Different from the traditional electrophilic polymerization
method
of thermoplastic elastomer, here, we adopted a new nucleophilic reaction
route, which did not need extreme high temperature and vacuum condition
to prepare a novel kind of semi-aromatic thermoplastic polyether amide
elastomers. First, difluoro-terminated semi-aromatic di-amide monomer
containing long chain ether (or 1,12-diaminododecane) was synthesized
through facile interfacial electrophilic substitution reaction. Then,
they were conducted to react with hydroquinone under atmospheric pressure
to yield polyether amide elastomer. Additionally, a small amount of
branched structure with trifluoro-terminated semi-aromatic amide monomer
was designed and further introduced into the polymer chain to adjust
the mechanical property. These semi-aromatic polyamide elastomers
were found to have excellent thermal properties with glass transition
temperature (T
g) of −39.5 to −34.8
°C, melting temperature (T
m) of 227.3–260.4
°C [which is much higher than that of the commercial products
such as Pebax5533 (Arkema, Paris, France) (T
m = 159 °C)], the 5% weight-loss temperature (T
d,5%) of 376.3–408.7 °C, and Vicat
softening temperature of 73.0–223.6 °C. The mechanical
properties of these resultant elastomers were good and can be controlled
with different copolymerization ratios of soft, hard, and branched
segments. The tensile strength, elongation at break, and elasticity
modulus were in the range of 9.8–23.4 MPa, 87.6–712.3%,
and 30.8–362.0 MPa, respectively. Besides, such a series of
copolymers showed a relatively low water absorption of 1.57–3.67%.
Interestingly, it was found that these resultant polyether amide elastomers
had better organic solvent resistance and acid–base corrosion
than the traditional TPAE-containing ester bond (−COO−)
in the polymer molecular chain. It can be potentially applied in the
chemical mechanical seal, especially in the high temperature and corrosion
environment.