T. Wang et al., SURFACE-STRUCTURES AND ADHESION ENHANCEMENT OF POLY(TETRAFLUOROETHYLENE) FILMS AFTER MODIFICATION BY GRAFT-COPOLYMERIZATION WITH GLYCIDYL METHACRYLATE, Journal of adhesion science and technology, 11(5), 1997, pp. 679-693
Surface modifications of Ar plasma-pretreated poly(tetrafluoroethylene
) (PTFE) film were carried out via near-UV light-induced graft copolym
erization with glycidyl methacrylate (GMA). The structure and chemical
composition of the copolymer surface and interface were studied by an
gle-resolved X-ray photoelectron spectroscopy (XPS). For PTFE substrat
e with a substantial amount of grafting, the grafted GMA polymer penet
rates or becomes partially submerged beneath a thin surface layer of d
ense substrate chains to form a stratified surface microstructure. The
concentration of the surface-grafted GMA polymer increases with the p
lasma pretreatment time, the near-UV light illumination time, and the
monomer concentration. The GMA graft copolymerized PTFE surfaces adher
e strongly to one another when brought into direct contact and cured (
i) in the presence of a diamine alone or (ii) in the presence of an ep
oxy adhesive (epoxy resin plus diamine curing agent). In the presence
of diamine alone, failure occurs in the interfacial region. For epoxy
adhesive-promoted adhesion, the failure mode is cohesive, i.e. it take
s place in the bulk of one of the delaminated PTFE films. The lap shea
r strengths in both cases increase with the amount of surface-grafted
epoxide polymer. The development of the adhesion strength depends on t
he concentration of the surface graft, the microstructure of the graft
copolymerized PTFE surface, the interfacial reactions, and the nature
of the bonding agent.