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Dynamics of water in supercooled aqueous solutions of glucose and poly(ethylene glycol)s as studied by dielectric spectroscopy

机译:介电谱研究葡萄糖和聚乙二醇过冷水溶液中水的动力学

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The dielectric behaviour of aqueous solutions of glucose,poly(ethylene glycol)s (PEGs) 200 and 600,and poly( vinyl pyr-rolidone) (PVP) has been examined at different concentrations in the frequency range of 10~6-10~(-6) Hz by dielectric spectroscopy and by using differential scanning calorimetry down to 77 K from room temperature.The shape of the relaxation spectra and the temperature dependence of the relaxation rates have been critically examined along with temperature dependence of dielectric strength.In addition to the so-called primary (alpha-) relaxation process,which is responsible for the glass-transition event at T_g,another relaxation process of comparable magnitude has been found to bifurcate from the main relaxation process on the water-rich side,which continues to the sub-T_g region,exhibiting relaxation at low frequencies.The sub-T_g process dominates the dielectric measurements in aqueous solutions of higher PEGs,and the main relaxation process is seen as a weak process.The sub-T_g process was not observed when water was replaced by methanol in the binary mixtures.These observations suggest that the sub-T_g process in the aqueous mixtures is due to the reorientational motion of the 'confined' water molecules.The corresponding dielectric strength shows a noticeable change at T_g,indicating a hindered rotation of water molecules in the glassy phase.The nature of this confined water appears to be anomalous compared to most other supercooled confined liquids.
机译:葡萄糖,聚乙二醇(PEG)200和600以及聚(乙烯基吡咯烷酮)(PVP)水溶液在10〜6-10〜 (-6)Hz是通过介电谱和从室温降至低至77 K的差示扫描量热法进行的。已严格研究了弛豫谱的形状和弛豫速率的温度依赖性以及介电强度的温度依赖性。与所谓的主要(α-)弛豫过程有关,后者负责T_g处的玻璃化转变,已发现另一个类似程度的弛豫过程与富水侧的主要弛豫过程分叉,并继续在较高的PEG水溶液中,sub-T_g过程主导着介电测量,而主要的弛豫过程被认为是一个弱过程。当二元混合物中的水被甲醇代替时,未观察到sub-T_g过程。这些观察结果表明,水性混合物中的sub-T_g过程是由于``受限''水分子的重新定向运动引起的。在T_g处显示出明显的变化,表明玻璃态中水分子的旋转受阻。与大多数其他过冷密闭液体相比,这种密闭水的性质似乎异常。

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