Search

Herein, an electrochemical sensor was developed for detecting heavy metal ions by using a carboimidazole grafted reduced graphene oxide (reduced graphene oxide-NH-carboimidazole, abbreviated as RGO-NH-Ci) modified electrode. The morphology of RGO-NH-Ci material was characterized by scanning electron microscopy (SEM). The electrochemical behaviors of the RGO-NH-Ci modified electrode toward heavy metal ions, including Hg 2 + and Pb 2 + , were investigated with differential pulse anodic stripping voltammetry (DPASV). Compared with pure reduced graphene oxide (RGO), RGO-NH-Ci modified electrode showed improved analytical performance in detecting the two metal ions owing to the strong complexing capacity of Ci and the presence of the amino groups. The detection limits were estimated to be 0.2 nM and 3.0 nM for Hg 2 + and Pb 2 + , respectively, under the optimized conditions. The developed method was also employed to detect the Hg 2 + and Pb 2 + in real water samples, and satisfactory results were obtained. [ABSTRACT FROM AUTHOR]

Toxic heavy-metal ions are well known to be severely harmful to human health. Therefore, the development of fast and sensitive methods for their detection has drawn a great attention in recent years. Herein, a sensitive electrochemical platform for the simultaneous determination of Cd 2 + , Pb 2 + , Cu 2 + , and Hg 2 + has been constructed based on N-doped graphene (NG) modified electrode using differential pulse stripping voltammetry (DPSV). NG was synthesized by a facile, efficient and green electrochemical method. The structure and composition of NG were studied by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron microscopy (XPS) techniques, chronocoulometry and N 2 adsorption–desorption measurements. The NG modified electrode showed excellent catalytic activity for selective detection of Cd 2 + , Pb 2 + , Cu 2 + , and Hg 2 + due to its particular structure and unique electronic properties. Under optimal conditions, the limits of detection were estimated to be 0.05 μM for Cd 2 + and Hg 2 + , 0.005 μM for Pb 2 + and Cu 2 + , respectively. Finally, the method was applied to the simultaneous detection of trace metal ions in the tap water samples. [ABSTRACT FROM AUTHOR]