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氨基酸型表面活性剂与长链醇形成的 α-凝胶的流变性:无机盐浓度的影响。

Rheology of α-Gel Formed by Amino Acid-Based Surfactant with Long-Chain Alcohol: Effects of Inorganic Salt Concentration.

机构信息

Department of Pure and Applied Chemistry, Faculty of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.

Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.

出版信息

Langmuir. 2021 Jun 15;37(23):7032-7038. doi: 10.1021/acs.langmuir.1c00626. Epub 2021 Jun 3.

Abstract

Mixtures of surfactants, long-chain alcohols, and water sometimes yield lamellar gels with hexagonally packed alkyl chains. This assembly is called "α-gel" or "α-form hydrated crystal." In this study, we characterized the rheological properties of α-gel prepared using disodium -dodecanoylglutamate (C12Glu-2Na), 1-hexadecanol (C16OH), and water at different NaCl concentrations. The α-gel structure was assessed using small- and wide-angle X-ray scattering (SWAXS). The SWAXS measurements revealed that an increased NaCl concentration (0-200 mmol dm) resulted in a decreased -spacing caused by the screening of electrostatic repulsion between lamellar bilayers. This led to an increased amount of excess water (i.e., the water present between the α-gel domains), and hence, the viscosity of the α-gel decreased in the range of the NaCl concentration. A further increase in the NaCl concentration (200-1000 mmol dm) resulted in decreased electrostatic repulsion between the α-gel domains and/or an increased number of α-gel domains (multilamellar vesicles). These effects increased the domain-to-domain interactions, leading to increased viscosity. Therefore, we concluded that the viscosity of the α-gel was controlled by the amount of excess water and the domain-to-domain interactions. Once the network structure collapsed under the strain, it was difficult to recover the original network structure. The low recoverability resulted from increased cohesion between the domains at high NaCl concentrations.

摘要

表面活性剂、长链醇和水的混合物有时会产生具有六方堆积烷基链的层状凝胶。这种组装体被称为“α-凝胶”或“α-形式水合晶体”。在这项研究中,我们使用二钠 - 十二酰基谷氨酸(C12Glu-2Na)、1-十六醇(C16OH)和水在不同 NaCl 浓度下制备α-凝胶,表征了其流变性质。使用小角和广角 X 射线散射(SWAXS)评估了α-凝胶结构。SWAXS 测量结果表明,增加 NaCl 浓度(0-200 mmol dm)会导致层状双层之间的静电排斥屏蔽作用降低,从而导致 - 间距减小。这导致了更多的过剩水(即,存在于α-凝胶域之间的水)的增加,因此,α-凝胶的粘度在 NaCl 浓度范围内降低。进一步增加 NaCl 浓度(200-1000 mmol dm)会导致α-凝胶域之间的静电排斥降低和/或α-凝胶域数量增加(多层层状囊泡)。这些效应增加了域间相互作用,导致粘度增加。因此,我们得出结论,α-凝胶的粘度受过剩水量和域间相互作用的控制。一旦在应变下网络结构崩溃,就很难恢复原始的网络结构。在高 NaCl 浓度下,由于域之间的内聚性增加,恢复性较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7c0/8280742/0a59f56aad5d/la1c00626_0002.jpg

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