Predicting Galvanic Corrosion of Aluminum Using Accelerated Laboratory Electrochemical Experiments

Abstract

Aluminum (Al) alloys are the most commonly used non-ferrous metals (approximately 25 million tons per year) for various technical applications and is the second most commonly used metal alloy after steel. Al alloys are also used in combination with other metals or materials to get specific desirable properties for applications such as transportation, construction, electrical appliances, and consumer goods. However, a system of dissimilar materials can lead to potential corrosion problems such as galvanic and crevice corrosion. In this work, atmospheric galvanic corrosion of Al alloy was predicted by combining electrochemical techniques and accelerated laboratory corrosion tests. Three different galvanic couples were analyzed where 6061-T6 Al alloy was coupled with a passivating metal (304 stainless steel), noble metal (copper), and a carbon fiber-reinforced polymer matrix composite (CFR PMC). The galvanic current flowing between the anode and cathode was measured using the zero-resistance ammeter (ZRA) technique in the humidity-chamber setup, cyclic corrosion test chamber following a modified GM9540P cycle, and an outdoor exposure test site. Electrolytes with varying amounts of chloride contents were used to simulate different atmospheric conditions. Four separate equations based on Faraday's law were developed to calculate the corrosion rate in grams per meter square per day (gmd) by relating the time of wetness (TOW) to the galvanic current measured from the accelerated laboratory experiments. The total exposure time was divided into wet periods (Twet) and dry periods (Tdry). The surface morphology of Al samples from the galvanic couples was studied using a scanning electron microscope (SEM), and elemental surface analysis was conducted using energy-dispersive X-ray Spectroscopy (EDXA). Figure 1