2021
DOI: 10.1016/j.apcatb.2020.119597
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Synthesis of CQDs@FeOOH nanoneedles with abundant active edges for efficient electro-catalytic degradation of levofloxacin: Degradation mechanism and toxicity assessment

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Cited by 66 publications
(18 citation statements)
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“…† It was reported that the Environmental Science: Nano Paper main degradation pathways of LEV involve quinolone ring destruction, piperazine ring removal, defluorination and ringopening processes. [50][51][52][53] Herein, according to the detected intermediates and previous reports, 48,51,[54][55][56][57][58] small molecules that cannot be completely degraded.…”
Section: Synergistic Removal Of Lev and Crijvi)mentioning
confidence: 76%
See 1 more Smart Citation
“…† It was reported that the Environmental Science: Nano Paper main degradation pathways of LEV involve quinolone ring destruction, piperazine ring removal, defluorination and ringopening processes. [50][51][52][53] Herein, according to the detected intermediates and previous reports, 48,51,[54][55][56][57][58] small molecules that cannot be completely degraded.…”
Section: Synergistic Removal Of Lev and Crijvi)mentioning
confidence: 76%
“…It was reported that the main degradation pathways of LEV involve quinolone ring destruction, piperazine ring removal, defluorination and ring-opening processes. 50–53 Herein, according to the detected intermediates and previous reports, 48,51,54–58 three possible degradation routes were proposed and are presented in Scheme 2. Route I mainly involves the oxidation and destruction of the piperazine ring.…”
Section: Resultsmentioning
confidence: 95%
“…Subsequently, the opening of benzene rings lead to the production of L16 (m/z = 80) and L17 (m/z = 54). Finally, intermediate L17 products might be continuously broken into small-molecule organic acids and mineralization products [49][50][51][52][53][54][55][56].…”
Section: Possible Degradation Routes Of Lvxmentioning
confidence: 99%
“…Hydrogen peroxide (H 2 O 2 ), persulfates, and ozone (O 3 ) are the most common commercial oxidants used in AOPs. In particular, peroxymonosulfate (PMS) can be easily activated by both homogeneous and heterogeneous catalytic systems. Compared with • OH (1.8–2.7 V), SO 4 •– possesses a high redox potential (2.5–3.1 V), high selectivity, and relatively longer half-life (30–40 μs). , Transition metal ions and metal oxides (Co, Mn, Fe, Cu, etc.) have been widely used to activate PMS and to produce a hydroxyl radical ( • OH) and sulfate radical (SO 4 •– ). The rapid redox circulation of multi-valence metal sites is the key to promoting the utilization efficiency of PMS and peroxydisulfate (PDS). Single metal atoms anchored on N rich sites are electropositive sites to adsorb and activate persulfates. , In addition, the morphology, oxidation states, and crystallographic phases of the MnO x are controlled to analyze the structure–performance relationships. Nevertheless, metal-based catalysts are highly effective, but the potential secondary pollution and post-treatment limit their practical application …”
Section: Introductionmentioning
confidence: 99%