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戊糖和己糖基碳水化合物聚合物的热降解动力学和机理。

Kinetics and mechanism of thermal degradation of pentose- and hexose-based carbohydrate polymers.

机构信息

Department of Chemistry, University of Sargodha, Sargodha 40100, Pakistan.

出版信息

Carbohydr Polym. 2012 Oct 15;90(3):1386-93. doi: 10.1016/j.carbpol.2012.07.008. Epub 2012 Jul 9.

Abstract

This work aims at study of thermal degradation kinetics and mechanism of pentose- and hexose-based carbohydrate polymers isolated from Plantago ovata (PO), Salvia aegyptiaca (SA) and Ocimum basilicum (OB). The analysis was performed by isoconversional method. The materials exhibited mainly two-stage degradation. The weight loss at ambient-115°C characterized by low activation energy corresponds to loss of moisture. The kinetic triplets consisting of E, A and g(α) model of the materials were determined. The major degradation stage represents a loss of high boiling volatile components. This stage is exothermic in nature. Above 340°C complete degradation takes place leaving a residue of 10-15%. The master plots of g(α) function clearly differentiated the degradation mechanism of hexose-based OB and SA polymers and pentose-based PO polymer. The pentose-based carbohydrate polymer showed D(4) type and the hexose-based polymers showed A(4) type degradation mechanism.

摘要

本工作旨在研究从车前草(PO)、埃及鼠尾草(SA)和罗勒(OB)中分离得到的戊糖和己糖基碳水化合物聚合物的热降解动力学和机理。分析采用等转化率法进行。这些材料主要表现出两阶段降解。环境温度-115°C 下的失重,其活化能较低,对应于水分的损失。确定了材料的动力学三参数 E、A 和 g(α)模型。主要降解阶段代表高沸点挥发性成分的损失。该阶段本质上是放热的。在 340°C 以上,完全降解发生,留下 10-15%的残渣。g(α)函数的主图清楚地区分了基于己糖的 OB 和 SA 聚合物以及基于戊糖的 PO 聚合物的降解机理。基于戊糖的碳水化合物聚合物表现出 D(4)型,而基于己糖的聚合物表现出 A(4)型降解机理。

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