Abstract
Solute ionic electrification of the O:H–O bond modulates significantly the critical pressures, temperatures, and gelation times for transiting aqueous solution into solid by dispersing the boundaries of the quasisolid phase. High-pressure in situ Raman spectrometrics revealed that transiting NaX solutions into ice VI and then into ice VII phase requires higher excessive pressures at 298 K temperature. The ΔPC varies in the order of Hofmeister series: X = I > Br > Cl > F ~ 0. Meanwhile, salting stiffens the ωH and elongates the dOO throughout the course of compressure when transiting phase VII to phase X at even higher pressure. Recovering the electrification-shortened H–O bond needs excessive energy for the same sequence of phase transitions. Concentration dependence of the NaI solution indicates a different mechanism from that of solution type but it is similar to heating on the Liquid-VI-VII phase transition dynamics.
• Solvent O:H–O phonon relaxation by electrification mediates the T C for phase transition by dispersing the quasisolid phase boundaries.
• The ΔE L loss depresses the T N for ice/quasisolid transition; the ΔE H gain elevates the T m for liquid/quasisolid transition.
• Liquid/VI, VI/VII, and VII/XI phase transition at constant T C requires excessive ΔP C to recover the electrification-deformed H–O bond; mechanical impulsion raises but ionic electrification depresses the freezing temperature of the quasisolid (supercooled) water by modifying the O:H energy.
• Colloidal gelation at constant T C and P C takes time that follows the Hofmeister series but the concentration dependence is less conclusive because of the involvement of other kinds of ions.
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References
C.Q. Sun, Hofmeister pressures for liquid/VI and VI/VII phase transition. Communicated
Q. Zeng, Y. Zhou, W. Kai, B. Zou, C.Q. Sun, NaI concentration resolved critical pressures for the solution-ice VI-ice VII transition at room temperature. Communicated (2015)
J. Niehaus, W. Cantrell, Contact freezing of water by salts. J. Phys. Chem. Lett. (2015)
M. van der Linden, B.O. Conchúir, E. Spigone, A. Niranjan, A. Zaccone, P. Cicuta, Microscopic origin of the Hofmeister effect in gelation kinetics of colloidal silica. J. Phys. Chem. Lett. 2881–2887 (2015)
Q. Zeng, Y. Zhou, W. Kai, B. Zou, C.Q. Sun, Room temperature icing of NaX solution by compression (X = F, Cl, Br, I). Communicated (2015)
C.Q. Sun, X. Zhang, W.T. Zheng, Hidden force opposing ice compression. Chem. Sci. 3, 1455–1460 (2012)
Q. Zeng, Y. Zhou, W. Kai, B. Zou, C.Q. Sun, Solution room temperature phase precipitation under compression. Communicated (2015)
X. Zhang, P. Sun, Y. Huang, T. Yan, Z. Ma, X. Liu, B. Zou, J. Zhou, W. Zheng, C.Q. Sun, Water’s phase diagram: from the notion of thermodynamics to hydrogen-bond cooperativity. Prog. Solid State Chem. 43, 71–81 (2015)
Y. Zhou, Y. Huang, Y. Gong, C.Q. Sun, Skin preferential occupancy of the I− anion in NaI-water solution. Communicated (2016)
N.R. Gokhale, J.D. Spengler, Freezing of freely suspended, supercooled water drops by contact nucleation. J. Appl. Meteorol. 11(1), 157–160 (1972)
W.A. Cooper, A possible mechanism for contact nucleation. J. Atmos. Sci. 31(7), 1832–1837 (1974)
N. Fukuta, A study of the mechanism of contact ice nucleation. J. Atmos. Sci. 32(8), 1597–1603 (1975)
C. Gurganus, A.B. Kostinski, R.A. Shaw, Fast imaging of freezing drops: no preference for nucleation at the contact line. J. Phys. Chem. Lett. 2(12), 1449–1454 (2011)
R.A. Shaw, A.J. Durant, Y. Mi, Heterogeneous surface crystallization observed in undercooled water. J. Phys. Chem. B 109(20), 9865–9868 (2005)
R.G. Knollenberg, A laboratory study of the local cooling resulting from the dissolution of soluble ice nuclei having endothermic heats of solution. J. Atmos. Sci. 26(1), 115–124 (1969)
X. Zhang, T. Yan, Y. Huang, Z. Ma, X. Liu, B. Zou, C.Q. Sun, Mediating relaxation and polarization of hydrogen-bonds in water by NaCl salting and heating. PCCP 16(45), 24666–24671 (2014)
Y. Xu, L. Li, P. Zheng, Y.C. Lam, X. Hu, Controllable gelation of methylcellulose by a salt mixture. Langmuir 20(15), 6134–6138 (2004)
Y. Xu, C. Wang, K. Tam, L. Li, Salt-assisted and salt-suppressed sol-gel transitions of methylcellulose in water. Langmuir 20(3), 646–652 (2004)
L.E. Bove, R. Gaal, Z. Raza, A.-A. Ludl, S. Klotz, A.M. Saitta, A.F. Goncharov, P. Gillet, Effect of salt on the H-bond symmetrization in ice. Proceedings of the National Academy of Sciences 112(27), 8216–8220 (2015)
Y. Bronstein, P. Depondt, L.E. Bove, R. Gaal, A.M. Saitta, F. Finocchi, Quantum versus classical protons in pure and salty ice under pressure. Phys. Rev. B 93(2), 024104 (2016)
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Sun, C.Q., Sun, Y. (2016). Aqueous Solution Phase Transition. In: The Attribute of Water. Springer Series in Chemical Physics, vol 113. Springer, Singapore. https://doi.org/10.1007/978-981-10-0180-2_14
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DOI: https://doi.org/10.1007/978-981-10-0180-2_14
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