Hemicellulose acetates were prepared under homogeneous reaction conditions
in the system N,N-dimethylacetamide/lithium chloride by reacting the native
hemicelluloses with acetic anhydride in the presence of 4-dimethylaminopyr
idine within 72 h at 60-85 degrees C. The products obtained were characteri
sed by means of Fourier transform infrared chromatography, gel permeation c
hromatography, and thermal analysis. The degree of substitution of acetylat
ed hemicelluloses ranged between 0.74 and 1.49 as a function of experimenta
l conditions. Under an optimum reaction condition (85 degrees C, 60 h), ove
r 80% hydroxyl groups in native hemicelluloses were acetylated. The molecul
ar weight measurements showed that a significant degradation and hydrolysis
of the products appeared at only a prolonging period of 72 h. It was found
that the thermal stability of the products increased by esterification. (C
) 1999 Elsevier Science B.V. All rights reserved.