The underpotential determination of lead using the laboratory-made gold electrode flow cell
The analysis of lead(II) by continuous flow square-wave anodic stripping voltammetry (SWASV) at a gold electrode flow cell is described. Various experimental variables have been optimized to yield low detection limit and good precision. The detection limits for a 30 s and 600 s electrodeposition wer...
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th-cmuir.6653943832-601722018-09-10T03:48:38Z The underpotential determination of lead using the laboratory-made gold electrode flow cell Prinya Masawat Saisunee Liawruangrath Biochemistry, Genetics and Molecular Biology Chemistry Materials Science Mathematics Physics and Astronomy The analysis of lead(II) by continuous flow square-wave anodic stripping voltammetry (SWASV) at a gold electrode flow cell is described. Various experimental variables have been optimized to yield low detection limit and good precision. The detection limits for a 30 s and 600 s electrodeposition were 3.5 and 0.38 μg L-1, respectively. The recoveries were found to be 113 ± 1.8 % and 108 ± 2.3 % (n=5) in spiked drinking water samples and 110 ± 4.8 % and 106 ± 3.4% (n=5) in spiked tap water samples. Reproducibility on measurement of solution containing 5 μg L-1 lead(II) (%R.S.D., n = 20) was 2.1 %. Measurements in the presence of typical interferences such as copper(II), cadmium(II), zinc(II), iron(II), chromium(VI), and mercury are also reported. 2018-09-10T03:38:59Z 2018-09-10T03:38:59Z 2008-05-01 Journal 01252526 2-s2.0-67650286894 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67650286894&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60172 |
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Biochemistry, Genetics and Molecular Biology Chemistry Materials Science Mathematics Physics and Astronomy Prinya Masawat Saisunee Liawruangrath The underpotential determination of lead using the laboratory-made gold electrode flow cell |
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The analysis of lead(II) by continuous flow square-wave anodic stripping voltammetry (SWASV) at a gold electrode flow cell is described. Various experimental variables have been optimized to yield low detection limit and good precision. The detection limits for a 30 s and 600 s electrodeposition were 3.5 and 0.38 μg L-1, respectively. The recoveries were found to be 113 ± 1.8 % and 108 ± 2.3 % (n=5) in spiked drinking water samples and 110 ± 4.8 % and 106 ± 3.4% (n=5) in spiked tap water samples. Reproducibility on measurement of solution containing 5 μg L-1 lead(II) (%R.S.D., n = 20) was 2.1 %. Measurements in the presence of typical interferences such as copper(II), cadmium(II), zinc(II), iron(II), chromium(VI), and mercury are also reported. |
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Journal |
author |
Prinya Masawat Saisunee Liawruangrath |
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Prinya Masawat Saisunee Liawruangrath |
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Prinya Masawat |
title |
The underpotential determination of lead using the laboratory-made gold electrode flow cell |
title_short |
The underpotential determination of lead using the laboratory-made gold electrode flow cell |
title_full |
The underpotential determination of lead using the laboratory-made gold electrode flow cell |
title_fullStr |
The underpotential determination of lead using the laboratory-made gold electrode flow cell |
title_full_unstemmed |
The underpotential determination of lead using the laboratory-made gold electrode flow cell |
title_sort |
underpotential determination of lead using the laboratory-made gold electrode flow cell |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67650286894&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60172 |
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