Catalytic Transformation of Nitroarenes to Amines over Ba (1-x) Sr x TiO 3 (0 < x < 1) Perovskites in Water.
Iwona Kuźniarska-BiernackaBarbara Garbarz-GlosElżbieta SkibaWaldemar ManiukiewiczMarta MonteiroWojciech BąkDariusz SzydłowskiCristina FreirePublished in: Molecules (Basel, Switzerland) (2024)
This work is focused on the application of lanthanide-free perovskite Ba 1-x Sr x TiO 3 (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 Ba 2+ by Sr 2+ 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) Sr x TiO 3 (0 < x < 1) series were evaluated in reduction of 4-NPh in water using NaBH 4 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) Sr x TiO 3 (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).
Keyphrases
- electron microscopy
- solid state
- high resolution
- quantum dots
- visible light
- crystal structure
- solar cells
- room temperature
- single molecule
- mass spectrometry
- highly efficient
- magnetic resonance imaging
- high efficiency
- gold nanoparticles
- high speed
- magnetic resonance
- risk assessment
- data analysis
- dual energy
- simultaneous determination