4.8 Article

Ionic liquid enables highly efficient low temperature desalination by directional solvent extraction

期刊

NATURE COMMUNICATIONS
卷 12, 期 1, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41467-020-20706-y

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资金

  1. National Science Foundation [1510826, CHE 1665440, 1956170, CBET 2031431]
  2. Sustainable Energy Initiative (SEI) part of the Center for Sustainable Energy at Notre Dame (ND Energy)
  3. Center for Research Computing at the University of Notre Dame
  4. NSF through XSEDE [TG-CTS100078]
  5. Direct For Mathematical & Physical Scien
  6. Division Of Chemistry [1956170] Funding Source: National Science Foundation
  7. Directorate For Engineering
  8. Div Of Chem, Bioeng, Env, & Transp Sys [1510826] Funding Source: National Science Foundation

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Seawater desalination is critical in addressing the global water scarcity challenge. A new non-membrane desalination technology called Directional Solvent Extraction (DSE) can utilize low temperature waste heat and achieve higher desalination rates by using ionic liquids as directional solvents. This research demonstrates the potential for significantly advancing DSE technology as a solution to the challenges in the global water-energy nexus.
Seawater desalination plays a critical role in addressing the global water shortage challenge. Directional Solvent Extraction (DSE) is an emerging non-membrane desalination technology that features the ability to utilize very low temperature waste heat (as low as 40 degrees C). This is enabled by the subtly balanced solubility properties of directional solvents, which do not dissolve in water but can dissolve water and reject salt ions. However, the low water yield of the state-of-the-art directional solvent (decanoic acid) significantly limits its throughput and energy efficiency. In this paper, we demonstrate that by using ionic liquid as a new directional solvent, saline water can be desalinated with much higher production rate and thus significantly lower the energy and exergy consumptions. The ionic liquid identified suitable for DSE is [emim][Tf2N], which has a much (similar to 10x) higher water yield than the currently used decanoic acid. Using molecular dynamics simulations with Gibbs free energy calculations, we reveal that water dissolving in [emim][Tf2N] is energetically favorable, but it takes significant energy for [emim][Tf2N] ions to dissolve in water. Our findings may significantly advance the DSE technology as a solution to the challenges in the global water-energy nexus.

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