Development of an analytical method for the determination of arsenic in gasoline samples by hydride generation-graphite furnace atomic absorption spectrometry

被引:27
作者
Becker, Emilene M. [2 ,3 ]
Dessuy, Morgana B. [1 ]
Boschetti, Wiliam [1 ]
Vale, Maria Goreti R. [1 ,4 ]
Ferreira, Sergio L. C. [4 ,5 ]
Welz, Bernhard [4 ,6 ]
机构
[1] Univ Fed Rio Grande do Sul, Inst Quim, BR-91501970 Porto Alegre, RS, Brazil
[2] Univ Fed Pampa, Bage, RS, Brazil
[3] Univ Fed Pelotas, Pelotas, RS, Brazil
[4] Univ Fed Bahia, Inst Nacl Ciencia & Tecnol CNPq, INCT Energia & Ambiente, Salvador, BA, Brazil
[5] Univ Fed Bahia, Inst Quim, Salvador, BA, Brazil
[6] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
关键词
Gasoline; Sample preparation; Arsenic determination; In-situ trapping; HG-GF AAS; VAPOR GENERATION; NAPHTHA; PRECONCENTRATION; OPTIMIZATION; DIGESTION; ELEMENTS; MERCURY; METALS; DIESEL; OIL;
D O I
10.1016/j.sab.2012.04.006
中图分类号
O433 [光谱学];
学科分类号
070207 [光学];
摘要
The purpose of the present work was to optimize the conditions for the determination of arsenic in gasoline with hydride generation-graphite furnace atomic absorption spectrometry after acid digestion using a full two-level factorial design with center point. The arsine was generated in a batch system and collected in a graphite tube coated with 150 mu g Ir as a permanent modifier. The sample volume, the pre-reduction conditions, the temperature program and modifier mass were kept fixed for all experiments. The estimated main effects were: reducing agent concentration (negative effect), acid concentration (negative effect) and trapping temperature (positive effect). It was observed that there were interactions between the variables. Moreover, the curvature was significant, indicating that the best conditions were at the center point. The optimized parameters for arsine generation were 2.7 mol L-1 hydrochloric acid and 1.6% (w/v) sodium tetrahydroborate. The optimized conditions to collect arsine in the graphite furnace were a trapping temperature of 250 degrees C and a collection time of 30s. The limit of detection was 6.4 ng L-1 and the characteristic mass was 24 pg. Two different systems for acid digestion were used: a digester block with cold finger and a microwave oven. The concentration of arsenic found with the proposed method was compared with that obtained using a detergendess microemulsion and direct graphite furnace determination. The results showed that the factorial design is a simple tool that allowed establishing the appropriate conditions for sample preparation and also helped in evaluating the interaction between the factors investigated. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:102 / 106
页数:5
相关论文
共 25 条
[1]
Atomic spectrometric methods for the determination of metals and metalloids in automotive fuels - A review [J].
Andrade Korn, Maria das Gracas ;
Sodre dos Santos, Denilson Santana ;
Welz, Bernhard ;
Rodrigues Vale, Maria Goreti ;
Teixeira, Alete Paixao ;
Lima, Daniel de Castro ;
Ferreira, Sergio Luis Costa .
TALANTA, 2007, 73 (01) :1-11
[2]
Vapor generation and atom traps: Atomic absorption spectrometry at the ng/L level [J].
Ataman, O. Yavuz .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2008, 63 (08) :825-834
[3]
Direct determination of arsenic in petroleum derivatives by graphite furnace atomic absorption spectrometry: A comparison between filter and platform atomizers [J].
Becker, Emilene ;
Rampazzo, Roger T. ;
Dessuy, Morgana B. ;
Vale, Maria Goreti R. ;
da Silva, Marcia M. ;
Welz, Bernhard ;
Katskov, Dmitri A. .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2011, 66 (05) :345-351
[4]
Multiple response optimization for Cu, Fe and Pb determination in naphtha by graphite furnace atomic absorption spectrometry with sample injection as detergent emulsion [J].
Brum, Daniel M. ;
Lima, Claudio F. ;
Robaina, Nicolle F. ;
Fonseca, Teresa Cristina O. ;
Cassella, Ricardo J. .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2011, 66 (05) :338-344
[5]
Multivariate optimization of the determination of zinc in diesel oil employing a novel extraction strategy based on emulsion breaking [J].
Cassella, Ricardo J. ;
Brum, Daniel M. ;
Lima, Claudio F. ;
Caldas, Luiz Fernando S. ;
de Paula, Carlos Eduardo R. .
ANALYTICA CHIMICA ACTA, 2011, 690 (01) :79-85
[6]
Stabilization of aviation gasoline as detergent emulsion for lead determination by electrothermal atomic absorption spectrometry [J].
Cassella, Ricardo J. ;
Brum, Daniel M. ;
Lima, Claudio F. ;
Fonseca, Teresa Cristina O. .
FUEL PROCESSING TECHNOLOGY, 2011, 92 (05) :933-938
[7]
Extraction induced by emulsion breaking: a novel strategy for the trace metals determination in diesel oil samples by electrothermal atomic absorption spectrometry [J].
Cassella, Ricardo J. ;
Brum, Daniel M. ;
de Paula, Carlos Eduardo R. ;
Lima, Claudio F. .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2010, 25 (11) :1704-1711
[8]
Direct determination of arsenic and antimony in naphtha by electrothermal atomic absorption spectrometry with microemulsion sample introduction and iridium permanent modifier [J].
Cassella, RJ ;
Barbosa, BARS ;
Santelli, RE ;
Rangel, AT .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2004, 379 (01) :66-71
[9]
Atomization of volatile compounds for atomic absorption and atomic fluorescence spectrometry: On the way towards the ideal atomizer [J].
Dedina, Jiri .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 2007, 62 (09) :846-872
[10]
APPLICATION OF THE FURNACE ATOMIC-ABSORPTION METHOD FOR THE DETECTION OF ARSENIC IN BIOLOGICAL SAMPLES BY MEANS OF THE HYDRIDE TECHNIQUE [J].
DRASCH, G ;
MEYER, LV ;
KAUERT, G .
FRESENIUS ZEITSCHRIFT FUR ANALYTISCHE CHEMIE, 1980, 304 (2-3) :141-142