Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions

The performance of a carbon paste electrode (CPE) modified with SBA-15 nanostructured silica organofunctionalised with 2-benzothiazolethiol in the simultaneous determination of Pb(II), Cu(II) and Hg(II) ions in natural water and sugar cane spirit ( cachaça) is described. Pb(II), Cu(II) and Hg(II) we...

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Veröffentlicht in:Talanta (Oxford) 2008-03, Vol.75 (1), p.15-21
Hauptverfasser: Cesarino, Ivana, Marino, Glimaldo, Matos, Jivaldo do Rosário, Cavalheiro, Éder Tadeu Gomes
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Marino, Glimaldo
Matos, Jivaldo do Rosário
Cavalheiro, Éder Tadeu Gomes
description The performance of a carbon paste electrode (CPE) modified with SBA-15 nanostructured silica organofunctionalised with 2-benzothiazolethiol in the simultaneous determination of Pb(II), Cu(II) and Hg(II) ions in natural water and sugar cane spirit ( cachaça) is described. Pb(II), Cu(II) and Hg(II) were pre-concentrated on the surface of the modified electrode by complexing with 2-benzothiazolethiol and reduced at a negative potential (−0.80 V). Then the reduced products were oxidised by DPASV procedure. The fact that three stripping peaks appeared on the voltammograms at the potentials of −0.48 V (Pb 2+), −0.03 V (Cu 2+) and +0.36 V (Hg 2+) in relation to the SCE, demonstrates the possibility of simultaneous determination of Pb 2+, Cu 2+ and Hg 2+. The best results were obtained under the following optimised conditions: 100 mV pulse amplitude, 3 min accumulation time, 25 mV s −1 scan rate in phosphate solution pH 3.0. Using such parameters, calibration graphs were linear in the concentration ranges of 3.00–70.0 × 10 −7 mol L −1 (Pb 2+), 8.00–100.0 × 10 −7 mol L −1 (Cu 2+) and 2.00–10.0 × 10 −6 mol L −1 (Hg 2+). Detection limits of 4.0 × 10 −8 mol L −1 (Pb 2+), 2.0 × 10 −7 mol L −1 (Cu 2+) and 4.0 × 10 −7 mol L −1(Hg 2+) were obtained at the signal noise ratio (SNR) of 3. The results indicate that this electrode is sensitive and effective for simultaneous determination of Pb 2+, Cu 2+ and Hg 2+ in the analysed samples.
doi_str_mv 10.1016/j.talanta.2007.06.032
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Pb(II), Cu(II) and Hg(II) were pre-concentrated on the surface of the modified electrode by complexing with 2-benzothiazolethiol and reduced at a negative potential (−0.80 V). Then the reduced products were oxidised by DPASV procedure. The fact that three stripping peaks appeared on the voltammograms at the potentials of −0.48 V (Pb 2+), −0.03 V (Cu 2+) and +0.36 V (Hg 2+) in relation to the SCE, demonstrates the possibility of simultaneous determination of Pb 2+, Cu 2+ and Hg 2+. The best results were obtained under the following optimised conditions: 100 mV pulse amplitude, 3 min accumulation time, 25 mV s −1 scan rate in phosphate solution pH 3.0. Using such parameters, calibration graphs were linear in the concentration ranges of 3.00–70.0 × 10 −7 mol L −1 (Pb 2+), 8.00–100.0 × 10 −7 mol L −1 (Cu 2+) and 2.00–10.0 × 10 −6 mol L −1 (Hg 2+). Detection limits of 4.0 × 10 −8 mol L −1 (Pb 2+), 2.0 × 10 −7 mol L −1 (Cu 2+) and 4.0 × 10 −7 mol L −1(Hg 2+) were obtained at the signal noise ratio (SNR) of 3. 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Pb(II), Cu(II) and Hg(II) were pre-concentrated on the surface of the modified electrode by complexing with 2-benzothiazolethiol and reduced at a negative potential (−0.80 V). Then the reduced products were oxidised by DPASV procedure. The fact that three stripping peaks appeared on the voltammograms at the potentials of −0.48 V (Pb 2+), −0.03 V (Cu 2+) and +0.36 V (Hg 2+) in relation to the SCE, demonstrates the possibility of simultaneous determination of Pb 2+, Cu 2+ and Hg 2+. The best results were obtained under the following optimised conditions: 100 mV pulse amplitude, 3 min accumulation time, 25 mV s −1 scan rate in phosphate solution pH 3.0. Using such parameters, calibration graphs were linear in the concentration ranges of 3.00–70.0 × 10 −7 mol L −1 (Pb 2+), 8.00–100.0 × 10 −7 mol L −1 (Cu 2+) and 2.00–10.0 × 10 −6 mol L −1 (Hg 2+). Detection limits of 4.0 × 10 −8 mol L −1 (Pb 2+), 2.0 × 10 −7 mol L −1 (Cu 2+) and 4.0 × 10 −7 mol L −1(Hg 2+) were obtained at the signal noise ratio (SNR) of 3. 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Pb(II), Cu(II) and Hg(II) were pre-concentrated on the surface of the modified electrode by complexing with 2-benzothiazolethiol and reduced at a negative potential (−0.80 V). Then the reduced products were oxidised by DPASV procedure. The fact that three stripping peaks appeared on the voltammograms at the potentials of −0.48 V (Pb 2+), −0.03 V (Cu 2+) and +0.36 V (Hg 2+) in relation to the SCE, demonstrates the possibility of simultaneous determination of Pb 2+, Cu 2+ and Hg 2+. The best results were obtained under the following optimised conditions: 100 mV pulse amplitude, 3 min accumulation time, 25 mV s −1 scan rate in phosphate solution pH 3.0. Using such parameters, calibration graphs were linear in the concentration ranges of 3.00–70.0 × 10 −7 mol L −1 (Pb 2+), 8.00–100.0 × 10 −7 mol L −1 (Cu 2+) and 2.00–10.0 × 10 −6 mol L −1 (Hg 2+). Detection limits of 4.0 × 10 −8 mol L −1 (Pb 2+), 2.0 × 10 −7 mol L −1 (Cu 2+) and 4.0 × 10 −7 mol L −1(Hg 2+) were obtained at the signal noise ratio (SNR) of 3. The results indicate that this electrode is sensitive and effective for simultaneous determination of Pb 2+, Cu 2+ and Hg 2+ in the analysed samples.</abstract><cop>Amsterdam</cop><cop>Oxford</cop><pub>Elsevier B.V</pub><pmid>18371840</pmid><doi>10.1016/j.talanta.2007.06.032</doi><tpages>7</tpages></addata></record>
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subjects 2-Benzothiazolethiol
Analytical chemistry
Cachaça
Carbon paste electrode
Chemistry
Exact sciences and technology
Indexing in process
Q1
SBA-15 nanostructured silica
Well water
title Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions
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