A novel elongational device is used to investigate the capillary thinning p
rocess of threads of dilute and semidilute aqueous polymer solutions. It is
shown that the end regions of the threads do not play an essential role in
the thinning process, so that a simple theory describing the self-thinning
of the liquid thread is appropriate to describe the experiments with polym
er solutions carried out with this device. Aqueous solutions of four differ
ent polymers (all polyacrylamide based) are studied using the elongational
device. It is shown that the elasticity of the polymers is dominated by pol
yacrylamide chains and that the effect of branching and topological structu
re of macromolecules is negligible. The time-dependent decrease of the thre
ad diameter can be divided into two stages. The first is a viscoelastic one
where macromolecular coils are stretched by die elongational how, and the
second is a quasi-Newtonian one, where full stretching has already been ach
ieved, resulting in a very high but constant elongational viscosity. At the
first stage the rheological behavior of the solutions studied is character
ized by a constant relaxation time, whereas at the second one it is by a co
nstant elongational viscosity. For polymer macromolecules of relatively low
stability, mechanical degradation of the molecules is found during their s
tretching in a self-thinning capillary thread. (C) 2000 The Society of Rheo
logy. [S0148-6055(00)01003-8].