Catalytic Transformation of Nitroarenes to Amines over Ba(1−x)SrxTiO3 (0 < x < 1) Perovskites in Water

Author:

Kuźniarska-Biernacka Iwona1,Garbarz-Glos Barbara2ORCID,Skiba Elżbieta3ORCID,Maniukiewicz Waldemar3ORCID,Monteiro Marta1ORCID,Bąk Wojciech2,Szydłowski Dariusz4,Freire Cristina1ORCID

Affiliation:

1. REQUIMTE/LAQV, Departamento de Química e Bioquímica, Faculdade de Ciencias, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal

2. Institute of Technology, University of the National Education Commission, Podchorążych 2, 30-084 Kraków, Poland

3. Institute of General and Ecological Chemistry, Lodz University of Technology, Żeromskiego 116, 90-924 Łódź, Poland

4. Evidence Law and Forensic Technology, University of the National Education Commission, Podchorążych 2, 30-084 Kraków, Poland

Abstract

This work is focused on the application of lanthanide-free perovskite Ba1−xSrxTiO3 (0 < x < 1) in valorization of toxic pollutants as 4-nitrophenol (4-NPh). The series of perovskites were fabricated by facile, one-step solid-state preparation method and characterized via various techniques: elemental analysis (Inductively Coupled Plasma Optical Emission Spectrometry, ICP-OES), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR) and dielectric properties (impedance spectroscopy, IS). The methods confirmed the assumed composition, structure and high purity of the materials. The results showed that substitution of Ba2+ by Sr2+ in the perovskite crystal lattice influenced the dielectric properties of samples and the size of the grains. The absorption and catalytic properties of Ba(1−x)SrxTiO3 (0 < x < 1) series were evaluated in reduction of 4-NPh in water using NaBH4 as reducing agent. No adsorption of 4-NPh was found for all the materials during 180 min of contact (experiment without reducing agent), and the best catalytic performance was found for the Ba(1−x)SrxTiO3 (x = 0.3) sample. The catalytic transformation of 4-NPh to 4-APh follows a pseudo-first-order model, and the catalysts can be easily regenerated via mild annealing (300 °C).

Funder

FCT

Institute of General and Ecological Chemistry of Lodz University of Technology

Publisher

MDPI AG

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