Abstract

As a sensitive and selective analytical technique, gold nanoparticles-based colorimetric sensing was characterized by its simplicity and cost-effectiveness. Specific methods have been extensively developed for different targets in diverse samples. In this study, a label-free method for sensing Co(2+) in aqueous solutions was described. The target was achieved by the induced aggregation of thiosulfate (S(2)O(3)(2-)) stabilized gold nanoparticles (AuNPs) in the presence of ethylenediamine (en). Co(2+) first reacted with en and formed complexes of Co(en)(3)(2+) in aqueous solutions, which was followed by the oxidation of Co(en)(3)(2+) to Co(en)(3)(3+) by dissolved oxygen. Co(en)(3)(3+) then attacked S(2)O(3)(2-) ligands adsorbed on the AuNPs' surfaces, forming positively charged (en)(2)CoS(2)O(3)(+) on the AuNPs' surfaces, which reduced the surface charges of AuNPs and induced the aggregation of AuNPs. The process was accompanied by a red-shift in the adsorption spectrum and a visible colour change from wine red to blue. Potential effects of relevant experimental conditions, including pH, concentrations of S(2)O(3)(2-) and en, and incubation time were evaluated for optimization of the method. The proposed method is sensitive (LOD = 0.0 4 μM or 2.36 ppb) and selective (by at least 100-fold over other metal ions except for Cu(2+)) toward Co(2+) with a linear range from 0.1 to 0.7 μM. The cost-effective method allows rapid and simple determination of the concentrations of Co(2+) ions in drinking water.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.