期刊
ACS CATALYSIS
卷 12, 期 8, 页码 4333-4343出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.1c05847
关键词
reductive decomposition; Ni3Mo3N; hydrodeoxygenation; palmitic acid; bifunctional catalyst; alkanes
资金
- National Natural Science Foundation of China [21972099]
- Application Foundation Program of Sichuan Province [2021YJ0305]
- 111 project [B17030]
- Spanish Ministry of Science and Innovation [RTI2018-89237-CO2-R1]
- Generalitat Valenciana
- China Scholarship Council (CSC)
This study discovers that bimetallic Ni-Mo nitrides can be obtained by a non-nitridation method and serve as efficient catalysts for the hydrodeoxygenation reaction in the production of liquid fuels from biomass. The Ni3Mo3N samples show high selectivity and activity in the hydrodeoxygenation of palmitic acid, and they can be recycled with slight decay in catalytic activity.
In the context of the preparation of liquid fuelsderived from biomass with zero CO2footprint, fatty acids appearas suitable feedstocks. However, reduction of carboxylic acidgroups usually requires harsh reaction conditions and thedevelopment of efficient solid catalysts. Herein, bimetallic Ni-Mo nitrides have been obtained by a procedure not involvingnitridation of the corresponding oxide, but reductive decom-position of the tris(ethylenediamine)nickel molybdate at temper-atures between 550 and 700 degrees C. Successful formation of the Ni3Mo3N nitride is confirmed by X-ray diffraction. Ni3Mo3N samplesare found to be efficient catalysts for the hydrodeoxygenation of palmitic acid to C15/C16alkanes with a combined selectivity over 90and 100% palmitic acid conversion and higher activity than analogous Ni-Mo nitrides obtained by NH3nitridation of NiMoO4.Ni3Mo3N is found recyclable with only a slight decay in the catalytic activity upon consecutive reuses attributable to theneutralization of acid sites. The present results show an opportunity that bimetallic nitrides offer as robust advanced solid catalystsfor reactions of biomass conversion requiring harsh conditions.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据