首页> 外文期刊>Journal of Molecular Liquids >On the physico-chemical basis of self-nanosegregation giving magnetically-induced birefringence in dibutyl phosphate/bis(2-ethylhexyl) amine systems
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On the physico-chemical basis of self-nanosegregation giving magnetically-induced birefringence in dibutyl phosphate/bis(2-ethylhexyl) amine systems

机译:在磷酸二丁基/双(2-乙基己基)胺系统中磁诱导的双折射的自纳中聚四甲酸的物理化学基础

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摘要

Dibutyl phosphate (DBP)/bis(2-ethylhexyl) amine (BEEA) liquid mixtures can show optical birefringence when exposed to a magnetic field. It has been hypothesized that this is a consequence of self-segregation characterizing these systems giving formation of anisotropic local assemblies which are able to re-orient undermagnetic field. In thiswork, an ab-initio Density Functional Theory computermodeling coupledwith synchrotron X-Ray Scattering (XRS) experiments carried out at various BEEAmolar ratio (X) and temperatures (10 <= T <= 60 degrees C) permitted to highlight the physical origin of this effect: a DBP-to-BEEA proton transfer with formation of an inherently anisotropic DBP-BEEA ion pair constituting the building block of highly structured ionic liquid nanodomains. At nonequimolar compositions (X not equal 0.5) such ionic liquids domains are dispersed in the component in excess. At X > 0.5 the ionic liquids nanodomains are dispersed in excess of poorly structured BEEA, creating the ideal assumptions for the formation of a two-phase dispersed system, as confirmed by Guinier analysis in the small angle regime of the XRS spectra, explaining the system capability to become birefringent in reaction to external magnetic field. These information can be transferred to other amphiphiles-based mixtures for the piloted design of new magnetic field responsive materials with advanced applications. (C) 2020 Elsevier B.V. All rights reserved.
机译:磷酸二丁酯(DBP)/双(2-乙基己基)胺(Beea)液体混合物可以在暴露于磁场时显示光学双折射。已经假设这是自偏析表征这些系统的后果,其形成能够重新定向在底部的区域的各向异性局部组件。在这方面,AB-Initio密度泛函理论计算机耦合耦合的同步X射线散射(XRS)实验在各种牛排比(X)和温度(10 <= T <= 60摄氏度)允许突出显示物理来源这种效果:具有构成高度结构化离子液体纳米膜的构建结构块的固有各向异性DBP-Bea离子对的DBP-to-eaa质子转移。在非Quimolar组合物(x不等于0.5),这种离子液体结构域分散在多余的组分中。在X> 0.5处,离子液体纳米型纳米型纳米液体分散超过结构较差的贝亚,从而产生了两相分散系统的理想假设,如XRS光谱的小角度制度中的Guinier分析所确认的那样,解释了系统能力成为外部磁场反应的双折射。这些信息可以转移到其他基于两种基于两种基于两种的混合物,用于使用先进的应用程序的新磁场响应材料设计。 (c)2020 Elsevier B.v.保留所有权利。

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