Influence of Rapid Heat Treatment on the Photocatalytic Activity and Stability of Strontium Titanates against a Broad Range of Pollutants

Author:

Abedi Mahsa1,Szamosvölgyi Ákos1ORCID,Sápi András1ORCID,Kukovecz Ákos1,Kónya Zoltán1ORCID,Gyulavári Tamás1ORCID,Pap Zsolt123ORCID

Affiliation:

1. Department of Applied and Environmental Chemistry, University of Szeged, Rerrich Béla Sqr. 1, 6720 Szeged, Hungary

2. Nanostructured Materials and Bio-Nano-Interfaces Center, Interdisciplinary Research Institute on Bio-Nano-Sciences, Babes-Bolyai University, Treboniu Laurian Str. 42, 400271 Cluj-Napoca, Romania

3. Institute of Research-Development-Innovation in Applied Natural Sciences, Babes-Bolyai University, Fântânele Str. 30, 400294 Cluj-Napoca, Romania

Abstract

Strontium titanate (STO) photocatalysts were prepared via a slightly modified Pechini sol–gel method. A unique rapid calcination technique with a short exposure time was used to obtain crystalline products. The samples were characterized by X-ray diffractometry, scanning electron microscopy, diffuse reflectance spectroscopy, infrared spectroscopy, nitrogen adsorption–desorption measurements, and X-ray photoelectron spectroscopy. Their photocatalytic activity was evaluated by the photocatalytic oxidation of phenol, oxalic acid, and chlorophenol under UV light irradiation using commercial STO as a reference. These pollutants, together with glucose and propanol, were used to investigate the stability of the samples against various functional groups. All our samples exhibited higher photocatalytic activity than the commercial STO reference. With increasing calcination temperature, the crystallinity and primary crystallite sizes increased while the band gaps and specific surface areas decreased. The photocatalytic activity of the most efficient sample was explained by the presence of SrCO3 on its surface. The STO catalysts were highly stable as they largely retained their crystalline composition after exposure to chemicals with different functional groups. Finally, we compared the costs associated with the unique calcination technique with a more conventional one and found that our method is ~35% more cost-effective.

Funder

National Research, Development and Innovation Office

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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