Comparative and Structural Characterization of Organosolv and Alkali Lignins from Abaca Fiber

• Published in: International journal of polymer analysis & characterization 1998-11, Vol.4 (6), p.517-530
• Main Authors: Sun, Runcang, Xiao, Bing, Fang, Jianmin, Goodwin, Andy, Lawther, J. Mark
• Format: Article
• Language: English
• Subjects: 13C-NMR; Abaca fiber; Alkali lignin; Alkaline nitrobenzene oxidation; FT-1R; Molecular weight; Organosolv lignin; Phenolic acids and aldehydes
• ISSN: 1023-666X; 1563-5341
• DOI: 10.1080/10236669808009732

In ihis study, one organosolv lignin preparation and two alkali lignin preparations were extracted with 95% ethanol, 1% NaOH from abaca fiber, and 17.5% NaOH from the fiber holocellulose. respectively. The three lignin preparations were compared using spectroscopic and degradative techniques. The very small chemical differences between the one organosolv lignin and two alkali lignin preparations were mainly that the organosolv lignin contained 3.70% neutral sugars and 1.88% uronic acids. The two alkali lignin preparations, however, were relatively free of neutral sugars and had lower uronic acid content. The weight-average molecular weights (Mw) of the lignins ranged between 2,160 and 3.340. All three lignin preparations showed a large proportion of syringyl units and fewer guaiacyl and p-hydroxyphenyl units. The lignin preparation B, extracted with 1% NaOH at 25°C for 0.5 h, is mainly composed of β-O-4 and 3-3 ether bonds, together with some β-β and β-5 carbon-carbon linkages between the lignin structural units. Furthermore, it was found that p-coumaric acids and uronic acids were eslerified to lignin. while ferulic acids are etherified to lignin molecules.