We present an experimental comparative study of the effect of elasticity of the continuous liquid in generation of droplets in microfluidic flow focusing devices. For a wide range of values of dynamic viscosity of the Newtonian droplet phase we compare the dynamics of the formation of droplets in three different Newtonian and non-Newtonian, viscoelastic (Boger) fluid pairs of the same (and nearly constant) shear viscosities. In both Newtonian and viscoelastic systems we find similar regimes of operation of the system: (i) dripping without satellites, (ii) dripping with single satellites, (iii) formation of multiple satellites, and (iv) jetting. We find that the elasticity of the focusing liquid stabilizes the jets facilitating formation of smaller droplets, and leads to transitions between various regimes at lower ratios of flow and at lower values of the capillary numbers in comparison to the Newtonian focusing liquids. We also show that the polydispersity of Newtonian droplets produced in non-Newtonian continuous phases depend significantly on the viscosity of the droplet phase while this dependence is minor when the continuous liquid is Newtonian.

In this paper we present the synthesis route and electrochemical properties of new class of ionic liquids (ILs) obtained from lithium derivate TDI (4,5-dicyano-2-(trifluoromethyl)imidazolium) anion. ILs synthesized by us were EMImTDI, PMImTDI and BMImTDI, i.e. TDI anion with 1-alkyl-3-methylimidazolium cations, where alkyl meant ethyl, propyl and butyl groups. TDI anion contains fewer fluorine atoms than LiPF₆ and thanks to C–F instead of P–F bond, they are less prone to emit fluorine or hydrogen fluoride due to the rise in temperature. Use of IL results in non-flammability, which is making such electrolyte even safer for both application and environment. The thermal stability of synthesized compounds was tested by DSC and TGA and no signal of decomposition was observed up to 250 °C. The LiTDI salt was added to ILs to form complete electrolytes. The structures of tailored ILs with lithium salt were confirmed by X-ray diffraction patterns. The electrolytes showed excellent properties regarding their ionic conductivity (over 3 mS cm⁻¹ at room temperature after lithium salt addition), lithium cation transference number (over 0.1), low viscosity and broad electrochemical stability window. The ionic conductivity and viscosity measurements of pure ILs are reported for reference.