Thermodynamics of the interaction of HCl with D-galactose in water at 278.15–318.15 K

Jianji Wang, K. Zhuo, Qiufen Zhang, Zhenning Yan, Han-qing Wang
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引用次数: 14

Abstract

Thermodynamic parameters of the interaction of HCl with D-galactose in water have been determined from electromotive force measurements at 10 K intervals from 278.15 to 318.15 K. Standard Gibbs energies of transfer of HCl from water to aqueous solutions of 5, 10, 15 wt.% D-galactose were evaluated. Comparison of pair interaction parameters of HCl–D-galactose was made with those of HCl–D-glucose and HCl–D-arabinose. The difference between these parameters was interpreted in terms of the stereochemistry of these monosaccharides. An enthalpy–entropy compensation has been observed with the pair interaction parameters for the HCl–sugar–water systems at each given temperature studied. The salting constants, kS, of D-galactose, D-glucose, D-fructose, D-arabinose, and sucrose by HCl in water were calculated from (a) the Debye–MacAulay theory (DMT); (b) Conway–Desnoyers–Smith theory (CDST); (c) the internal pressure theory developed by McDevit–Long (IPT); (d) the scaled particle theory (SPT). The results show that the calculated values of kS are reasonably in agreement with the experimental ones.
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278.15 ~ 318.15 K时水中HCl与d -半乳糖相互作用的热力学
在278.15 ~ 318.15 K的10 K间隔内,通过电动势测量确定了HCl与d -半乳糖在水中相互作用的热力学参数。计算了HCl从水中转移到5%、10%、15% d -半乳糖水溶液的标准吉布斯能。将半乳糖的对相互作用参数与葡萄糖和阿拉伯糖进行了比较。这些参数之间的差异是根据这些单糖的立体化学来解释的。在研究的每个给定温度下,对氢-糖-水体系的相互作用参数进行了焓-熵补偿。根据(a) Debye-MacAulay理论(DMT)计算d -半乳糖、d -葡萄糖、d -果糖、d -阿拉伯糖和蔗糖在盐酸溶液中的盐化常数kS;(b) conway - desnoyer - smith理论;(c)由McDevit-Long (IPT)提出的内压理论;(d)缩放粒子理论(SPT)。结果表明,k的计算值与实验值基本吻合。
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