Three-dimensional porous La(OH)3/g-C3N4 adsorption-photocatalytic synergistic removal of tetracycline
- PMID: 38403828
- DOI: 10.1007/s11356-024-32546-0
Three-dimensional porous La(OH)3/g-C3N4 adsorption-photocatalytic synergistic removal of tetracycline
Abstract
La(OH)3/g-C3N4 composites were successfully synthesized via one-step calcination using urea, melamine, and La(NO3)3·nH2O as raw materials, and applied to UV-induced photocatalytic tetracycline (TC) removal. Comprehensive characterization by an X-ray diffraction (XRD), Fourier transform infrared reflection (FT-IR), high-resolution transmission electron microscope (HRTEM), and other techniques analyzed effects of La3+ doping, especially N vacancies and cyano groups as active sites. Compared to pure g-C3N4 and La(OH)3, synthesized La(OH)3/g-C3N4 composites exhibited a three-dimensional porous nanosheet structure with specific surface area of 83.62 m2/g and equilibrium TC adsorption capacity up to 285.59 mg/g; La(OH)3 doping significantly improved composite structure. After dispersing 10 mg La-CN-0.5 photocatalyst in 60 mL 40 mg/L TC solution, TC removal reached 91.08% in 30 min under UV irradiation, exhibiting excellent performance. Additionally, La-CN-0.5 showed significant adsorption-photocatalytic synergism, with the quasi-primary kinetic constant increased by 1.83-fold. The efficiency of high tetracycline (TC) concentration treatment through adsorption photocatalytic degradation by La-CN-0.5 was confirmed by the utilization of free radical trapping and electron spin resonance (ESR) tests. The significant involvement of ∙O2-, ∙OH, and h+ in this process was observed. These findings propose that the prepared La-CN-0.5 material exhibits a unique capability for adsorption photocatalysis, providing a promising approach for the efficient removal of high TC concentrations.
Keywords: Active sites; Adsorption; One-step calcination; Photocatalysis; Removal; Synergy; Tetracycline.
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
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