The transformation of CO2 into polymeric materials
is
an important and hot research topic from the viewpoint of renewable
resources and environmental effects. Herein, a series of polyureas
have been synthesized by polycondensation from CO2 with
diamines of 1,12-diaminododecane (DAD) and/or 4,7,10-trioxa-1,13-tridecanediamine
(TTD). The properties of polyureas synthesized were characterized
by FTIR, 1H NMR, 13C NMR, XRD, DSC, TGA, and
DMA. The polyureas synthesized from CO2 with a mixture
of diamines presented high performances compared to those of polyureas
synthesized from CO2 with a single diamine. The thermal
and mechanical properties were improved largely by the variation in
the crystallization and the chain flexibility depending on the changes
in the density and/or intensity of hydrogen bonds. With increasing
amounts of TTD from 0 to 100% in weight, the melting (T
m), crystallization (T
c),
and glass transition (T
g) temperatures
decreased from 207 to 116 °C, from 181 to 54 °C, and from
66 to −34 °C, respectively. When the TTD content was increased
from 0 to 50 wt %, the Young’s modulus decreased from 1170
to 406 MPa, and the tensile strength decreased from 53.3 to 42.9 MPa.
However, the elongation at break increased from 13 to 330%. Furthermore,
the chain length of aliphatic diamines and polyetheramines had a significant
effect on the mechanical properties. The initial decomposition temperature
(T
d,5%) is >295 °C, about 110
°C
higher than the T
m (116–207 °C),
which is advantageous for the postprocessing. The mechanical properties
of the polyureas synthesized herein are superior to those of polycarbonate
and polyamide 6. Thus, polyureas synthesized from the renewable and
cheap resources, CO2 and diamines, will find wide potential
applications in the field of polymeric materials.