Bismuth-dispersed xerogel-based composite films for trace Pb(II) and Cd(II) voltammetric determination
| dc.contributor.author | Dimovasilis, P.A., | en |
| dc.contributor.author | Prodromidis, M.I. | en |
| dc.date.accessioned | 2015-11-24T16:53:13Z | |
| dc.date.available | 2015-11-24T16:53:13Z | |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9989 | |
| dc.rights | Default Licence | - |
| dc.subject | Bismuth-modified xerogel | en |
| dc.subject | Bismuth precursors | en |
| dc.subject | Determination of Cd(II) and Pb(II) ions | en |
| dc.subject | Stripping voltammetry | en |
| dc.title | Bismuth-dispersed xerogel-based composite films for trace Pb(II) and Cd(II) voltammetric determination | en |
| heal.abstract | We report for the first time the synthesis of bismuth-modified (3-mercaptopropyl) trimethoxysilane (MPTMS) and its application for the determination of lead and cadmium by anodic stripping voltammetry. Xerogels made from bismuth-modified MPTMS and mixtures of it with tetraethoxysilane, under basic conditions (NH3·H2O), were characterized with scanning electron microscopy, energy dispersive spectroscopy, infrared spectroscopy and electrochemical methods. Bismuth-modified xerogels were mixed with 1.5% (v/v) Nafion in ethanol and applied on glassy carbon electrodes. During the electrolytic reductive deposition step, the bismuth compound on the electrode surface was reduced to metallic bismuth. The target metal cations were simultaneously reduced to the respective metals and were preconcentrated on the electrode surface by forming an alloy with bismuth. Then, an anodic voltammetric scan was applied in which the metals were oxidized and stripped back into the solution; the voltammogram was recorded and the stripping peak heights were related to the concentration of Cd(II) and Pb(II) ions in the sample. Various key parameters were investigated in detail and optimized. The effect of potential interferences was also examined. Under optimum conditions and for preconcentration period of 4 min, the 3σ limit of detection was 1.3 μg L�1 for Pb(II) and 0.37 μg L�1 for Cd(II), while the reproducibility of the method was 4.2% for lead (n = 5, 10.36 μg L�1 Pb(II)) and 3.9% for cadmium (n = 5, 5.62 μg L�1 Cd(II)). Finally, the sensors were applied to the determination of Cd(II) and Pb(II) ions in water samples. | en |
| heal.access | campus | - |
| heal.fullTextAvailability | TRUE | - |
| heal.identifier.primary | 10.1016/j.aca.2013.01.040 | - |
| heal.identifier.secondary | http://www.sciencedirect.com/science/article/pii/S0003267013001888 | - |
| heal.journalName | Analytica Chimica Acta | en |
| heal.journalType | peer reviewed | - |
| heal.language | en | - |
| heal.publicationDate | 2013 | - |
| heal.publisher | Elsevier | en |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.type | journalArticle | - |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.type.en | Journal article | en |
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