4.7 Article

Novel Hg (II) selective fluorescent green sensor based on carbon dots synthesized from starch and functionalized with methimazole

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ecoenv.2021.112043

关键词

Carbon dots; Mercury(II); Methimazole; Starch; Water

资金

  1. FAPEMIG (Fundacao de Amparo a Pesquisa do Estado de Minas Gerais), Brazil [CEX-APQ-02436-15]
  2. CAPES (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior), Brazil
  3. CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)
  4. FINEP (Financiadora de Estudos e Projetos), Brazil

向作者/读者索取更多资源

A green synthesis method for water-soluble photoluminescent carbon dots (CDs) functionalized with methimazole (MTZ) was described, with starch from rice as the natural source. The CDs were characterized using fluorescence techniques, FTIR, and UV-Vis spectroscopy, showing selective response to Hg2+ ions after MTZ functionalization. The method achieved a low detection limit of 1.8 x 10(-7) mol L-1 for Hg2+ in water samples.
We describe a green new method for the synthesis of water-soluble photoluminescent carbon dots (CDs) that were functionalized with methimazole (MTZ) and applied to determine Hg2+ based on the fluorescence extinction. Starch obtained from rice was used as a natural source for the production of CDs by hydrothermal treatment. Also, it was proposed a factorial design to optimize the parameters for CD synthesis and the results showed that the luminescence intensity is a function of temperature and not of the heating time in the hydro thermal process. The synthesized CDs were characterized using fluorescence techniques, Fourier transform infrared spectroscopy (FTIR), and UV-Vis spectroscopy. Through transmission electron microscopy (TEM) and dynamic light scattering (DLS), it was found the formation of CDs on a nanometer scale with an average size of 11 nm. The functionalization with MTZ, eliminated all interferences from other metals, indicating a selective response to Hg2+ ions. The method was applied to Hg2+ determination in waters. Under optimal conditions, was obtained a limit of detection of 1.8 x 10(-7) mol L-1 with a linear range from 3.3 x 10(-7) to 50.0 x 10(-6) mol L-1. Therefore, the proposed method can be considered a simple, selective, and precise alternative that minimizes the number of reagents used for Hg2+ determination in natural waters, and can be applied on a large scale in environmental analyzes.

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