Surfactant-mediated gelation by 12-hydroxyoctadecanoic acid in a nonionic surfactant system

被引:0
|
作者
Aramaki, Kenji [1 ]
Maeda, Miho [1 ]
Murokasa, Yuka [1 ]
Mata, Jitendra [2 ]
Caldero, Gabriela [3 ,4 ]
Rodriguez-Abreu, Carlos [3 ,4 ]
机构
[1] Yokohama Natl Univ, Grad Sch Environm & Informat Sci, Tokiwadai 79-7,Hodogaya Ku, Yokohama 2408501, Japan
[2] Australian Nucl Sci & Technol Org ANSTO, Australian Ctr Neutron Scattering, Lucas Heights, NSW 2234, Australia
[3] CSIC, Inst Quim Avanzada Cataluna IQAC, Jordi Girona 18-26, Barcelona 08034, Spain
[4] Biomed Res Networking Ctr Bioengn Biomat & Nanomed, Jordi Girona 18-26, Barcelona 08034, Spain
关键词
Low-molecular-weight gelator; Rheological property; Small- and wide-angle X-ray scattering spectroscopy; Sol-gel temperature; Surfactant-mediated gelation; Supramolecular hydrogel; Orthogonal system; SANS; GELLED POLYMERIZABLE MICROEMULSIONS; 12-HYDROXYSTEARIC ACID; CHIRAL MESOPHASES; SOLID-STATE; TRANSITION; NANOSCALE;
D O I
10.1016/j.colsurfa.2024.134258
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
In this study, we present a hydrogel fabrication utilizing a water-insoluble, low-molecular-weight organogelator by the surfactant-mediated gelation (SMG). Specifically, we employed a nonionic surfactant (poly(oxyethylene) sorbitan monooleate, Tween 80) and an organogelator (12-hydroxyoctadecanoic acid, 12-HOA) to produce hydrogels. Gelation experiments conducted at varying concentrations of surfactant and gelator demonstrated successful hydrogel formation in the water/Tween 80/12-HOA system. Moreover, we observed a significant dependence of surfactant concentration on gelation ability. The sol-gel transition temperature was found to be influenced by both the gelator and surfactant concentrations. Optical and electron microscopy analyses revealed that the SMG hydrogels comprised an entangled network of fibers with micrometer-scale widths, formed as bundles of submicron-wide fibers, and further composed of fine fibers measuring several tens of nanometers in width. These fine fibers exhibited a left-handed helical structure. Small- and wide-angle X-ray scattering corroborated the presence of a lamellar structure within the fine fibers, displaying a triclinic subcell morphology. The coexistence of micelles with the fiber network was confirmed through small-angle neutron scattering and UV-vis spectroscopy. Furthermore, dynamic viscoelasticity tests demonstrated that the SMG hydrogels exhibited typical solid-like properties indicative of gel behavior.
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页数:8
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