Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR

Abstract Cellulose forms crystalline fibrils, via biosynthesis, that can be just a few nanometers wide. The crystallinity is a structural factor related to material performance. Recently, many routes to isolate these fibrils as nanocellulose have been developed, and there exist various types of nano...

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Main Authors: Kazuho Daicho, Shuji Fujisawa, Kayoko Kobayashi, Tsuguyuki Saito, Jun Ashida
Format: Article
Language:English
Published: SpringerOpen 2020-09-01
Series:Journal of Wood Science
Subjects:
Online Access:http://link.springer.com/article/10.1186/s10086-020-01909-9
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spelling doaj-04fd8aafaf864a9e8ae4516db0f8cf192020-11-25T03:35:00ZengSpringerOpenJournal of Wood Science1435-02111611-46632020-09-016611710.1186/s10086-020-01909-9Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMRKazuho Daicho0Shuji Fujisawa1Kayoko Kobayashi2Tsuguyuki Saito3Jun Ashida4Graduate School of Agricultural and Life Sciences, The University of TokyoGraduate School of Agricultural and Life Sciences, The University of TokyoDivision of Forest and Biomaterials Science, Graduate School of Agriculture, Kyoto UniversityGraduate School of Agricultural and Life Sciences, The University of TokyoJEOL LtdAbstract Cellulose forms crystalline fibrils, via biosynthesis, that can be just a few nanometers wide. The crystallinity is a structural factor related to material performance. Recently, many routes to isolate these fibrils as nanocellulose have been developed, and there exist various types of nanocellulose with different crystallinities. Quantitative assessment of the crystallinity of nanocellulose is thus essential to advance knowledge in the high performance and functionality of such materials. Solid-state 13C cross-polarization/magic-angle spinning (CP/MAS) nuclear magnetic resonance (NMR) spectroscopy is a strong tool to investigate the structural features and dynamics of solid cellulose. The crystallinity is often evaluated by using the NMR signal ratio of the C4 crystalline and noncrystalline regions as a crystallinity index (CI) value. To calculate the CI value, it is necessary to examine the dependence of the contact time (CT) for CP on the signal intensity and set the optimum CT at a maximum of the signal intensity. However, the dependence has not been investigated for evaluation of the CI value of various cellulose samples with different crystal sizes. Here, we optimized the CT for evaluation of the CI value of cellulose with different crystal sizes. The error in the CI at the optimized CT was ~ 3%. At the optimized CT, the structural change after surface modification by TEMPO-oxidation was also analyzed from the NMR spectra of the C6 region. The relationship between the CI value and the degree of oxidation shows that it is possible to evaluate the degree of oxidation from the NMR spectra irrespective of the crystallinity of cellulose. Furthermore, the C4-based CI value was linearly correlated with the C6-based trans-gauche (tg) ratio, which is approximated by a function, CI = 0.9 tg ratio.http://link.springer.com/article/10.1186/s10086-020-01909-913C CP/MAS NMRCrystallinityNanocelluloseTEMPO-oxidation
collection DOAJ
language English
format Article
sources DOAJ
author Kazuho Daicho
Shuji Fujisawa
Kayoko Kobayashi
Tsuguyuki Saito
Jun Ashida
spellingShingle Kazuho Daicho
Shuji Fujisawa
Kayoko Kobayashi
Tsuguyuki Saito
Jun Ashida
Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR
Journal of Wood Science
13C CP/MAS NMR
Crystallinity
Nanocellulose
TEMPO-oxidation
author_facet Kazuho Daicho
Shuji Fujisawa
Kayoko Kobayashi
Tsuguyuki Saito
Jun Ashida
author_sort Kazuho Daicho
title Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR
title_short Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR
title_full Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR
title_fullStr Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR
title_full_unstemmed Cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13C NMR
title_sort cross-polarization dynamics and conformational study of variously sized cellulose crystallites using solid-state 13c nmr
publisher SpringerOpen
series Journal of Wood Science
issn 1435-0211
1611-4663
publishDate 2020-09-01
description Abstract Cellulose forms crystalline fibrils, via biosynthesis, that can be just a few nanometers wide. The crystallinity is a structural factor related to material performance. Recently, many routes to isolate these fibrils as nanocellulose have been developed, and there exist various types of nanocellulose with different crystallinities. Quantitative assessment of the crystallinity of nanocellulose is thus essential to advance knowledge in the high performance and functionality of such materials. Solid-state 13C cross-polarization/magic-angle spinning (CP/MAS) nuclear magnetic resonance (NMR) spectroscopy is a strong tool to investigate the structural features and dynamics of solid cellulose. The crystallinity is often evaluated by using the NMR signal ratio of the C4 crystalline and noncrystalline regions as a crystallinity index (CI) value. To calculate the CI value, it is necessary to examine the dependence of the contact time (CT) for CP on the signal intensity and set the optimum CT at a maximum of the signal intensity. However, the dependence has not been investigated for evaluation of the CI value of various cellulose samples with different crystal sizes. Here, we optimized the CT for evaluation of the CI value of cellulose with different crystal sizes. The error in the CI at the optimized CT was ~ 3%. At the optimized CT, the structural change after surface modification by TEMPO-oxidation was also analyzed from the NMR spectra of the C6 region. The relationship between the CI value and the degree of oxidation shows that it is possible to evaluate the degree of oxidation from the NMR spectra irrespective of the crystallinity of cellulose. Furthermore, the C4-based CI value was linearly correlated with the C6-based trans-gauche (tg) ratio, which is approximated by a function, CI = 0.9 tg ratio.
topic 13C CP/MAS NMR
Crystallinity
Nanocellulose
TEMPO-oxidation
url http://link.springer.com/article/10.1186/s10086-020-01909-9
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