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• W3146952469 abstract "This work demonstrates for the first time the potential application of a novel nonradical oxidation system consisting of N/S co-doped ordered mesoporous carbon (NS-CMK-3) and peroxymonosulfate (PMS). The results showed that the NS-CMK-3 catalyst effectively activated PMS to completely degrade pharmaceutical acetaminophen (ACT). The catalytic performance of NS-CMK-3 was ~20 and 10 times better than that of pristine CMK-3 and single N-doped one (N-CMK-3), respectively. The oxidative system could also remove other pollutants (i.e., sulfathiazole, trans-ferulic acid, orange G, and phenol). A higher content of N (5.3 at.%) and a distribution of graphite-N (28.1%) were determined in NS-CMK-3 than in N-CMK-3. The synergistic effect of N/S co-doping (i.e., graphite-N and thiophene-S) resulted in the enhanced catalytic performance. The activation of PMS by NS-CMK-3 primarily followed two nonradical pathways (i.e., singlet oxygen and catalyst surface-bound reactive PMS complexes), supported by quenching experiments and electron paramagnetic resonance measurements. The p-benzoquinone (p-BQ) and ACTdimer were main degradation products. The removal of total organic carbon (TOC) was ≈27%, suggesting nonradicals could mineralize ACT. The NS-CMK-3 not only demonstrated superior stability owing to a removal efficiency that was still as high as 98% in the fifth recycle run, but also significantly decreased the potential effects of water constituents (e.g., Cl−, NO3−, HCO3−, and humic acid) on the removal process. The NS-CMK-3/PMS oxidative system offers a novel strategy to carry out environmental remediation via nonradical processes." @default.
• W3146952469 created "2021-04-13" @default.
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• W3146952469 date "2021-08-01" @default.
• W3146952469 modified "2023-10-16" @default.
• W3146952469 title "Dual nonradical degradation of acetaminophen by peroxymonosulfate activation with highly reusable and efficient N/S co-doped ordered mesoporous carbon" @default.
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• W3146952469 doi "https://doi.org/10.1016/j.seppur.2021.118697" @default.
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