; chemical modifier; palladium; magnesium

资金

  1. funding agency in Japan: The Japan Society for the Promotion of Science KAKENHI [19550077]
  2. Grants-in-Aid for Scientific Research [19550077] Funding Source: KAKEN

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Effectiveness of Pd/Mg chemical modifier for the accurate direct determination of zinc in marine/lacustrine sediments by graphite furnace atomic absorption spectrometry (GF-AAS) using slurry samples was evaluated. A calibration curve prepared by aqueous zinc standard solution with addition of Pd/Mg chemical modifier is used to determine the zinc concentration in the sediment. The accuracy of the proposed method was confirmed using Certified Reference Materials, NMIJ CRM 7303-a (lacustrine sediment) from National Metrology Institute of Japan, National Institute of Advanced Industrial Science and Technology, Japan, and MESS-3 (marine sediment) and PACS-2 (marine sediment) from National Research Council, Canada. The analytical results obtained by employing Pd/Mg modifier are in good agreement with the certified values of all the reference sediment materials. Although for NRC MESS-3 an accurate determination of zinc is achieved even without the chemical modifier, the use of Pd/Mg chemical modifier is recommended as it leads to establishment of a reliable and accurate direct analytical method. One quantitative analysis takes less than 15 minutes after we obtain dried sediment samples, which is several tens of times faster than conventional analytical methods using acid digested sample solutions. The detection limits are 0.13 mu g g(-1) (213.9 nm) and 16 mu g g(-1) (307.6 nm), respectively, in sediment samples, when 40 mg of dried powdered samples are suspended in 20mL of 0.1 mol L(-1) nitric acid and a 10 mu l portion of the slurry sample is measured. The precision of the proposed method is 8-15% (RSD).

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