Structural features and thermal degradation properties of various lignin macromolecules obtained from poplar wood (Populus albaglandulosa)

Four different lignins obtained from poplar wood (milled wood lignin: ML, organosolv lignin: OL, ionic liquid lignin: IL and Klason lignin: ML) were subjected to several types of chemical/thermal analyses to compare their structural features and thermal decomposition properties. The ML, OL, IL and KL yield from poplar wood was 5.5, 3.9, 5.8, 19.5 wt%, respectively. Functional group analysis revealed that during the OL and ML extraction processes, the condensation reaction involved with phenolic hydroxyl groups of lignins significantly prevailed, which led to a highly condensed OL and ML structure. Thermogravimetric analysis (TGA) results showed that OL and ML thermal stability was much higher than that of ML and IL The derivatization followed by reductive cleavage (DFRC) data showed that the thermal stability was highly associated with the frequency of arylglycerol-beta-aryl ether (beta-O-4) linkages in the lignin polymers. Pyrolysis-GC/MS (Py-GC/MS) analysis confirmed that acetic acid and several types of phenolic compounds were the main lignin pyrolysis products. The maximum sum of ML (13.8 wt%), OL (9.9 wt%) and IL (11.8 wt%) pyrolysis products was obtained at the pyrolysis temperature of 600 degrees C, whereas ML (1.6 wt%) was significantly lower due to its high thermal stability and condensation degree. The S- and G-type pyrolysis products (S/G) ratio varied from 1.61 to 1.93 for ML, 2.28 to 5.28 for OL, 2.06 to 2.86 for IL and 1.40 to 2.20 for la, depending on the pyrolysis temperature, which ranged between 400 degrees C and 700 degrees C. (C) 2013 Elsevier Ltd. All rights reserved.