Abstract

Glyceline, a deep eutectic solvent comprising glycerol and choline chloride, is a green nonaqueous solvent with potential industrial applications. Molecular mechanisms of surfactant self-assembly in deep eutectic solvents are expected to differ from those in their constituent polar components and are not well understood. Here we report the observation of self-assembled SDS fractal dendrites with dimensions up to ∼mm in glyceline at SDS concentrations as low as cSDS ∼ 0.1 wt%. The prevalence of these dendritic fractal aggregates led to the formation of a gel phase at SDS concentrations above ≥1.9 wt% (the critical gelation concentration cCGC). The gel microscopic structure was visualised using polarised light microscopy (PLM); rheology measurements confirmed the formation of a colloidal gel, where the first normal stress difference was negative and the elastic modulus was dominant. Detailed nano-structural characterisation by small-angle neutron scattering (SANS) further confirmed the presence of fractal aggregates. Such SDS aggregation or gelation has not been observed in water at such low surfactant concentrations, whereas SDS has been reported to form lamellar aggregates in glycerol (a component of glyceline). We attribute the formation of the SDS fractal dendrites to the condensation of counterions (i.e. the choline ions) around the SDS aggregates - a diffusion-controlled process, leading to the aggregate morphology observed. These unprecedented results shed light on the molecular mechanisms of surfactant self-assembly in deep eutectic solvents, important to their application in industrial formulation.

Highlights

  • Deep eutectic solvents (DES)[1,2] are green, non-volatile, and they are good solvents for many inorganic and organic species.[3,4] Their green credentials are of interest in many industrial applications ranging from electroplating[5,6,7,8,9] to personal care products

  • The microscopic structure of this fracto-eutectogel was visualised with polarising light microscopy (PLM) and its nanostructure studied with small-angle neutron scattering (SANS)

  • Protonated sodium dodecyl sulfate (h-SDS) (Sigma-Aldrich, 498.0%) was recrystallised three times from ethanol, and its purity was checked with 1H NMR. h-Glycerol (Fisher Scientific, 498.0%) and d-glycerol (Sigma–Aldrich, 498.0% and 498.0 atom%D) were used as received. h-Choline chloride (Sigma– Aldrich, 498.0%) and d9-trimethyl-choline chloride (SigmaAldrich, 498.0% and 498.0 atom%D) were used as received. h-/d-glyceline was prepared by mixing h-/d-choline chloride and h-/d-glycerol in a 1 : 2 molar ratio in a shaker incubator (Stuart SI505) at 550 rpm at 60 1C for two hours (2 h)

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Summary

Introduction

Deep eutectic solvents (DES)[1,2] are green, non-volatile, and they are good solvents for many inorganic and organic species.[3,4] Their green credentials are of interest in many industrial applications ranging from electroplating[5,6,7,8,9] to personal care products. Surfactant self-assembly has been investigated in both reline and glyceline (comprising choline chloride and glycerol in a 1 : 2 molar ratio).[23,24,25] It has been found that the interfacial self-assembly behaviour of surfactants in the DES is similar to that in aqueous systems. SDS forms globular micelles in water under the same condition, whilst SDS lamellar gels in glycerol (a glyceline constituent hydrogen-bonding rich solvent) have been reported recently.[30] The microscopic structure of this fracto-eutectogel was visualised with polarising light microscopy (PLM) and its nanostructure studied with small-angle neutron scattering (SANS). The unprecedented observation of the microscopic fractal structures as a result of SDS self-organisation in glyceline points to different molecular interactions in DES compared to aqueous systems or single-component hydrogen-bonding rich solvents

Materials
Viscometry and oscillation rheology
SANS data analysis
Surface tensiometry
Surface tensiometry measurements of SDS in glyceline
The formation of a gel in glyceline
Rheological properties of the fracto-eutectogel
Microscopic structure of the ordered surfactant mesophase
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