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Microemulsion system formed with new piperazinium-based surface-active ionic liquid

JOURNAL OF MOLECULAR LIQUIDS [2023]
Bingying Wang, Zaisheng Zhu, Jiayu Yin, Xiaoxing Lu
ABSTRACT

The intensive use of ionic liquid (IL) in various researches and applications induces the imperative need of specific functional ILs. Present work introduces a novel piperazinium-based surface-active IL (SAIL) which shows great potential for the preparation of microemulsion (ME), namely 1-(2-hydroxyethyl)piperazinium laurate ([HEP][C 11 CO 2 ]). Important fundamental physicochemical properties have been investigated, revealing higher surface activity for the SAIL than common surfactants. [HEP][C 11 CO 2 ] is able to solubilize different oil components and water with short-chain alcohol as cosurfactant, forming stable ME in a wide range of ratio of water to oil, and a broad microemulsion region covering over 50 % of the pseudo-ternary phase diagram can be found. The structural transition of water-in-oil to bicontinuous occurs at the water content of 0.60 to 0.65 for the SAIL/1-butanol/ n -heptane/water systems at the ratios of SAIL to 1-butanol of 1:1 and 1:2, as confirmed by electrical conductivity measurements. Moreover, the solubilization of oil and water was investigated in the presence of NaCl, KCl or MgCl 2 , and the optimal salinity was determined. While Mg 2+ induces formation of emulsion probably due to the poor solubility of Mg 2+ /[C 11 CO 2 ] − complexes, the ME system is much more stable with the presence of monovalent ions like Na + and K + . For the NaCl-contained system, the salinity window of the bicontinuous phase changes from 0.030 to 0.025 and 0.020 when the temperature rises from 15 °C to 25 °C and 35 °C, which mainly results from the enhanced hydrophobic interactions and the weakened electrostatic interactions. Present studies elucidate that [HEP][C 11 CO 2 ] is feasible to form various microemulsion systems which may have extensive potential in further applications like size-controlled syntheses and oil recovery.

MATERIALS

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