Abstract

The idea of active cellulose is based on the initial induction period that is observed during thermogravimetric analysis of cellulose. The role of the reducing ends of cellulose samples (Avicel PH-101 and Whatman No. 42) was studied in relation to active cellulose formation, because our previous studies suggested that these end groups have lower thermal stabilities. Elimination of the reducing ends from Avicel PH-101 by reduction with NaBH4 substantially prolonged the induction period. These features were only characteristic of Avicel PH-101, with a leveling-off degree of polymerization (DP) of DP¯n 218. Formation of water-soluble oligosaccharides was also lower (240°C/60min). For Whatman No. 42 cellulose with a higher DP (DP¯n 2170), similar elimination of the reducing ends had almost no effect on the weight-loss behavior. The reducing group analysis data showed that a large number of new reducing ends were formed in Whatman cellulose during DP reduction as the initial pyrolysis process. Based on these differences arising from the initial DP of cellulose, a mechanism for active cellulose was proposed: thermal decomposition of reducing end groups, which are originally present or are formed during pyrolysis in crystalline cellulose, activates the following pyrolysis reactions. The molecular mechanism for activation is also discussed; we propose that it includes hydrogen-bond rearrangement in the initiation of pyrolytic reactions such as depolymerization (transglycosylation) and dehydration, based on our previous proposal that proton donation (acting as an acid catalyst) through hydrogen bonding is a fundamental mechanism for these pyrolytic reactions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.