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Lee, Jae Sung
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Copper- and vanadium-catalyzed methane oxidation into oxygenates with in situ generated H2O2 over Pd/C

Alternative Title
Copper- and vanadium-catalyzed methane oxidation into oxygenates with in situ generated H2O2 over Pd/C
Author(s)
Park, Eun DuckHwang, Yoo-ShikLee, Chul WooLee, Jae Sung
Issued Date
2003-07
DOI
10.1016/S0926-860X(03)00125-X
URI
https://scholarworks.unist.ac.kr/handle/201301/12525
Fulltext
http://www.sciencedirect.com/science/article/pii/S0926860X0300125X#
Citation
APPLIED CATALYSIS A-GENERAL, v.247, no.2, pp.269 - 281
Abstract
Copper- and vanadium-catalyzed oxidation of methane into methyl trifluoroacetate and formic acid with in situ generated H2O2 from H-2 and O-2 over Pd/C was investigated in trifluoroacetic acid (TFA) and/or trifluoroacetic anhydride (TFAA) as a solvent. Metallic palladium was responsible for the in situ generation of hydrogen peroxide from dihydrogen and dioxygen. Divalent copper hydroperoxide and monoperoxomonovanadate, VO(O-2)(+), seemed to be related to C-H bond activation. The radical chain reaction did not occur in either copper- or vanadium-catalyzed methane oxidation. However, methyl radical appeared to be produced in vanadium system but not in copper system. (C) 2003 Elsevier Science B.V. All rights reserved
Publisher
ELSEVIER SCIENCE BV
ISSN
0926-860X

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