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Enhancing catalytic activity and pore structure of metal-organic framework-808 via ligand competition for biodiesel production from microalgal lipids at reduced temperatures
被引:9
|作者:
Qian, Lei
[1
]
Cheng, Jun
[1
,2
]
Xin, Kai
[1
]
Guo, Hao
[1
]
Mao, Yuxiang
[1
]
Tu, Jiacan
[3
]
Yang, Weijuan
[1
]
机构:
[1] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Peoples R China
[2] Chongqing Univ, Key Lab Low grade Energy Utilizat Technol & Syst, Minist Educ, Chongqing 400044, Peoples R China
[3] Zhejiang Lanyou Energy Co Ltd, Zhoushan 316013, Peoples R China
关键词:
Metal -organic framework;
Heterogeneous catalyst;
Hierarchical pore;
FAME;
Microalgae;
DFT;
ZIRCONIA;
HYDROGEN;
UIO-66;
MOFS;
D O I:
10.1016/j.biortech.2023.129533
中图分类号:
S2 [农业工程];
学科分类号:
0828 ;
摘要:
Catalysts with hierarchical porous structures and increased active defects play a crucial role in catalyzing the conversion of microalgae lipids. However, the template methods used for pore expansion and the acidification process employed to enhance activity are cumbersome and prone to deactivation. It is necessary to propose a simple and versatile synthetic approach to overcome these challenges. By modulating N,N-dimethylformamide basicity with formic acid, MOF-808 exhibited enhanced coordination of benzene-1,3,5-tricarboxylic acid to Zrclusters, creating three types of functional defects. These defects increased pore size from 1.63 nm to 5.34 nm and enhanced catalyst acidity by 22.8%, while maintaining high porosity. The active catalytic sites were confirmed to be defect sites (exposed Zr4+) through density functional theory. Compared to regular MOF-808, catalyst MOF-808-3/1 shows enhanced hierarchical porosity and increased acidity, enabling efficient conversions at reduced reaction temperature (100 degrees C) and pressure (352 kPa) compared to 200 degrees C and 4036 kPa, respectively.
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页数:10
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