ABSTRACT
To explore the mechanism and pathway for pollutant degradation in seawater by heterogeneous photocatalysts, the degradation of tetracycline (TC) in pure water and simulated seawater with different mesoporous TiO2 under the excitation of visible light was first investigated; then the effect of different salt ions on the photocatalytic degradation process was clarified. Combined with radical trapping experiments, electron spin resonance (ESR) spectroscopy, and intermediate product analysis, the main active species for photodegrading pollutants and the pathway of TC degradation in simulated seawater were investigated. The results showed that the photodegradation for TC in simulated seawater was significantly inhibited. Compared with the TC photodegradation in pure water, the reaction rate of the chiral mesoporous TiO2 photocatalyst for TC was reduced by approximately 70%, whereas the achiral mesoporous TiO2 photocatalyst could hardly degrade TC in seawater. Anions in simulated seawater had little effect on photodegradation, but Mg2+ and Ca2+ ions significantly inhibited the TC photodegradation process. Whether in water or simulated seawater, the active species generated by the catalyst after excitation by visible light were mainly holes, and each salt ion did not inhibit the generation of active species; thus, the degradation pathway both in simulated seawater and in water was the same. However, Mg2+ and Ca2+ would be enriched around the highly electronegative atoms in TC molecules, hindering the attack of holes to highly electronegative atoms in TC molecules, thereby inhibiting the photocatalytic degradation efficiency.
