Scientific Paper
Heavy Metal Detection Methods in Water using Quartz Crystal Microbalance
Abstract
According to the World Health Organization, long-term exposures to heavy metal toxicants such as arsenic (As) and lead (Pb), even at the parts per billion (ppb, μg/L) level, can cause severe health problems such as cancer, skin lesions, and cardiovascular diseases. Therefore, an accurate and rapid heavy metal toxicant monitoring technique is needed. This research investigated the proof-of-the concept of a portable sensor for detecting As and Pb in water. The sensor system utilized a Quartz Crystal Microbalance – QCM (openQCM w-i2) system interfaced with a computer as the sensing platform. It was further integrated with a peristaltic pump and required tubing to create the integrated sensing system. It used a 10 MHz AT-cut quartz crystal gold electrode as the sensing substrate. For the determination of As in water, dithiothreitol (DTT) was used as the ligand to be deposited on the gold electrode using the Self-assembly-monolayer method (SAM). For the determination of Pb, a combination of ligands (Chitosan, Glutaraldehyde, and lead ionophore II – CGL) was used and deposited on the gold electrode using the spin-coating method. The system was tested for As in water with specific concentrations (0, 50, 100, and 200 ppb) under laboratory conditions. Similarly, the system was tested for Pb in water with different concentrations (0, 10, 25, 50, and 100 ppb) under laboratory conditions. The resulted change of frequency (with respect to time, in seconds) of the QCM system to different concentrations of the individual analyte was recorded. Subsequently, the recorded data were analyzed to determine the correlation model and coefficient of determination, R2. The maximum R2 values for detecting As and Pb were 0.963 and 0.991, respectively. Thus, this proof-of-the-concept study using the developed QCM-based sensing system for detecting As and Pb in water was successful.
Abstract reproduced from the published article under its CC BY 4.0 licence; copyright remains with the authors.
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