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Related Concept Videos

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Constant Volume Calorimetry

Calorimeters are useful to determine the heat released or absorbed by a chemical reaction. Coffee cup calorimeters are designed to operate at constant (atmospheric) pressure and are convenient to measure heat flow (or enthalpy change) accompanying processes that occur in solution at constant pressure. A different type of calorimeter that operates at constant volume, colloquially known as a bomb calorimeter, is used to measure the energy produced by reactions that yield large amounts of heat and...
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Calorimetry is a technique used to measure the amount of heat involved in a chemical or physical process or to measure the heat transferred to or from a substance. The heat is exchanged with a calibrated and insulated device called the calorimeter. Calorimetry experiments are based on the assumption that there is no heat exchange between the insulated calorimeter and the external environment. The well-insulated calorimeters prevent the transfer of heat between the calorimeter and its external...
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Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
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Published on: December 20, 2016

Reverse dynamic calorimetry of a viscous ionic liquid.

Wei Huang1, Ranko Richert

  • 1Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287-1604, USA.

The Journal of Chemical Physics
|November 18, 2009
PubMed
Summary

In ionic liquids, the electric modulus relaxes faster than structural relaxation near the glass transition temperature (Tg). This study compares thermal relaxation and electric modulus timescales in a supercooled ionic liquid.

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Area of Science:

  • Physical Chemistry
  • Materials Science
  • Condensed Matter Physics

Background:

  • Ionic liquids exhibit complex dynamics near their glass transition temperature (Tg).
  • Understanding the relationship between electrical and structural relaxation is crucial for predicting material properties.

Purpose of the Study:

  • To compare the time scales of thermal relaxation and electric modulus in the supercooled ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate.
  • To investigate the dynamics of ionic liquids under high electric fields.

Main Methods:

  • Utilizing a high-field impedance setup to apply sinusoidal electric fields (up to 387 kV/cm, 0.2 Hz-56 kHz).
  • Measuring time-resolved configurational temperature (indicating structural relaxation) and low-field dielectric properties simultaneously.

Main Results:

  • The electric modulus (macroscopic field M) was found to relax significantly faster than structural relaxation indicators (thermal relaxation, solvation dynamics, probe rotation) near Tg.
  • This faster relaxation of the electric modulus was observed despite the liquid being composed of mobile ions.

Conclusions:

  • The electric modulus does not solely reflect the structural relaxation time scale in deeply supercooled ionic liquids.
  • Discrepancies highlight the complex interplay between electrical response and molecular dynamics in these materials.