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Liquid phase hydrogenation of CO2 to formate using palladium and ruthenium nanoparticles supported on molybdenum carbide
被引:22
|作者:
Mitchell, Claire E.
[1
]
Terranova, Umberto
[1
]
Alshibane, Ihfaf
[2
]
Morgan, David J.
[1
]
Davies, Thomas E.
[1
]
He, Qian
[1
]
Hargreaves, Justin S. J.
[2
]
Sankar, Meenakshisundaram
[1
]
de Leeuw, Nora H.
[1
]
机构:
[1] Cardiff Univ, Sch Chem, Cardiff Catalysis Inst, Cardiff CF10 4AT, S Glam, Wales
[2] Glasgow Univ, Sch Chem, Glasgow G12 8QQ, Lanark, Scotland
基金:
英国工程与自然科学研究理事会;
关键词:
CARBON-DIOXIDE HYDROGENATION;
FORMIC-ACID;
MOLECULAR-HYDROGEN;
CATALYTIC-HYDROGENATION;
BIMETALLIC CATALYSTS;
METHANOL SYNTHESIS;
ROOM-TEMPERATURE;
WATER;
ENERGY;
ADSORPTION;
D O I:
10.1039/c9nj02114k
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
We report the development of palladium nanoparticles supported on Mo2C as an active catalyst for the liquid-phase hydrogenation of CO2 to formate under mild reaction conditions (100 degrees C and 2.0 MPa of a 1 : 1 CO2 : H-2 mixture). A series of Pd/Mo2C catalysts were synthesised via the modified wet-impregnation (MIm) and sol-immobilization (SIm) techniques and evaluated for CO2 hydrogenation, in an aqueous 1 M NaOH solution. MIm catalysts synthesised using PdCl2 dissolved in a 2 M HCl solution gave the highest formate yield with turnover numbers of up to 109 after 19 h. We further report the crucial role of base and the pH of the reaction medium for the hydrogenation of CO2 to formate. Based on stability studies, electron microscopic characterisation and density functional theory calculations we found that Ru has a stronger affinity than Pd to Mo2C resulting in the development of a stable bimetallic RuPd/Mo2C catalyst for the hydrogenation of CO2 to formate.
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页码:13985 / 13997
页数:13
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