Surfactant/biosurfactant mixing: Adsorption of saponin/nonionic surfactant mixtures at the air-water interface

被引:34
|
作者
Tucker, I. M. [1 ]
Burley, A. [1 ]
Petkova, R. E. [1 ]
Hosking, S. L. [1 ]
Thomas, R. K. [2 ]
Penfold, J. [2 ,3 ]
Li, P. X. [3 ]
Ma, K. [3 ]
Webster, J. R. P. [3 ]
Welbourn, R. [3 ]
机构
[1] Port Sunlight Lab, Unilever Res & Dev, Quarry Rd East, Wirral, Merseyside, England
[2] Univ Oxford, Phys & Theoret Chem Lab, South Parks Rd, Oxford, England
[3] Rutherford Appleton Lab, STFC, ISIS Facil, Didcot, Oxon, England
基金
“创新英国”项目;
关键词
Mixed surfactants; Adsorption; Saponins; Escin; Nonionic surfactants; Neutron reflectivity; Air-water interface; Pseudo phase approximation; QUILLAJA BARK SAPONIN; AIR/WATER INTERFACE; LAYERS; HYDRATION; RHEOLOGY; IMPACT; FOOD;
D O I
10.1016/j.jcis.2020.04.061
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 naturally occurring biosurfactants present in a wide range of plant species. They are highly surface active glycosides, and are used to stabilise foams and emulsions in foods, beverages and cosmetics. They have great potential for an even wider range of applications, especially when mixed with different synthetic surfactants. Understanding those mixing properties are key to the exploitation of saponins in that wider range of potential applications. The surface adsorption properties of the saponin, escin, with two conventional nonionic surfactants, polyethylene glycol surfactants, have been studied at the air-water interface using neutron reflectivity, NR, and surface tension, ST. Although the saponin and polyethylene glycol, CnEOm, surfactants are both nonionic the disparity in the relative surface activities and packing constraints result in non-ideal mixing. Comparison with the predictions of the pseudo phase approximation requires the inclusion of the quadratic, cubic and quartic terms in the expansion of the excess free energy of mixing to explain the variations in the surface composition. For escin/pentaethylene glycol monododecyl ether, C12EO5, the interaction is attractive and close to ideal. For escin/octaethylene glycol monododecyl ether, C12EO8, it is repulsive and close to the criteria for demixing. The differences in mixing behaviour are attributed to greater packing constraints imposed by the larger ethylene oxide headgroup of the C12EO8 compared to C12EO5. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:385 / 392
页数:8
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