Silver Nanoparticles Capped with p-Hydroxybenzoic Acid for Colorimetric Determination of Cu(II)
Abstract
ABSTRACT. Silver nanoparticles (AgNPs) have attracted significant attention from researchers and are widely used in the development of chemical sensors due to their unique surface plasmon resonance properties. This study focuses on a colorimetric method for determining Cu(II) using AgNPs capped with p-hydroxybenzoic acid. The AgNPs were synthesized through a chemical reduction process, using p-hydroxybenzoic acid as both a reducing and capping agent. The resulting AgNPs exhibited a yellow color and displayed a characteristic absorption peak at 420 nm, with an average particle size of about 60 nm. These nanoparticles were then used for the colorimetric detection of Cu(II) in the presence of ethylenediaminetetraacetic acid (EDTA), which serves as a ligand. The addition of Cu(II) to the mixture of AgNPs and EDTA induced nanoparticle aggregation, leading to a decrease in absorption intensity at 420 nm and the emergence of a new peak at 680 nm. A linear correlation was established between the concentration of Cu(II) and the absorbance ratio at 680 nm to 420 nm. The limits of detection and quantitation for determining Cu(II) were found to be 0.4 × 10⁻³ M and 1.4 × 10⁻³ M, respectively, with a recovery rate of 104%. These results demonstrate that AgNPs capped with p-hydroxybenzoic acid, combined with EDTA, can provide a simple colorimetric determination of Cu(II) and offer insight into ligand-mediated aggregation behavior in AgNPs-based sensing systems.
Keywords: colorimetry; copper; hydroxybenzoic acid; nanoparticles; silver; water
Authors agree with the statements below:
- Authors automatically transfer the copyright to the MOLEKUL journal and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
- Authors are able to enter into separate permission for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgment of its initial publication in this journal.









