Hydrogenolysis of 5-hydroxymethylfurfural to 2,5-dimethylfuran over supported Pt–Co bimetallic catalysts under mild conditions
Highly dispersed Pt–Co bimetallic catalysts were deposited on multi-walled carbon nanotubes (MWCNTs) by atomic layer deposition. High-resolution TEM and TPR analyses verified the formation of Pt–Co bimetallic particles. Catalysts were applied for the hydrogenolysis of 5-hydroxymethyfurfural (HMF) to...
Saved in:
Published in | Green chemistry : an international journal and green chemistry resource : GC Vol. 20; no. 12; pp. 2894 - 2902 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
2018
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Highly dispersed Pt–Co bimetallic catalysts were deposited on multi-walled carbon nanotubes (MWCNTs) by atomic layer deposition. High-resolution TEM and TPR analyses verified the formation of Pt–Co bimetallic particles. Catalysts were applied for the hydrogenolysis of 5-hydroxymethyfurfural (HMF) to 2,5-dimethyfuran (DMF). A high yield of DMF (>90%) was achieved in the hydrogenolysis of HMF over the optimized Pt–Co/MWCNTs catalyst after 8 h of reaction time under 10 bar H
2
at 160 °C. Through a series of experiments and comparison, the synergistic effect among Pt, Co, and MWCNTs was investigated. The results revealed that the synergistic effect between Pt–Co and MWCNTs played an important role in the improvement of selectivity to DMF for Pt–Co/MWCNTs bimetallic catalysts. In addition, steric hindrance appeared when Co loading in Pt–Co/MWCNTs was high and it affected the activity of the Pt–Co bimetallic catalysts. However, moderate activity can inhibit the production of byproducts and thereby improve the yield of DMF. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 AC02-06CH11357 USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities Division |
ISSN: | 1463-9262 1463-9270 1463-9270 |
DOI: | 10.1039/C8GC00716K |