Modifying the Hydrogenation Activity of Zeolite Beta for Enhancing the Yield and Selectivity for Fuel-Range Alkanes from Carbon Dioxide

被引:6
作者
Dokania, Abhay [1 ]
Ramirez, Adrian [1 ]
Shterk, Genrikh [1 ]
Cerrillo, Jose Luis [1 ]
Gascon, Jorge [1 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, KAUST Catalysis Ctr KCC, Thuwal 23955, Saudi Arabia
关键词
CO2; conversion; Fischer-Tropsch synthesis; heterogeneous catalysis; paraffins; zeolites; CATALYTIC-HYDROGENATION; DIRECT CONVERSION; LIGHT OLEFINS; CO2; AROMATICS; TRANSFORMATION; ISOPARAFFINS;
D O I
10.1002/cplu.202200177
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In order to empower a circular carbon economy for addressing global CO2 emissions, the production of carbon-neutral fuels is especially desired, since addressing the global fuel demand via this route has the potential to significantly mitigate carbon emissions. In this study, we report a multifunctional catalyst combination consisting of a potassium promoted iron catalyst (Fe-K) and platinum containing zeolite beta (Pt-beta) which produces an almost entirely paraffinic mixture (up to C-10 hydrocarbons) via CO2 hydrogenation in one step. Here, the Fe catalyst is responsible for modified Fischer-Tropsch synthesis from CO2 while Pt-beta is instrumental in tuning the product distribution almost entirely towards paraffins (both linear and branched) presumably via a combination of cracking and hydrogenation. The optimal temperature of operation was estimated to be 325 degrees C for the production of higher paraffins (C-5-C-10) with a selectivity of ca. 28 % at a CO2 conversion of ca. 31 %.
引用
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页数:6
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