2022
DOI: 10.1016/j.jes.2021.04.014
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Tetracycline removal via adsorption and metal-free catalysis with 3D macroscopic N-doped porous carbon nanosheets: Non-radical mechanism and degradation pathway

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Cited by 40 publications
(5 citation statements)
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“…Although the introduction of N‐rGO did not improve the reaction rate (if compared to the reaction only using PSM), the complete conversion of the organics into water and CO 2 was observed, revealing the excellent catalytic performance of these materials. In the recent past, melamine was successfully employed for the synthesis of 3D macroscopic N ‐doped porous carbonaceous nanosheets (NPCN) [38] . With this material, tetracycline (TC) was removed up to 96 % after the addition of persulphate as an oxidizing agent.…”
Section: Opportunities In Thermocatalysismentioning
confidence: 99%
See 1 more Smart Citation
“…Although the introduction of N‐rGO did not improve the reaction rate (if compared to the reaction only using PSM), the complete conversion of the organics into water and CO 2 was observed, revealing the excellent catalytic performance of these materials. In the recent past, melamine was successfully employed for the synthesis of 3D macroscopic N ‐doped porous carbonaceous nanosheets (NPCN) [38] . With this material, tetracycline (TC) was removed up to 96 % after the addition of persulphate as an oxidizing agent.…”
Section: Opportunities In Thermocatalysismentioning
confidence: 99%
“…In the recent past, melamine was successfully employed for the synthesis of 3D macroscopic N-doped porous carbonaceous nanosheets (NPCN). [38] With this material, tetracycline (TC) was removed up to 96 % after the addition of persulphate as an oxidizing agent. No less significant, NPCN proved its stability in 4 subsequent recycles, removing up to 80 % of TC, thereby demonstrating that the catalytic efficiency was not altered over time by the reaction environment during the recycling tests and by the washing/restoring procedures.…”
Section: N-doped Carbonaceous Materialsmentioning
confidence: 99%
“…The intermediate products of TC degradation were analyzed by LC-MS to further investigate the degradation mechanism of the BM0.5%/PS/Vis system, and two possible TC degradation pathways were finally obtained (Figure 9). In pathway I, TC formed intermediate P1 (m/z = 460) through hydroxylation first, [53] followed by N-methyl demethylation, and the amide and hydroxyl groups were lost, resulting in the intermediate P2 (m/z = 389). [54] P2 underwent C─N bond cleavage, removal of hydroxyl, methyl groups and other processes, and then P3 was obtained (m/z = 328), [55] followed by cyclization to obtain P4 (m/z = 192).…”
Section: Activity Performance Analysismentioning
confidence: 99%
“…Interestingly, toroidal structures of tetracyclines were related to several readily ionizable functional and electron-rich groups (e.g. dimethylphenol groups and amino groups) that were susceptible to attack by reactive agents (Shen et al 2022).…”
Section: Photocatalytic Mechanismmentioning
confidence: 99%