Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6903
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dc.contributor.authorVan der Horst, Charltonen_US
dc.contributor.authorSilwana, Bongiween_US
dc.contributor.authorIwuoha, Emmanuelen_US
dc.contributor.authorSomerset, Vernonen_US
dc.date.accessioned2019-03-05T08:19:42Z-
dc.date.available2019-03-05T08:19:42Z-
dc.date.issued2018-
dc.identifier.urihttp://hdl.handle.net/11189/6903-
dc.descriptionArticleen_US
dc.description.abstractThe emission of toxic compounds by increasing anthropogenic activities affects human health and the environment. Heavy road traffic and mining activities are the major anthropogenic activities contributing to the presence of metals in the environment. The release of palladium (Pd), platinum (Pt), and rhodium (Rh) into the environment increases the levels of contamination in soils, road sediments, airborne particles, and plants. These Pd, Pt, and Rh in road dusts can be soluble and enter aquatic environment posing a risk to environment and human health. The aim of this study is to determine the levels of Pd, Pt, and Rh with spectroscopy and voltammetric methods. Potential interferences by other metal ions (Na(I), Fe(III), Ni(II), Co(II)) in voltammetric methods have also been investigated in this study. At all the sampling sites very low concentrations of Pd, Pt, and Rh were found at levels that range from 0.48 ± 0.05 to 5.44 ± 0.11 ng/g (dry weight (d.wt)) for Pd(II), with 17.28 ± 3.12 to 81.44 ± 3.07 pg/g (d.wt) for Pt(II), and 14.34 ± 3.08 to 53.35 ± 4.07 pg/g (d.wt) for Rh(III). The instrumental limit of detection for Pd, Pt, and Rh for Inductively Coupled Plasma Quadrupole-based Mass Spectrometry (ICP-QMS) analysis was found to be 3 × 10−6 µg/g, 3 × 10−6 µg/g and 1 × 10−6 µg/g, respectively. In the case of voltammetric analysis the instrumental limit of detection for Pd(II), Pt(II), and Rh(III) for differential pulse adsorptive stripping voltammetry was found to be 7 × 10−8 µg/g, 6 × 10−8 µg/g, and 2 × 10−7 µg/g, respectively. For the sensor application, good precision was obtained due to consistently reproduced the measurements with a reproducibility of 6.31% for Pt(II), 7.58% for Pd(II), and 5.37% for Rh(III) (n = 10). The reproducibility for ICP-QMS analysis were 1.58% for Pd(II), 1.12% for Pt(II), and 1.37% for Rh(III) (n = 5). In the case of repeatability for differential pulse adsorptive stripping voltammetry (DPAdSV) and ICP-QMS, good standard deviations of 0.01 for Pd(II); 0.02 for Pt(II), 0.009 for Rh(III) and 0.011 for Pd, 0.019 for Pt and 0.013 for Rh, respectively.en_US
dc.description.sponsorshipThis study was financially supported by the National Research Foundation (NRF) of South Africa and partially by the Council for Scientific and Industrial Research (CSIR). The research laboratories at the Cape Peninsula University of Technology and the University of the Western Cape are also acknowledged.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofEnvironmenten_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/-
dc.subjectInductive coupled plasma spectroscopyen_US
dc.subjectdifferential pulse adsorptive stripping voltammetryen_US
dc.subjectdust; soilen_US
dc.subjectplatinum group metalsen_US
dc.subjectextraction methodsen_US
dc.titleSpectroscopic and Voltammetric Analysis of Platinum Group Metals in Road Dust and Roadside Soilen_US
dc.type.patentArticleen_US
dc.identifier.doi10.3390/environments5110120-
Appears in Collections:Appsc - Journal Articles (not DHET subsidised)
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