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Mild synthesis of benzylated bamboo in LiCl/DMSO solution
Author(s) -
Li MingFei,
Sun ShaoNi,
Xu Feng,
Sun RunCang
Publication year - 2011
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.35551
Subject(s) - bamboo , crystallinity , fourier transform infrared spectroscopy , cellulose , magic angle spinning , polymer chemistry , benzyl chloride , thermal stability , materials science , nuclear chemistry , chemistry , nuclear magnetic resonance spectroscopy , organic chemistry , chemical engineering , catalysis , composite material , engineering
Benzylated bamboo was mildly synthesized in nonaqueous medium without mercerization pretreatment. The ball‐milled bamboo was firstly preswelled in lithium chloride/dimethyl sulfoxide (LiCl/DMSO) solution and then reacted with benzyl chloride in the presence of solid NaOH with varying molar ratios of benzyl chloride to OH groups of bamboo (1–4), reaction times (1–8 h), and temperatures (60–90°C). Benzylated bamboo products with yields from 51.1 to 106.9% and with degrees of substitution [DS, apparent value evaluated by Fourier transform infrared (FTIR) spectra] between 0.2 and 1.2 were synthesized. FTIR and 13 C cross polarization/magic angle spinning nuclear magnetic resonance (CP/MAS NMR) spectroscopy confirmed the incorporation of benzyl groups into bamboo; SEM observations of the highly benzylated bamboo showed porous surface with small irregular slices ascribed to the disruption of intermolecular and intramolecular hydrogen bonds between cellulose. Because of the degradation of amorphous components, the crystallinity decreased negligibly after modification and the thermal stability increased slightly but was lower than that of cellulose. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012