Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Rb-promoted Fe/CeO2 nanocatalyst for aniline conversion into azoxybenzene, DFT calculations and mechanism

Khan, Afsar ; Xiao, Sa ; Xie, Yu ; Kaya, Savaş ; Zareen, Shah LU ; Muhammad, Nisar ; Parveen, Kousar and Xu, Dayong (2024) In New Journal of Chemistry 49(3). p.921-934
Abstract

Selectivity control of aniline oxidation and low reactant conversion in traditional synthesis methods are great challenges, and it is desirable to develop a green, low-cost and highly efficient catalytic route toward value-added products. Herein, an Rb-promoted Fe/CeO2 nanocatalyst was prepared to understand the effects of Rb-promoter on the catalytic performance for the selective oxidation of aniline to azoxybenzene using H2O2 as an oxidant. The 0.1 M Rb-4% Fe/CeO2 (Rb-Fe/CeO2) catalyst showed a high aniline conversion of 100% with 91% selectivity of azoxybenzene. This is because the existence of Rb contributes to the electron transportation property, decreases activation energy... (More)

Selectivity control of aniline oxidation and low reactant conversion in traditional synthesis methods are great challenges, and it is desirable to develop a green, low-cost and highly efficient catalytic route toward value-added products. Herein, an Rb-promoted Fe/CeO2 nanocatalyst was prepared to understand the effects of Rb-promoter on the catalytic performance for the selective oxidation of aniline to azoxybenzene using H2O2 as an oxidant. The 0.1 M Rb-4% Fe/CeO2 (Rb-Fe/CeO2) catalyst showed a high aniline conversion of 100% with 91% selectivity of azoxybenzene. This is because the existence of Rb contributes to the electron transportation property, decreases activation energy and leads to lattice distortion of Fe/CeO2 and further formation of oxygen vacancies and Ce3+, which contributes to improving the activity of Fe/CeO2 nanocatalysts for aniline conversion reaction. The Rb used to modify Fe/CeO2 nanocatalysts can not only passivate the strong Brønsted acid sites and stability of Fe/CeO2 but also enhance the Fe dispersion and induce an electron-rich chemical environment for the supported Fe species and promote the activation of the substrate. All these effects lead to the desirable catalytic performance. The increased basic strength of the cation-promoted catalyst improves the electron density of the active Fe species, resulting in a higher yield of the desired aromatic azo compounds. This compensates for electronic deficiencies in the Fe, enhancing its catalytic activity without interference. Experiments were conducted as a function of catalyst loading (20-100 mg), time (2-24 h), temperature (25-100 °C), types of solvent and solvent amount (0.5-2 ml) in 50 ml round bottom flask with reflux condenser. Our work proposes a facile approach to develop and promote non-noble metal catalysts for the effective conversion of aniline into azoxybenzene under mild reaction conditions.

(Less)
Please use this url to cite or link to this publication:
author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
New Journal of Chemistry
volume
49
issue
3
pages
14 pages
publisher
Royal Society of Chemistry
external identifiers
  • scopus:85212712430
ISSN
1144-0546
DOI
10.1039/d4nj04200j
language
English
LU publication?
yes
id
199de250-c1ba-4cbb-8d58-8ee9ea3d063c
date added to LUP
2025-01-28 12:54:24
date last changed
2025-04-04 15:07:45
@article{199de250-c1ba-4cbb-8d58-8ee9ea3d063c,
  abstract     = {{<p>Selectivity control of aniline oxidation and low reactant conversion in traditional synthesis methods are great challenges, and it is desirable to develop a green, low-cost and highly efficient catalytic route toward value-added products. Herein, an Rb-promoted Fe/CeO<sub>2</sub> nanocatalyst was prepared to understand the effects of Rb-promoter on the catalytic performance for the selective oxidation of aniline to azoxybenzene using H<sub>2</sub>O<sub>2</sub> as an oxidant. The 0.1 M Rb-4% Fe/CeO<sub>2</sub> (Rb-Fe/CeO<sub>2</sub>) catalyst showed a high aniline conversion of 100% with 91% selectivity of azoxybenzene. This is because the existence of Rb contributes to the electron transportation property, decreases activation energy and leads to lattice distortion of Fe/CeO<sub>2</sub> and further formation of oxygen vacancies and Ce<sup>3+</sup>, which contributes to improving the activity of Fe/CeO<sub>2</sub> nanocatalysts for aniline conversion reaction. The Rb used to modify Fe/CeO<sub>2</sub> nanocatalysts can not only passivate the strong Brønsted acid sites and stability of Fe/CeO<sub>2</sub> but also enhance the Fe dispersion and induce an electron-rich chemical environment for the supported Fe species and promote the activation of the substrate. All these effects lead to the desirable catalytic performance. The increased basic strength of the cation-promoted catalyst improves the electron density of the active Fe species, resulting in a higher yield of the desired aromatic azo compounds. This compensates for electronic deficiencies in the Fe, enhancing its catalytic activity without interference. Experiments were conducted as a function of catalyst loading (20-100 mg), time (2-24 h), temperature (25-100 °C), types of solvent and solvent amount (0.5-2 ml) in 50 ml round bottom flask with reflux condenser. Our work proposes a facile approach to develop and promote non-noble metal catalysts for the effective conversion of aniline into azoxybenzene under mild reaction conditions.</p>}},
  author       = {{Khan, Afsar and Xiao, Sa and Xie, Yu and Kaya, Savaş and Zareen, Shah and Muhammad, Nisar and Parveen, Kousar and Xu, Dayong}},
  issn         = {{1144-0546}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{921--934}},
  publisher    = {{Royal Society of Chemistry}},
  series       = {{New Journal of Chemistry}},
  title        = {{Rb-promoted Fe/CeO<sub>2</sub> nanocatalyst for aniline conversion into azoxybenzene, DFT calculations and mechanism}},
  url          = {{http://dx.doi.org/10.1039/d4nj04200j}},
  doi          = {{10.1039/d4nj04200j}},
  volume       = {{49}},
  year         = {{2024}},
}