Ultraoriented polymer fibers have elastic modulus E as large as 350 GP
a and tensile strength sigma(b) as large as 7 GPa in materials with a
density rho approximate to 1200 Kg/m(3). Keys to achieving these prope
rties are near perfect orientation of polymer chains along the fiber a
xis and reduction of the number of chain ends. The two materials that
have been most thoroughly studied are polyethylene (PE) and poly(p-phe
nylene terephthalamide) (PPTA). Various schemes for calculating the el
astic modulus are reviewed, together with estimates of effects of impe
rfect chain orientation and the presence of chain ends. Fracture of fi
bers is treated in terms of covalent bond scission and/or chain slip o
riginating at chain ends. Under laboratory conditions the experimental
modulus E can be >90% of the theoretical modulus. It appears that fra
cture is more sensitive to chain end defects, limiting practical stren
gth to less than 25% of the ultimate strength predicted from bond scis
sion models.