CO2 hydrogenation to methane over Ni/ZrO2 and Ni/CeO2 catalysts: experimental and DFT studies

被引:3
|
作者
Li, Dan [1 ,3 ]
Ding, Xin [1 ,3 ]
Liu, Xu [1 ,3 ]
Cheng, Jiahui [1 ,3 ]
Jiang, Zhao [2 ,3 ]
Guo, Yang [1 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Energy & Power Engn, Key Lab Thermo Fluid Sci & Engn, Minist Educ, Xian 710049, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Xian 710049, Shaanxi, Peoples R China
[3] Sichuan Digital Econ Ind Dev Res Inst, Chengdu 610036, Sichuan, Peoples R China
关键词
NI-BASED CATALYSTS; ENHANCED ACTIVITY; SUPPORTED NI; TEMPERATURE; ADSORPTION; ENERGY; ZRO2; NANOPARTICLES; NANOCRYSTALS; COMBUSTION;
D O I
10.1007/s10853-023-08814-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this paper, performance of ZrO2 and CeO2 supported Ni catalysts on CO2 hydrogenation reaction was investigated in continuous flow reactor. The results revealed that Ni/ZrO2 catalyst exhibited superior performance compared to Ni/CeO2, with a CO2 conversion rate of 71.84%, a CH4 formation rate of 21.03 mmol g(-1) h(-1), and excellent reaction stability at 400 & DEG;C. And the activation energy of Ni/ZrO2 was lower than that of Ni/CeO2. N-2 adsorption-desorption, SEM, XRD, XPS, CO2-TPD and O-2-TPO analysis results suggest that Ni/ZrO2 is a multi-stage pore material, which has slit holes formed by the accumulation of sheet-like particles, as well as a superior dispersion of Ni on ZrO2. Moreover, Ni/ZrO2 shows higher alkalinity and remarkable resistance to carbon accumulation. DFT calculations demonstrated that CO2 can be more easily adsorbed on ZrO2 surface, and one O-terminus of CO2 is closer to top sites of ZrO2, which is favorable for electron transfer and promotes the activation of CO2.
引用
收藏
页码:12584 / 12595
页数:12
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