z-logo
Premium
Intrinsic Iron‐Containing Multiwalled Carbon Nanotubes as Electro‐Fenton Catalyst for the Conversion of Benzene to Redox‐Active Surface‐Confined Quinones
Author(s) -
Vishnu Nandimalla,
Kumar Annamalai Senthil
Publication year - 2016
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.201600052
Subject(s) - hydroquinone , cyclic voltammetry , catalysis , redox , fourier transform infrared spectroscopy , inorganic chemistry , carbon nanotube , raman spectroscopy , nuclear chemistry , benzene , chemistry , electrochemistry , materials science , photochemistry , chemical engineering , electrode , organic chemistry , nanotechnology , engineering , physics , optics
Multiwalled carbon nanotubes containing an iron impurity (2.1 wt %) (MWCNT‐Fe*) were used to modify a glassy carbon electrode (GCE/MWCNT‐Fe*), which was subsequently exploited for the electrochemical oxidation of benzene (BZ) to redox‐active and surface‐confined quinones (BZO) in H 2 O 2 containing pH 2 HCl–KCl. Physicochemical and electrochemical characterization methods, such as transmission electron microscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, UV/Vis spectroscopy, liquid chromatography coupled mass spectroscopy, and cyclic voltammetry studies with naked Fe 3+/2+ , catechol (CA), and hydroquinone (HQ), evidenced that, in the presence of H 2 O 2 , the intrinsic iron impurity in MWCNT‐Fe* follows the electro‐Fenton reaction to oxidize BZ to BZO (CA+HQ) on the surface of MWCNT‐Fe* (i.e. GCE/MWCNT‐Fe*@BZO). Electro‐catalytic oxidation of hydrazine was demonstrated as a model system for the application of the GCE/MWCNT‐Fe*@BZO catalyst.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom