Go to:
Logótipo
Você está em: Start > Publications > View > Reaction Mechanism of Aerobic Oxidation of Alcohols Conducted on Activated-Carbon-Supported Cobalt Oxide Catalysts
Publication

Reaction Mechanism of Aerobic Oxidation of Alcohols Conducted on Activated-Carbon-Supported Cobalt Oxide Catalysts

Title
Reaction Mechanism of Aerobic Oxidation of Alcohols Conducted on Activated-Carbon-Supported Cobalt Oxide Catalysts
Type
Article in International Scientific Journal
Year
2011
Authors
Junjiang J Zhu
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Jose L Figueiredo
(Author)
FEUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Arne Thomas
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Journal
Vol. 17
Pages: 7112-7117
ISSN: 0947-6539
Publisher: Wiley-Blackwell
Indexing
Scientific classification
FOS: Natural sciences > Chemical sciences
Other information
Authenticus ID: P-002-R46
Abstract (EN): Catalytic performances and the reaction mechanism of Co(3)O(4)/AC (AC=activated carbon) for aerobic oxidation of alcohols carried out in the liquid phase were investigated. Co(3)O(4)/AC shows a high activity for aerobic oxidation of benzyl alcohol, comparable to noble metal catalysts (e. g., Au/AC) even in the absence of additives or promoters (e. g., NaOH). Changing preparation conditions, such as treatment temperature and/or time, can affect the catalytic performances of Co(3)O(4)/AC, due to decomposition of surface groups of the carbon support. Careful studies show that low alcohol conversions are obtained with either Co(3)O(4) or AC alone, which indicates that the high conversion observed over the Co(3)O(4)/AC is due to a synergistic effect between Co(3)O(4) and AC. Parallel experiments using a high-surface-area covalent triazine framework or oxygen-inert carbon nitride as support for the Co(3)O(4) catalyst also show lower conversions, which suggest that the ability of AC (in Co(3)O(4)/AC) to activate molecular oxygen is essential for the reaction. FTIR and XPS spectra taken from catalysts before and after the reaction confirm that oxygen activation proceeds mainly on the carbon support. As a result, it can be assumed that the alcohol dehydrogenation step proceeds on the metal oxide, whereas the oxygen activation step occurs mainly on the carbon support.
Language: English
Type (Professor's evaluation): Scientific
Contact: ciaczjj@gmail.com; jlfig@fe.up.pt
No. of pages: 6
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same journal

Inside Cover: The Catalytic Mechanism of the Marine-Derived Macrocyclase PatGmac (Chem. Eur. J. 37/2016) (2016)
Another Publication in an International Scientific Journal
Natercia F Bras; Ferreira, P; Calixto, AR; Jaspars, M; Houssen, W; Naismith, JH; Pedro A Fernandes; Ramos, MJ
Developments Towards Regioselective Synthesis of 1,2-Disubstituted Benzimidazoles (2011)
Another Publication in an International Scientific Journal
Luisa C R Carvalho; Eduarda Fernandes; Manuel M B Marques
Water Stable Zr-Benzenedicarboxylate Metal-Organic Frameworks as Photocatalysts for Hydrogen Generation (2010)
Article in International Scientific Journal
Claudia Gomes Silva; Ignacio Luz; Francesc X L I Llabres i Xamena; Avelino Corma; Hermenegildo Garcia
Understanding ribonucleotide reductase inactivation by gemcitabine (2007)
Article in International Scientific Journal
Nuno M F S A Cerqueira; Pedro A Fernandes; Maria L Ramos

See all (33)

Recommend this page Top
Copyright 1996-2024 © Faculdade de Arquitectura da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z  I Guest Book
Page created on: 2024-09-02 at 08:00:48 | Acceptable Use Policy | Data Protection Policy | Complaint Portal