The properties of a 100 penetration grade bitumen are modified considerably
, and in a number of ways by the addition of 10 to 40 parts per hundred (pp
h) of a homopolystyrene and graft, block and random copolymers of styrene w
ith butadiene and acrylonitrile. At low temperatures some blends have a sim
ilar stiffness to or even lower stiffness than the bitumen, but generally t
he blends are more than one order of magnitude stiffer, even when a rubber
is added. The contrasting behavior is displayed by a polystyrene and a high
impact polystyrene, similar to3% to 4% of grafted rubber on the latter bei
ng sufficient to cause the enhancement, even at the 10 pph level, by two di
fferent random styrene-butadiene copolymers, and also by blends consisting
of different amounts of SBS block copolymer. Some polymers apparently trigg
er a Hartley inversion of the micellar structure of the asphaltene micelles
. High law temperature stiffness correlates roughly with a lower Tg, as mea
sured by the peak maximum in the E " plots of the dynamic mechanical therma
l analysis (DMTA) and by the steps in the differential scanning calorimetry
(DSC) curves at temperatures below 0 degreesC. Tan delta maxima and DSC tr
aces detected the glass transition in the continuous phase and in the dispe
rsed phases, but none of these amorphous polymers formed a crystalline phas
e, though the DSC traces of the polystyrene and the SBS blends suggested th
at the polymer-rich phases underwent an aging/ordering process on cooling.
Our SBS blends differ in phase inversion behavior and the pattern of loss p
rocesses from others that had a smaller asphaltene component.