ABSTRACT
The formation of a protective layer of γ-methacryloxypropyltrimethoxysilane (γ-MPS) on copper is studied by diffuse reflectance infrared spectroscopy (DRIFT), gravimetric chemical (weight loss) and electrochemical (cyclic voltammetry and potentiodynamic polarization) measurements. By simple immersion in the silanic bath (90/5/5 v/v ethanol/water/silane), this agent immediately physisorbed on copper, but the protective effects are poor. Thiolate and siloxane band formation improve the performances of the silanic layer on the surface of copper especially after heat treatment process. Chemical and electrochemical measurements show that the protective action of heat treatment (HT/Cu-MPS) process is higher than that of aged process (aged/Cu-MPS).
Subject(s)
Copper/chemistry , Methacrylates/chemistry , Silanes/chemistry , Corrosion , Electrochemical Techniques , Spectrophotometry, InfraredABSTRACT
The hydrolysis of three alkoxy-silane coupling agents, gamma-methacryloxypropyl trimethoxy silane (MPS), gamma-aminopropyl triethoxy silane (APS), and gamma-diethylenetriaminopropyl trimethoxy silane (TAS), was carried out in ethanol/water solutions (80/20 w/w) at different pH values and followed by 1H, 13C and 29Si NMR spectroscopy. Acidic media were found to stabilize the hydrolyzed forms. As expected, the formation of silanol groups was followed by their self-condensation to generate oligomeric structures, yielding, ultimately, solid homopolycondensated structures, as analyzed by 29Si and 13C high-resolution solid-state NMR. Hydrolyzed MPS in acidic media was then successfully adsorbed onto a cellulose surface and the ensuing substrates submitted to thermal treatment at 110-120 degrees C under reduced pressure, in order to create covalent bonds between cellulose and the coupling agent.