The fracture behavior of blends of nylon 6 and acrylonitrile-butadiene-styr
ene (ABS) compatibilized with an imidized acrylic (IA) polymer was examined
by Izod impact testing and single-notch three-point bend (SEN3PB) instrume
nted Dynatup tests. The effects of the method of fracture surface measureme
nt, ABS content, specimen thickness, compatibilizer content and fracture zo
ne geometry were investigated. Blends containing a fixed (5 wt.% IA) compat
ibilizer content were tough over a broad range of ABS contents; the optimum
toughness occurred near 50 wt.% ABS. A dual-mode of fracture was observed
in SEN3PB specimens whose Izod impact samples with the same composition had
ductile-brittle transition temperatures near room temperature. In these SE
N3PB samples, ductile deformation occurred in samples with shorter ligament
lengths, whereas brittle failure prevailed in samples with longer ligament
lengths. The critical Ligament length at which the ductile-to-brittle tran
sition occurs was shown to be dependent on the compatibilizer content and s
pecimen thickness. These dual modes of fracture were rationalized in terms
of a plane-strain to plane-stress transition. For blends that were super to
ugh and had good low temperature toughness as judged by Izod impact testing
, the toughness of SEN3PB specimens was generally insensitive to specimen t
hickness; these blends were fully ductile over the entire range of ligament
lengths. The size of the stress-whitened zone was examined for fractured S
EN3PB specimens that were fully ductile over the entire range of ligament l
engths. Among specimens of a given composition, the size of the stress-whit
ened zones was geometrically similar and independent of the size of the ori
ginal ligament. However, when ductile samples of different composition were
compared, the size of the stress-whitened zone was not necessarily proport
ional to the energy dissipated during plastic deformation. This may be a re
sult of the presence of different modes of energy absorption in the nylon 6
or SAN matrix phase. (C) 1999 Elsevier Science Ltd. All rights reserved.