Porous polyimide films were prepared in two steps. The first step was the p
reparation of poly(urethane-imide) films by a reaction between a phenol-ter
minated polyurethane prepolymer and poly(amide acid) obtained from pyromell
itic dianhydride (PMDA) and oxydianiline (ODA) followed by thermal treatmen
t at 200 degrees C. The second step was the pyrolysis of the poly(urethanei
mide) films. Upon thermal treatment of the poly(urethane-imide) films at 30
0 to 400 degrees C, the thermally less stable urethane domains decomposed,
leaving porous polyimide films. The presence of pores was confirmed from th
e scanning electron microscope (SEM) picture of the surface and the cross s
ection of the films. The size distribution of the pores was narrow. With in
creasing urethane content, the apparent density decreased but the size of t
he pore did not increase so much. Instead, the number of pores increased. T
ensile measurements revealed that, with increasing urethane component the t
ensile modulus did not vary very much, but the elongation and thus the tens
ile strength decreased. Viscoelastic analyses showed that all the porous po
lyimide films had a high glass transition temperature, above 400 degrees C,
and storage moduli were maintained up to 400 degrees C.