Abstract
In the proposed method, microwave-assist heating and AgNO3/trisodium citrate were used to create the polyvinylpyrrolidone-capped silver nanoparticles (PVP-AgNPs) sensor. This sensor had a peroxidase-like activity that could catalytically oxidize O-phenylenediamine (OPD, colourless) into 2,3-diaminophenazine (ox-OPD, greenish-yellow colour) in the presence of H2O2, otherwise, in the presence of Hg2+, this pass has been effectively inhibited. The degree of colour fading was directly correlated with Hg2+ concentration. These results indicated the selectivity of Hg2+ ions toward PVP-AgNPs after establishing the PVP-AgNPs/OPD/H2O2 system. This selectivity was proved by the negative results obtained from other mon-, di-, and trivalent ions such as Na+, K+, Ca2+, Mg2+, Ba2+, Co2+, Ni2+, Cd2+, and Cr3+, instead of Hg2+. Consequently, a reliable, selective, and eco-effective spectrophotometric approach was designed for the detection of Hg2+ in various types of water samples. LOD was extended to lower than 0.1 mu M, and a fading in the obtained colour was shown by the naked eye at a concentration higher than 1.5 mu M of Hg2+. The elemental details for preparing the used PVP-AgNPs, such as particle size, morphology, polydispersity index (PdI), and their UV-visible spectrum, were identified by SEM technique, TEM, UV-visible spectrophotometer, and zeta-sizer device. Thus, the peroxidase mimicking the activity of OPD/H2O2 was confirmed by a fluorescence technique. The greenness profile of this work was confirmed after applying a reported assessment tool.