The fracture energy required to delaminate PMDA/ODA polyimide films from al
uminum substrates was determined using the circular blister test. Films wer
e prepared by spin coating the polyamic acid of PMDA and ODA onto polished
aluminum substrates, by vapor co-deposition of PMDA and ODA monomers onto p
olished aluminum substrates, or by spin-coating the polyamic acid onto poli
shed aluminum substrates that were first coated with thin layers of gamma -
aminopropyltriethoxysilane (gamma -APS). Elastic and elastoplastic analyses
were used to extract the fracture energies from the blister test results.
Elastoplastic analysis provided fracture energies that ranged from 579J/m(2
) for spin-coated films on polished substrates to 705 J/m(2) for vapor-depo
sited films on polished substrates and to 750 J/m(2) for spin-coated films
on silanated substrates. These values were intermediate between those provi
ded by the two different elastic analyses. Differences in fracture energy d
etermined by the three different analysis methods were related to plastic d
eformation in the films and, in the case of the two elastic analyses, to di
fferences in the approach used to extract the fracture energy from experime
ntal results. Failure of specimens prepared by spin-coating PMDA/ODA films
onto aluminum substrates occurred cohesively within the polymer, near the i
nterface between well imidized polymer in the bulk of the films and poorly
imidized polymer in a layer near the aluminum surface. For the case of spec
imens prepared by vapor codeposition of PMDA and ODA monomers, failure occu
rred within the vapor deposited films, close to the aluminum/film interface
. Failure of spin-coated films on silanated substrates occurred mostly with
in the gamma -APS but leaving "islands" of polyimide and silane on the alum
inum.