The formation of N-acetyl chitosan gels in an acetic acid-water-propan
ediol solution was studied. Side reactions arising from the esterifica
tion of 1,2-propanediol by acetic anhydride, and hydrolysis of acetic
anhydride were studied, as well as their possible role on the gel form
ation. The gels were studied by FTIR and H-1 NMR spectroscopy. Indepen
dently of the initial acetylation degree of chitosan, a minimal acetyl
ation degree is required for gelation (80%). The final acetylation deg
ree of the gels increases with the molar ratio acetic anhydride/amine,
but does not reach 100%. An increase in temperature favours the molec
ular mobility, inter-and intra-molecular hydrogen bondings and hydroph
obic interactions, responsible for gelation which appears to depend on
two parameters: a critical acetylation degree and a critical molecula
r weight allowing the aggregation of the polymer chains. The nature of
the solvent used to avoid chitosan side reactions during gelation (et
hanol or propanediol) does not influence the chemical structure of the
gel but only the kinetics of gelation. (C) 1997 Elsevier Science Ltd.