A novel approach to Hg2+ determination in water samples using carbon dots based on paper and fluorescence digital image analysis

Author:

Maia Matheus Valentin1ORCID,Suarez Willian Toito1ORCID,dos Santos Vagner Bezerra2ORCID,de Oliveira Severino Carlos Bezerra3ORCID,de Almeida João Paulo Barbosa2

Affiliation:

1. Department of Chemistry Federal University of Viçosa – UFV, Centro de Ciências Exatas e Tecnologia Viçosa Brazil

2. Fundamental Chemistry Department Federal University of Pernambuco – UFPE Recife Brazil

3. Department of Chemistry Federal Rural University of Pernambuco – UFRPE Recife Brazil

Abstract

AbstractBACKGROUNDThis work proposes the use of a simple, inexpensive method for the hydrothermal synthesis of fluorescent carbon dot nanoparticles (CDs) from rice starch aimed at the determination of Hg2+ in water. The proposed method involved using a paper‐based analytical device coupled to a 3D plate, with a UV‐LED chamber and a smartphone for the acquisition and analysis of the fluorescence digital images of the CDs.RESULTSThe size of the carbon dots ranged from 0.5 to 3 nm, with an average particle size of ~1 nm. The functionalization of carbon dots with methimazole allowed a high selective for Hg2+ determination. The results obtained showed a linear response R2 of 0.997 and Hg2+ concentration in the range of 0.5–45.0 μmol L−1 with a limit of detection and limit of quantitation of 0.23 and 0.62 μmol L−1, respectively. The results of the study show that there were no significant differences, at 95% confidence level, between the data obtained from the application of the proposed method and the reference method.CONCLUSIONThe proposed method is in line with the principles of green chemistry, as it involves the use of renewable sources for starch extraction and a hydrothermal synthesis process that does not employ toxic reagents. In addition, the method employs only 15 μL reagent/sample. © 2024 Society of Chemical Industry (SCI).

Funder

Fundação de Amparo à Pesquisa do Estado de Minas Gerais

Publisher

Wiley

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