Ultrasound assisted mercury extraction from soil and sediment

被引:66
作者
Collasiol, A [1 ]
Pozebon, D [1 ]
Maia, SM [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Inst Quim, BR-9150970 Porto Alegre, RS, Brazil
关键词
Hg; sediment; soil; ultrasonic; CV-AAS;
D O I
10.1016/j.aca.2004.04.021
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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) HNO3 assisted by ultrasonic irradiation (during 90-120 s) when sample particles size are less than or equal to 120 mum. 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) KCI in addition to 30% (v/v) HNO3 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 mug Hg l(-1) and a LOQ (10s) of 0.012 mug Hg g(-1) are typically attained. These are based on 800 mul of sample solution and 1.000 g of sample mass in 20 ml. The RSD of 10 consecutive runs of the sample is < 5%. The proposed method was finally applied for the determination of Hg in real samples of soil, river sediment and marine sediment. The same samples were also analysed using a digestion method giving similar results. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 164
页数:8
相关论文
共 20 条
[1]   Selective extractions to assess the biogeochemically relevant fractionation of inorganic mercury in sediments and soils [J].
Bloom, NS ;
Preus, E ;
Katon, J ;
Hiltner, M .
ANALYTICA CHIMICA ACTA, 2003, 479 (02) :233-248
[2]   Room temperature sonolysis-based advanced oxidation process for degradation of organomercurials: Application to determination of inorganic and total mercury in waters by flow injection-cold vapor atomic absorption spectrometry [J].
Capelo, JL ;
Lavilla, I ;
Bendicho, C .
ANALYTICAL CHEMISTRY, 2000, 72 (20) :4979-4984
[3]   Determination of cadmium, mercury and lead in soil samples by slurry sampling electrothermal vaporization inductively coupled plasma mass spectrometry [J].
Chen, SF ;
Jiang, SJ .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1998, 13 (10) :1113-1117
[4]   Trace determination of mercury: A review [J].
Clevenger, WL ;
Smith, BW ;
Winefordner, JD .
CRITICAL REVIEWS IN ANALYTICAL CHEMISTRY, 1997, 27 (01) :1-26
[5]   Feasibility study for a BCR sediment methyl mercury reference material production. [J].
Filippelli, M .
CHEMOSPHERE, 1999, 39 (07) :1199-1210
[6]   Determination of mercury in mineral coal using cold vapor generation directly from slurries, trapping in a graphite tube, and electrothermal atomization [J].
Flores, EMM ;
Welz, B ;
Curtius, AJ .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2001, 56 (09) :1605-1614
[7]   DETERMINATION OF TOTAL MERCURY IN WATERS AND URINE BY FLOW-INJECTION ATOMIC-ABSORPTION SPECTROMETRY PROCEDURES INVOLVING ONLINE AND OFF-LINE OXIDATION OF ORGANOMERCURY SPECIES [J].
HANNA, CP ;
TYSON, JF ;
MCINTOSH, S .
ANALYTICAL CHEMISTRY, 1993, 65 (05) :653-656
[8]   Results of a complex round robin test with four river sediments [J].
Heininger, P ;
Pelzer, J ;
Henrion, R ;
Henrion, G .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1998, 360 (3-4) :344-347
[9]  
HORVAT M, 2001, ELEMENT SPECIATION E, pCH7
[10]   Reagent generation assisted by ultrasonic irradiation [J].
Korn, M ;
Andrade, MVAS ;
Borges, SS ;
Sousa, CS ;
Oliveira, FS .
JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2003, 14 (02) :254-258