Catalytic Oxidation of 5-Hydroxymethylfurfural into 2,5-Diformylfuran Using V-Containing Heteropoly Acid Catalysts
Научная публикация
| Общее |
Язык:
Английский,
Жанр:
Статья (Full article),
Статус опубликования:
Опубликована,
Оригинальность:
Оригинальная
|
| Журнал |
Reaction Kinetics, Mechanisms and Catalysis
ISSN: 1878-5190
, E-ISSN: 1878-5204
|
| Вых. Данные |
Год: 2020,
Том: 130,
Номер: 1,
Страницы: 403-415
Страниц
: 13
DOI:
10.1007/s11144-020-01782-z
|
| Ключевые слова |
2,5-Diformylfuran; Heteropoly acids; Homogeneous catalysis; 5‐Hydroxymethylfurfural; Oxidation |
| Авторы |
Rodikova Yulia
1
,
Zhizhina Elena
1
|
| Организации |
| 1 |
Department of Fine Organic Synthesis and Renewable Energy Source, Boreskov Institute of Catalysis SB RAS, Pr. Akad. Lavrentieva 5, Novosibirsk 630090, Russian Federation
|
|
Информация о финансировании (1)
|
1
|
Российский фонд фундаментальных исследований
|
18-33-00073
|
2,5-Diformylfuran (DFF) is an attractive and challenging compound that can be synthesized with good selectivity by the oxidation of bio-based 5‐hydroxymethylfurfural (5-HMF) using specific catalysts. Vanadium-containing heteropoly acids (PMoV HPAs) are highly active oxidation catalysts whose activity can be tuned by changing vanadium(V) (VV) content. This study reports the preparation of a number of PMoV HPAs with different VV amount and type of outer-sphere cation and investigating their catalytic performance in 5-HMF-to-DFF conversion. The characterization of synthesized HPAs by simple instrumental methods (pH-measurement, potentiometry, and titration analysis) and NMR revealed retaining Keggin structure and increasing oxidation potential with rising VV amount. The complete optimization of reaction conditions allowed one to reach a DFF yield of 92% using Co2H6P3Mo18V7O84 at 110 °C in water/MIBK for 90 min under atmospheric pressure. The described method of 5-HMF oxidation is based on using effective soft oxidants that can be easily recycled and reused at least five times without significant loss of catalytic activity.