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dc.contributor.authorPrinya Masawaten_US
dc.contributor.authorSaisunee Liawruangrathen_US
dc.date.accessioned2018-09-10T03:38:59Z-
dc.date.available2018-09-10T03:38:59Z-
dc.date.issued2008-05-01en_US
dc.identifier.issn01252526en_US
dc.identifier.other2-s2.0-67650286894en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=67650286894&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60172-
dc.description.abstractThe 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.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.subjectMathematicsen_US
dc.subjectPhysics and Astronomyen_US
dc.titleThe underpotential determination of lead using the laboratory-made gold electrode flow cellen_US
dc.typeJournalen_US
article.title.sourcetitleChiang Mai Journal of Scienceen_US
article.volume35en_US
article.stream.affiliationsNaresuan Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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