共 50 条
A facial strategy to synthesize Pd/Co3O4 nanosheets with enhanced performance for methane catalytic oxidation
被引:27
|作者:
Yang, Nating
[1
,2
]
Ni, Shenglin
[1
]
Sun, Yuhan
[1
]
Zhu, Yan
[1
,3
]
机构:
[1] Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engneering, Nanjing 210093, Jiangsu, Peoples R China
来源:
MOLECULAR CATALYSIS
|
2018年
/
452卷
关键词:
Thermal-stability;
Palladium based catalyst;
Metal-support interaction;
Catalytic oxidation;
LOW-TEMPERATURE;
PD CATALYSTS;
SURFACE-CHEMISTRY;
COMBUSTION;
CO3O4;
WATER;
PD/GAMMA-AL2O3;
DEACTIVATION;
SUPPORT;
AL2O3;
D O I:
10.1016/j.mcat.2018.03.016
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:
Pd-based catalysts that prepared by traditional impregnation or co-precipitate method show remarkable activity for catalytic oxidation of hydrocarbon, unfortunately they tend to deactivate in the long-term reaction process or at high temperature by sintering and transformation of active species. We now report a facile strategy to synthesize Pd/Co3O4 with superior catalytic durability for the methane catalytic oxidation. In this method, Pd ions coordinate with -CoOCH2COOH that derived from Co precursor and form the Pd-Co precursor complex at first, this complex was further calcined into Pd/Co3O4 catalysts with strong interaction between Pd and cobalt oxide. Methane catalytic oxidation experiment demonstrated that such Pd-based catalyst possesses intrinsically enhanced catalytic activity and exhibits a high resistance toward deactivate in the harsh reaction condition, in sharp contrast to the conventional catalysts prepared via impregnation or deposition-precipitation routes. TEM, XPS, O-2-TPO, and isotopic experiments further indicate that the Pd/Co3O4 could form stronger interaction between PdO and Co3O4 and produce more actives species during long-term reaction.
引用
收藏
页码:28 / 35
页数:8
相关论文