摘要

A new method for analysis of trace mercury in water samples was developed, based on the combination of preconcentration/separation using dithizone-modified nanometer titanium. dioxide (TiO2) as a solid phase extractant and determination by cold vapor atomic adsorption spectrometry (CVAAS). Dithizone was dissolved with alcohol and loaded on the surface of nano-sized TiO2 powders by stirring. The static adsorption behavior of Hg2+ on the dithizone-modified nanoparticles was investigated in detail. It was found that excellent adsorption ratio for Hg2+ could be obtained in die pH range of 7-8 with an oscillation time of 15 min, and a 5 mL of 3.5 mol center dot L-1 HCI solution could quantitatively elute Hg2+ from nanometer TiO2 powder. Common coexisting ions caused no obvious influence on the determination of mercury. The mechanisms for the adsorption and desorption were discussed. The detection limit (3 sigma) for Hg2+ was calculated to be 5 ng center dot L-1. The proposed method was applied to the determination of Hg2+ in a mineral water sample and a Zhujiang River water sample. By the standard addition method, the average recoveries were found to be 94.4%-108.3% with RSD (n = 5) of 2.9%-3.5%.