<p>This work investigates the adsorption of Mn<sup>2+</sup> ions on hydrothermally synthesized Nb<sub>2</sub>O<sub>5</sub> nanoparticles obtained via an oxidant peroxo method, with particular emphasis on the role of functional groups present on the nanoparticle surface. Orthorhombic Nb<sub>2</sub>O<sub>5</sub> was formed at a mild temperature (100&#xa0;°C), yielding nanocrystalline particles with high colloidal stability and a strongly negative surface charge. FTIR and zeta potential analyses reveal a carbonyl and hydroxyl-rich surface that promotes electrostatic attraction toward Mn<sup>2+</sup> species. Adsorption experiments demonstrate rapid Mn<sup>2+</sup> uptake, reaching equilibrium within minutes, with kinetics best described by a pseudo-first-order model, indicating a physisorption-dominated process. Equilibrium data are best fitted by the Freundlich and Redlich–Peterson isotherms, reflecting surface heterogeneity and multilayer adsorption, with an experimental adsorption capacity approaching 116.67&#xa0;mg&#xa0;g<sup>−1</sup>. These findings demonstrate that hydrolyzed Nb<sub>2</sub>O<sub>5</sub> is an efficient and tunable adsorbent for Mn<sup>2+</sup> removal, offering strong potential for water treatment and environmental remediation applications.</p> Graphical abstract <p></p>

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Exploring the role of hydrolyzed Nb2O5 surfaces in manganese ion adsorption

  • Allef Leite,
  • Jeferson Almeida Dias,
  • Gelson Tavares da Silva,
  • Rodrigo Leandro Bonifácio,
  • Caue Ribeiro,
  • Vagner Romito de Mendonça,
  • Tania Regina Giraldi

摘要

This work investigates the adsorption of Mn2+ ions on hydrothermally synthesized Nb2O5 nanoparticles obtained via an oxidant peroxo method, with particular emphasis on the role of functional groups present on the nanoparticle surface. Orthorhombic Nb2O5 was formed at a mild temperature (100 °C), yielding nanocrystalline particles with high colloidal stability and a strongly negative surface charge. FTIR and zeta potential analyses reveal a carbonyl and hydroxyl-rich surface that promotes electrostatic attraction toward Mn2+ species. Adsorption experiments demonstrate rapid Mn2+ uptake, reaching equilibrium within minutes, with kinetics best described by a pseudo-first-order model, indicating a physisorption-dominated process. Equilibrium data are best fitted by the Freundlich and Redlich–Peterson isotherms, reflecting surface heterogeneity and multilayer adsorption, with an experimental adsorption capacity approaching 116.67 mg g−1. These findings demonstrate that hydrolyzed Nb2O5 is an efficient and tunable adsorbent for Mn2+ removal, offering strong potential for water treatment and environmental remediation applications.

Graphical abstract