Issue 35, 2024

Selective adsorption and photodegradation of residual norfloxacin in water using a mTiO2 based inorganic molecularly imprinted magnetic photocatalyst

Abstract

In this study, a mesoporous TiO2 (mTiO2) based inorganic molecularly imprinted magnetic photocatalyst was prepared for the selective adsorption and photodegradation of residual antibiotics in water. Direct molecularly imprinted TiO2 shells were coated on nano-Fe3O4 (Fe3O4@TiO2) through a sol–gel imprinting technique using norfloxacin (NOR) as a template, then the amorphous imprinted TiO2 shells were transformed into mesoporous crystalline anatase (Fe3O4@mTiO2) by a microwave-assisted hydrothermal method, and Ag NPs were simultaneously in situ reduced on the surface (Fe3O4@mTiO2@Ag) to enhance the photodegradation performance. The as-prepared inorganic molecularly imprinted Fe3O4@mTiO2@Ag (MIFTA) nanocomposites showed excellent specificity for the target molecule NOR, and the adsorption capacity was as high as 135.7 μg mg−1, which was 1.4 to 2.3 times higher than that of other fluoroquinolone antibiotics. The photodegradation rate of MIFTA for NOR was 0.0129 min−1, which was about 3.1 times faster than that of non-imprinted Fe3O4@mTiO2@Ag (NIFTA). In addition, the used MIFTA nanocomposites can be easily recycled by magnetic separation and subsequent water elution. These results indicate that prepared MIFTA nanocomposites were expected to provide an efficient, environment friendly, and low-cost approach for the selective removal of residual antibiotics in water.

Graphical abstract: Selective adsorption and photodegradation of residual norfloxacin in water using a mTiO2 based inorganic molecularly imprinted magnetic photocatalyst

Supplementary files

Article information

Article type
Paper
Submitted
03 Jul 2024
Accepted
06 Aug 2024
First published
07 Aug 2024

New J. Chem., 2024,48, 15567-15576

Selective adsorption and photodegradation of residual norfloxacin in water using a mTiO2 based inorganic molecularly imprinted magnetic photocatalyst

L. Zheng, W. Liao, J. Wu, Q. Long, Y. Luo, X. Li, L. Huang, L. Jia, H. Li and K. Liu, New J. Chem., 2024, 48, 15567 DOI: 10.1039/D4NJ03014A

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