4.6 Article

Impact of physical and chemical parameters on square wave anodic stripping voltammetry for trace Pb2+ detection in water

期刊

ANALYST
卷 147, 期 15, 页码 3542-3557

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2an00724j

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资金

  1. Department of Chemistry at the University of Cincinnati
  2. NSF [2016484]
  3. Translational Impacts
  4. Dir for Tech, Innovation, & Partnerships [2016484] Funding Source: National Science Foundation

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Exposure to lead in drinking water is a global problem. The Square wave anodic stripping voltammetry (SWASV) technique is commonly used for detecting trace Pb2+ ions. This study investigated the impact of water quality parameters on the SWASV technique and found that conductivity and temperature were positively correlated with the peak height, while pH, alkalinity, free chlorine, and copper were inversely correlated.
Exposure to lead, a toxic heavy metal, in drinking water is a worldwide problem. Lead leaching from lead service lines, the main contamination source, and other plumbing materials is controlled by the plumbosolvency of water. Square wave anodic stripping voltammetry (SWASV) has been greatly explored as a rapid and portable technique for the detection of trace Pb2+ ions in drinking water. However, the impact of water quality parameters (WQP) on the SWASV technique is not well understood. Herein, SWASV was employed to detect 10 mu g L-1 Pb2+ and determine trends in the stripping peak changes in simulated water samples while individually varying the pH, conductivity, alkalinity, free chlorine, temperature, and copper levels. The pH and conductivity were controlled using the buffer 3-(N-morpholino)propanesulfonic acid (MOPS), and NaNO3, respectively and kept at pH = 7.0 and conductivity = 500 mu S cm(-1) when exploring other WQPs. The working electrode, a gold-nanoparticle-modified carbon nanotube fiber cross-section (AuNP-CNTf-CS) electrode provided sufficiently sharp and prominent peaks for 10 mu g L-1 Pb2+ detection as well as good reproducibility, with a relative error of 5.9% in simulated water. We found that conductivity, and temperature had a proportional relationship to the peak height, and pH, alkalinity, free chlorine, and copper had an inverse relationship. In addition, increasing the copper concentration caused broadening and shifting of the Pb2+ stripping peak. At extremely low conductivities (<100 mu S cm(-1)), the voltammograms became difficult to interpret owing to the formation of inverted and distorted peaks. These trends were then also observed within a local drinking water sample in order to validate the results.

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