journal article·2019-10-28

Solvent Tuning the Selective Hydrogenation of Levulinic Acid into Biofuels over Ni-Metal Organic Framework-Derived Catalyst

Hong Xu, Di Hu, Zixiao Yi, Zuotong Wu, Man Zhang, Kai Yan

ACS Applied Energy Materials· Volume 2· Issue 10
Publisher page

Abstract

We demonstrated that the direct change of solvent could tune the highly selective synthesis of biofuels γ-valerolactone (GVL) or levulinate esters from the hydrogenation levulinic acid (LA) over magnetic Ni/C catalysts fabricated from a nickel–metal organic framework (Ni-MOF) precursor. Yields were 98.2% and 86.1% of GVL with almost perfect selectivity when 1,4-dioxane and isopropanol were used as the solvent, respectively. Levulinate esters (86.5% yield of methyl levulinate and 45.6% yield of ethyl levulinate) were synthesized in methanol and ethanol solvents under identical conditions. This work offers an attractive strategy for the selective production of biofuels in the process of biomass feedstocks.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Catalysis for Biomass Conversion · Catalysis and Hydrodesulfurization Studies · Supercapacitor Materials and Fabrication

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Environmental Science and Engineering, Sun Yat-sen University, 135 Xingang Xi Road, Guangzhou 510275, P. R. China

Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, Guangzhou 510275, P. R. China

Funding

Sun Yat-sen University · Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Central Committee of the Communist Party of China · Guangdong Province

References (29)

Show source-provided references
1. 10.1126/science.115921010.1126/science.1159210 ↗
2. 10.1016/j.apcatb.2015.04.03010.1016/j.apcatb.2015.04.030 ↗
3. 10.1016/j.rser.2019.05.03910.1016/j.rser.2019.05.039 ↗
4. 10.1039/b922014c10.1039/b922014c ↗
5. 10.1016/j.jallcom.2019.05.35010.1016/j.jallcom.2019.05.350 ↗
6. 10.1016/j.apcatb.2018.03.03310.1016/j.apcatb.2018.03.033 ↗
7. 10.1021/cs401177p10.1021/cs401177p ↗
8. 10.1038/ncomms754010.1038/ncomms7540 ↗
9. 10.1002/cssc.20170146910.1002/cssc.201701469 ↗
10. 10.1021/acssuschemeng.9b0266510.1021/acssuschemeng.9b02665 ↗
11. 10.1039/C4CY00504J10.1039/C4CY00504J ↗
12. 10.1016/j.fuel.2019.11620810.1016/j.fuel.2019.116208 ↗
13. 10.1039/C5RA24305J10.1039/C5RA24305J ↗
14. 10.1021/acs.energyfuels.6b0120710.1021/acs.energyfuels.6b01207 ↗
15. 10.1007/s11244-008-9047-610.1007/s11244-008-9047-6 ↗
16. 10.1126/science.118436210.1126/science.1184362 ↗
17. 10.1039/C8SE00274F10.1039/C8SE00274F ↗
18. 10.1016/j.apcata.2012.03.02010.1016/j.apcata.2012.03.020 ↗
19. 10.1039/C9GC00482C10.1039/C9GC00482C ↗
20. 10.1021/jacs.8b0931010.1021/jacs.8b09310 ↗
21. 10.1021/acssuschemeng.8b0287610.1021/acssuschemeng.8b02876 ↗
22. 10.1039/C8GC02001A10.1039/C8GC02001A ↗
23. 10.1016/j.rser.2015.07.02110.1016/j.rser.2015.07.021 ↗
24. 10.1039/C7TA06671F10.1039/C7TA06671F ↗
25. 10.1039/C5GC01604E10.1039/C5GC01604E ↗
26. 10.1021/acsnano.5b0242010.1021/acsnano.5b02420 ↗
27. 10.1002/adma.20100411010.1002/adma.201004110 ↗
28. 10.1039/C7NJ04398H10.1039/C7NJ04398H ↗
29. 10.1021/acs.chemrev.5b0073110.1021/acs.chemrev.5b00731 ↗