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Compressibility of Lithium Hexafluorophosphate Solutions in Two Carbonate Solvents.
Wang, Andrew A; Persa, Delia; Helin, Sara; Smith, Kirk P; Raymond, Jason L; Monroe, Charles W.
Afiliação
  • Wang AA; Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.
  • Persa D; The Faraday Institution, Becquerel Avenue, Harwell Campus, Didcot OX11 0RA, U.K.
  • Helin S; Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.
  • Smith KP; Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.
  • Raymond JL; Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.
  • Monroe CW; Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, U.K.
J Chem Eng Data ; 68(4): 805-812, 2023 Apr 13.
Article em En | MEDLINE | ID: mdl-37084176
Speed-of-sound measurements are performed to establish how the isentropic bulk modulus K s of the electrolyte system comprising lithium hexafluorophospate (LiPF6) in blends of propylene carbonate (PC) and ethyl methyl carbonate (EMC) varies with salt molality m, mass fraction of PC in the PC:EMC cosolvent f, and temperature T. Bulk moduli are calculated by combining acoustic time-of-flight data between parallel walls of a liquid-filled cuvette with densitometric data for a sequence of binary and ternary salt solutions. Correlations are presented to yield K s (m, f, T) accurately for nine compositions spanning the range m = 0-2 mol kg-1 and f = 0-1, at temperatures T ranging from 283.15 to 313.15 K. Electrolyte compressibility varies most with solvent ratio, followed by salt content and temperature, with K s ranging from 1 to 3 GPa. Composition-dependent acoustical properties elucidate the nature of speciation and solvation states in bulk electrolytes, and could be useful to identify the features of individual phases within solution-permeated porous electrodes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article