On-line electrochemical preconcentration and flame atomic absorption spectrometric determination of manganese in urine samples

被引:25
作者
Burguera, M
Burguera, JL
Rivas, D
Rondón, C
Carrero, P
Alarcón, OM
de Peña, YP
Brunetto, MR
Gallignani, M
Márquez, OP
Márquez, J
机构
[1] Univ Los Andes, Fac Sci, Dept Chem, Mol Spect Lab, Merida 5101A, Venezuela
[2] Univ Los Andes, Fac Sci, Dept Chem, Electrochem Lab, Merida 5101A, Venezuela
关键词
manganese; electrochemical preconcentration; flame atomic absorption spectrometry detection; flow injection manifold; urine samples;
D O I
10.1016/j.talanta.2005.06.056
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive and selective method was developed for the determination of traces of manganese in urine using on-line electrochemical preconcentration followed by flame atomic absorption spectrometry detection. A home made flow-through polypropylene cell (4.5 cm long x 0.8 cm diameter filled with glass marbles) with an effective inner volume of 0.5 ml containing a working and a counter electrode, both of glassy carbon and a Pt pseudo reference electrode was located in a flow injection manifold specially designed for the purpose of this work. The manganese was deposited from buffer solution of NH3/NH4Cl at pH 9.00 through an oxidizing process at a current of 400 mA during 7 min. A flow of HCl 0.1 mol l(-1) at 4 ml min(-1) through the cell, chemically dissolved the deposit. A small portion (15 mu l) of the concentrate was introduced in a continuously flowing system by means of a timing device and was then carried to the detector for the manganese quantification. All electrochemical and spectroscopic variables as well as possible interferences in both systems were systematically studied. The relative standard deviations for ten consecutive measurements of manganese solutions of 2.0 and 20 mu g l(-1) were of 2.3 and 1.5%, respectively, while for a sample processed five times was less then 5%. The accuracy of the developed procedure was evaluated by adding known amounts of manganese standard to urine samples and following the whole procedure. Recoveries within the range 97.2-102.8% were obtained. To further prove the accuracy, a Seronorm Trace Elements in Urine, Batch 403125 sample with a reported concentration of 13 p g Mn l(-1) was also analyzed. The experimental value obtained was of 12.7 +/- 0.1 mu g l(-1), which does not differ significantly from the reported amount (p < 0.05). A preconcentration factor of 40, a linear range between 0.015 and 60 p,g l(-1) and a limit of detection of 15 ng l(-1) permitted the determination of manganese in real urine samples from non-exposed subjects in the range 0.5-2.8 mu g l(-1). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:219 / 225
页数:7
相关论文
共 28 条
[11]  
*IMM GMBH, 1993, SPUR FORSCH DIAGN
[12]   Simultaneous determination of cobalt and manganese in urine by electrothermal atomic absorption spectrometry. Method development using a simplex optimization approach [J].
Iversen, BS ;
Panayi, A ;
Camblor, JP ;
Sabbioni, E .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1996, 11 (08) :591-594
[13]  
Keen C L, 1987, HDB TOXICITY INORGAN
[14]  
Leach R M, 1978, World Rev Nutr Diet, V32, P123
[15]   Direct and simultaneous determination of copper, chromium, aluminum, and manganese in urine with a multielement graphite furnace atomic absorption spectrometer [J].
Lin, TW ;
Huang, SD .
ANALYTICAL CHEMISTRY, 2001, 73 (17) :4319-4325
[16]  
LINCH AL, 1974, BIOL THRESHOLD LIMIT
[17]   Voltammetric trace metal determinations by cathodic and anodic stripping voltammetry in environmental matrices in the presence of mutual interference [J].
Locatelli, C ;
Torsi, G .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 509 (01) :80-89
[18]  
Miller J. C., 1993, STAT ANAL CHEM
[19]  
MONTAGUD AH, 109 NTP I NAC SEG HI
[20]   Determination of dissolved manganese(II) in coastal and estuarine waters by differential pulse cathodic stripping voltammetry [J].
Roitz, JS ;
Bruland, KW .
ANALYTICA CHIMICA ACTA, 1997, 344 (03) :175-180