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image of Pd/ZrO₂-TiO₂ Catalyst for Reductive Amination of Furfural: Exploring Solvent and N-Substrate Effects
  • oa Pd/ZrO₂-TiO₂ Catalyst for Reductive Amination of Furfural: Exploring Solvent and N-Substrate Effects

  • Authors: Alex A. Fernández-Andrade1, Daviel Gómez2, Konstanza Ortiz-Araya3, Cristian H. Campos4 and Luis E. Arteaga-Pérez5
  • 1 Laboratory of Thermal and Catalytic Processes (LPTC-UBB), Department of Process Engineering and Bioproducts, Engineering Faculty, Universidad del Bio-Bio, Concepción 4030000, Chile 2 Instituto de Tecnología Química, Universitat Politècnica de València-Consejo Superior de Investigaciones Científicas (UPV-CSIC), Avenida de los Naranjos s/n, Valencia 46022, Spain 3 Laboratory of Gas Cromatography and Analytical Pyrolysis (LCGPA-UBB), Department of Process Engineering and Bioproducts, Engineering Faculty, Universidad del Bio-Bio, Concepción 4030000, Chile 4 Universidad Andres Bello sede Concepción, Facultad de Ciencias Exactas, Departamento de Ciencias Químicas, Autopista Concepción-Talcahuano 7100, Talcahuano, Chile 5 Department of Chemical Engineering, Faculty of Engineering, Universidad de Concepcion, Concepción, 4030000, Chile
  • Source: Johnson Matthey Technology Review
    Available online: 13 August 2025
  • DOI: https://doi.org/10.1595/205651326X17550851489133
    • Received: 23 May 2025
    • Revised: 12 Aug 2025
    • Accepted: 13 Aug 2025
    • Published online: 13 Aug 2025

Abstract

The valorization of furfural (FUR) through reductive amination is a sustainable alternative for producing secondary aromatic amines; however, this process holds relevant scientific challenges associated to reaction conditions, catalytic materials as well as on the understanding of reaction mechanisms. This study systematically investigates the effect of the solvent and N-substrates nature on the reductive amination of FUR using a bifunctional Pd/ZrO2-TiO2 catalyst. The catalyst presented an anatase TiO2 phase, high Pd dispersion (22%), and a predominance of weak Lewis’s acid sites. The solvent screening demonstrated that methanol provided a balance of hydrogen-bonding ability and dielectric constant, which favor H₂ dissociation at metal sites and imine adsorption at acid sites, thus favoring N-furfurylaniline (FFA) selectivity. Among the tested substrates the 3-Fluoroaniline resulted in the highest yield and selectivity to secondary amine FFA (YFFA = 76%; SFFA = 82%), due to increased electrophilicity of the C=N group, while ortho substituents generated hysteric hindrance, limiting FFA formation. These findings could contribute to the rational design of catalysts and the selection of more suitable reaction systems for the reductive amination of FUR.

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2025-08-13
2025-08-22
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  • Article Type: Research Article
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