Tandem Conversion of CO2 to Valuable Hydrocarbons in Highly Concentrated Potassium Iron Catalysts

The alarming atmospheric concentration and continuous emissions of carbon dioxide (CO2) require immediate action. As a result of advances in CO2 capture and sequestration technologies (generally involving point sources such as energy generation plants), large amounts of pure CO2 will soon be availab...

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Published inChemCatChem Vol. 11; no. 12; pp. 2879 - 2886
Main Authors Ramirez, Adrian, Ould‐Chikh, Samy, Gevers, Lieven, Chowdhury, Abhishek Dutta, Abou‐Hamad, Edy, Aguilar‐Tapia, Antonio, Hazemann, Jean‐Louis, Wehbe, Nimer, Al Abdulghani, Abdullah J., Kozlov, Sergey M., Cavallo, Luigi, Gascon, Jorge
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 19.06.2019
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Abstract The alarming atmospheric concentration and continuous emissions of carbon dioxide (CO2) require immediate action. As a result of advances in CO2 capture and sequestration technologies (generally involving point sources such as energy generation plants), large amounts of pure CO2 will soon be available. In addition to geological storage and other applications of the captured CO2, the development of technologies able to convert this carbon feedstock into commodity chemicals may pave the way towards a more sustainable economy. Here, we present a novel multifunctional catalyst consisting of Fe2O3 encapsulated in K2CO3 that can transform CO2 into olefins via a tandem mechanism. In contrast to traditional systems in Fischer‐Tropsch reactions, we demonstrate that when dealing with CO2 conversion (in contrast to CO), very high K loadings are key to activate CO2 via the well‐known ‘potassium carbonate mechanism’. The proposed catalytic process is demonstrated to be as productive as existing commercial processes based on synthesis gas while relying on economically and environmentally advantageous CO2 feedstock. Potassium carbonate‐iron catalyst for tandem conversion of CO2: The potassium carbonate activates the CO2 while undergoing several transformation, yielding KOOCH and releasing CO. This CO is subsequently hydrogenated to olefins on the iron nanoparticles via Fisher‐Tropsch.
AbstractList The alarming atmospheric concentration and continuous emissions of carbon dioxide (CO2) require immediate action. As a result of advances in CO2 capture and sequestration technologies (generally involving point sources such as energy generation plants), large amounts of pure CO2 will soon be available. In addition to geological storage and other applications of the captured CO2, the development of technologies able to convert this carbon feedstock into commodity chemicals may pave the way towards a more sustainable economy. Here, we present a novel multifunctional catalyst consisting of Fe2O3 encapsulated in K2CO3 that can transform CO2 into olefins via a tandem mechanism. In contrast to traditional systems in Fischer‐Tropsch reactions, we demonstrate that when dealing with CO2 conversion (in contrast to CO), very high K loadings are key to activate CO2 via the well‐known ‘potassium carbonate mechanism’. The proposed catalytic process is demonstrated to be as productive as existing commercial processes based on synthesis gas while relying on economically and environmentally advantageous CO2 feedstock.
The alarming atmospheric concentration and continuous emissions of carbon dioxide (CO2) require immediate action. As a result of advances in CO2 capture and sequestration technologies (generally involving point sources such as energy generation plants), large amounts of pure CO2 will soon be available. In addition to geological storage and other applications of the captured CO2, the development of technologies able to convert this carbon feedstock into commodity chemicals may pave the way towards a more sustainable economy. Here, we present a novel multifunctional catalyst consisting of Fe2O3 encapsulated in K2CO3 that can transform CO2 into olefins via a tandem mechanism. In contrast to traditional systems in Fischer‐Tropsch reactions, we demonstrate that when dealing with CO2 conversion (in contrast to CO), very high K loadings are key to activate CO2 via the well‐known ‘potassium carbonate mechanism’. The proposed catalytic process is demonstrated to be as productive as existing commercial processes based on synthesis gas while relying on economically and environmentally advantageous CO2 feedstock. Potassium carbonate‐iron catalyst for tandem conversion of CO2: The potassium carbonate activates the CO2 while undergoing several transformation, yielding KOOCH and releasing CO. This CO is subsequently hydrogenated to olefins on the iron nanoparticles via Fisher‐Tropsch.
Author Chowdhury, Abhishek Dutta
Al Abdulghani, Abdullah J.
Hazemann, Jean‐Louis
Cavallo, Luigi
Ramirez, Adrian
Ould‐Chikh, Samy
Gascon, Jorge
Aguilar‐Tapia, Antonio
Abou‐Hamad, Edy
Wehbe, Nimer
Gevers, Lieven
Kozlov, Sergey M.
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Snippet The alarming atmospheric concentration and continuous emissions of carbon dioxide (CO2) require immediate action. As a result of advances in CO2 capture and...
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SubjectTerms Alkenes
Carbon dioxide
Carbon sequestration
Cascade chemical reactions
Catalysis
Catalysts
CO2 conversion
Conversion
Economics
Fisher-Tropsch
Hydrogenation
Olefins
Organic chemistry
Point sources
Potassium
Potassium carbonate
Raw materials
Synthesis gas
Title Tandem Conversion of CO2 to Valuable Hydrocarbons in Highly Concentrated Potassium Iron Catalysts
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcctc.201900762
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