MICROSTRUCTURAL EXAMINATION OF SEMIINTERPENETRATING NETWORKS OF POLY(N,N-DIMETHYLACRYLAMIDE) WITH CELLULOSE OR CHITIN SYNTHESIZED IN LITHIUM-CHLORIDE N,N-DIMETHYLACETAMIDE
Sl. Williamson et al., MICROSTRUCTURAL EXAMINATION OF SEMIINTERPENETRATING NETWORKS OF POLY(N,N-DIMETHYLACRYLAMIDE) WITH CELLULOSE OR CHITIN SYNTHESIZED IN LITHIUM-CHLORIDE N,N-DIMETHYLACETAMIDE, Macromolecules, 31(23), 1998, pp. 8134-8141
Semi-interpenetrating networks (SIPNs) of poly(N,N-dimethylacrylamide)
(DMAm) containing cellulose of chitin were prepared in 9%LiCl/N,N-dim
ethylacetamide (DMAc) as the homogeneous reaction medium. N,N-Methylen
ebisacrylamide (MBAm) was utilized as the cross-linking agent with 2,2
'-azobisisobutyronitrile (AIBN) as the initiator. The respective SIPNs
contained 25, 12, and 6 wt % cellulose or 6 wt % chitin. A control DM
Am hydrogel (without polysaccharide) was also synthesized in 9%LiCl/DM
Ac. The 25 wt % cellulose DMAm SIPN was found to be unique, differing
from the other compositions prepared, possessing a 6-fold higher modul
us than the DMAm control. The enhancement in mechanical stiffness was
attributed to intimate molecular interactions and complexation between
cellulose and DMAm. The presence of the extended cellulose chains wit
hin the DMAm matrix creates a more open network in the nonsolvated sta
te as reflected in DSC and fluorescence experiments. It is this molecu
lar level interaction of cellulose with DMAm that enhances the physica
l properties in the first SIPN composite to utilize unmodified cellulo
se and chitin. In the solvated state, the microdispersed polysaccharid
e hydrogen bonds with the DMAm matrix increases the rigidity of the ne
twork yet allows reversible hydration as reflected in rheology, equili
brium swelling, and fluorescence experiments.