The thermal conductivities of mixtures of ionic liquids
(ILs) and
fluorocarbon gases are necessary for the design of a variety of engineering
and separation applications. Here, a transient hot-wire technique
was used to measure the liquid thermal conductivities of 1-ethyl-3-methylimidazolium
bis(trifluoromethylsulfonyl)amide ([EMIm][Tf2N]) and 1-n-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide
([HMIm][Tf2N]) in vapor–liquid equilibrium with
the hydrofluorocarbon gas, 1,1,1,2-tetrafluoroethane (R-134a), at
(298.15, 323.15, 348.15) K for [HMIm][Tf2N] and (298.15,
348.15, 398.15) K for [EMIm][Tf2N] and pressures up to
28 bar. The thermal conductivity of the gas-saturated ionic liquid
exhibits a very small and relatively linear decrease with increasing
pressure (composition) of R-134a even to relatively high compositions
(∼80% mol). Only at very high molar compositions of the gas
(∼90+% mol) does the thermal conductivity significantly decrease
toward that of the value of pure saturated liquid R-134a. However,
no simple mixing rule of the pure component properties could correlate
the trends in composition. As some potential applications require
higher temperatures, the system of [EMIm][Tf2N]/R-134a
was measured at 398.15 K. Generally, a longer alkyl-chain length on
the cation, such as [HMIm][Tf2N], experiences a steeper
decrease in thermal conductivity with increasing R-134a composition
than with the [EMIm] cation.