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Dielectric relaxation study of m-Fluoroaniline and methanol mixture using time domain reflectometry

机译:使用时域反射测定法的M-氟二苯胺和甲醇混合物的介电弛豫研究

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The dielectric relaxation studies of liquids and liquid mixtures is a tool to understand intermolecular interaction along with molecular dynamics. Although m-Fluoroaniline (MFA) has higher dipole moment than methanol (MT) has dielectric constant less than that of methanol. H-bonds appear in methanol but not in m-Fluoroaniline. The dielectric behavior, dielectric relaxation mechanism of these pure liquids and their binary mixtures helps to understand nature of interactions between dipoles and effects of molecular bonding. Higher dielectric constant and relaxation time of of pure methanol compared to those of m-Fluoroaniline are due to presence of H-bonding and parallel alignment of electric dipoles. In pure m-Fluoroaniline spatial correlation between molecules appear only through dipole-dipole interactions. To study these aspects the Time domain Reflectometry technique has been used to obtain complex dielectric spectra of binary mixture of MT and MFA in the frequency range of 10 MHz to 10 GHz at various temperatures the results are presented
机译:液体和液体混合物的介电弛豫研究是理解分子间相互作用以及分子动力学的工具。虽然M-氟二苯胺(MFA)具有比甲醇(MT)更高的偶极矩,但具有小于甲醇的介电常数。 H键在甲醇中出现,但不含M-氟硅氧烷。这些纯液体的介电行为,介电弛豫机制及其二元混合物有助于了解偶极子与分子键合的相互作用的性质。与M-氟苯胺相比,纯甲醇的较高介电常数和弛豫时间是由于存在H键合和电偶极孔的平行对准的存在。在纯的M-氟胆碱中,分子之间的空间相关仅通过偶极 - 偶极相互作用出现。为了研究这些方面,已经使用时域反射测定技术在10MHz至10GHz的频率范围内获得MT和MFA的二元混合物的复杂介电光谱,在各种温度下呈现结果

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