Sol–gel coatings on metals for corrosion protection

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. However, hexavalent chromium species are responsible for several diseases, including DNA damage and cancer, which is the main reason for banning Cr-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. 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. 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). 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. ZrO2/CeO2), [4] b-cyclodextrin-inhibitor complexes, hollow polypropylene fibers, and conducting polyaniline 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. 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 case of aluminum alloys used for aerospace applications. The recently developed technology of layer-by-layer (LbL) deposition of oppositely charged species (polyelectrolytes, nanoparticles, enzymes, dendrimers) from their solutions on the substrate surface represents an interesting approach to prepare reservoirs with regulated storage/release properties assembled with nanometer-thickness precision. LbL coatings are of practical interest in photonics (optical filters, luminescent coatings), electrocatalysis (electrodes for DNA transfer, enzyme-catalyzed oxidation), as membranes, and chemical reactors. LbL-assembled polyelectrolyte multilayers reveal controlled permeability properties. Depending on the nature of the assembled monolayers, the permeability of multilayer films can be controlled by changing pH, ionic strength, and temperature, or by applying magnetic or electromagnetic fields. Polyelectrolyte assemblies have never been used in corrosion-protection coatings, although storage of corrosion inhibitors in polyelectrolyte multilayers can confer several advantages: they can prevent a negative effect of the corrosion inhibitor on the stability of the coating, decrease the influence of the coating polymerization on the inhibitor, and provide intelligent release of the corrosion inhibitor, as the permeability C O M M U N IC A TI O N S

Layer‐by‐Layer Assembled Nanocontainers for Self‐Healing Corrosion Protection

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...

Anticorrosion Coatings with Self-Healing Effect Based on Nanocontainers Impregnated with Corrosion Inhibitor

Nanostructured sol-gel coatings doped with cerium nitrate as pre-treatments for AA2024-T3 Corrosion protection performance

Sol–gel derived films exhibit a high potential as substitutes for the environmentally unfriendly chromate metal-surface pre-treatment methods. Inorganic sol–gel derived films offer good adhesion between metals and organic paint. However, they cannot provide adequate corrosion protection due to their high crack-forming potential. Introduction of an organic component to an inorganic sol–gel system leads to the formation of thicker, more flexible and functionalized films with enhanced compatibility to different organic top coatings. Incorporation of nanoparticles in the hybrid sol–gel systems increases the corrosion protection properties due to lower porosity and lower cracking potential along with enhancement of the mechanical properties. Furthermore, the incorporation of inorganic nanoparticles can be a way to insert corrosion inhibitors, preparing inhibitor nanoreservoirs for “self-repairing” pre-treatments with controlled release properties.

Sol–gel coatings for corrosion protection of metals

Sol–gel coatings were investigated as potential replacements for chromate-based surface treatments on aircraft aluminum alloys. Unlike chromate based treatments current sol–gel coatings do not have the ability to leach corrosion inhibitors upon coating damage and minimize corrosion of the unprotected area. As an alternative, environmentally compliant non-chromate inhibitors of Ce(NO3)3, NaVO3 and Na2MoO4 were incorporated into a Zr-epoxy sol–gel. Results are reported on the coatings chemical analysis and their corrosion protection performance based on electrochemical studies. Aluminum alloy 2024-T3 test coupons coated with protective sol–gel films were found to provide considerable corrosion protection. The improved performance characteristics were derived from the sol–gel ability to form a uniform, low defect, barrier coating. Coatings doped with Ce(NO3)3 had barrier properties at least as good as the standard sol–gel coatings. Coatings with Na2MoO4 and NaVO3 did not provide adequate corrosion protection. The use of corrosion inhibitors within organically modified sol–gel coatings is discussed.

N.N. Voevodin

Papers

Potentiodynamic evaluation of sol–gel coatings with inorganic inhibitors