We study the elasto-capillary self-thinning and ultimate breakup of three p
olystyrene-based ideal elastic fluids by measuring the evolution in the fil
ament diameter as slender viscoelastic threads neck and eventually break. W
e examine the dependence of the transient diameter profile and the time to
breakup on the molecular weight, and compare the observations with simple t
heories for breakup of slender viscoelastic filaments. The evolution of the
transient diameter profile predicted by a multimode FENE-P model quantitat
ively matches the data provided the initial stresses in the filament are ta
ken into account. Finally, we show how the transient uniaxial extensional v
iscosity of a dilute polymer solution can be estimated from the evolution i
n the diameter of the necking filament. The resulting "apparent extensional
viscosity" profiles are compared with similar results obtained from a fila
ment stretching rheometer. Both transient profiles approach the same value
for the steady state extensional viscosity, which increases with molecular
weight in agreement with the Rouse-Zimm theory. The apparent discrepancy in
the growth rate of the two transient curves can be quantitatively explaine
d by examining the effective stretch rate in each configuration. Filament t
hinning studies and filament stretching experiments thus form complementary
experiments that lead to consistent measures of the transient extensional
viscosity of a given test fluid. (C) 2001 The Society of Rheology.