Heterogeneous degradation of organic contaminant by peroxydisulfate catalyzed by activated carbon cloth
An eco-friendly material, activated carbon cloth (ACC) was used as the heterogeneous catalyst in activation of peroxydisulfate (PDS) for the efficient degradation of organic pollutant in water. Besides, the effects of several parameters in the ACC/PDS process including initial pH, PDS concentration,...
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Veröffentlicht in: | Chemosphere (Oxford) 2020-01, Vol.238, p.124611-124611, Article 124611 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | An eco-friendly material, activated carbon cloth (ACC) was used as the heterogeneous catalyst in activation of peroxydisulfate (PDS) for the efficient degradation of organic pollutant in water. Besides, the effects of several parameters in the ACC/PDS process including initial pH, PDS concentration, reaction temperature, stirring speed and co-existing anions were investigated. Under optimum conditions, almost complete removal (98.6%) of AO7 in 60 min and 67.4% of total organic carbon (TOC) removal within 180 min were obtained, accompanied by the remarkable destruction of azo band and naphthalene ring on AO7. The electron paramagnetic resonance and radical quenching experiments were carried out to identify the reactive radicals in the ACC/PDS process. Surface characteristic techniques such as XRD, BET, SEM, FTIR, XPS were applied to analysis the change of crystal structure, surface area, surface morphology, functional groups on the surface of fresh and spent ACC samples. Hydroxyl groups (C‒OH) and π-π transitions significantly affected the catalytic activity of ACC. The intermediate products of AO7 oxidation were identified by LC-MS and the corresponding degradation pathway was proposed.
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•Activated carbon cloth (ACC) in monolithic form was applied to catalyze PDS.•Effects of reaction parameters on AO7 removal were evaluated.•SO4.•−, HO• and •C were identified in ACC/PDS system•Surface function groups are responsible for the adsorption and activation of ACC. |
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ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2019.124611 |