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Applied catalysis. B, Environmental, 2022-04, Vol.303, p.120926, Article 120926
2022

Details

Autor(en) / Beteiligte
Titel
Enhancement of persulfate activation by Fe-biochar composites: Synergism of Fe and N-doped biochar
Ist Teil von
  • Applied catalysis. B, Environmental, 2022-04, Vol.303, p.120926, Article 120926
Ort / Verlag
Amsterdam: Elsevier B.V
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Persulfate-based (PS-based) advanced oxidation process is a promising technology for degradation of organic pollutants. PS activation needs efficient and economical catalysts and heterogeneous Fe-carbon composites are competitive. Herein, novel N-doped biochar-loaded nanoscale zero-valent iron (nZVI) composites (Fe@N-BC) were synthesized and evaluated for PS activation. Detailed characterization data indicated that graphitic and pyridine N structures were introduced by N-doping, which enhanced the anchoring, dispersion and loading of amorphous nZVI on biochar. Remarkably, the optimized Fe@N-BC material, Fe@N2-BC900, presented excellent catalytic performance for PS activation for lindane removal. The N-doped defects in biochar acted as reactive bridges and accelerated the electron transfer between nZVI and PS, showing strong synergistic effects toward nZVI. O2•− and 1O2 were the dominant active species in catalytic systems. Additionally, Fe@N2-BC900 catalyst showed effectiveness over a wide pH range for lindane removal. This work provides a new approach to the rational design and application of Fe@N-BC for persulfate activation in pollution control, which is certified by deep exploration of reaction mechanism. [Display omitted] •Graphitic and pyridine N atoms reinforced the anchor, dispersion and loading of nZVI.•Synergistic effects of Fe and N species enhanced the PS activation.•Fe-N @ BC activated PS to generate O2•− and 1O2 for γ-HCH degradation.•N-doped defects acted as reactive bridge to accelerate the electron transfer.
Sprache
Englisch
Identifikatoren
ISSN: 0926-3373
eISSN: 1873-3883
DOI: 10.1016/j.apcatb.2021.120926
Titel-ID: cdi_proquest_journals_2622303057

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