On-line arsenic co-precipitation on ethyl vinyl acetate turning-packed mini-column followed by hydride generation-ICP OES determination

被引:54
作者
Gil, R. A.
Ferrua, N.
Salonia, J. A.
Olsina, R. A.
Martinez, L. D.
机构
[1] Natl Univ San Luis, Fac Chem Biochem & Pharm, Dept Analyt Chem, RA-5700 San Luis, Argentina
[2] Consejo Nacl Invest Cient & Tecn, CONICET, Ciudad Buenos Aires, Argentina
关键词
inorganic arsenic; EVA turnings as adsorbent and as mechanical filter; On-line co-precipitation/solid phase extraction; HG-ICP OES; water samples;
D O I
10.1016/j.jhazmat.2006.09.051
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
An alternative and new system for on-line preconcentration of arsenic by sorption on a mini-column associated to hydride generation - inductively coupled plasma - optical emission spectrometry determination was studied. It is based on the sorption of arsenic on a column packed with ethyl vinyl acetate (EVA) turnings and the use of La(HI) as co-precipitant reagent. This polymeric material was employed here for the first time as filling material for column preconcentration. It could work both as adsorbent and as sieve material. Sample and co-precipitant agent (lanthanum nitrate) were off-line mixed and merged with ammonium buffer solution (pH 10.0), which promoted precipitation and quantitative collection on the small EVA turnings. The arsenic preconcentrated by co-precipitation with lanthanum hydroxide precipitate was subsequently eluted with hydrochloric acid, which was the medium used for hydride generation. Considering a flow rate of 5 ml/min, three enrichment factors were obtained, 28-, 38-and 45-fold at three different sampling times, 60, 120 and 180 s; respectively. The detection limits (3 s) obtained for each case were 0.013, 0.009 and 0.007 mu g/l. Additionally, the calculated precisions expressed as relatively standard deviation (R.S.D.) were 0.9, 1.3 and 1.1%. Satisfactory results were obtained for the determination of arsenic in standard reference material NIST 1643e Trace Elements in Water and drinking water samples. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:431 / 436
页数:6
相关论文
共 34 条
[1]   Determination of arsenic(III) and total arsenic(III,V) in water samples by resin suspension graphite furnace atomic absorption spectrometry [J].
Anezaki, K ;
Nukatsuka, I ;
Ohzeki, K .
ANALYTICAL SCIENCES, 1999, 15 (09) :829-834
[2]   Determination of arsenic(III) by flow injection solid phase extraction coupled with on-line hydride generation atomic absorption spectrometry using a PTFE turnings-packed micro-column [J].
Anthemidis, Aristidis N. ;
Martavaltzoglou, Evdoxia K. .
ANALYTICA CHIMICA ACTA, 2006, 573 :413-418
[3]   Determination of arsenic in sediment and soil slurries by electrothermal atomic absorption spectrometry using W-Rh permanent modifier [J].
Barbosa, F ;
Lima, ÉC ;
Krug, FJ .
ANALYST, 2000, 125 (11) :2079-2083
[4]   Determination of arsenic in biological fluids by electrothermal atomic absorption spectrometry [J].
Campillo, N ;
Viñas, P ;
López-García, I ;
Hernández-Córdoba, M .
ANALYST, 2000, 125 (02) :313-316
[5]  
Cerutti S, 2005, ATOM SPECTROSC, V26, P125
[6]   High performance liquid chromatography - atomic fluorescence spectrometric determination of arsenic species in beer samples [J].
Coelho, NMM ;
Parrilla, CN ;
Cervera, ML ;
Pastor, A ;
de la Guardia, A .
ANALYTICA CHIMICA ACTA, 2003, 482 (01) :73-80
[7]   Determination of heavy metals by inductively coupled plasma mass spectrometry after on-line separation and preconcentration [J].
Dressler, VL ;
Pozebon, D ;
Curtius, AJ .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1998, 53 (11) :1527-1539
[8]  
Fang Z., 1993, FLOW INJECTION SEPAR
[9]   Voltammetric measurement of arsenic in natural waters [J].
Feeney, R ;
Kounaves, SP .
TALANTA, 2002, 58 (01) :23-31
[10]   Fast automated determination of toxicologically relevant arsenic in urine by flow injection hydride generation atomic absorption spectrometry [J].
Guo, T ;
Baasner, J ;
Tsalev, DL .
ANALYTICA CHIMICA ACTA, 1997, 349 (1-3) :313-318