Ultrasound assisted mercury extraction from soil and sediment
A method for mercury (Hg) determination in soil, river sediment and marine sediment without sample digestion is investigated. Mercury determination is performed by cold vapour atomic absorption spectrometry (CV-AAS) using a flow injection system. Mercury quantitatively leaches out from the investiga...
Gespeichert in:
Veröffentlicht in: | Analytica chimica acta 2004-08, Vol.518 (1), p.157-164 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | A method for mercury (Hg) determination in soil, river sediment and marine sediment without sample digestion is investigated. Mercury determination is performed by cold vapour atomic absorption spectrometry (CV-AAS) using a flow injection system. Mercury quantitatively leaches out from the investigated marine sediment into 30% (v/v) HNO
3 assisted by ultrasonic irradiation (during 90–120
s) when sample particles size are ≤120
μm. Similar conditions can be applied for Hg determination in river sediment and soil, excepting the time of sonication which needs to be increased to 180
s and KCl is also added to the extraction medium. The presence of 0.15% (m/v) KCl in addition to 30% (v/v) HNO
3 is seen to be effective for quantitative Hg leaching. The certified samples PACS-2 and MESS-3 (both marine sediment from NRCC), Buffalo River (NIST 8704), Montana Soil (NIST 2710) and the non-certified river sediment sample RS-3 were analysed. The attained results were well within the 95% confidence level of the certificate or close to information value. Samples were analysed using aqueous standard calibration. A characteristic mass of 25
pg, a LOD (3s) of 0.2
μg
Hg
l
−1 and a LOQ (10s) of 0.012
μg
Hg
g
−1 are typically attained. These are based on 800
μl of sample solution and 1.000
g of sample mass in 20
ml. The RSD of 10 consecutive runs of the sample is |
---|---|
ISSN: | 0003-2670 1873-4324 |
DOI: | 10.1016/j.aca.2004.04.021 |