The potential benefits from using a novel vinyl-terminated long alkyl-chain self-assembling silane (VTS) have been investigated. A relatively high water contact-angle of 83° was found for water on the VTS-pretreated soda-lime glass surface. This revealed that the degree of hydrophobicity of this surface was far more pronounced than for the ultrasonically-cleaned glass surface or the γ-glycidoxypropyltrimethoxy silane (GPS)-pretreated glass surface, which gave contact angles of 14° and 42°, respectively. Further, good agreement between the measured and the theoretical contact angles for a fully adsorbed vinyl-terminated self-assembled monolayer surface implied that the VTS molecules were adsorbed with the vinyl-terminal groups orientated away from the glass surface. Indeed, X-ray photoelectron spectroscopy (XPS) analysis confirmed that the VTS molecules were adsorbed as a monolayer with the vinyl-terminal groups orientated away from the glass surface. Double-cantilever beam joints were prepared using these various pretreated-glass substrates, using an epoxy adhesive, and they were tested employing a fracture-mechanics approach. The adhesive fracture energy, G c , of the VTS-pretreated glass/epoxy joints was found to be far lower in value than for the ultrasonically-cleaned joints or the GPS-pretreated joints. The potential applications of this novel long alkyl-chain silane are two-fold: (a) the relatively very poor adhesion of the VTS pretreatment enables this silane to be used as an excellent abhesive layer, i.e. as a release agent, and (b) the presence of reactive vinyl-terminal groups might allow this silane to be activated to form functional groups that may then react with an adhesive, such as an epoxy resin, and so act as an excellent adhesion promoter to increase the durability of the adhesive joint.Keywords: Abhesion, accelerated testing, durability, glass, monolayers, organosilane adhesion promoters, XPS 2
IntroductionCommercially-available short alkyl-chain silane primers have been used extensively to decrease the susceptibility of the adhesive-substrate interface to attack by water, see for example [1][2][3]. The ability of these silanes to promote enhanced adhesion to metallic and ceramic substrates is a result of the specific interaction, via a condensation reaction, between the silanols of the hydrolysed silane with hydroxyl groups present on the surface of the substrate to form covalent bonds [1][2]. Typically there is also a functional terminalgroup at the other end of the silane molecule which may react with the adhesive. Thus, silanes may 'couple', via covalent bonding, the substrate to the adhesive.However, such commercially-available silane primers have a relatively short alkylchain in their chemical structure, and typically adsorb onto the surface of the substrate as disordered multilayer layers. For example, γ-glycidoxypropyltrimethoxysilane (GPS)typically adsorbs with approximately 50 % of the silanol groups pointing upwards and 50 % pointing downwards [4], and typically forms a mult...