Electrocatalytic Oxidation of 5-(Hydroxymethyl)furfural Using High-Surface-Area Nickel Boride

被引:362
|
作者
Barwe, Stefan [1 ]
Weidner, Jonas [1 ]
Cychy, Steffen [2 ]
Morales, Dulce M. [1 ]
Dieckhofer, Stefan [1 ]
Hiltrop, Dennis [2 ]
Masa, Justus [1 ]
Muhler, Martin [2 ]
Schuhmann, Wolfgang [1 ]
机构
[1] Ruhr Univ Bochum, Fac Chem & Biochem, CES, Analyt Chem, Univ Str 150, D-44780 Bochum, Germany
[2] Ruhr Univ Bochum, Fac Chem & Biochem, Lab Ind Chem, Univ Str 150, D-44780 Bochum, Germany
关键词
ATR-IR; electrocatalysis; electrosynthesis; HMF oxidation; nickel boride; SELECTIVE AEROBIC OXIDATION; 2,5-FURANDICARBOXYLIC ACID; MILD CONDITIONS; ELECTROCHEMICAL OXIDATION; CATALYZED OXIDATION; HYDROGEN-PRODUCTION; WATER; HMF; NANOPARTICLES; NANOCATALYST;
D O I
10.1002/anie.201806298
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical oxidation of the biorefinery product 5-(hydroxymethyl)furfural (HMF) to 2,5-furandicarboxylic acid (FDCA), an important platform chemical for the polymer industry, is receiving increasing interest. FDCA-based polymers such as polyethylene 2,5-furandicarboxylate (PEF) are sustainable candidates for replacing polyethylene terephthalate (PET). Herein, we report the highly efficient electrocatalytic oxidation of HMF to FDCA, using Ni foam modified with high-surface-area nickel boride (NixB) as the electrode. Constant potential electrolysis in combination with HPLC revealed a high faradaic efficiency of close to 100% towards the production of FDCA with a yield of 98.5%. Operando electrochemistry coupled to ATR-IR spectroscopy indicated that HMF is oxidized preferentially via 5-hydroxymethyl-2-furancarboxylic acid rather than via 2,5-diformylfuran, which is in agreement with HPLC results. This study not only reports a low-cost active electrocatalyst material for the electrochemical oxidation of HMF to FDCA, but additionally provides insight into the reaction pathway.
引用
收藏
页码:11460 / 11464
页数:5
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