期刊
RSC ADVANCES
卷 8, 期 20, 页码 10907-10913出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ra00584b
关键词
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资金
- National Natural Science Foundation of China [21266023]
- National First-rate Discipline Construction Project of Ningxia [NXYLXK2017A04]
- Chunhui Project of Ministry of Education of China
In this work, a mesoporous silica microsphere (MSM) was selected as a support to prepare a bimetallic supported catalyst (15% W-5% Ni/MSM) by a co-impregnation method that was simple and easy to conduct. We wished to improve the capability of catalytic conversion of biomass into ethylene glycol (EG) and 1,2-propylene glycol (1,2-PG). 15% W-5% Ni/MSM was examined on microcrystalline cellulose (cellulose) and corn stalks in a one-pot catalytic process, and total yields of EG and 1,2-PG reached up to 82.40 wt% and 62.60 wt%, respectively. This remarkable catalytic performance of W-Ni/MSM catalyst could be attributed to the synergistic effect between the active sites of Ni and W and the unique structure of MSM, which was suitable for mass transfer and metal loading. Based on physicochemical characterizations, the metal component was well-distributed on the surface of the MSM, and the metallic Ni, W and WO3 of the fresh catalyst were converted mainly into NiWO4 during the catalytic conversion of cellulose. To shed light on the reaction mechanism of the catalyzed hydrogenation of biomass, a possible process involving the formation of HxWO3 homogeneous catalysts, cellulose hydrolysis, C-C cleavage and hydrogenation conversion to 1,2-PG and EG was illustrated. Furthermore, the reusability of W-Ni/MSM catalyst was tested and we explored the cause of decreased diols yields. In summary, this work provides important guidance to rationally design effective catalysts for biomass conversion.
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