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Micellization Behavior of Conventional Cationic Surfactants within Glycerol-Based Deep Eutectic Solvent.
Ramesh Kumar Banjare1, Manoj Kumar Banjare1,2, Kamalakanta Behera3
1MATS School of Sciences, MATS University, Pagariya Complex, Pandari, Raipur, C.G. 492009, India.
ACS Omega
|August 18, 2020
Summary
This study investigates cationic surfactants in deep eutectic solvents (DES), revealing they form self-assembled nanostructures. These findings are valuable for understanding colloidal solutions containing DES and water mixtures.
Area of Science:
- Colloid and Surface Science
- Supramolecular Chemistry
- Materials Science
Background:
- Deep eutectic solvents (DES) offer unique properties for self-assembly.
- Cationic surfactants are key components in various colloidal systems.
- Understanding surfactant behavior in DES is crucial for developing new materials.
Purpose of the Study:
- To investigate the aggregation behavior of cationic surfactants in an aqueous glycerol-based DES.
- To characterize the self-assembled nanostructures formed by these surfactants.
- To elucidate the intermolecular interactions governing micelle formation in DES.
Main Methods:
- Synthesis and characterization of a glycerol-based DES using FTIR and 1H NMR spectroscopy.
- Investigation of surfactant aggregation using surface tension, conductivity, fluorescence, and dynamic light scattering (DLS).
- Analysis of intermolecular interactions via FTIR, 1H NMR, and 2D NOESY spectroscopy.
Main Results:
- Cetyldimethylethanolammonium bromide (CDMEAB) and cetyltributylphosphonium bromide (CTBPB) form self-assembled nanostructures in the aqueous DES.
- Interfacial properties and thermodynamic parameters were determined, showing the influence of DES on surfactant aggregation.
- FTIR and NMR analyses confirmed hydrogen bonding and electrostatic interactions between surfactant head groups and DES components.
Conclusions:
- Cationic surfactants self-assemble into nanostructures within aqueous glycerol-based DES.
- The head groups of surfactants interact with DES via H-bonding and electrostatic forces, influencing micellar structure.
- Results provide insights into the colloidal behavior of DES-water mixtures, relevant for materials science applications.
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