葡萄糖在酸性溶液中的降解动力学研究*

Kenneth R. Heimlich , Alfred N. Martin
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引用次数: 46

摘要

在不同温度下对葡萄糖在酸溶液中的降解进行了研究。从5-羟甲基糠醛(5HMF)的初始形成速率得到的分解反应的一级速率常数始终高于在超过100°c的温度下长时间葡萄糖消耗测量的结果。在100°时,5-羟甲基糠醛的形成速率随着分解早期时间的增加而增加。在较高温度下,速率常数与阿伦尼乌斯图不一致。这表明在较低温度下发生机理变化的可能性。速率数据符合一级连续反应的动力学表达式。计算值与实验值吻合,表明反应是阶梯式的。从不同酸浓度的降解中得到的数据表明,速率常数不随正态性线性变化。在二恶烷-水混合物中的分解表明,速率常数的对数与介电常数的倒数呈线性变化。
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A Kinetic Study of Glucose Degradation in Acid Solution*

The degradation of glucose in acid solution was carried out at various temperatures. The first-order rate constants for the decomposition reaction, obtained from the initial rate of formation of 5-hydroxymethylfurfural (5HMF), were consistently higher than those calculated from glucose depletion measurements over long periods of time at temperatures above 100°. At 100° the rate of formation of 5-HMF increased with time for the early portion of the break-down. The rate constant did not coincide with the Arrhenius plot for higher temperatures. This indicates the possibility of a change of mechanism at lower temperatures. The rate data was fitted to kinetic expressions for first-order consecutive reactions. Agreement between calculated and experimental values indicates that the reaction proceeds by the step-wise mechanism. Data obtained from degradation in varying acid concentrations show that the rate constant does not vary linearly with normality. Decomposition in dioxane-water mixtures indicates that the logarithm of the rate constant varies linearly with the reciprocal of the dielectric constant.

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