Simultaneous determination of cadmium and lead in wine by electrothermal atomic absorption spectrometry
A method has been developed for the direct simultaneous determination of Cd and Pb in white and red wine by electrothermal atomic absorption spectrometry (ET-AAS) using a transversely heated graphite tube atomizer (THGA) with longitudinal Zeeman-effect background correction. The thermal behavior of...
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Veröffentlicht in: | Spectrochimica acta. Part B: Atomic spectroscopy 2001-10, Vol.56 (10), p.1987-1993 |
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container_end_page | 1993 |
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container_issue | 10 |
container_start_page | 1987 |
container_title | Spectrochimica acta. Part B: Atomic spectroscopy |
container_volume | 56 |
creator | Freschi, Gian P.G Dakuzaku, Carolina S de Moraes, Mercedes Nóbrega, Joaquim A Gomes Neto, José A |
description | A method has been developed for the direct simultaneous determination of Cd and Pb in white and red wine by electrothermal atomic absorption spectrometry (ET-AAS) using a transversely heated graphite tube atomizer (THGA) with longitudinal Zeeman-effect background correction. The thermal behavior of both analytes during pyrolysis and atomization stages were investigated in 0.028 mol l
−1 HNO
3 and in 1+1 v/v diluted wine using mixtures of Pd(NO
3)
2+Mg(NO
3)
2 and NH
4H
2PO
4+Mg(NO
3)
2 as chemical modifiers. With 5 μg Pd+3 μg Mg as the modifiers and a two-step pyrolysis (10 s at 400°C and 10 s at 600°C), the formation of carbonaceous residues inside the atomizer was avoided. For 20 μl of sample (wine+0.056 mol l
−1 HNO
3, 1+1, v/v) dispensed into the graphite tube, analytical curves in the 0.10–1.0 μg l
−1 Cd and 5.0–50 μg l
−1 Pb ranges were established. The characteristic mass was approximately 0.6 pg for Cd and 33 pg for Pb, and the lifetime of the tube was approximately 400 firings. The limits of detection (LOD) based on integrated absorbance (0.03 μg l
−1 for Cd, 0.8 μg l
−1 for Pb) exceeded the requirements of Brazilian Food Regulations (decree #55871 from Health Department), which establish the maximum permissible level for Cd at 200 μg l
−1 and for Pb at 500 μg l
−1. The relative standard deviations (
n=12) were typically |
doi_str_mv | 10.1016/S0584-8547(01)00331-7 |
format | Article |
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−1 HNO
3 and in 1+1 v/v diluted wine using mixtures of Pd(NO
3)
2+Mg(NO
3)
2 and NH
4H
2PO
4+Mg(NO
3)
2 as chemical modifiers. With 5 μg Pd+3 μg Mg as the modifiers and a two-step pyrolysis (10 s at 400°C and 10 s at 600°C), the formation of carbonaceous residues inside the atomizer was avoided. For 20 μl of sample (wine+0.056 mol l
−1 HNO
3, 1+1, v/v) dispensed into the graphite tube, analytical curves in the 0.10–1.0 μg l
−1 Cd and 5.0–50 μg l
−1 Pb ranges were established. The characteristic mass was approximately 0.6 pg for Cd and 33 pg for Pb, and the lifetime of the tube was approximately 400 firings. The limits of detection (LOD) based on integrated absorbance (0.03 μg l
−1 for Cd, 0.8 μg l
−1 for Pb) exceeded the requirements of Brazilian Food Regulations (decree #55871 from Health Department), which establish the maximum permissible level for Cd at 200 μg l
−1 and for Pb at 500 μg l
−1. The relative standard deviations (
n=12) were typically <8% for Cd and <6% for Pb. The recoveries of Cd and Pb added to wine samples varied from 88 to 107% and 93 to 103%, respectively. The accuracy of the direct determination of Cd and Pb was checked for 10 table wines by comparing the results with those obtained for digested wine using single-element ET-AAS, which were in agreement at the 95% confidence level.</description><identifier>ISSN: 0584-8547</identifier><identifier>EISSN: 1873-3565</identifier><identifier>DOI: 10.1016/S0584-8547(01)00331-7</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Cadmium ; Direct analysis ; Lead ; Simultaneous graphite furnace atomic absorption spectrometry ; Wine</subject><ispartof>Spectrochimica acta. Part B: Atomic spectroscopy, 2001-10, Vol.56 (10), p.1987-1993</ispartof><rights>2001 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-4605133022d0388ec39014003bbfd0e81c48d8d5a64e4f5878fc79e41b8af813</citedby><cites>FETCH-LOGICAL-c404t-4605133022d0388ec39014003bbfd0e81c48d8d5a64e4f5878fc79e41b8af813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0584-8547(01)00331-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids></links><search><creatorcontrib>Freschi, Gian P.G</creatorcontrib><creatorcontrib>Dakuzaku, Carolina S</creatorcontrib><creatorcontrib>de Moraes, Mercedes</creatorcontrib><creatorcontrib>Nóbrega, Joaquim A</creatorcontrib><creatorcontrib>Gomes Neto, José A</creatorcontrib><title>Simultaneous determination of cadmium and lead in wine by electrothermal atomic absorption spectrometry</title><title>Spectrochimica acta. Part B: Atomic spectroscopy</title><description>A method has been developed for the direct simultaneous determination of Cd and Pb in white and red wine by electrothermal atomic absorption spectrometry (ET-AAS) using a transversely heated graphite tube atomizer (THGA) with longitudinal Zeeman-effect background correction. The thermal behavior of both analytes during pyrolysis and atomization stages were investigated in 0.028 mol l
−1 HNO
3 and in 1+1 v/v diluted wine using mixtures of Pd(NO
3)
2+Mg(NO
3)
2 and NH
4H
2PO
4+Mg(NO
3)
2 as chemical modifiers. With 5 μg Pd+3 μg Mg as the modifiers and a two-step pyrolysis (10 s at 400°C and 10 s at 600°C), the formation of carbonaceous residues inside the atomizer was avoided. For 20 μl of sample (wine+0.056 mol l
−1 HNO
3, 1+1, v/v) dispensed into the graphite tube, analytical curves in the 0.10–1.0 μg l
−1 Cd and 5.0–50 μg l
−1 Pb ranges were established. The characteristic mass was approximately 0.6 pg for Cd and 33 pg for Pb, and the lifetime of the tube was approximately 400 firings. The limits of detection (LOD) based on integrated absorbance (0.03 μg l
−1 for Cd, 0.8 μg l
−1 for Pb) exceeded the requirements of Brazilian Food Regulations (decree #55871 from Health Department), which establish the maximum permissible level for Cd at 200 μg l
−1 and for Pb at 500 μg l
−1. The relative standard deviations (
n=12) were typically <8% for Cd and <6% for Pb. The recoveries of Cd and Pb added to wine samples varied from 88 to 107% and 93 to 103%, respectively. The accuracy of the direct determination of Cd and Pb was checked for 10 table wines by comparing the results with those obtained for digested wine using single-element ET-AAS, which were in agreement at the 95% confidence level.</description><subject>Cadmium</subject><subject>Direct analysis</subject><subject>Lead</subject><subject>Simultaneous graphite furnace atomic absorption spectrometry</subject><subject>Wine</subject><issn>0584-8547</issn><issn>1873-3565</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkM1KAzEURoMoWKuPIGQluhi9mSQz6UpE_IOCi3YfMskdjcxMapIqfXunrbh1dTfnXPgOIecMrhmw6mYBUolCSVFfArsC4JwV9QGZMFXzgstKHpLJH3JMTlL6AIBSlnJC3ha-X3fZDBjWiTrMGHs_mOzDQENLrXG9X_fUDI52aBz1A_32A9JmQ7FDm2PI76NiOmpy6L2lpkkhrnZ-Wu2AHnPcnJKj1nQJz37vlCwfH5b3z8X89enl_m5eWAEiF6ICyTiHsnTAlULLZ8DEOKlpWgeomBXKKSdNJVC0UtWqtfUMBWuUaRXjU3Kxf7uK4XONKeveJ4tdtx-oy1KV5UxWIyj3oI0hpYitXkXfm7jRDPS2qt5V1dtkGpjeVdX16N3uPRxHfHmMOlmPg0Xn47hWu-D_-fAD-oSArg</recordid><startdate>20011031</startdate><enddate>20011031</enddate><creator>Freschi, Gian P.G</creator><creator>Dakuzaku, Carolina S</creator><creator>de Moraes, Mercedes</creator><creator>Nóbrega, Joaquim A</creator><creator>Gomes Neto, José A</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20011031</creationdate><title>Simultaneous determination of cadmium and lead in wine by electrothermal atomic absorption spectrometry</title><author>Freschi, Gian P.G ; Dakuzaku, Carolina S ; de Moraes, Mercedes ; Nóbrega, Joaquim A ; Gomes Neto, José A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-4605133022d0388ec39014003bbfd0e81c48d8d5a64e4f5878fc79e41b8af813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Cadmium</topic><topic>Direct analysis</topic><topic>Lead</topic><topic>Simultaneous graphite furnace atomic absorption spectrometry</topic><topic>Wine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Freschi, Gian P.G</creatorcontrib><creatorcontrib>Dakuzaku, Carolina S</creatorcontrib><creatorcontrib>de Moraes, Mercedes</creatorcontrib><creatorcontrib>Nóbrega, Joaquim A</creatorcontrib><creatorcontrib>Gomes Neto, José A</creatorcontrib><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Spectrochimica acta. Part B: Atomic spectroscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Freschi, Gian P.G</au><au>Dakuzaku, Carolina S</au><au>de Moraes, Mercedes</au><au>Nóbrega, Joaquim A</au><au>Gomes Neto, José A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous determination of cadmium and lead in wine by electrothermal atomic absorption spectrometry</atitle><jtitle>Spectrochimica acta. Part B: Atomic spectroscopy</jtitle><date>2001-10-31</date><risdate>2001</risdate><volume>56</volume><issue>10</issue><spage>1987</spage><epage>1993</epage><pages>1987-1993</pages><issn>0584-8547</issn><eissn>1873-3565</eissn><abstract>A method has been developed for the direct simultaneous determination of Cd and Pb in white and red wine by electrothermal atomic absorption spectrometry (ET-AAS) using a transversely heated graphite tube atomizer (THGA) with longitudinal Zeeman-effect background correction. The thermal behavior of both analytes during pyrolysis and atomization stages were investigated in 0.028 mol l
−1 HNO
3 and in 1+1 v/v diluted wine using mixtures of Pd(NO
3)
2+Mg(NO
3)
2 and NH
4H
2PO
4+Mg(NO
3)
2 as chemical modifiers. With 5 μg Pd+3 μg Mg as the modifiers and a two-step pyrolysis (10 s at 400°C and 10 s at 600°C), the formation of carbonaceous residues inside the atomizer was avoided. For 20 μl of sample (wine+0.056 mol l
−1 HNO
3, 1+1, v/v) dispensed into the graphite tube, analytical curves in the 0.10–1.0 μg l
−1 Cd and 5.0–50 μg l
−1 Pb ranges were established. The characteristic mass was approximately 0.6 pg for Cd and 33 pg for Pb, and the lifetime of the tube was approximately 400 firings. The limits of detection (LOD) based on integrated absorbance (0.03 μg l
−1 for Cd, 0.8 μg l
−1 for Pb) exceeded the requirements of Brazilian Food Regulations (decree #55871 from Health Department), which establish the maximum permissible level for Cd at 200 μg l
−1 and for Pb at 500 μg l
−1. The relative standard deviations (
n=12) were typically <8% for Cd and <6% for Pb. The recoveries of Cd and Pb added to wine samples varied from 88 to 107% and 93 to 103%, respectively. The accuracy of the direct determination of Cd and Pb was checked for 10 table wines by comparing the results with those obtained for digested wine using single-element ET-AAS, which were in agreement at the 95% confidence level.</abstract><pub>Elsevier B.V</pub><doi>10.1016/S0584-8547(01)00331-7</doi><tpages>7</tpages></addata></record> |
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source | Access via ScienceDirect (Elsevier) |
subjects | Cadmium Direct analysis Lead Simultaneous graphite furnace atomic absorption spectrometry Wine |
title | Simultaneous determination of cadmium and lead in wine by electrothermal atomic absorption spectrometry |
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