Selective electrocatalytic oxidation of 2,5-dihydroxymethylfuran in aqueous medium: a chromatographic analysis of the reaction products

Citation
A. Al Baradii et al., Selective electrocatalytic oxidation of 2,5-dihydroxymethylfuran in aqueous medium: a chromatographic analysis of the reaction products, ELECTR ACT, 44(16), 1999, pp. 2779-2787
Citations number
20
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ELECTROCHIMICA ACTA
ISSN journal
00134686 → ACNP
Volume
44
Issue
16
Year of publication
1999
Pages
2779 - 2787
Database
ISI
SICI code
0013-4686(1999)44:16<2779:SEOO2I>2.0.ZU;2-B
Abstract
The electrocatalytic oxidation of 2.5-dihydroxymethylfuran (DHMF) was carri ed out on platinum and nickel electrodes in alkaline medium. Suitable opera ting conditions of HPLC analyses were found to determine each reaction prod uct formed during the anodic oxidation. When electrolysis was conducted on a bare Pt electrode or on a NiOOH anode, DHMF is converted only into 5-hydr oxymethylfurfural (HMF). Conversely, the electrooxidation of DHMF on Pt, mo dified in situ by lead adatoms, yielded selectively 61% 2,5-furandialdehyde (FDC). In all the cases, HMF was the primary reaction product. (C) 1999 El sevier Science Ltd. All rights reserved.