Lead contamination in drinking water can be caused by
various types
of lead: lead ions, soluble lead complexes, and lead particulates.
Traditional detection methods such as inductively coupled plasma mass
spectroscopy (ICP-MS) and atomic absorption spectroscopy (AAS) can
detect all types of lead because of sample preparation. Nevertheless,
these methods are expensive and require trained personnel. As electrochemical
techniques are less expensive, portable, and easy to use, they are
a promising alternative for lead detection in drinking water. However,
electrochemistry is typically only able to detect lead ions. In this
work, lead scales collected from a lead pipe are characterized to
determine the types of lead compounds present within the lead corrosion
scale. Subsequently, membrane electrolysis (ME) is used to acidify
a drinking water solution containing lead corrosion scales, allowing
for the dissociation of the particulate lead into lead ions. Square-wave
anodic stripping voltammetry (SWASV) is then applied to determine
the current associated with the lead ions being stripped off the working
electrode, which originated from the particulates in the scales. Standard
addition is used to determine the concentration of lead associated
with the current response. This technique is compared to ICP-MS, and
the relative errors between the two methods show that ME combined
with SWASV is a viable approach for detecting lead contamination in
drinking water due to lead corrosion scales.