The molten-salt-mediated oxidative dehydrogenation (MM-ODH) of ethane (CH) 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) emissions. Here, stepwise experimentation with LiCO-NaCO-KCO (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 (CH) and carbon monoxide (CO) yields. Of fifteen screened LNK compositions, nine exhibited ethylene yields greater than 50 % at 800 °C while maintaining CH selectivities of 85 % or higher. LNK salts rich in LiCO content yielded more ethylene and CO on average than their counterparts, and net CO 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 CH. 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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http://dx.doi.org/10.1002/cssc.202401473 | DOI Listing |
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