Carbon-Supported Hyperbranched Polyethyleneimines: Exploring into Polyamine/Anion Interactions to Design Efficient Polymer-Based Energy and Scavenger Materials
The anion-complexation mechanism and anion-adsorption capacity of a hybrid material based on hyperbranched polyethyleneimine (HBPEI) covalently bonded onto an activated carbon (AC) is presented. The anion-scavenger behavior of this hybrid material toward CrO<sub>4</sub><sup>2-</sup>, PO<sub>4</sub><sup>3-</sup>, AsO<sub>4</sub><sup>3-</sup> and HgCl<sub>4</sub><sup>2-</sup> was explored by direct potentiometric and adsorption measurements, which revealed a novel approach to predict the interactions between the supported polymeric complexing units and the different anions. The results were analyzed by considering the reactivity data of the HBPEI/anion (HBPEI free in solution) and AC-HBPEI/anion systems. The results corroborated that the AC-HBPEI hybrid material is an excellent anion-complexing material, whose anion adsorption ability is defined by the complexing properties of the HBPEI molecules toward the anions. This assessment provides a straightforward tool to determine the type and strength of the interactions involved in supported polymer-based/anion systems, which can provide valuable information for predicting and designing efficient energy and scavenger materials.
Authors
- Manuel Melguizo (ORCID: https://orcid.org/0000-0002-2210-9547)
- Antonio Peñas (ORCID: https://orcid.org/0000-0003-1408-8376)
- Michele Melchionna (ORCID: https://orcid.org/0000-0001-9813-9753)
- Rafael López-Garzón (ORCID: https://orcid.org/0000-0001-7176-1913)
- M.L. Godino-Salido (ORCID: https://orcid.org/0000-0003-3257-4431)
- Celeste García-Gallarín (ORCID: https://orcid.org/0000-0001-8455-9837)
Institutions
- University of Trieste (IT)
- Universidad de Jaén (ES)
Publication Details
- Journal
- Polymers
- Published
- 2025-03-15
- DOI
- https://doi.org/10.3390/polym17060786
- Primary Topic
- Molecular Sensors and Ion Detection
- Type
- article
- Field-Weighted Citation Impact
- 0.00