Stearoylated hemicelluloses with degrees of substitution 0.20-1.71 were pre
pared by a rapid reaction of wheat straw hemicelluloses with stearoyl chlor
ide using 4-dimethylaminopyridine as catalyst and triethylamine as acid acc
eptor in a homogeneous N,N-dimethylformamide and lithium chloride system. U
nder optimum conditions approximately 92% of the free hydroxyl groups in na
tive hemicelluloses were stearoylated in 30 min at 75 degrees C. Molecular
weight measurements showed only minimal degradation (less than or equal to
8%) of hemicellulosic chains during the rapid reactions at 75 degrees C for
10-35 min, while a noticeable degradation (similar to 20%) of the stearoyl
ated hemicelluloses was observed during the reaction at 85 degrees C. Diffe
rential thermal analysis studies revealed an increase of the thermal stabil
ity of the stearoylated hemicelluloses. (C) 2000 Elsevier Science Ltd. All
rights reserved.