Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, 1 Brookings Dr, St. Louis, MO, 63130, USA.
ChemSusChem. 2020 Sep 7;13(17):4557-4566. doi: 10.1002/cssc.202000942. Epub 2020 Jun 15.
Many valorization approaches for lignin rely on its organic solvent (organosolv) extraction. However, the severity of the extraction conditions required to obtain high lignin extraction generally results in low-quality lignin for downstream processing. To better understand the secondary reaction pathways and kinetics related to molecular alterations that result from organosolv extraction under extreme conditions, extractions were conducted at temperatures of 150, 180, and 210 °C. Lignin was collected at residence times between 0.25 and 18 h and analyzed by NMR techniques to quantify the concentrations of key chemical moieties that appear or disappear upon reactions of lignin molecules during and after their fractionation from biomass. The kinetics of chemical moiety evolution was modeled as processes in-series. In these models, pseudo first-order kinetics were used to describe the change in concentration of chemical moieties on extracted lignin as a function of residence time.
许多木质素的增值方法都依赖于其有机溶剂(有机溶剂)提取。然而,为了获得高木质素提取率而需要的提取条件的苛刻程度通常会导致下游处理的木质素质量较低。为了更好地理解在极端条件下通过有机溶剂提取导致分子变化的次级反应途径和动力学,在 150、180 和 210°C 的温度下进行了提取。在 0.25 到 18 小时的停留时间内收集木质素,并通过 NMR 技术进行分析,以定量关键化学部分的浓度,这些化学部分在木质素分子从生物质中分级分离过程中和之后的反应中出现或消失。化学部分演化的动力学被建模为串联过程。在这些模型中,拟一级动力学用于描述提取木质素中化学部分浓度随停留时间的变化。