PMID- 38467998 OWN - NLM STAT- MEDLINE DCOM- 20240419 LR - 20240419 IS - 1614-7499 (Electronic) IS - 0944-1344 (Linking) VI - 31 IP - 17 DP - 2024 Apr TI - MXene-supported MIL-88A(Fe) as persulfate activator for removal of tetracycline. PG - 25273-25286 LID - 10.1007/s11356-024-32677-4 [doi] AB - The poor conductivity, poor stability, and agglomeration of iron-based metal organic framework MIL-88A(Fe) limit its application as persulfate (PS) activator in water purification. Herein, MXene-supported MIL-88A(Fe) composites (M88A/MX) were synthesized to enhance its adsorption and catalytic capability for tetracycline (TC) removal. Scanning electron microscope (SEM), X-ray diffractometer (XRD), Fourier transform infrared spectrometer (FT-IR), and X-ray photoelectron spectroscopy (XPS) were used to characterize prepared materials, confirming the successful attachment of MIL-88A(Fe) to the surface of MXene. M88A/MX-0.2 composites, prepared with 0.2 g MXene addition, exhibit optimal degradation efficiency, reaching 98% under conditions of 0.2 g/L M88A/MX-0.2, 1.0 mM PS, 20 ppm TC, and pH 5. The degradation rate constants of M88A/MX-0.2 were 0.03217 min(-1), which was much higher than that of MIL-88A(Fe) (0.00159 min(-1)) and MXene (0.00626 min(-1)). The removal effects of reaction parameters, such as dosage of M88A/MX-0.2 and PS; initial solution pH; and the presence of the common co-existing constituents (humic acid and the inorganic anions) were investigated in detail. Additionally, the reuse of M88A/MX-0.2 showed that the composites had good cycling stability by recurrent experiments. The results of electron paramagnetic resonance (EPR) and quenching experiments indicated that .OH, .SO(4)(-), and .O(2)(-) were involved in the M88A/MX-0.2/PS system where persulfate oxidation process was activated with prepared M88A/MX-0.2. In addition, the intermediates of photocatalytic degradation were determined by HPLC-MS, and the possible degradation pathways of the target molecules were inferred. This study offered a new avenue for sulfate-based degradation of Fe-based metal organic framework. CI - (c) 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. FAU - Chen, Junxia AU - Chen J AD - State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China. FAU - Yang, Zhenzhen AU - Yang Z AD - State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China. FAU - Li, Weigang AU - Li W AD - State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China. FAU - Yang, Yuying AU - Yang Y AD - State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China. FAU - Zhu, Feng AU - Zhu F AD - Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, 210009, China. FAU - Huo, Zongli AU - Huo Z AD - Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, 210009, China. FAU - Zhou, Qing AU - Zhou Q AUID- ORCID: 0000-0003-3957-7408 AD - State Key Laboratory of Pollution Control and Resource Reuse, School of Environment, Nanjing University, Nanjing, 210023, China. zhouqing@nju.edu.cn. LA - eng PT - Journal Article DEP - 20240311 PL - Germany TA - Environ Sci Pollut Res Int JT - Environmental science and pollution research international JID - 9441769 RN - 0 (Metal-Organic Frameworks) RN - 0 (MXene) RN - F8VB5M810T (Tetracycline) RN - 0 (Anti-Bacterial Agents) RN - 0 (Nitrites) RN - 0 (Transition Elements) SB - IM MH - *Metal-Organic Frameworks/chemistry MH - Spectroscopy, Fourier Transform Infrared MH - Tetracycline MH - Anti-Bacterial Agents MH - *Nitrites MH - *Transition Elements OTO - NOTNLM OT - Free radical production OT - MIL-88A(Fe) OT - MXene OT - Persulfate activation OT - Tetracycline degradation EDAT- 2024/03/12 06:43 MHDA- 2024/04/19 06:42 CRDT- 2024/03/12 00:44 PHST- 2023/11/27 00:00 [received] PHST- 2024/02/23 00:00 [accepted] PHST- 2024/04/19 06:42 [medline] PHST- 2024/03/12 06:43 [pubmed] PHST- 2024/03/12 00:44 [entrez] AID - 10.1007/s11356-024-32677-4 [pii] AID - 10.1007/s11356-024-32677-4 [doi] PST - ppublish SO - Environ Sci Pollut Res Int. 2024 Apr;31(17):25273-25286. doi: 10.1007/s11356-024-32677-4. Epub 2024 Mar 11.