Interface catalysis over AlPO4/Al2O3 with F-Al-O species for resource utilization of hydrofluorocarbon greenhouse gas

被引:0
|
作者
Sun, Yiwei [1 ]
Wei, Xiaoli [1 ]
Liu, Fangcao [1 ]
Liu, Bing [1 ]
Zhao, Jiaming [1 ]
Bi, Yubao [1 ]
Han, Wenfeng [1 ]
机构
[1] Zhejiang Univ Technol, Inst Ind Catalysis, State Key Lab Breeding Base Green Chem Synth Techn, Hangzhou 310014, Zhejiang, Peoples R China
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2025年 / 13卷 / 02期
基金
中国国家自然科学基金;
关键词
Hydrofluorocarbons (HFCs); Dehydrofluorination; Interface; F-Al-O; OXYGEN VACANCIES; DEHYDROFLUORINATION; TEMPERATURE; PERFORMANCE; PHOSPHORUS; STABILITY; OXIDATION; FLUORIDE; CF3I;
D O I
10.1016/j.jece.2025.115929
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Developing effective techniques to produce and stabilize highly active metastable F-Al-O species in HFCs dehydrofluorination system without being over-fluorinated to Al-F is a major challenge. Herein, we report a new strategy for the formation and stabilization of metastable species. Using NaH2PO4 as a P source, phosphoric acid groups are modified to the surface of Al2O3 leading to the fabrication of AlPO4/Al2O3 interface. P and Al2O3 bond to form Al-O-P structure at the interface and stabilize F-Al-O in the dehydrofluorination system. Further studies show that AlPO4/Al2O3 interface increase the oxygen vacancy content of catalyst and accelerate the conversion of HFC-152a on the catalyst surface. Meanwhile, AlPO4/Al2O3 interface improves the surface acidity of Al2O3, endue a large number of Lewis weak acid sites, reducing the carbon accumulation of catalyst, and improving the stability of catalyst. The activity test showed that AlPO4/Al2O3 interface shows high catalytic performance (74.2 %) and excellent stability (50 h) for 1,1-difluoroethane dehydrogenation compared with Al2O3 (30 % and low stability) without P modification.
引用
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页数:11
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