High catalytic performance of CuCe/Ti for CO oxidation and the role of TiO2

被引:5
作者
Chang, Tingting [1 ]
Wang, Ziyan [2 ]
Wang, Zhimiao [1 ,3 ]
An, Hualiang [1 ,3 ]
Li, Fang [1 ,3 ]
Xue, Wei [1 ,3 ]
Wang, Yanji [1 ,3 ,4 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Hebei Prov Key Lab Green Chem Technol & High Effic, Tianjin 300130, Peoples R China
[2] CSIC, Purificat Equipment Res Inst, Handan 056027, Peoples R China
[3] Tianjin Key Lab Chem Proc Safety, Tianjin 300130, Peoples R China
[4] Hebei Ind Technol Res Inst Green Chem Ind, Hebei 061100, Peoples R China
来源
CHINESE JOURNAL OF CHEMICAL ENGINEERING | 2023年 / 62卷
基金
中国国家自然科学基金;
关键词
CO oxidation; TiO2 crystal phase; CuCe/Ti; Reaction mechanism; PREFERENTIAL OXIDATION; CUO-CEO2; CATALYSTS; OXYGEN VACANCIES; CERIA; TEMPERATURE; REDUCTION; PT/CEO2; OXIDE; CUO; AU/TIO2;
D O I
10.1016/j.cjche.2023.08.004
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
CuCe/Ti-A and CuCe/Ti-R catalysts were prepared using anatase TiO2 (TiO2-A) and rutile TiO2 (TiO2-R) as supports using the incipient wetness impregnation method for the carbon monoxide (CO) oxidation reaction and were compared with a CuCe-C catalyst prepared using the co-precipitation method. The CuCe/ Ti-A catalyst exhibited the highest activity, with complete CO conversion at 90 degrees C, when the gas hourly space velocity was 24000 ml center dot g(-1)center dot h(-1) and the CO concentration was approximately 1% (vol). A series of characterizations of the catalysts revealed that the CuCe/Ti-A catalyst has a larger specific surface area, more Cu+ species and oxygen vacancies, and the Cu species of CuCe/Ti-A catalyst is more readily reduced. In situ FT-IR results indicate that the bicarbonate species generated on the CuCe/Ti-A catalyst have lower thermal stability than the carbonate species on CuCe/Ti-R, and will decompose more readily to form CO2. Therefore, CuCe/Ti-A has excellent catalytic activity for CO oxidation. (c) 2023 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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