Molten‐Salt‐Mediated Chemical Looping Oxidative Dehydrogenation of Ethane with <i>In‐Situ</i> Carbon Capture and Utilization

The molten-salt-mediated oxidative dehydrogenation (MM-ODH) of ethane (C<sub>2</sub>H<sub>6</sub>) via a chemical looping scheme represents an effective carbon capture and utilization (CCU) method for the valorization of ethane-rich shale gas and concurrent mitigation of carbon dioxide (CO<sub>2</sub>) emissions. Here, stepwise experimentation with Li<sub>2</sub>CO<sub>3</sub>-Na<sub>2</sub>CO<sub>3</sub>-K<sub>2</sub>CO<sub>3</sub> (LNK) ternary salts (i) assessed how each component of the LNK mixture impacted ethane MM-ODH performance and (ii) explored physicochemical and thermodynamic mechanisms behind melt-induced changes to ethylene (C<sub>2</sub>H<sub>4</sub>) and carbon monoxide (CO) yields. Of fifteen screened LNK compositions, nine exhibited ethylene yields greater than 50 % at 800 °C while maintaining C<sub>2</sub>H<sub>4</sub> selectivities of 85 % or higher. LNK salts rich in Li<sub>2</sub>CO<sub>3</sub> content yielded more ethylene and CO on average than their counterparts, and net CO<sub>2</sub> capture per cycle reached a maximum of ~75 %. Extended MM-ODH cycling also demonstrated long-term stability of a high-performing LNK medium. Density functional theory (DFT) calculations and ab initio molecular dynamics (AIMD) simulations suggested that the molten salt does not directly activate C<sub>2</sub>H<sub>6</sub>. Meanwhile, an empirical model informed by experimental data and reaction thermodynamics adequately predicted overall MM-ODH performance from LNK composition and provided insights into the system's primary drivers.

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Publication Details

Journal
ChemSusChem
Published
2024-10-27
DOI
https://doi.org/10.1002/cssc.202401473
Citations
3
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
0.32

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article

Molten‐Salt‐Mediated Chemical Looping Oxidative Dehydrogenation of Ethane with In‐Situ Carbon Capture and Utilization

Dennis Chacko, M. Housley, Kyle Vogt‐Lowell, Kunran Yang et al.
3 citations
ChemSusChem
Catalysis and Oxidation Reactions
0.32
article

Molten‐Salt‐Mediated Chemical Looping Oxidative Dehydrogenation of Ethane with In‐Situ Carbon Capture and Utilization

Dennis Chacko, M. Housley, Kyle Vogt‐Lowell, Kunran Yang, Junchen Liu, Fanxing Li, Jace Carsten
article en
3 citations

Abstract

The molten-salt-mediated oxidative dehydrogenation (MM-ODH) of ethane (C<sub>2</sub>H<sub>6</sub>) via a chemical looping scheme represents an effective carbon capture and utilization (CCU) method for the valorization of ethane-rich shale gas and concurrent mitigation of carbon dioxide (CO<sub>2</sub>) emissions. Here, stepwise experimentation with Li<sub>2</sub>CO<sub>3</sub>-Na<sub>2</sub>CO<sub>3</sub>-K<sub>2</sub>CO<sub>3</sub> (LNK) ternary salts (i) assessed how each component of the LNK mixture impacted ethane MM-ODH performance and (ii) explored physicochemical and thermodynamic mechanisms behind melt-induced changes to ethylene (C<sub>2</sub>H<sub>4</sub>) and carbon monoxide (CO) yields. Of fifteen screened LNK compositions, nine exhibited ethylene yields greater than 50 % at 800 °C while maintaining C<sub>2</sub>H<sub>4</sub> selectivities of 85 % or higher. LNK salts rich in Li<sub>2</sub>CO<sub>3</sub> content yielded more ethylene and CO on average than their counterparts, and net CO<sub>2</sub> capture per cycle reached a maximum of ~75 %. Extended MM-ODH cycling also demonstrated long-term stability of a high-performing LNK medium. Density functional theory (DFT) calculations and ab initio molecular dynamics (AIMD) simulations suggested that the molten salt does not directly activate C<sub>2</sub>H<sub>6</sub>. Meanwhile, an empirical model informed by experimental data and reaction thermodynamics adequately predicted overall MM-ODH performance from LNK composition and provided insights into the system's primary drivers.

ChemSusChemVol. 18(6)
North Carolina State University (US), Newcastle University (GB)
U.S. Department of Energy, Office of Fossil Energy and Carbon Management
Openalex Percentile: Top 53%
Catalysis and Oxidation Reactions
0.32
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