Kinetic study of chitosan-tripolyphosphate complex reaction and acid-resistive properties of the chitosan-tripolyphosphate gel beads prepared by in-liquid curing method
Fl. Mi et al., Kinetic study of chitosan-tripolyphosphate complex reaction and acid-resistive properties of the chitosan-tripolyphosphate gel beads prepared by in-liquid curing method, J POL SC PP, 37(14), 1999, pp. 1551-1564
Chitosan gel beads were prepared using am in-liquid curing method by the io
notropic crosslinking with sodium tripolyphosphate. Crosslinking characteri
stics of the chitosan-TPP beads were improved by the modification of in-liq
uid curing mechanism of the beads in TPP solution. Chitosan gel beads cured
in pH value lower than 6 were really ionic-crosslinking controlled, wherea
s chitosan gel beads cured in pH values higher than 7 were coacervation-pha
se :inversion controlled accompanied with slightly ionic-crosslinking depen
dence. According to the result, significantly increasing the ionic-crosslin
king density of chitosan beads could be achieved by transferring the pH val
ue of the curing agent, TPP, from basic to acidic. The swelling behavior of
various chitosan beads in acid appeared to depend on the ionic-crosslinkin
g density of the chitosan-TPP beads that were deeply affected by the curing
mechanism of the beads. The mechanism of chitosan-TPP beads swollen in wea
k acid was chain-relaxation controlled, while the mechanism of chitosan-TPP
beads swollen in strong acid seem to be not only chain-relaxation but also
chain-scission controlled. Chitosan-TPP beads prepared in acidic TPP solut
ion decreased the chain-scission ability due to the increase of ionic cross
linking density of the beads. By the transition of curing mechanism, the sw
elling degree of chitosan-TPP beads was depressed, and the disintegration o
f chitosan-TPP beads would not occur in strong acid. The mechanism of ionic
-crosslinking reaction of chitosan beads could be investigated by an unreac
ted core model, and the curing mechanism of the chitosan beads is mainly di
ffusion controlled when higher than 5% of chitosan was employed. (C) 1999 J
ohn Wiley & Sons, Inc.