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  • Energy absorbancy and freezing-temperature tunability of NaCl solutions during ice formation

    Author(s)
    Shen, Y
    Wei, X
    Wang, Y
    Shen, Y
    Li, L
    Huang, Y
    Ostrikov, KK
    Sun, CQ
    Griffith University Author(s)
    Ostrikov, Ken
    Year published
    2021
    Metadata
    Show full item record
    Abstract
    Freezing-thawing cycling of salt solutions is ubiquitously important to fields varying from biochemistry to agriculture, climate, and geological engineering. However, understanding the dynamics of energy exchange and freezing-temperature TN shift during phase transition of the concentrated solutions remains elusive despite intensive investigations since the discovery of Homeister series in 1888. Here we address this issue by focusing on the performance of the hydrogen bond (O:H–O) in the fraction fS molecules of the hydrating supersolid phase and in the remaining fraction fO molecules of the pristine phase during NaCl solution ...
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    Freezing-thawing cycling of salt solutions is ubiquitously important to fields varying from biochemistry to agriculture, climate, and geological engineering. However, understanding the dynamics of energy exchange and freezing-temperature TN shift during phase transition of the concentrated solutions remains elusive despite intensive investigations since the discovery of Homeister series in 1888. Here we address this issue by focusing on the performance of the hydrogen bond (O:H–O) in the fraction fS molecules of the hydrating supersolid phase and in the remaining fraction fO molecules of the pristine phase during NaCl solution ice formation. The supersolid formation is related to the effect of ionic polarization that shortens and stiffens the H–O bond, while lengthening and weakening the O:H non-bonding interactions in the hydration cells. The supersolid phase is gel-like, less dense, viscoelastic, and mechanically and thermally stable. We demonstrate that the polarization-weakening of the O:H non-bonding interactions of the supersolid phase reduces the TN of the solution and that the H–O cooling contraction in the quasisolid (QS) phase of the pristine water absorbs energy during the Liquid-QS-Ice transition of solution. At fS = 1, neither TN nor energy absorption is resolved within the range of 273 ± 20 K. The least saturation number of molecules is 10 per pair of Na+ and Cl− ions. These findings shall help to develop solutions with tunable TN for practical applications and to understand the mechanism of energy exchange during phase transition in the temperature and time domains.
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    Journal Title
    Journal of Molecular Liquids
    Volume
    344
    DOI
    https://doi.org/10.1016/j.molliq.2021.117928
    Subject
    Physical chemistry
    Publication URI
    http://hdl.handle.net/10072/410529
    Collection
    • Journal articles

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