Determining copper ions in water using electrochemiluminescence
Abstract
The detection of copper ions in aqueous solution using electrochemiluminescence (ECL) is reported. ECL is generated by reducing Cu2+ ions to Cu+ with hydroxylamine hydrochloride and then complexing with the chelating agent 2,9-dimethyl-1,10-phenanthroline (dmp) to form Cu(dmp)2+, followed by oxidation in the presence of tri-n-propylamine (TPrA). The ECL intensity peaks a potential corresponding to oxidation of both TPrA and Cu(dmp)2+, indicating that the emission is from a Cu(dmp)2+ metal-to-ligand charge transfer excited state. Conditions for ECL emission were optimized and used to generate a calibration curve that was linear over the 0.1–5 mg/l (ppm) range. The theoretical limit of detection was 6 μg/l (ppb), with a practical limit of detection of 0.1 ppm. The ECL of several metal ions other than copper with dmp, and effects on Cu(dmp)2+ ECL were also examined.
Department(s)
Chemistry and Biochemistry
Document Type
Article
DOI
https://doi.org/10.1016/s0003-2670(01)01357-5
Keywords
electrochemiluminescence, copper, neocuproine
Publication Date
2001
Recommended Citation
High, Brian, David Bruce, and Mark M. Richter. "Determining copper ions in water using electrochemiluminescence." Analytica chimica acta 449, no. 1-2 (2001): 17-22.
Journal Title
Analytica chimica acta
