Search

A novel synthesis of gold nanoparticles is reported by chemical reduction of chloroauric acid with polyethylenimine and trisodium citrate. The use of polyethylenimine and trisodium citrate provided a convenient route to produce gold nanoparticles with diameters between 3.7 and 11.8 nm. The resulting nanoparticles were characterized by ultraviolet-visible spectroscopy, transmission electron microscopy, and zeta potential measurements. Transmission electron microscopy provided imaging of the shape and size of the nanoparticles. In order to characterize the solubility of the gold nanoparticles for application as an electrochemical sensor, the zeta potential, hydrodynamic diameter, electrophoretic mobility, and surface area-to-volume ratio were determined. The gold nanoparticles were incorporated on a glassy carbon electrode to produce an amperometric sensor for the determination of arsenic. [ABSTRACT FROM AUTHOR]

A combined homogeneous assay and colorimetric determination method using gold nanoparticles was developed for rapid determination of lead(II) in contaminated natural waters. The presence of lead(II) in the colloidal gold suspension causes a change in the absorbance of the suspension. An increase in the absorption property at 595 nm is accompanied by a change in the size of the gold nanoparticles. High concentrations of lead cause aggregation of the gold colloids. Colloidal gold nanoparticles were synthesized using tannic acid as the reducing agent; this reagent allowed selective determination of lead in 10 µL of water, with a detection limit of 310 ng mL−1with an analysis time of 5 min. The coefficient of variation for lead(II) within the working range of the assay (520 ng mL−1–13 µg mL−1) varied from 1.3% to 9.2%. The limit of detection using this method with a sample volume of 50 µL was 60 ng mL−1. The coefficient of variation for lead over the working range of the determined concentrations (80 ng mL−1–25 µg mL−1) varied from 0.2% to 9.3%, while the values for the inter-day assay (n = 8) were less than 10%. The method was employed for the analysis of river, lake, marsh, and spring water; the recovery of lead was determined to be 72.5%–130% for 10 µL of water and 93.6%–114.7% for 50 µL. [ABSTRACT FROM PUBLISHER]