We examine the roles of several types of intramolecular interactions in the
behavior of the steady elongational flow properties of infinitely dilute p
olymer solutions. In particular, bond stretching bond bending, bond torsion
, and nonbonded intramolecular interactions are included. Geometric and rhe
ological properties are calculated using Monte Carlo integration. We observ
e that bond bending and nonbonded interactions result in significant change
s over the traditional bond stretching predictions, but bond torsion plays
only a minor role. Bond bending results in more abrupt chain expansion with
increasing elongation rate, and the corresponding increase in the elongati
onal viscosity is also more steep. Nonbonded interactions cause the chain t
o be more spheroidal at lower elongation rates, and they result in a minimu
m in the elongational viscosity at an intermediate elongation rate-presumab
ly as a result of excluded-volume effects causing the chain to be slightly
more expanded.