NiAl2O4 as a beneficial precursor for Ni/Al2O3 catalysts for the dry reforming of methane

被引:0
|
作者
Kwon, Yongtak [1 ]
Eichler, J. Ehren [2 ]
Mullins, C. Buddie [1 ,2 ]
机构
[1] Univ Texas Austin, John J McKetta Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
关键词
Dry reforming of methane; Ni/Al2O3; catalyst; Nickel aluminate; CO2; utilization; X-RAY-DIFFRACTION; CARBON-DIOXIDE; SYNTHESIS GAS; COKING RESISTANCE; NI/GAMMA-AL2O3; CATALYSTS; PARTIAL OXIDATION; NICKEL; ALUMINA; TEMPERATURE; PERFORMANCE;
D O I
10.1016/j.jcou.2022.102112
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have studied the catalytic behavior of different Ni/Al2O3 catalysts for the dry reforming of methane which originate from different Ni metal sources: NiO and also non-stoichiometric and stoichiometric Ni/Al2O4. After complete reduction of the stoichiometric Ni/Al2O4 precursor at high temperatures, the resulting Ni/Al2O3 catalyst had more dispersed Ni particles of smaller size and with stronger interactions with alumina. Accordingly, this catalyst was more active and stable, developing only a moderate amount of carbon deposits which were less graphitized. On the other hand, the catalyst formed from NiO showed low initial activity and notable deactivation resulting from the encapsulation and separation of Ni metal particles from the support by more graphitic carbons, which was facilitated by the weaker metal-support interactions. In contrast to what is frequently reported, here we provide evidence which suggests that the Ni/Al2O4 species should be considered the most beneficial precursor for Ni metal in a Ni/Al2O3 catalyst for the dry reforming of methane even though a high reduction temperature (>950 degrees C) is needed to activate it.
引用
收藏
页数:10
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