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Voltammetry as an Alternative Tool for Trace Metal Detection in Peloid Marine Sediments
Author(s) -
Ciglenečki Irena,
BuraNakić Elvira,
Inzelt György
Publication year - 2007
Publication title -
electroanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 128
eISSN - 1521-4109
pISSN - 1040-0397
DOI - 10.1002/elan.200703877
Subject(s) - anodic stripping voltammetry , trace metal , sulfide , voltammetry , chemistry , inductively coupled plasma mass spectrometry , environmental chemistry , seawater , cyclic voltammetry , analytical chemistry (journal) , metal , electrochemistry , mass spectrometry , electrode , chromatography , geology , oceanography , organic chemistry
Here was demonstrated for the first time a possible application of abrasive stripping voltammetry in the direct measurement of trace metals in anoxic, sulfidic marine sediments (peloid mud) from a small and shallow (0.2–1 m) marine lagoon in Central Dalmatia, Croatia. Trace amounts of sample compounds are transferred to the graphite electrode surface and electrochemical reduction or oxidation processes are followed by the cyclic voltammetry in seawater or 0.55 M NaCl as electrolyte. After a preelectrolysis at potentials ranging from −1.0 to −1.5 V (vs. SCE) a well‐defined anodic stripping peak corresponding to the oxidation of metal deposits generated at deposition potentials is obtained around −0.74 V (vs. SCE). The same samples were studied by anodic stripping voltammetry at the Hg electrode and inductively coupled plasma‐mass spectrometer (ICP‐MS). ICP‐MS showed higher concentrations of trace metals such as Al, Fe, Mo, Mn. A relatively high concentration of reduced sulfur species (RSS) (10 −3 M) is determined electrochemically in porewater of the peloid mud, indicating that the magnitude of metal enrichment in the sediments is probably controlled by precipitation with sulfide.