Search

Abstract Precursor solubility is a crucial factor in industrial applications, dominating the outcome of reactions and purification steps. The outcome and success of thermodynamic modelling of this industrially important property with equations of states, such as Perturbed‐Chain Statistical Associating Fluid Theory (PC‐SAFT), vastly depends on the quality of the pure‐component parameters. The pure‐component parameters for low‐volatile compounds such as ionic liquids (ILs) have been commonly estimated using mixture properties, e. g. the osmotic pressure of aqueous solutions. This leads to parameters that depend on the solvent, and transferability to other mixtures often causes poor modeling results. Mixture‐independent experimental properties would be a more suitable basis for the parameter estimation offering a way to universal parameter sets. Model parameters for ILs are available in the literature [10.1016/j.fluid.2012.05.029], but they were estimated using pure‐IL density data. The present work focuses on a step towards a more universal estimation strategy that includes new experimental vapor‐pressure data of the pure IL. ILs exhibit an almost negligible vapor pressure in magnitude of usually 10−5 Pa even at elevated temperatures. In this work, such vapor‐pressure data of a series of 1‐ethyl‐3‐methyl‐imidazolium‐based [C2mim]‐ILs with various IL‐anions (e. g. tetrafluoroborate [BF4]−, hexafluorophosphate [PF6]−, bis(trifluoromethylsulfonyl)imide [NTf2]−) were experimentally determined and subsequently used for PC‐SAFT parameter estimation. The so‐determined parameters were used to predict experimental molecular precursor solubility in ILs and infinitely diluted activity coefficients of various solvents in ILs. The parameters were further compared to modeling results using classical parametrization methods (use of liquid‐density data only for the molecular PC‐SAFT and the ion‐based electrolyte PC‐SAFT). As a result, the modeled precursor solubilities using the new approach are much more precise than using the classical parametrization methods, and required binary parameters were found to be much smaller (if needed). In sum, including the pure‐component vapor‐pressure data of ILs opens the door towards parameter estimation that is not biased by mixture data. This procedure might be suitable also for polymers and for all kind of ionic species but needs extension to ion‐specific parametrization in the long term.

Abstract S‐alkyltetrahydrothiophenium, [CnTHT]+ bis(trifluorosulfonyl)imide, [NTf2]− room temperature ionic liquids (ILs) and tetraphenylborate, [BPh4]− salts with alkyl chain lengths from C4 to C10 have been prepared. The ILs and salts were characterized and their purity verified by 1H‐ and 13C‐nuclear magnetic resonance, elemental analysis, ion chromatography, Karl‐Fischer titration, single crystal X‐ray diffraction as well as thermogravimetric analysis. The experimentally determined density and viscosity decrease with increasing temperature. The experimental solubility of the [CnTHT][NTf2]‐ILs in water (75 to 2.2 mg/L for C4 to C10) was modelled with very good agreement by Perturbed Chain Statistical Associating Fluid Theory (PC‐SAFT), based on the extremely low vapor pressures for the [CnTHT][NTf2]‐ILs measured in this work (4.15 to 0.037 ⋅ 10−7×psat for C4 to C10). PC‐SAFT is able to predict and correlate different thermodynamic properties by estimating the Helmholtz residual energy.

Abstract The two ionic compounds [Ph4P][NTf2] and Cs[NTf2] were qualified to be suitable liquid materials for different high temperature applications. Development and optimization of these application techniques require knowledge of the thermodynamic properties of vaporization. Vapor pressures and vaporization enthalpies have been measured by using quartz‐crystal microbalance. Solubility parameters and miscibility of ionic liquids in practically relevant solvents were assessed.

Abstract A series of nine different known ionic liquids or low melting salts was synthesised and purified. They are composed of the [NTf2]– (bis(trifluoromethane)sulfonimide), [OTf]– (trifluoro‐methane‐sulfonate), or [B(CN)4]– (tetracyanidoborate) anion and [Ph4P]+ (tetraphenylphosphonium), [Ph3BzP]+ (triphenylbenzyl phosphonium), [nBu4P]+ (tetra‐nbutylphosphonium), [nBuPh3P]+ (tri‐phenyl‐nbutylphosphonium), [nBu4N]+ (tetra‐nbutylammonium), or the [PPN]+ (bis(triphenylphosphine)iminium) cation. Precise vapour pressure data and enthalpies of vaporisation were measured using the Quartz Crystal Microbalance (QCM) method and evaluated. Structure‐property relations are established using the obtained data as well as literature known data of ILs with alkyl‐substituted imidazolium cations. It turns out that ILs with the tetracyanidoborate anion have even higher values of the enthalpy of vaporisation than those with the common [NTf2]− or [OTf]− anion and therefore are even less volatile.