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Self-assembly in saponin/surfactant mixtures: Escin and sodium dodecylsulfate
被引:11
|作者:
Tucker, I. M.
[1
]
Burley, A.
[1
]
Petkova, R. E.
[1
]
Hosking, S. L.
[1
]
Webster, J. R. P.
[2
]
Li, P. X.
[2
]
Ma, K.
[2
]
Doutch, J.
[2
]
Penfold, J.
[2
,3
]
Thomas, R. K.
[3
]
机构:
[1] Port Sunlight Lab, Unilever Res & Dev, Quarry Rd East, Wirral, Merseyside, England
[2] Rutherford Appleton Lab, STFC, ISIS Facil, Harwell Campus, Didcot, Oxon, England
[3] Univ Oxford, Phys & Theoret Chem Lab, South Parks Rd, Oxford, England
基金:
“创新英国”项目;
关键词:
Saponins;
Escin;
Sodium dodecylsulfate;
Surfactant mixtures;
Self-assembly;
Micelles;
Small angle neutron scattering;
D O I:
10.1016/j.colsurfa.2021.127019
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Saponins are a class of bio-surfactants obtained from a wide variety of plant species. They are surface active glycosides which are used in the stabilisation of foams and emulsions in many food, drink and cosmetic applications. Their wider utilisation and application will involve their mixture with different synthetic and bioderived surfactants, proteins and polymers. Understanding the mixing properties of saponins with other surfactants at surfaces and in self-assembly is key to their wider exploitation; and the focus here is on triterpenoid saponin escin and the anionic surfactant sodium dodecylsulfate, SDS. Previous analysis of the surface adsorption and critical micelle concentration, cmc, data using the pseudo phase approximation, PPA, indicate that the micelle mixing is more non-ideal than the surface mixing. The non-ideality is associated with the packing constraints arising from the quite different molecular structures and how this impacts upon the mixture selfassembly is probed here. To address specifically the self-assembly properties of saponin-surfactant mixtures, small angle neutron scattering, SANS, has been used to explore the nature of mixed micelles of escin and SDS. The SANS data for the escin / SDS mixtures are modelled as globular ellipsoidal micelles. The micelles exhibit an overall increase in size and aggregation number as the solution becomes richer in escin, and the evolution in micelle size goes through a minimum at relatively rich SDS solutions. The results illustrate the impact of the disparity in the molecular structures of escin and SDS on the self-assembly, and provides an insight into the factors affecting the departure from ideal mixing.
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