T. Nakashima et al., Morphology and mechanical properties of poly(vinyl alcohol) and starch blends prepared by gelation/crystallization from solutions, COLLOID P S, 279(7), 2001, pp. 646-654
In an attempt to produce biodegradation materials, poly(vinyl alcohol) (PVA
) starch (ST) blends were prepared by gelation/crystallization from semidil
ute solutions in dimethyl sulfoxide (Me2SO) and water mixtures and elongate
d up to 8 times. The content of mixed solvent represented as Me2SO/H2O (vol
ume percent) was set to be 60/ 40 assuring the greatest drawability of PVA
homopolymer films. The PVA/ST compositions chosen were 1/1, 1/3, and 1/5. T
he elongation up to 8 times could be done for the 1/1 blend but any elongat
ion was impossible for blends whose ST content was beyond 50%. When the ble
nds were immersed in water at 20 or 83 degreesC, the solubility became cons
iderable for an undrawn blend with 1/5 composition and a drawn 1/1 blend wi
th lambda = 8. To avoid this phenomenon, cross-linking of PVA chains was ca
rried out by formalization under formaldehyde vapor. Significant improvemen
t could be established by tile cross-linking of PVA chains. For the 1/1 ble
nd, the amount of ST dissolved in water at 23 degreesC was less than 3% for
the undrawn state and 25% for the drawn film. The decrease in the ST conte
nt was enough for use as biodegradation materials. Namely, the water conten
t relating to the biodegradation in soil is obviously different from such a
serious experimental condition that a piece of blend film was immersed in
a water bath. At temperatures above 0 degreesC, the storage modulus of the
formalization blends became slightly higher than those of the nonformalizat
ion blends. The Young's modulus of the drawn films with a draw ratio of 8 t
imes was 2 GPa at 20 degreesC.