木质素
玻璃化转变
残余物
工业化学
材料科学
化学
复合材料
有机化学
聚合物
生化工程
数学
算法
工程类
作者
Åke Henrik-Klemens,Fabio Caputo,Roujin Ghaffari,Gunnar Westman,Ulrica Edlund,Lisbeth Olsson,Anette Larsson
出处
期刊:Holzforschung
[De Gruyter]
日期:2024-03-05
卷期号:78 (4): 216-230
被引量:1
摘要
Abstract The glass transition temperatures ( T g ) of native, residual, and technical lignins are important to lignocellulose pulping, pulp processing and side stream utilization; however, how the structural changes from native to residual and technical lignin influences T g has proven difficult to elucidate. Since the T g of macromolecules is greatly influenced by the molecular weight, low-molecular-weight fractions, such as milled wood lignin (MWL), are poor representatives of lignin in the cell wall. To circumvent this problem, lignins of both high yield and purity were isolated from Norway spruce and softwood kraft pulp using the enzymatic mild acidolysis lignin (EMAL) protocol. Technical softwood kraft lignin was also fractionated into groups of different molecular weights, to acquire lignin that spanned over a wide molecular-weight range. A powder sample holder for dynamic mechanical analysis (DMA), was used to determine the T g of lignins, for which calorimetric methods were not sensitive enough. The T g s of EMAL were found to be closer to their in situ counterparts than MWL.
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