Role of Na in the stability enhancement of CeO2 catalysts for ketonization of propionic acid

被引:2
作者
Liu, Zihao [1 ]
Guo, Yonghua [1 ,2 ]
Wang, Hua [1 ]
Zhu, Xinli [1 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Collaborat Innovat Ctr Chem Sci & Engn, Key Lab Green Chem Technol,Minist Educ, Tianjin 300072, Peoples R China
[2] China Oilfield Serv Ltd, COSL Prod Optimizat, Tianjin 300452, Peoples R China
[3] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
CeO2; Sodium doping; Propionic acid; Ketonization; Acid-base pair; Biomass conversion; CARBOXYLIC-ACIDS; ACETIC-ACID; CERIA; OXIDATION; BIOMASS; OXIDE; CO; CONVERSION; KETONES; FUELS;
D O I
10.1016/j.apcata.2024.119593
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
A series of CeO2 catalysts with varying Na content were tested for vapor-phase ketonization of propionic acid at 350 degrees C. Na+ diffuses into the CeO2 lattice and excess NaOx accumulates on the surface, which dilutes surface contiguous and partially covers Ce -O acid-base pairs. The intrinsic reaction rate in terms of surface area always decreased with increasing Na, likely originated from the altered acid-base property and the increased distance and steric hindrance between enolate and carboxylate for C -C coupling. On the other hand, the stability was significantly improved, with almost no deactivation being observed for Na0.1Ce0.9Ox. This improvement is resulted from the dilution and/or coverage effects of NaOx, which significantly reduces accumulation of inactive bidentate propionate. This work demonstrates a strategy of dilution and/or coverage of surface acid-base pairs by alkaline metal oxides to reduce bidentate carboxylate and therefore to enhance the stability of metal oxide catalysts toward ketonization of carboxylic acids.
引用
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页数:12
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