In this study, flexible Nylon-6 was reinforced by semi- or wholly-arom
atic polyamides; poly(m-phenylene isophthalamide) (PmIA), poly(4,4'-di
phenylmethane terephthalamide) (PMA), and poly(4,4'-diphenylsulfone te
rephthalamide) (PSA). Various high molecular weight block copolyamides
were synthesized by solution polymerization using p-aminophenylacetic
acid (p-APA) as a coupling agent. Their thermal properties have shown
that the block copolyamides exhibit higher T-g and T-m, and better th
ermal stability than those of Nylon-6, especially PmIA modified Nylon-
6. The order of their thermal properties of aromatic modified Nylon-6
copolyamides is PmIA > PMA > PSA. Moreover, the T-g and T-m of multibl
ock copolyamides are higher than those of triblock copolyamides. From
the wide-angle X-ray diffraction pattern, it is found that the tribloc
k copolyamides have two diffraction peaks, i.e., 2 theta = 20.5 degree
s and 24 degrees. However, the multiblock has only one peak at 2 theta
= 20 degrees, indicating a different crystal structure for multiblock
copolyamides. For the mechanical properties, it is found that the mul
tiblock copolyamides have a more significant reinforcing effect than t
he triblock copolyamides. Also, the order of the physical properties o
f aromatic modified Nylon-6 copolyamides, such as tensile strength, is
PmIA > PMA > PSA, but for the elongation PSA > PMA > PmIA.