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Publication

Zero-valent iron supported on nitrogen-containing activated carbon for catalytic wet peroxide oxidation of phenol

Title
Zero-valent iron supported on nitrogen-containing activated carbon for catalytic wet peroxide oxidation of phenol
Type
Article in International Scientific Journal
Year
2014
Authors
S. A. Messele
(Author)
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J. J. M. Órfão
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F. Stüber
(Author)
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C. Bengoa
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A. Fortuny
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A. Fabregat
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J. Font
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Journal
Vol. 154
Pages: 329-338
ISSN: 0926-3373
Publisher: Elsevier
Indexing
Scientific classification
CORDIS: Technological sciences > Engineering
FOS: Engineering and technology
Other information
Authenticus ID: P-009-7BB
Abstract (EN): Zero-valent iron supported catalysts were prepared through modifying an activated carbon (AC) support with different nitrogen containing precursors; (ethylenediamine, urea and melamine) and impregnating it with 3 wt% of iron. The supports were characterized by N-2 adsorption at -196 degrees C, elemental analysis (EA), the pH at the point of zero charge (pH(pzc)) and temperature programmed desorption (TPD). The iron catalysts were also characterized by temperature programmed reduction (TPR). Subsequently, the catalysts were tested in the adsorption and wet peroxidation of phenol. The results from the different characterization techniques demonstrate that the nitrogen-containing groups are successfully introduced into the carbon surface via all the precursors used. The tests of the different modified carbons as adsorbents/catalysts indicated that the adsorption capacity and the efficiency in phenol oxidation are governed by the specific surface area and functional groups present. Both surface chemistry and textural properties of carbons are influenced by the nitrogen source and the type of oxygen functionalities preexisting on the surface. The modified carbon-supported iron catalysts revealed significantly enhanced phenol removal efficiency, reaching over 85% conversion after 3 h, and showed interesting catalytic stability.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 10
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