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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Phase behavior of an aqueous mixture of octaethylene glycol dodecyl ether revealed by DSC, FT-IR, and C-13 NMR measurements
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Phase behavior of an aqueous mixture of octaethylene glycol dodecyl ether revealed by DSC, FT-IR, and C-13 NMR measurements

机译:通过DSC,FT-IR和C-13 NMR测量揭示八乙二醇十二烷基醚的水性混合物的相行为

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The phase behavior of an aqueous mixture of octaethylene glycol dodecyl ether (C12E8) was investigated by means of differential scanning calorimetry (DSC), Fourier transform infrared (FT-IR) spectroscopy, and C-13 nuclear magnetic resonance (C-13 NMR) spectroscopy. The phase diagram in the temperature range from -10 to 70 degreesC was constructed on the basis of DSC experiments, according to which four mesophases, that is, L-a, V-1, H-1, and I-1, appear in this mixture system depending on the composition and temperature. The FT-IR measurements as a function of composition and temperature revealed the events occurring in the mixture associated with the phase transformation. When the mixture transforms from solid to mesophases, the hydrogen bonds between terminal OH groups of the surfactant molecules are broken. Accompanied by this phase transformation, the ordered conformational structure of both the polyoxyethylene (POE) and alkyl chains is mostly broken, and the residual order in the chain is lost gradually by the increase in temperature of the mesophases. Based on the analysis of NMR line width, a qualitative picture was drawn concerning the molecular motion of the surfactant in various phases. No NMR signal is observed for the solid phase because surfactant molecules are highly immobilized. In the H-1 and L-a phases, the POE chain of the surfactant molecule can undergo segmental motion to some extent, whereas the motion of the alkyl chain is rather restricted. The molecular motion of the surfactants in the V-1 phase is quite rapid and is close to that in the liquid phase despite the highly viscous nature of that phase. The motion of the POE chain in the I-1 phase is somewhat restricted compared with that in the liquid phase probably due to the enhanced hydration of the POE chain in the spherical micelles constituting the I-1 phase. [References: 27]
机译:通过差示扫描量热法(DSC),傅里叶变换红外(FT-IR)光谱和C-13核磁共振(C-13 NMR)研究了八乙二醇十二烷基醚(C12E8)水性混合物的相行为光谱学。根据DSC实验构建了-10至70℃温度范围内的相图,据此混合物中出现了四个中间相,即La,V-1,H-1和I-1。系统取决于成分和温度。 FT-IR测量值是成分和温度的函数,揭示了混合物中发生的与相变有关的事件。当混合物从固相转变为中间相时,表面活性剂分子的末端OH基团之间的氢键断裂。伴随这种相变,聚氧乙烯(POE)和烷基链的有序构象结构大多被破坏,并且中间相温度的升高逐渐失去了链中的残留顺序。根据NMR线宽的分析,得出了关于表面活性剂在各个相中分子运动的定性图。由于表面活性剂分子高度固定,因此未观察到固相的NMR信号。在H-1和L-a相中,表面活性剂分子的POE链可能在某种程度上经历分段运动,而烷基链的运动受到很大限制。尽管表面活性剂具有很高的粘性,但它们在V-1相中的分子运动非常迅速,并且与液相中的分子运动相近。与液相相比,在I-1相中POE链的运动受到一定限制,这可能是由于在构成I-1相的球形胶束中POE链的水合作用增强了。 [参考:27]

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