Decomposition of glucose with in situ deoxygenation in a low H2 pressure environment - Pt. II: Bimetallic catalysts

被引:2
|
作者
Rogers, Kyle A. [1 ]
Zheng, Ying [1 ,2 ]
机构
[1] Univ New Brunswick, Dept Chem Engn, 15 Dineen Dr, Fredericton, NB E3B 5A3, Canada
[2] Western Univ, Dept Chem & Biochem Engn, 1150 Richmond St, London, ON N6A 3K7, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
Deoxygenation; Water-gas-shift; Glucose; Decomposition; Bimetallic catalysts; GAS SHIFT REACTION; BIO-OIL; PHASE HYDRODEOXYGENATION; HYDROGEN-PRODUCTION; BIOMASS; PYROLYSIS; CELLULOSE; NI; FE; PD;
D O I
10.1016/j.apcata.2019.03.013
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bimetallic catalysts, CoFe, NiFe, PdFe, and PtCo were studied for their ability to perform in situ deoxygenation of glucose decomposition production at 350 degrees C. Catalysts were prepared via co-impregnation and sequential impregnation methods on SiO2 in combinations of 4 wt% and 0.5 wt% for the two metals. Easily identifiable furanic compounds in the products were used to establish an understanding of deoxygenation activity. Co-impregnated 0.5%Co4%Fe/SiO2 and sequentially impregnated (Fe first) 0.5%Ni4%Fe/SiO2 catalysts provided the most favourable results. Thanks to the alloying of Co and Fe which stabilized Fe, the 0.5%Co4%Fe/SiO2 catalyst eliminated furfural content and maintained a higher output of H-2. The 0.5%Ni4%Fe/SiO2 catalyst required the Ni and Fe phases to remain uninterrupted to perform their synergistic roles which boosted DMF content and overall reduced solid residue.
引用
收藏
页码:10 / 19
页数:10
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