Abstract
Abstract 13C-NMR spectroscopy has been used to characterize the lignins extracted by an organosolv flow-through process from spruce TMP, bleached TMP (BTMP) and yellowed BTMP (YBTMP). In general, the 13C-NMR spectra of these lignins are similar to that of spruce MWL, indicating that the lignins underwent limited structural changes. Thus they may be an acceptable substrate for lignin structural study. However, these lignins appear to have a significant amount of condensed aromatic carbons assigned mainly to β-5, 5-5 and diarylmethane structures. These were likely formed during the organosolv cook, or initially present in TMP and extracted with this organosolv process. On the other hand, the hydrogen peroxide bleaching causes little change in the lignin overall structure. As a favorable effect, elimination of the coniferaldehyde structures can clearly be seen. The photoyellowing appears to result in the creation of aromatic carbonyl and carboxyl groups. This suggests that oxidative cleavage of Cα, Cβb bonds...
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.