4.8 Article

Capillary and Electrodynamic Forces-Driven Separation Detection of Metal Ions Using a Disposable Microfluidic Sensor with a Composite Electrode

Journal

ANALYTICAL CHEMISTRY
Volume 95, Issue 45, Pages 16701-16709

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.3c03518

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In this study, a disposable microfluidic channel sensor printed on a plastic platform was developed for analyzing heavy metal ions. Precise separation and detection of multiple targets were achieved by applying an AC potential and optimizing various experimental variables. The sensor exhibited low detection limits and a wide linear dynamic range, and its reliability was validated through analysis of real water samples.
A disposable microfluidic channel sensor printed on a plastic platform was developed to analyze heavy metal ions (HMIs) as a model target species. Precise separation and detection of multiple targets were established by symmetrically applying a small AC potential on the carbon channel walls to induce an electrodynamic force. The separation device was constructed by covering it with a plastic lid to achieve capillary action in the channel. The sample flow rate was regulated by the hydrophilicity of the lid plastic and electrodynamic convection by the AC field, which was characterized by the contact angle measurement and the additional electrodynamic force. The flow variables and their relevance to the capillary phenomena were demonstrated, and the analytical parameters were optimized. The working electrode was modified with poly(diamino terthiophene) anchored with nanosized graphene oxide (pDATT/GO) to enhance the detection performance. The experimental variables for separating and detecting the target species were optimized according to the AC frequency and amplitude, sample flow rate, electrolytes, pH, temperature, and applied potential for detection. The linear dynamic ranges were between 0.1 and 200.0 ppb, with detection limits of 0.04 +/- 0.023, 0.29 +/- 0.05, 0.07 +/- 0.011, and 0.14 +/- 0.06 ppb for Cu2+ Cd2+, Hg2+, and Pb2+, respectively. Finally, the reliability of the proposed method was evaluated through analysis of HMIs in real water samples. The results were matched to those obtained through parallel analysis using ICP-MS at a 95% confidence level.

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