Synthesis of Bentonite/MIL-68(AL) composite for Hg2+ adsorption and electrochemical detection
Heavy metal contamination, particularly mercury ions (Hg2+), represents a critical environmental issue due to their toxicity and persistence in the environment. In this study, a composite based on the MOF MIL-68(Al) and bentonite (B/MIL-68(Al)) was synthesized and characterized to evaluate its performance in the adsorption and electrochemical detection of Hg2+. Structural characterization by XRD and FTIR confirmed the integration of the MOF into the bentonite, while textural analyses revealed a significant increase in surface area (430 m2 g−1) and microporosity, enhancing its adsorptive capacity. The material was employed in the modification of screen-printed gold electrodes (SPEAu), improving their conductivity and electrochemical response for Hg2+ detection via differential pulse anodic stripping voltammetry, achieving a detection limit of 10.14 μg L−1. Additionally, adsorption studies demonstrated that the composite exhibited a higher Hg2+ removal capacity compared to pure bentonite, fitting the Freundlich model, which suggests adsorption on heterogeneous sites with variable affinities. These findings highlight the potential of the B/MIL-68(Al) composite as a promising material for environmental remediation and the development of sensitive and selective electrochemical sensors for Hg2+ detection in aqueous media.
Authors
- Matías Rafti (ORCID: https://orcid.org/0000-0003-3393-358X)
- Jimena S. Tuninetti
- Lisette Ruiz Bravo (ORCID: https://orcid.org/0000-0001-5858-051X)
- Jaime Fernando Martínez Suárez (ORCID: https://orcid.org/0000-0003-2381-3509)
- Pedro Luis Gomis Díaz
Institutions
- Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (AR)
- Universidad de la Amazonia (CO)
Publication Details
- Journal
- Discover Electrochemistry.
- Published
- 2025-12-18
- DOI
- https://doi.org/10.1007/s44373-025-00070-6
- Primary Topic
- Adsorption and biosorption for pollutant removal
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministerio de Ciencia y Tecnología