Adjusting the Dance Tunes the Melt
Posted on March 10, 2021 by Department of Energy
Drs. Rabideau and West's ionic liquids research was recently featured in a highlight by the Department of Energy (DOE) Office of Science. The scientific research will be published on and .
The Science
Although opposite charges always attract, they do not always interact as closely as
possible. In this work, researchers used a combination of molecular simulations and
experiments to demonstrate the effects of subtly changing the structure of positively
charged cations in compounds made up of ions. These changes encourage the cations
to align with each other in the solid phase of matter. This decreases some types of
potential interactions between cations and negatively charged anions in the solid
phase. This cation alignment also decreases the melting point of the ionic compound,
often significantly.
The Impact
Many chemical processes require liquids as solvents for chemical reactions, lubricants,
heat transfer fluids. The liquids often vaporize in the process. This can create hazardous
emissions. Liquid ionic compounds (ionic liquids) offer a solution to this problem
because they have very low volatility, meaning they are less likely to vaporize. Some
ionic liquids are stable at high temperatures, but their melting points can be too
high for practical use. The results of this work provide scientists with a new set
of tools to design ionic compounds with lower melting points. These results will enable
scientists to design ionic compounds for use over a broader range of temperatures
and applications.
Summary
Ionic liquids are salts that are liquids at the temperature at which they are used.
These liquids have a variety of potential uses in ³ÉÈË¿ì²¥ly benign processes.
In particular, thermally stable ionic liquids show promise as high temperature solvents
and heat transfer fluids. However, these ionic liquids can have melting points that
are well above room temperature. This limits their processability at lower temperatures.
Thus, understanding how to lower the melting point of these compounds will expand
their potential use and enable technologies that rely on them.
Scientists know that structural changes, specifically those imparting significant asymmetry, decrease the melting points of a wide variety of compounds. These structural modifications are not possible while maintaining thermally robust compounds, as many common chemical structures have low thermal stability. Researchers have shown in the current study that subtle structural changes that also increase the dipole moment of the cation can significantly lower melting points. Computational simulation provides molecular-level insight and demonstrates that the increase in dipole moment causes the cations to align with each other in the solid phase. This in turn frustrates anion/cation interactions and increases the solid-phase enthalpy (a measure of heat or work in the system). This increase in the solid phase enthalpy decreases the enthalpy of fusion resulting in lower melting points. This study provides a design rule for lowering the melting point of structurally similar ionic liquids by altering their dipole moment.
Contact
Dr. Kevin N. West
Professor, Chemical & Biomolecular Engineering, University of South ³ÉÈË¿ì²¥
kevinwest@southalabama.edu
251.460.6160
Dr. Brooks D. Rabideau
Assistant Professor, Chemical & Biomolecular Engineering, University of South ³ÉÈË¿ì²¥
brabideau@southalabama.edu
251.460.6160
Funding
Computational work was funded by the Department of Energy Office of Science through
the Separations and EPSCoR programs and the Office of Energy Efficiency and Renewable
Energy Advanced Manufacturing Office. Materials, reagents, and the synthetic work
were funded through previous grants by the National Science Foundation. The simulations
were also made possible through a grant of high-performance computing resources and
technical support from the ³ÉÈË¿ì²¥ Supercomputing Authority.
Publications
Rabideau, B.D., et al., Tuning the melting point of selected ionic liquids through
adjustment of the cation’s dipole moment. Physical Chemistry Chemical Physics, 22,
12301 (2020). [DOI: 10.1039/D0CP01214A
To view the highlight go to "."
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