Quantification of lead particulates requires laborious sample acidification and/or digestion in acidic environment, therefore lead quantification is limited to laboratories with trained personnel and expensive instrumentation. These technologies are not easily accessible to the public, and the large number of portable methods available to public today are characterized by their qualitative nature, and requirement of additional reagents. Unlike labor intense expensive instruments, electrochemical methods are inexpensive, fast and portable but they are blind to non-electroactive lead species or particulate forms of lead. They are limited to the detection of ionic or electroactive analytes. This talk will report an electrochemical method for the detection and quantification of lead contaminant in drinking waters that results from particulate forms of lead, mostly present as scales. We will present the fundamentals of membrane electrolysis for reagent-free sample preparation and detection of Pb2+. Also, we will present the characterization of real particulates/scales extracted from lead service lines from the Cincinnati area. We think this method will contribute to the development of on-site, quantitative methods of lead detection, and can assist to the research and understanding of drinking water contamination. Perhaps it could help to determine what triggers lead intermittent release to residential tap water. This work has the potential to address the lack of that instrumentation because it employs a robust technology based on anionic exchange membrane and controlled electrolysis for in-situ generation of nitric acid, that eliminates the need of external reagent or sample treatments. For its trace detection, it employs a well stablished Anodic Striping Voltammetry method.
Read full abstract