Journal
CRYSTALS
Volume 12, Issue 11, Pages -Publisher
MDPI
DOI: 10.3390/cryst12111621
Keywords
deep eutectic solvents; surfactants; self-assembly; liquid crystals; small-angle scattering
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This study examines the self-assembly of surfactants in a common deep eutectic solvent, and demonstrates the influence of solvent composition on the assembly behavior. The results show evidence of micelle formation and provide insights into the critical micelle concentration and micelle structure. The study also explores the effects of different diols and ternary solvents on self-assembly, highlighting the importance of solvent composition in modulating assembly behavior.
The common Deep Eutectic Solvent (DES) 'ethaline' (1:2 choline chloride:ethylene glycol) was examined here as a basis for the self-assembly of the surfactant dodecyltrimethylammonium bromide (C(12)TAB). A phase diagram was constructed, showing evidence for a L-1 (micellar) phase, confirmed by tensiometry to have a room temperature critical micelle concentration (CMC) of 1.2 wt.%. Small angle neutron scattering (SANS) measurements indicate formation of interacting globular micelles with slightly smaller apparent radii than in water. The apparent mesophase/multiphase region was studied using SWAXS, demonstrating rich mesoscopic lyotropic liquid crystalline phase behaviour, with evidence for lamellar L-alpha peaks, alongside potential co-crystalline phases. We attempted to tailor the self-assembly by studying binary DES containing longer diols including 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, and 1,5-pentanediol, and ternary DES where the HBD component was a 1:1 ethylene glycol:diol mixture. However, synchrotron SAXS showed that only ternary 'propethaline' mixtures displayed signs of self-assembly and micellization, perhaps due to the reduction in calculated Gordon parameter, which decreases linearly with increasing alkyl chain length. Systematic differences were thus observed in the ability of the solvents to modulate assembly, from globular micelles in ChCl:EG, to weaker assembly in long-tail DES, and complete solubilisation in butaline and pentaline.
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