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Thermal decomposition of mercerized linter cellulose and its acetates obtained from a homogeneous reaction

机译:由均相反应获得的丝光棉绒纤维素及其乙酸酯的热分解

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Cellulose acetates with different degrees of substitution (DS, from 0.6 to 1.9) were prepared from previously mercerized linter cellulose, in a homogeneous medium, using N,N-dimethylacetamide/lithium chloride as a solvent system. The influence of different degrees of substitution on the properties of cellulose acetates was investigated using thermogravimetric analyses (TGA). Quantitative methods were applied to the thermogravimetric curves in order to determine the apparent activation energy (Ea) related to the thermal decomposition of untreated and mercerized celluloses and cellulose acetates. Ea values were calculated using Broido's method and considering dynamic conditions. Ea values of 158 and 187 kJ mol-1 were obtained for untreated and mercerized cellulose, respectively. A previous study showed that C6OH is the most reactive site for acetylation, probably due to the steric hindrance of C2 and C3. The C6OH takes part in the first step of cellulose decomposition, leading to the formation of levoglucosan and, when it is changed to C6OCOCH3, the results indicate that the mechanism of thermal decomposition changes to one with a lower Ea. A linear correlation between Ea and the DS of the acetates prepared in the present work was identified.
机译:使用N,N-二甲基乙酰胺/氯化锂作为溶剂体系,在均匀介质中,由先前光化的棉短绒纤维素在均匀介质中制备具有不同取代度(DS从0.6至1.9)的醋酸纤维素。使用热重分析(TGA)研究了不同取代度对乙酸纤维素性能的影响。为了确定与未处理的丝光化纤维素和醋酸纤维素的热分解有关的表观活化能(Ea),将定量方法应用于热重曲线。使用Broido方法并考虑动态条件计算Ea值。对于未处理的和丝光处理的纤维素,Ea值分别为158和187 kJ mol-1。先前的研究表明,C6OH是乙酰化反应最活跃的位点,这可能是由于C2和C3的空间位阻。 C6OH参与了纤维素分解的第一步,导致了左旋葡聚糖的形成,当将其变为C6OCOCH3时,结果表明热分解的机理转变为Ea较低的一种。鉴定了在本工作中制备的乙酸的Ea与DS的线性相关性。

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