Structure of cellulose and microcrystalline cellulose from various wood species, cotton and flax studied by X-ray scattering

By K. Leppänen, S. Andersson, M. Torkkeli, M. Knaapila, N. Kotelnikova, R. Serimaa. 2009

252 citations recorded by the source corpus.

Subfields: Biomaterials, Biomedical Engineering, Polymers and Plastics

View Paper: https://www.semanticscholar.org/paper/cb6ad113fcd0fb54c83c4070634cd5cd8d81e125

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In Biomaterials

1. U. Agarwal
2. I. Kontro
3. R. Reiner
4. S. Ralph
5. Kirsi Svedström
6. Patrik Ahvenainen
7. Orlando J. Rojas

In Biomedical Engineering

1. U. Agarwal
2. I. Kontro
3. Kirsi Svedström
4. Patrik Ahvenainen
5. Orlando J. Rojas

Citations in the corpus

• Comparison of sample crystallinity determination methods by X-ray diffraction for challenging cellulose I materials (2016, background): “…balsa (86 and 159 g/cm3, respectively) (Borrega et al. 2015), spruce-pine sulphite pulp and nata de coco (Parviainen et al. 2014), birch pulp (Testova et al. 2014), bamboo (Dixon et al. 2015), and MCC from birch sulphite, poplar kraft and cotton linters (Leppänen et al. 2009) were analyzed.”
• Cellulose polymorphy, crystallite size, and the Segal Crystallinity Index (2013, unknown): “There are numerous technologies for determination of crystallinity (Newman 1999; Park et al. 2009; Schenzel et al. 2005; Schwanninger et al. 2004), with one of the most widely used being X-ray diffraction (Leppänen et al. 2009).”
• Cellulose I crystallinity determination using FT–Raman spectroscopy: univariate and multivariate methods (2010, methodology): “Some of the frequently used techniques for estimating cellulose crystallinity are wide-angle X-ray scattering (WAXS) (Segal et al. 1959; Jayme and Knolle 1964; Leppänen et al. 2009), solid state (13)C cross-polarization/magic-angle spinning (CP/MAS) nuclear magnetic resonance (NMR) spectroscopy (Hor”