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One-step alcoholysis of lignin into small-molecular aromatics: Influence of temperature solvent and catalyst

机译:木质素一步醇解为小分子芳烃:温度溶剂和催化剂的影响

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摘要

Lignin valorization is a challenge because of its complex structure and high thermal stability. Supercritical alcoholysis of lignin without external hydrogen in a self-made high-pressure reactor is investigated under different temperatures (450–500 °C) and solvents as well as catalysts by using a reactant suspension mode. Small-molecular arenes and mono-phenols (C7-C12) are generated under short residence time of 30 min. High temperature (500 °C) favors efficient deoxy-liquefaction of lignin (70%) and formation of small-molecular arenes (C6-C9). Solvents methanol and ethanol demonstrate much more synergistic effect on efficient deoxy-liquefaction of lignin than propanol. The catalyst Cu-C has the optimal activity and selectivity in methanol (70% of conversion, 83.93% of arenes), whereas Fe-SiC possesses the optimal catalytic deoxygenation in ethanol, resulting in the formation of arenes other than phenols. Further analysis indicates that lignin is converted into arenes by efficient cleavages of C—O ether bonds and C—C bonds under high temperature and pressure.
机译:由于木质素的结构复杂且具有很高的热稳定性,因此木质素的增值是一个挑战。通过使用反应物悬浮模式,在自制的高压反应器中研究了木质素在没有外部氢的情况下的超临界醇解作用,该温度是在不同温度(450–500 C)和溶剂以及催化剂的作用下进行的。小分子芳烃和单酚(C7-C12)是在30分钟的短停留时间内生成的。高温(500 C)有利于木质素的高效脱氧液化(70%)和形成小分子芳烃(C6-C9)。与丙醇相比,溶剂甲醇和乙醇对木质素的有效脱氧液化表现出更多的协同作用。催化剂Cu-C在甲醇中具有最佳的活性和选择性(转化率70%,芳烃的83.93%),而Fe-SiC在乙醇中具有最佳的催化脱氧作用,导致形成苯酚以外的芳烃。进一步的分析表明,木质素通过在高温和高压下有效裂解C-O醚键和C-C键而转化为芳烃。

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