Thermal imidization of poly(amic acid) precursors on surface-modified poly(tetrafluoroethylene) films via graft copolymerization with glycidyl methacrylate

A novel method for preparing composites of polyimides (PI) laminated to poly(tetrafluoroethylene) (PTFE) films is reported. PI/PTFE composites were developed through thermal imidization of poly(amic acid) (PAA) precursors on surface-modified PTFE films. Surface modification of PTFE films was carried out via Ar plasma pretreatment of the films, followed by UV-induced graft copolymerization with glycidyl methacrylate (GMA). The surface composition and topography of the graft copolymerized PTFE films and the delaminated PI and PTFE surfaces were characterized by X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM), respectively. The adhesion strengths of the PI (imidized PAA) on the GMA graft copolymerized PTFE films were evaluated as a function of various thermal imidization schedules. The adhesion reliability of the PI/PTFE composites was tested by a series of hydrothermal cycles. The development of strong Tpeel adhesion strengths of about 8 N/cm with excellent reliability for the PI/PTFE composites was attributable to the synergistic effect of coupling the curing of the epoxide functional groups of the grafted GMA chains with the imidization process of the PAA and the fact that the GMA chains were covalently tethered onto the PTFE surface. The PI/PTFE composites delaminated via cohesive failure inside the PTFE substrates. The delaminated PI film with a covalently adhered 'rough' PTFE surface layer exhibited a water contact angle as high as 140°.     

Surface modifications of EVA copolymers induced by low pressure RF plasmas from different gases and their relation to adhesion properties

Two ethylene vinyl acetate (EVA) copolymers (12 and 20 wt% of vinyl acetate,VA, content) have been treated with low pressure RF plasmas from non-oxidizing gases (Ar, N₂) and oxidizing gases (air, a mixture of 4N₂: 6O₂ (v/v), O₂ and CO₂). The formation of polar moieties on both EVAs was more noticeable by treatment with plasmas from non-oxidizing gases than from oxidizing ones (the higher the reactivity, the lower the difference with respect to untreated EVA surfaces). The surface etching with the non-oxidizing plasmas, giving rise to a high roughness, depends on the wt% of VA in the composition of the copolymer because of the different resistances of VA (low) and PE (high) to the non-oxidizing plasma particles bombardment. The adhesion properties obtained using a polyurethane adhesive (PU) showed high T-peel strength values and adhesion failure in EVAs treated with plasmas from oxidizing gases, due to roughness produced causing mechanical interlocking of the adhesive. Lower T-peel strength values were obtained with non-oxidizing plasmas: the values for EVA12 being, in general, lower than those obtained for EVA20. The durability of the treated EVAs/PU adhesive joints after ageing in humidity and temperature was quite good.     

Evidence for formation of metallo-siloxane bonds by comparison of dip-coated and electrodeposited silane films

It has been amply demonstrated that thin films of organofunctional silanes deposited by dipping or spraying on metals, such as aluminum, can provide protection against various forms of corrosion. In this paper we show that denser films with higher pore resistance and better corrosion protection performance can be obtained if the silane film is produced by electrodeposition rather than by dipping. In such a process the silane reacts with the metal oxide in a different way, and in the case of aluminum, aluminate ions seem to be incorporated into the silane film. The resulting films can protect aluminum alloys against uniform and pitting forms of corrosion in a salt solution for more than 1000 h, which is comparable to the standard chromate-based treatments. This paper discusses the protection mechanism in some detail. An important aspect of this work is that the use of XPS and TOFSIMS to analyze electrodeposited silane films provided direct evidence for the presence of O₂Al(O–Si–O) and OAl(O–Si–O)₂ groups at the silane–aluminum oxide interface. Such bonds have been suggested, but they have largely remained elusive over the years.     

Gas-phase surface functionalization of multi-walled carbon nanotubes with vacuum UV photo-oxidation

For bulk processing of carbon nanotubes, an important first step in adhesion to the nanotubes is often liquid-phase functionalization through chemical oxidation with acids (e.g., nitric and sulfuric), peroxides and/or potassium permanganate. In comparison, gas-phase photo-oxidation can be an alternative to introduce oxygenated functional groups on the surfaces of carbon nanotubes without the generation of liquid waste. In the present study, vacuum UV photo-oxidation of multi-walled carbon nanotube (MWNT) paper was investigated downstream from an Ar microwave plasma. X-ray Photoelectron Spectroscopy (XPS) was used to detect the carbon- and oxygen-containing functional groups in the top 2–5 nm of the sample's surface. The current results are compared to previous investigations using MWNT powder and single-walled carbon nanotube (SWNT) paper showing decreased levels of oxidation in MWNT samples.     

UV-Ozone Surface Treatment of SBS Rubbers Containing Fillers: Influence of the Filler Nature on the Extent of Surface Modification and Adhesion

SBS rubbers containing different loadings of calcium carbonate and/or silica fillers were surface treated with UV-ozone to improve their adhesion to polyurethane adhesive. The surface modifications produced on the treated filled SBS rubbers have been analyzed by contact angle measurements, ATR-IR spectroscopy, XPS and SEM. The adhesion properties have been evaluated by T-peel strength tests on treated filled SBS rubber/polyurethane adhesive/leather joints. The UV-ozone treatment improved the wettability of all rubber surfaces, and chemical (oxidation) and morphological modifications (roughness, ablation, surface melting) were produced. The increase in the time of UV-ozone treatment to 30 min led to surface cleaning (removal of silicon-based moieties) due to ablation and/or melting of rubber layers and also incorporation of more oxidized moieties was produced. Although chemical modifications were produced earlier in an unfilled rubber for short time of treatment with UV-ozone, they were more noticeable in filled rubbers for extended length of treatment, mainly for S6S and S6T rubbers containing silica filler. The oxidation process seemed to be inhibited for S6C and S6T rubbers (containing calcium carbonate filler). On the other hand, the S6S rubber containing silica filler and the lowest filler loading showed the higher extent of modification as a consequence of the UV-ozone treatment. The UV-ozone increased the joint strength in all joints, more noticeably in the rubbers containing silica filler, in agreement with the greater extents of chemical and morphological modifications produced by the treatment in these rubbers. Finally, the nature and content of fillers determined the extent of surface modification and adhesion of SBS rubber treated with UV-ozone.     

X-Ray photoemission study of plasma modified polyethylene surfaces

X-Ray photoelectron spectroscopy (XPS) was used to determine plasma induced chemical species on the surface of polyethylene (PE). Argon plasmas were found to have no detectable chemical effect on the PE surface, whereas oxygen and nitrogen plasmas created new chemical species which altered the chemical reactivity of the PE surface. Oxygen plasmas were found to react more rapidly with the PE surface than nitrogen plasmas. The degree of incorporation of new chemical species in the near surface region is approximately 20 at. % at the saturation level for both oxygen and nitrogen plasmas. Core level spectra for oxygen and nitrogen plasma treated PE suggest the formation of primarily C-O-C species in the former and C-N species in the latter. Angle-resolved XPS measurements indicate that the depth of incorporation of new chemical species is confined to the top 25 A.     

Acid-base interfaces in fiber-reinforced polymer composites

The role of Lewis acid-base interactions at the fiber-matrix interface in composites is studied with both glass and Teflon fibers. In the glass fiber case, surface chemistry is modified with amino-, methacryloxy- and glycidoxy-silane coupling agents (A-1100, A-174 and A-187, respectively). Silane adsorption mechanisms as well as the properties of filament-wound, unidirectional epoxy and polyester composites are explained by a combination of X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and flow microcalorimetry. The heats of adsorption of pyridine and phenol prove that the coupling agents add acidic sites to the glass fiber surface as well as stronger basic sites. The subsequent adhesion of the matrix polymers and the short beam shear strengths of composites are explained on this basis. The Teflon fibers are first etched with sodium naphthalene solutions, and then sequentially hydroborated and acetylated, producing approximately monofunctional hydroxyl (acidic) and ester (basic) groups on the surfaces, as determined by XPS, FTIR, and electrophoretic mobility analyses. Composites prepared with the acetylated fibers and a chlorinated polyvinyl chloride (acidic) matrix are superior in tensile properties, and SEM fractography shows PTFE fibrillation, indicative of good fiber-matrix adhesion and stress transfer, in this case only.     

Characterization of films of organofunctional silanes by TOFSIMS and XPS

The structures of thin films formed by the silanes N-[2-(vinylbenzylamino)-ethyl]-3-aminopropyltrimethoxysilane (SAAPS) and γ-aminopropyltriethoxysilane (γ-APS) deposited onto mechanically polished zinc or mild steel from dilute aqueous solutions were determined using time-of-flight (TOF) SIMS and XPS. TOFSIMS gave structural information which was highly complementary to the XPS data. Aspects such as silane condensation and crosslinking, oxidation at elevated temperatures, the formation of metallosiloxane bonds, and incomplete hydrolysis were detected by TOFSIMS by virtue of its high mass resolution and unlimited mass range. The structures of the films were found to be strongly dependent on the nature of the substrate, the deposition conditions, and heat treatment of the films.     

Adhesion characteristics of plasma-treated polypropylene to mild steel

The ability of polypropylene (PP) to adhere to mild steel depends to a large extent on the surface characteristics of both PP and steel. The adhesion of PP was improved by treatment in a cold plasma from oxidizing gases (O₂, H₂O, etc.). This surface functionalization was followed ex situ by means of contact angle measurements and XPS (X-ray photelectron spectroscopy) analysis. The polymer/steel assembly was fabricated by hot-pressing in vacuum, or after exposure to ambient air. Adhesion to steel, as determined by the lap-shear test, increased when the PP was treated with Ar-containing plasma gas and joined to steel after exposure to room atmosphere. Correlations between the polarity, the atomic (O/C, N/C) ratio, the dispersive component of the surface energy, and the degree of PP/steel adhesion are discussed.     

Surface segregation and miscibility in blends of poly(vinylidene fluoride-co-hexafluoro-acetone) with poly(butyl acrylate)

The surface segregation in poly(butyl acrylate) (PBA)/poly(vinylidene fluoride-co-hexafluoro-acetone) [P(VDF-HFA)] blends was confirmed by X-ray photoelectron spectroscopy (XPS), and is thought to be caused because the surface tension of P(VDF-HFA) is smaller than that of PBA. The PBA/P(VDF-HFA) blends were miscible at room temperature and exhibited a lower critical solution temperature (LCST) phase behavior. Thus, it was considered that the surface segregation of the P(VDF-HFA) component in PBA/P(VDF-HFA) blends was caused by the difference in surface tension between the components. Depth profiles [In(<Ø₁ (d) -Ø^b ₁) vs. depth (d), where Ø₁ (d) and Ø^b ₁ are the volume fractions at depth d from the surface and into the bulk, respectively] for PBA/P(VDF-HFA) blends were constructed by the mean-field treatment. The ln(Ø₁(d) - Ø^b ₁) vs. d plots for the PBA/P(VDF-HFA) blends could be approximated by a straight line.