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Phase equilibria and volumetric and viscosity behavior of the aqueous double salt ionic liquid [EMIM][SCN]x [MeSO3](1-x)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F21%3A43922084" target="_blank" >RIV/60461373:22340/21:43922084 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0378381221002624" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0378381221002624</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/J.FLUID.2021.113199" target="_blank" >10.1016/J.FLUID.2021.113199</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Phase equilibria and volumetric and viscosity behavior of the aqueous double salt ionic liquid [EMIM][SCN]x [MeSO3](1-x)

  • Original language description

    Continuing our recent systematic studies on thermodynamic and thermophysical properties of binary aqueous ionic liquids (ILs), this work extends our investigations to aqueous double salt ionic liquids (DSILs). Specifically, the (water + [EMIM][SCN]x[MeSO3](1-x)) system is examined here: vapor-liquid and solid-liquid equilibria, volumetric and viscosity behaviors were experimentally determined at three DSIL compositions (x approx. 0.75, 0.5, and 0.25 or 0.20) and several water contents xw. Water activity was measured at seven temperatures from (288.15 to 318.15) K and for xw from 0.3 to 1, freezing temperature for xw from 0.8 to 1, density and dynamic viscosity at two temperatures (298.15 and 323.15 K) and for xw from 0 to 0.9. The acquired data were treated as those for the ternary system (water + [EMIM][SCN] + [EMIM][MeSO3]) and modeled coherently together with its binary subsystems. The ternary water activity data were successfully correlated by the extended NRTL model, adopting for the aqueous parent IL binaries the parameters we evaluated previously, and fitting just those remaining for the (IL + IL) pair. The established model was shown to predict perfectly the measured SLE data. This model further provides an otherwise hardly procurable insight into the energetics of the DSIL. As inferred from the model, the ([EMIM][SCN] + [EMIM][MeSO3]) binary system exhibits quite large positive deviations from ideality, its excess Gibbs energy stemming from the very endothermic mixing of the two ILs which is only partially compensated by the positive excess entropy. The (IL + IL) mixture exhibits a positive, but very small excess volume, only slightly increasing as temperature increases, while its viscosity is much greatly affected by both temperature and the DSIL composition. The viscosity deviation from the linear mixing rule is for the DSIL negative and large but obeying quite accurately the linear mixing rule of logarithmic viscosity. For the aqueous mixtures of both parent ILs, the logarithmic viscosity deviation is high and greatly composition asymmetric. Coherent and sufficiently accurate representation of the volumetric and viscosity data for the ternary system and all its binary subsystems was achieved by Padé approximants with temperature-dependent parameters amended with a ternary term. Compared to the neat [EMIM][MeSO3], [EMIM][SCN]x[MeSO3](1-x) with smaller contents of [EMIM][SCN] (x &lt; 0.2) and water (xw &lt; 0.2) shows higher water affinity, while having considerably lower viscosity. Thus, the use of this DSIL as a water absorption medium for desiccation and cooling applications was found to be very beneficial.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Fluid Phase Equilibria

  • ISSN

    0378-3812

  • e-ISSN

  • Volume of the periodical

    548

  • Issue of the periodical within the volume

    November 15

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    12

  • Pages from-to

    113199

  • UT code for WoS article

    000703573400013

  • EID of the result in the Scopus database

    2-s2.0-85113274202