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表面活性剂/非离子共聚物相互作用:一项十二烷基硫酸钠、动态光散射、等温滴定量热法和核磁共振研究。

Surfactant/nonionic copolymer interaction: a SLS, DLS, ITC, and NMR investigation.

作者信息

Taboada Pablo, Castro Emilio, Mosquera Víctor

机构信息

Laboratorio de Física de Coloides y Polímeros, Grupo de Sistemas Complejos, Departamento de Física de la Materia Condensada, Facultad de Física, Universidad de Santiago de Compostela, Spain.

出版信息

J Phys Chem B. 2005 Dec 15;109(49):23760-70. doi: 10.1021/jp0532061.

Abstract

The interactions between an oxyphenylethylene-oxyethylene nonionic diblock copolymer with the anionic surfactant sodium dodecyl sulfate (SDS) have been studied in dilute aqueous solutions by static and dynamic light scattering (SLS and DLS, respectively), isothermal titration calorimetry (ITC), and 13C and self-diffusion nuclear magnetic resonance techniques. The studied copolymer, S20E67, where S denotes the hydrophobic styrene oxide unit and E the hydrophilic oxyethylene unit, forms micelles of 15.6 nm at 25 degrees C, whose core is formed by the styrene oxide chains surrounded by a water swollen polyoxyethylene corona. The S20E67/SDS system has been investigated at a copolymer concentration of 2.5 g dm(-3), for which the copolymer is fully micellized, and with varying surfactant concentration up to approximately 0.15 M. When SDS is added to the solution, two different types of complexes are observed at various surfactant concentrations. From SLS and DLS it can be seen that, at low SDS concentrations, a copolymer-rich surfactant mixed micelle or complex is formed after association of SDS molecules to block copolymer micelles. These interactions give rise to a strong decrease in both light scattering intensity and hydrodynamic radius of the mixed micelles, which has been ascribed to an effective reduction of the complex size, and also an effect arising from the increasing electrostatic repulsion of charged surfactant-copolymer micelles. At higher surfactant concentrations, the copolymer-rich surfactant micelles progressively are destroyed to give surfactant-rich-copolymer micelles, which would be formed by a surfactant micelle bound to one or very few copolymer unimers. ITC data seem to confirm the results of light scattering, showing the dehydration and rehydration processes accompanying the formation and subsequent destruction of the copolymer-rich surfactant mixed micelles. The extent of interaction between the copolymer and the surfactant is seen to involve as much as carbon 3 (C3) of the SDS molecule. Self-diffusion coefficients corroborated light scattering data.

摘要

通过静态和动态光散射(分别为SLS和DLS)、等温滴定量热法(ITC)以及13C和自扩散核磁共振技术,研究了氧苯基乙烯-氧乙烯非离子二嵌段共聚物与阴离子表面活性剂十二烷基硫酸钠(SDS)在稀水溶液中的相互作用。所研究的共聚物S20E67中,S表示疏水性氧化苯乙烯单元,E表示亲水性氧乙烯单元,在25℃下形成15.6nm的胶束,其核心由被水溶胀的聚氧乙烯冠层包围的氧化苯乙烯链构成。在共聚物浓度为2.5g dm(-3)(此时共聚物完全胶束化)且表面活性剂浓度变化至约0.15M的条件下,对S20E67/SDS体系进行了研究。当向溶液中加入SDS时,在不同表面活性剂浓度下观察到两种不同类型的复合物。从SLS和DLS可以看出,在低SDS浓度下,SDS分子与嵌段共聚物胶束缔合后形成富含共聚物的表面活性剂混合胶束或复合物。这些相互作用导致混合胶束的光散射强度和流体动力学半径都大幅降低,这归因于复合物尺寸的有效减小,以及带电表面活性剂 - 共聚物胶束静电排斥增加所产生的效应。在较高表面活性剂浓度下,富含共聚物的表面活性剂胶束逐渐被破坏,形成富含表面活性剂的 - 共聚物胶束,这可能是由与一个或极少数共聚物单分子结合的表面活性剂胶束形成的。ITC数据似乎证实了光散射的结果,显示了伴随富含共聚物的表面活性剂混合胶束形成及随后破坏的脱水和再水合过程。共聚物与表面活性剂之间的相互作用程度似乎涉及到SDS分子的多达碳3(C3)。自扩散系数证实了光散射数据。

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