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Hydrogen network fluctuations of associating liquids:Dielectric relaxation of ethylene glycol oligomers and their mixtures with water

机译:缔合液体的氢网络波动:乙二醇低聚物及其与水的混合物的介电弛豫

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摘要

Complex dielectric spectra of ethylene glycol and of various derivatives as well as of mixtures of water with an ethylene glycol oligomer and with a poly(ethylene glycol)dimethyl ether oligomer have been measured.The spectra can be well represented by a Cole-Cole [Cole and Cole,J.Chem.Phys.9,341(1941)]spectral function.The extrapolated low frequency(static)permittivity of this function has been evaluated to yield the effective dipole orientation correlation factor of the liquids.The relaxation time of the ethylene glycols displays a characteristic dependence upon the ratio of concentrations of hydrogen bond donating and accepting groups,indicating two opposing effects.With increasing availability of hydrogen bonding sites effects of association and also of dynamical destabilization increase.Both effects exist also in the mixture of water with the oligomers.They are discussed in terms of a wait-and-switch model of dipole reorientation in associating liquids.Another feature in the dependence of the dielectric relaxation time of poly(ethylene glycol)/water mixtures upon mixture composition has been tentatively assigned to precritical demixing behavior of the binary liquids in some temperature range.
机译:已测量了乙二醇及其各种衍生物以及水与乙二醇低聚物和聚(乙二醇)二甲醚低聚物的混合物的复介电谱。该谱可以很好地表示为Cole-Cole [Cole和Cole,J.Chem.Phys.9,341(1941)]光谱函数。已对该函数的外推低频(静态)介电常数进行了评估,以得出液体的有效偶极子取向相关系数。乙二醇的弛豫时间氢键提供和接受基团的浓度比具有特征依赖性,表明两个相反的作用。随着氢键位的可用性增加,缔合作用和动态失稳作用也增加。根据缔合液体中偶极子重新定向的等待-切换模型对它们进行了讨论。聚乙二醇/水混合物的介电弛豫时间对混合物组成的影响已初步确定为在某些温度范围内二元液体的预临界混合行为。

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