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Acetophenone hydrogenation and consecutive hydrogenolysis with Pd/CNT catalysts: Highlighting the synergy between single atoms and nanoparticles by kinetic modeling
被引:4
作者:
Bernardin, Vincent
[1
]
Vanoye, Laurent
[1
]
Rivera-Careamo, Camila
[2
]
Serp, Philippe
[2
]
Favre-Reguillon, Alain
[1
,3
]
Philippe, Regis
[1
]
机构:
[1] Univ Lyon, Catalyse Polymerisat Procedes & Mat CP2M, CNRS, CPE Lyon,UCBL,UMR 5128, 43 Blvd 11 Novembre 1918, F-69100 Villeurbanne, France
[2] Univ Toulouse, ENSIACET, CNRS, LCC,UPR 8241, F-31030 Toulouse, France
[3] Conservatoire Natl Arts & Metiers, Dept Chim Vivant Sante, 292 Rue St Martin, F-75003 Paris, France
来源:
关键词:
Palladium single atom catalyst;
Palladium nanoparticles;
Carbon nanotubes;
Acetophenone;
Kinetic modeling;
Hydrogen;
SELECTIVE HYDROGENATION;
ALUMINA CATALYSTS;
DISPERSION;
ACIDITY;
SIZE;
D O I:
10.1016/j.cattod.2023.114196
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Understanding the cooperative action of palladium nanoparticles (NPs) and palladium single atoms (SAs) supported on Nis essential for developing more efficient supported transition metal catalysts. In this work, the comparison of a series of Pd-catalysts on CNTs having the same palladium loading (similar to 1.4 wt%) but involving different and controlled SA/NP ratios (between 2 and 200) is described. The hydrogenation of acetophenone into 1-phenylethanol and its consecutive hydrogenolysis to ethylbenzene are the chosen test reactions. Appropriate kinetic modeling of these two consecutive reactions was performed and allowed a quantitative assessment of the activity differences between catalysts as well as the demonstration of a synergy between the two palladium species (SAs and NPs). The maximum activity was clearly dependent on the distribution of the surface palladium between SAs and NPs, and interestingly, different optima for the two reactions are evidenced. This work may offer a new perspective for the design and synthesis of supported transition metal catalysts with targeted catalytic performance.
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页数:9
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