共 50 条
Expanding nonpolar pore surfaces in stable ethane-selective MOF to boost ethane/ethylene separation performance
被引:13
|作者:
Han, Yuejiang
[1
]
Meng, Lingyi
[3
,4
,5
]
Liu, Yongyao
[2
]
Li, Hengbo
[2
]
Ji, Zhenyu
[2
]
Zhou, Yunzhe
[2
]
Wu, Mingyan
[2
]
Han, Zhengbo
[1
]
机构:
[1] Liaoning Univ, Coll Chem, Shenyang 110036, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[3] Chinese Acad Sci, CAS Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[4] Chinese Acad Sci, Fujian Inst Res Struct Matter, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
[5] Chinese Acad Sci, Xiamen Inst Rare Earth Mat, Haixi Inst, Xiamen Key Lab Rare Earth Photoelect Funct Mat, Xiamen 361021, Peoples R China
关键词:
Metal -organic framework;
Non -polar pore surfaces;
C;
2;
H;
6;
4;
separation;
6-selective;
METAL-ORGANIC FRAMEWORKS;
ADSORPTION;
ETHYLENE;
PROPYLENE;
PROPANE;
BEHAVIOR;
D O I:
10.1016/j.seppur.2023.123642
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Ethylene is an important raw material in chemical production. Reducing energy consumption by one-step sep-aration of ethylene from C2H6/C2H4 mixtures is a significant and challenging task. Designing a material with high C2H6 selectivity and adsorption capacity is very demanding. Here, we report a method to improve the performance of C2H6/C2H4 separation. By changing the carboxylic ligand in UiO-67, we synthesized a new material called UiO-67-BN. At room temperature, compared with the base material UiO-67, the optimized ma-terial UiO-67-BN has a significant increase in the adsorption capacity of C2H6 and the selectivity of C2H6/C2H4 due to its suitable pore size and numerous non-polar aromatic rings on the pore surface. Theoretical calculation results reveal that the optimized material can provide more C-Heee pi interactions with C2H6. The breakthrough experiments demonstrate that UiO-67-BN can efficiently capture C2H6 from 50/50 and 1/99 C2H6/C2H4 mixtures at various conditions and realize one-step acquisition of C2H4.
引用
收藏
页数:7
相关论文