A recent structure determination of native cellulose has shown that it is composed of two different crystal structures, a two-chain monoclinic phase and a single-chain triclinic phase. In this article a molecular dynamics study of the two allomorphs is presented, and a general picture of structure a
Determination of cellulose Iα and Iβ in lignocellulosic materials
✍ Scribed by Helena Lennholm; Tomas Larsson; Tommy Iversen
- Book ID
- 102996344
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 646 KB
- Volume
- 261
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
A novel method to estimate the relative amounts of cellulose I a and I, in lignocellulosic materials has been developed . 13C-CP/MAS NMR spectra were recorded on 12 calibration samples containing cellulose of various degrees of crystallinity . Principal component analysis of the NMR data extracted qualitative information about the relative amounts of amorphous cellulose, cellulose I a, and cellulose I s in the calibration samples . A quantitative partial least-squares (PLS) model was established between estimates of amorphicity index, cellulose I . -content, and cellulose I n-content and the 13 C-CP/MAS NMR data of the calibration samples . The cellulose la and Is content in some chemical and high-yield pulps was predicted from their NMR spectra by use of the PLS model . The existence of substantial amounts of cellulose I a in the pulp samples was demonstrated with the PLS model .
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