Dy. Chao et al., STUDY OF THE SYNTHESIS AND PHYSICAL-PROPERTIES OF FIRE-RESISTANT POLYURETHANE IONOMERS, Journal of applied polymer science, 67(1), 1998, pp. 19-26
Fire-resistant polyurethane ionomers successfully synthesized at our l
aboratory have been proved by infrared spectra. In aqueous solution, t
he surface tension for fire-resistant polyurethane ionomers made by to
luene diisocyanate or isophorone diisocyanate was found to decrease su
bstantially with increasing concentration of 1,4-bis (2-hydroxyethyl)p
iperazine but to increase gradually with increasing phenylphosphonic a
cid or 1,4-bis( 2-hydroxyethyl)piperazine with the phenylphosphonic ac
id concentration used to prepare these ionomers. For 1,4-bis( 2-hydrox
yethyl) piperazine-based polyurethane ionomers made by toluene diisocy
anate or isophorone diisocyanate in aqueous solution, the number-avera
ge particle sizes of these ionomers decrease drastically with increasi
ng 1,4-bis(2-hydroxyethyl) piperazine concentration, as a result of in
tramolecular interaction. On the other hand, for both phenylphosphonic
acid and 1,4-bis (2-hydroxyethyl) piperazine with phenylphosphonic ac
id-based polyurethane ionomers, their average particle size increased
with increasing phenylphosphonic acid or 1,4-bis (2-hydroxyethyl)piper
azine with phenylphosphonic acid concentration. This may be attributed
to the results of intermolecular interaction. Obviously, the limiting
oxygen index values are seen to be higher for the isophorone diisocya
nate type than for the toluene diisocyanate type of fire-resistant pol
yurethane ionomer. In fact, our experimental results suggest that the
isophorone diisocyanate types of fire-resistant polyurethane ionomers
provide good fire-resistance. For self-cured films of fire-resistant p
olyurethane ionomers, the tensile strength at breaking point increases
with increasing the concentration of fire retardants, but the elongat
ion at breaking point for these ionomers, on the other hand, appears t
o decrease with increasing concentration of fire retardants. (C) 1998
John Wiley & Sons, Inc.