The corrosion of metals is one of the main destructive processes that leads to huge economic losses. Polymer coating systems are normally applied on a metal surface to provide a dense barrier against the corrosive species in order to protect metal structures from corrosive attack. When the barrier is damaged and the corrosive agents penetrate to the metal surface the coating system can not stop the corrosion process. The most effective solution so far for designing anticorrosion coatings for active protection of metals is to employ chromate-containing conversion coatings.[1] However, hexavalent chromium species are responsible for several diseases, including DNA damage and cancer, [2] which is the main reason for banning Cr 6+ -containing anticorrosion coatings in Europe from 2007. The deposition of thin inorganic or hybrid films on metallic surfaces has been suggested as a pretreatment to provide an additional barrier against the corrosion species and mainly to improve adhesion between the metal and polymer coating system.[3] The films are usually deposited by the plasma polymerization technique or the sol-gel route. Sol-gel-derived thin films that contain either inorganic (phosphates, vanadates, borates, and cerium and molybdenum compounds) or organic (phenylphosphonic acid, mercaptobenzothiazole, mercaptobenzoimidazole, triazole) inhibitors are investigated as substitutes for chromates. [3a-e] Among them, the highest activity is shown for sol-gel coatings with a cerium dopant of a critical concentration in the 0.2-0.6 wt % range. However, the negative effect of the free inhibitor occluded in the sol-gel matrix on the stability of the protective film is observed for all types of inhibitors (for instance, a higher concentration of Ce leads to the formation of microholes in the sol-gel film [3f] ). This shortcoming calls for the development of nanometer-scale reservoirs to isolate an inhibitor inside and prevent its direct interaction with the sol-gel matrix. Nanoreservoirs should be homogeneously distributed in the film matrix and should possess controlled and corrosion-stimulated inhibitor release to cure corrosion defects.Mixed-oxide nanoparticles (e.g. ZrO 2 /CeO 2 ), [4] b-cyclodextrin-inhibitor complexes, [3c] hollow polypropylene fibers, [5] and conducting polyaniline [6] have been explored as prospective reservoirs for corrosion inhibitors to be incorporated in the protective film. The common mechanism of the nanoreservoir activity is based on the slow release of inhibitor triggered by corrosion processes. Ion exchangers have also been investigated as 'smart' reservoirs for corrosion inhibitors. Chemically synthesized hydrocalmite behaves as an anion exchanger: adsorbing corrosive chloride ions and releasing corrosion-inhibiting nitrite anions. [7] Despite considerable efforts devoted to the development of new, complex anticorrosion systems, practically no single solution is able to fulfill the requirements of sufficient corrosion protection while avoiding chromates in the coating, especially in the ...
The development of active corrosion protection systems for metallic substrates is an issue of prime importance for many industrial applications. The present work shows a new contribution to the development of a new protective system with self-healing ability composed of hybrid sol−gel films doped with nanocontainers that release entrapped corrosion inhibitor in response to pH changes caused by corrosion process. A silica−zirconia based hybrid film was used in this work as an anticorrosion coating deposited on 2024 aluminum alloy. Silica nanoparticles covered layer-by-layer with polyelectrolyte layers and layers of inhibitor (benzotriazole) were randomly introduced into the hybrid films. The hybrid film with the nanocontainers reveals enhanced long-term corrosion protection in comparison with the undoped hybrid film. The scanning vibrating electrode technique also shows an effective self-healing ability of the defects. This effect is obtained due to regulated release of the corrosion inhibitor triggered by the corrosion processes started in the cavities. The approach described herein can be used in many applications where active corrosion protection of materials is required.
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