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Some physical properties of acetosolv lignins from bagasse
Author(s) -
Shukry N.,
Fadel S. M.,
Agblevor F. A.,
ElKalyoubi S. F.
Publication year - 2008
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.28059
Subject(s) - solubility , thermogravimetric analysis , fourier transform infrared spectroscopy , chemistry , gel permeation chromatography , differential scanning calorimetry , proton nmr , acetic acid , organic chemistry , carbon 13 nmr , polymer chemistry , polymer , chemical engineering , engineering , thermodynamics , physics
Acetosolv‐solubilized lignins were characterized by their solubility in different organic solvents, Fourier transform infrared, 13 C‐NMR, UV, gel permeation chromatography, differential scanning calorimetry, and thermogravimetric analysis. Solvents having a solubility parameter in the range of 10–12.7 and a hydrogen‐bonding parameter in the range of 3.6–5 were considered good solvents for acetosolv lignins. Fourier transform infrared spectra of the lignins were typical for lignins containing p‐hydroxy phenylpropane (H), guaiacyl (G), and syringyl (S) units. The lignins contained more conjugated and fewer nonconjugated CO groups, and the guaiacyl groups were etherified and condensed. 13 C‐NMR confirmed partial acetylation of the lignins and the presence of β‐ O ‐4 and β‐5 linkages. Acetosolv lignins also showed the typical UV spectrum of annual plants. The effects of the acetic acid concentration and pulping time on the molecular weights of the lignins were explained with the presieving and condensation concepts. The thermal behavior of the acetosolv lignins was also studied. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008