Biomedical segmented polyurethanes (SPU) are frequently processed by soluti
on-casting techniques in order to obtain multilayer films. For processing p
arameters setup empirical criteria is currently applied. However, the selec
ted conditions can strongly affect the physico-chemical properties of the f
inished articles and they must be accurately established In order to descri
be the SPU coating formation, balances of heat, mass and momentum transfer
must be considered.
To study the drying process, two new medical-grade SPU solutions commercial
ly available, Biospan(TM) and Chronoflex AR(TM), were dried at different te
mperatures. Desorption curves and drying rate, both as a function of temper
ature, were obtained from experimental data. The mathematical model to desc
ribe this process take into account the heat and mass transfer and film shr
inkage along the whole drying step. The diffusion coefficients and the cont
rol mechanism were determined from the best experimental data fitting.
To obtain the solvent concentration profile, residual solvent and film, thi
ckness at any time, heat and mass transfer balances were numerically solved
using an explicit finite-difference method. The formulations showed differ
ent behavior For Biospan drying, performed in the range from 50 degrees C t
o 80 degrees C, a two-stage process was observed The first one controlled b
y mass transfer in the gas phase and the second one with mb control. When 4
0 degrees C drying temperature was applied a mb control was found along the
whole process. This change could be attributed to the acrylic additive pre
sent in the SPU matrix, which has a glass transition temperature value in t
he range of the process temperature. Chronoflex samples showed a two-stage
process in all cases and lower diffusion coefficients than Biospan samples.