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Details

Autor(en) / Beteiligte
Titel
Reductive transformation of nitroaromatic compounds by Pd nanoparticles on nitrogen-doped carbon (Pd@NC) biosynthesized using Pantoea sp. IMH
Ist Teil von
  • Journal of hazardous materials, 2019-03, Vol.366, p.338-345
Ort / Verlag
Netherlands: Elsevier B.V
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • [Display omitted] •We propose a novel green synthesis method for Pd NPs supported on the N-doped carbon (Pd@NC).•The Pd@NC exhibited a high catalytic activity for the reductive transformation of nitroaromatic compounds.•Integrated XANES and DFT results suggest that the d-hole counts increase due to Pd 4d-C 2p hybridization in Pd@NC. Reductive transformation of nitroaromatic compounds is a central step in its remediation in wastewater, and therefore has invoked extensive catalytical research with rare metals such as palladium (Pd). Herein, we report Pantoea sp. IMH assisted biosynthesis for Pd@NC as an efficient catalyst for the reduction of nitroaromatics. Multiple complementary characterization results for Pd@NC evidenced the evenly dispersed Pd NPs on an N-doped carbon support. Pd@NC exhibited the superior catalytic activity in the reduction of nitroaromatic compounds (4-nitrophenol, 2-nitroaniline, 4-nitroaniline, and 2,6-dichloro-4-nitroaniline). The origin of the catalytic activity was explained by its unique electronic structure, as explored with X-ray absorption near-edge structure (XANES) spectroscopy and density functional theory (DFT) calculations. XANES analysis revealed an increase of 25.6% in the d-hole count in Pd@NC compared with Pd°, as the result of pd hybridization. In agreement with our experimental observations, DFT calculations suggested the formation of Pd-C bonds and charge re-distribution between Pd and the carbon layer, which contributed to the superior catalytic activity of Pd@NC.
Sprache
Englisch
Identifikatoren
ISSN: 0304-3894
eISSN: 1873-3336
DOI: 10.1016/j.jhazmat.2018.12.009
Titel-ID: cdi_crossref_primary_10_1016_j_jhazmat_2018_12_009

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