首页> 外文期刊>The Journal of Chemical Thermodynamics >Densities, viscosities, and excess properties of binary mixtures of two imidazolide anion functionalized ionic liquids with water at T = (293.15 to 313.15) K
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Densities, viscosities, and excess properties of binary mixtures of two imidazolide anion functionalized ionic liquids with water at T = (293.15 to 313.15) K

机译:两种咪唑化物阴离子官能化离子液体与水在T =(293.15至313.15)K时的二元混合物的密度,粘度和过量性质

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Densities and viscosities of binary mixtures of 8-hydrogen-1,8-diazabicyclo[5,4,0]-undec-7-enium imidazolide ([HDBU]IM) and 8-butyl-1,8-diazabicyclo[5,4,0]-undec-7-enium imidazolide ([BDBU]IM) ionic liquids (ILs) with water were measured at temperatures from T = (293.15 to 313.15) K. Excess molar volumes V-E and viscosity deviations Delta eta of the mixtures were calculated to study the intermolecular interactions and structural factors between ILs and water. The results show that the V-E values of the two mixtures are negative over the whole composition range, while the Delta eta values have positive deviations, indicating that the hydrogen bonding interactions between IL and water are dominant in the mixtures. Moreover, the absolute values of V-E (vertical bar V-E vertical bar) of {[HDBU]IM (1) + H2O (2)} system are larger than those of {[BDBU]IM (1) + H2O (2)} system at the same condition, indicating that the hydrogen bonding interactions between [HDBU]IM and water are stronger than those between [BDBU]IM and water. Both vertical bar V-E vertical bar and Delta eta values of the mixtures decrease with the increasing temperature, resulting from the decreasing the hydrogen bonding interactions between IL and water. Other derived properties of the studied systems, such as the apparent molar volumes, partial molar volumes, excess partial molar volumes, Gibbs free energy of activation for viscous flow, and excess Gibbs free energy of activation for viscous flow were also calculated from the experimental values. (C) 2015 Elsevier Ltd. All rights reserved.
机译:8-氢-1,8-二氮杂双环[5,4,0]-十一碳-7-咪唑啉([HDBU] IM)和8-丁基-1,8-二氮杂双环[5,4]的二元混合物的密度和粘度在0°C =(293.15至313.15)K的温度下,测定了水的0,-十一碳-7-咪唑啉([BDBU] IM)离子液体(ILs)。过量的摩尔体积VE和混合物的粘度偏差Δeta为用来研究IL和水之间的分子间相互作用和结构因素。结果表明,两种混合物的V-E值在整个组成范围内均为负值,而Delta eta值具有正偏差,表明IL和水之间的氢键相互作用在混合物中占主导地位。此外,{[HDBU] IM(1)+ H2O(2)}系统的VE(垂直条VE垂直条)的绝对值大于{[BDBU] IM(1)+ H2O(2)}系统的VE的绝对值在相同条件下,表明[HDBU] IM与水之间的氢键相互作用强于[BDBU] IM与水之间的氢键相互作用。混合物的垂直线V-E垂直线和Deltaη值均随温度升高而降低,这是由于IL与水之间的氢键相互作用降低所致。还从实验值中计算了研究系统的其他派生特性,例如表观摩尔体积,部分摩尔体积,过量的部分摩尔体积,粘性流的活化Gibbs自由能和粘性流的活化过量Gibbs自由能。 。 (C)2015 Elsevier Ltd.保留所有权利。

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