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Extended surfactants: Characterization and microemulsion properties.

机译:扩展表面活性剂:表征和微乳液性能。

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Extended surfactants are surfactants with intermediate polarity groups, such as polypropylene oxide (PO) and polyethylene oxide (EO), inserted between the hydrophilic head and the hydrocarbon tail. With this unique molecular structure, extended surfactants provide an enhanced interaction with both oil and water phases. This results in microemulsion formation with desirable low interfacial tension (IFT) and high solubilization properties, especially for highly hydrophobic oils and vegetable oils. Such formulations have numerous potential applications in enhanced subsurface remediation, drug delivery, and detergency. However, due to the limited amount of information available on these recently developed surfactants, there is no easy and adequate technique to guide the formulation selection process and microemulsion characteristics for extended surfactant systems. In addition to the challenge in characterization, extended surfactant-based microemulsions also struggle with their slow kinetics. Therefore this present work seeks to characterize extended surfactant hydrophilicity/lipophilicity, and at the same time, evaluate both equilibrium and kinetic properties of extended surfactant-based microemulsions. The thermodynamically derived model known as hydrophilic-lipophilic deviation (HLD) approach used in combination with microemulsion phase behavior was proposed as a simple, yet convenient tool for characterizing extended surfactant behavior and predicting the optimal conditions for microemulsion systems. To our knowledge, this is the first report of the extended surfactant hydrophilicity/lipophilicity index and interfacial morphology of the extended surfactant membranes (i.e. characteristic length and interfacial rigidity). The findings of this study not only emphasize the important role of inserting PO and EO groups on the hydrophilic-lipophilic nature of extended surfactants, but also demonstrate the impact these intermediate functional groups have on both equilibrium and dynamic microemulsion properties.
机译:扩展的表面活性剂是插入在亲水头和烃尾之间的具有中间极性基团的表面活性剂,例如聚环氧丙烷(PO)和聚环氧乙烷(EO)。具有这种独特的分子结构,扩展的表面活性剂可增强与油相和水相的相互作用。这导致形成具有所需的低界面张力(IFT)和高增溶性能的微乳液,特别是对于高疏水性油和植物油。这样的制剂在增强地下修复,药物递送和去污力方面具有许多潜在的应用。然而,由于关于这些新近开发的表面活性剂的可用信息量有限,因此没有简单而适当的技术来指导用于扩展表面活性剂体系的制剂选择过程和微乳液特性。除了表征方面的挑战外,扩展的基于表面活性剂的微乳液还因其缓慢的动力学而挣扎。因此,本发明旨在表征扩展的表面活性剂的亲水性/亲脂性,同时评估扩展的基于表面活性剂的微乳液的平衡和动力学性质。提出了一种热力学衍生模型,称为亲水-亲脂偏差(HLD)方法,与微乳相行为结合使用,是一种简单而方便的工具,用于表征扩展的表面活性剂行为并预测微乳体系的最佳条件。据我们所知,这是扩展的表面活性剂亲水性/亲脂性指数和扩展的表面活性剂膜的界面形态(即特征长度和界面刚度)的首次报道。这项研究的发现不仅强调了插入PO和EO基团对扩展表面活性剂的亲水-亲脂性质的重要作用,而且还证明了这些中间官能团对平衡和动态微乳液性能的影响。

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