Paving the way to transfer hydrogenation of CO2 with bio-derived glycerol over Ni supported zeolite catalysts

被引:0
|
作者
Rouse, Nicola [1 ]
Martin, Claudia Fernandez [1 ]
McCue, Alan J. [2 ]
Graca, Ines [1 ]
机构
[1] Univ Aberdeen, Sch Engn, Chem Proc & Mat Grp, Aberdeen AB24 3UE, Scotland
[2] Univ Aberdeen, Adv Ctr Energy & Sustainabil ACES, Sch Nat & Comp Sci, Dept Chem, Aberdeen AB24 3UE, Scotland
关键词
CO 2 transfer hydrogenation; Glycerol dehydrogenation; H; -donors; Formic acid; Lactic acid; Zeolites; CARBON-DIOXIDE CAPTURE; OF-THE-ART; LACTIC-ACID; NICKEL-CATALYSTS; PHASE HYDROGENOLYSIS; RENEWABLE HYDROGEN; ENHANCED ACTIVITY; BASE-FREE; CONVERSION; 1,2-PROPANEDIOL;
D O I
10.1016/j.apcata.2024.119971
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
The CO2 transfer hydrogenation with bio-glycerol over a Ni-zeolite was systematically studied to produce formic and lactic acids. The alkaline hydrothermal reactions without a catalyst and with Ni-zeolite heterogeneous catalyst were explored, focusing on the effects of base types and concentrations, reaction atmosphere and temperature. In alkaline hydrothermal reactions without catalyst, NaOH demonstrated superior performance at 1 M. A Ni/NaZSM-5 catalyst showed astounding performance giving 9.3 mol-L-1-g(-1) lactic acid and 6.5 mol-L-1-g(-1) formic acid at 250 degrees C after 2 h. Notably, the zeolite showed resistance to the highly basic conditions of the reaction medium. For the first time, CO2 conversion in aqueous phase was reported addressing the complexity of CO2 solubility. A reaction network was proposed including the diverse glycerol transformations not yet studied for this system. Overall, this study sheds light on the understanding of this complex reaction system and the potential of Ni-supported zeolites for sustainable CO2 utilisation.
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页数:19
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