Department of Chemistry, Christian-Doppler Laboratory, BOKU, University of Natural Resources and Life Sciences, Vienna, Muthgasse 18, A-1190 Vienna, Austria.
Biomacromolecules. 2011 Apr 11;12(4):871-9. doi: 10.1021/bm101555q. Epub 2011 Mar 10.
Celluloses from different origins were dissolved stepwise in N,N-dimethylacetamide/lithium chloride (9% v/w; DMAc/LiCl) with the aim to study the time course of the dissolution process, completeness of dissolution in the dissolved fractions, possible discrimination effects, and differences between the celluloses. Cellulosic pulps from both annual plants and different wood species were analyzed. The obtained fractions were subject to gel permeation chromatography (GPC) with multiple detection to monitor the development of molecular mass distribution (MMD), molecular mass, and recovered mass. The dissolution behavior of accompanying xylans was followed by quantitative analysis of the uronic acids by fluorescence labeling--GPC. The morphological changes at the remaining fibers in the stepwise dissolution were addressed by SEM. The time needed to dissolve completely the cellulosic pulp differed from species to species, mainly between pulps from annual plants and pulps from wood. Annual plants generally needed much longer to dissolve completely. In the beginning of the dissolution, the dissolved fractions of annual plants showed a distinct discrimination effect because they were enriched in hemicellulose. By contrast, wood pulps dissolve fast and without distinct changes in the MMD of the dissolved fractions over time. Bagasse pulp is an exception to the observation for annual plants and rather resembled the behavior of wood celluloses. Prolonged dissolution times, as often practiced in cellulose GPC, do not lead to any improvements regarding the determination of molecular mass, MMD, and recovered mass of injected sample, so that the dissolution times required for reliable GPC analysis can be significantly shortened, which will be important for biorefinery analytics with high numbers of samples.
从不同来源获得的纤维素在 N,N-二甲基乙酰胺/氯化锂(9%v/w;DMAc/LiCl)中逐步溶解,目的是研究溶解过程的时间进程、溶解在溶解部分的完全程度、可能的分辨效果以及纤维素之间的差异。分析了来自一年生植物和不同木材物种的纤维素浆。获得的级分通过凝胶渗透色谱(GPC)进行多次检测,以监测分子量分布(MMD)、分子量和回收质量的发展。通过荧光标记-GPC 对糖醛酸进行定量分析,跟踪伴随木聚糖的溶解行为。通过扫描电子显微镜(SEM)研究了分步溶解中剩余纤维的形态变化。完全溶解纤维素浆所需的时间因物种而异,主要是在一年生植物浆和木材浆之间。一年生植物通常需要更长的时间才能完全溶解。在溶解的开始阶段,一年生植物的溶解级分表现出明显的分辨效果,因为它们富含半纤维素。相比之下,木浆溶解速度快,溶解部分的 MMD 随时间没有明显变化。甘蔗渣浆是一年生植物观察的例外,其行为更类似于木纤维素。延长溶解时间,如在纤维素 GPC 中经常实践的那样,不会提高注入样品的分子量、MMD 和回收质量的测定,因此可以显著缩短用于可靠 GPC 分析的溶解时间,这对于具有大量样品的生物炼制分析将非常重要。