Alcohol-mediated Reduction of Biomass-derived Furanic Aldehydes via Catalytic Hydrogen Transfer

2019 ◽  
Vol 23 (20) ◽  
pp. 2168-2179 ◽  
Author(s):  
Yufei Xu ◽  
Jingxuan Long ◽  
Jian He ◽  
Hu Li

With the depletion of fossil energy, liquid biofuels are becoming one of the effective alternatives to replace fossil fuels. The catalytic transfer and hydrogenation of biomass-based furanic compounds into fuels and value-added chemicals has become a spotlight in this field. Gas hydrogen is often used as the H-donor for the hydrogenation reactions. It is a very straightforward and simple method to implement, but sometimes it comes with the danger of operation and the difficulty of regulation. In recent years, diverse liquid hydrogen donor reagents have been employed in the catalytic transfer hydrogenation (CTH) of biomass. Amongst those H-donors, alcohol is a kind of green and benign reagent that has been used in different biomass conversion reactions. This type of reagent is very convenient to use, and the involved operation process is safe, as compared to that of H2. In this review, the application of alcohols as liquid H-donors in the catalytic transfer hydrogenation of biomass-derived furanic compounds is depicted, and the representative reaction mechanisms are discussed. Emphasis is also laid on the selective control of product distribution in the described catalytic systems.

2020 ◽  
Vol 4 (7) ◽  
pp. 3654-3667 ◽  
Author(s):  
Atul S. Nagpure ◽  
Pranjal Gogoi ◽  
Nishita Lucas ◽  
Satyanarayana V. Chilukuri

Highly dispersed Ru nanoparticles supported on N-doped mesoporous carbon demonstrated an admirable catalytic activity in catalytic transfer hydrogenation of 5-hydroxymethylfurfural to 2,5-dimethylfuran and furfural to 2-methylfuran.


2021 ◽  
Author(s):  
Wenting Fang ◽  
Anders Riisager

Catalytic transfer hydrogenation/hydrogenolysis are economically and environmentally benign synthetic strategies to valorize renewable compounds derived from biomass. Simple and easy accessible assessable organic molecules such as, e.g. alcohols, formic acid/formate...


2020 ◽  
Vol 10 (5) ◽  
pp. 1843
Author(s):  
Beatriz García ◽  
Jovita Moreno ◽  
Gabriel Morales ◽  
Juan A. Melero ◽  
Jose Iglesias

Sorbitol production from glucose was studied through catalytic transfer hydrogenation (CTH) over Raney nickel catalysts in alcohol media, used as solvents and hydrogen donors. It was found that alcohol sugars, sorbitol and mannitol, can be derived from two hydrogen transfer pathways, one produced involving the sacrificing alcohol as a hydrogen donor, and a second one involving glucose disproportionation. Comparison between short-chain alcohols evidenced that ethanol was able to reduce glucose in the presence of Raney nickel under neutral conditions. Side reactions include fructose and mannose production via glucose isomerization, which occur even in the absence of the catalyst. Blank reaction tests allowed evaluating the extension of the isomerization pathway. The influence of several operation parameters, like the temperature or the catalyst loading, as well as the use of metal promoters (Mo and Fe-Cr) over Raney nickel, was examined. This strategy opens new possibilities for the sustainable production of sugar alcohols.


2021 ◽  
pp. 120429
Author(s):  
Christian O. Blanco ◽  
Ligia Llovera ◽  
Alberto Herrera ◽  
Romano Dorta ◽  
Giuseppe Agrifoglio ◽  
...  

Author(s):  
Bolla Srinivasarao ◽  
Yogita Y ◽  
Dhana Lakshmi Darsi ◽  
Krishna Kumari Pamula ◽  
N. Lingaiah

One pot conversion of furfural to -valerolactone by transfer hydrogenation has been achieved over bifunctional Zr and TPA located in mesoporous silica catalysts. Different catalysts with TPA and ZrO2 located...


2018 ◽  
Vol 7 (6) ◽  
pp. 1107-1112 ◽  
Author(s):  
Yunrui Zhang ◽  
Yingying Zhai ◽  
Minzhe Chu ◽  
Li Huo ◽  
Haijun Wang ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (64) ◽  
pp. 59753-59761 ◽  
Author(s):  
A. M. Hengne ◽  
B. S. Kadu ◽  
N. S. Biradar ◽  
R. C. Chikate ◽  
C. V. Rode

A bifunctional Ni/MMT catalyst for catalytic transfer hydrogenation of levulinic acid to γ-valerolactone with complete conversion and selectivity.


Sign in / Sign up

Export Citation Format

Share Document