Investigation and Discussion of Characteristics for Intermetallic Phases Common to Aluminum Alloys as a Function of Solution pH

This paper presents results for corrosion potentials, pitting potentials, and electrochemical characteristics for intermetallic particles commonly present in high strength aluminum-based alloys, for tests conducted in a 0.1 M NaCl solution of varying pH via the use of a microcapillary electrochemical cell. The intermetallics investigated were Mg_2Si, MgZn_2, Al_7Cu_2Fe, Al_2Cu, Al_2CuMg, and Al_3Fe. Elaboration of the results reveals that the electrochemical behavior of such compounds varies markedly with pH, with attendant ramifications for localized corrosion and protection in Al alloys. Examples of this are shown for AA7075-T651, where it is shown that the localized corrosion morphology is drastically different upon the bulk alloy depending on the pH of the test environment. A stochastic pitting is observed at an acid pH, near-neutral conditions result in a deterministic-type pitting, and a general corrosion is observed at an alkaline pH

Electrochemical Characteristics of Intermetallic Phases in Aluminum Alloys

This paper presents a survey of corrosion potentials, pitting potentials, and electrochemical characteristics for intermetallic particles commonly present in high-strength aluminum-based alloys. Results from relevant pure metals and solid solutions are also presented. It is seen that corrosion potentials and pitting potentials vary over a wide range for various intermetallics. Elaboration of the results reveals that the electrochemical behavior of intermetallics is more detailed than the simple noble or active classification based upon corrosion potential or estimated from the intermetallic composition. Intermetallics capable of sustaining the largest cathodic current densities are not necessarily those with the most noble Ecorr, similarly those with the least noble Ecorr will not necessarily sustain the largest anodic currents. The data herein was collected via the use of a microcapillary electrochemical cell facilitating electrode investigations upon intermetallic particles in the micrometer-squared range. This survey may be used as a tool for clarification of localized corrosion phenomena in Al alloys

Electrochemical Evaluation of Constituent Intermetallics in Aluminum Alloy 2024-T3 Exposed to Aqueous Vanadate Inhibitors

Experiments were conducted to determine how inhibiting forms of vanadate interact with complex Al alloy microconstituent intermetallics to impart corrosion protection. Cathodic polarization experiments on Al 2024-T3 indicate a strong correlation between inhibition and the presence of tetrahedrally coordinated vanadate. Anodic and cathodic polarization curves were measured on bulk synthesized Al_2Cu, Al_2CuMg, Al_7Cu_2Fe, and Al_20Cu_2Mn_3 in alkaline 0.5 M NaCl solutions with and without 10 mM NaVO_3. Vanadate additions generally decreased E_corr, increased E_pit, and decreased the cathodic kinetics of all tested materials. Because of decreased cathodic kinetics, open-circuit potentials (OCPs) were shifted in the active direction in aerated solutions when vanadate was present. This shift pins the OCP just below the observed pitting potential for Al_2CuMg in vanadate solution, effectively preventing breakdown and subsequent support of rapid oxygen reduction by Cu-enriched clusters. E_corr, E_pit, E_rp, i_corr, i_pass, and i at −1.3 V_SCE data from polarization experiments were summarized in cumulative distribution plots, and averages are presented in tabulated format. Scanning electron microscopy images of Al 2024-T3 used for 4 h of OCP measurement show that vanadate greatly decreased circumferential trenching around intermetallic particles in both aerated and deaerated solutions. Potentiostatic hold experiments were used to show suppression of Al_2CuMg dissolution in vanadate solutions

Examining the Personal and Institutional Determinants of Research Productivity in Hospitality and Tourism Management

The transition toward a post-capitalist knowledge-oriented economy has resulted in an increasingly competitive academic environment, where the success of faculty is dependent on their research productivity. This study examines the personal and institutional determinants of the quantity and quality of the research productivity of hospitality and tourism management faculty in US institutions. A survey of 98 faculty found that a different set of determinants impact the quantity and quality aspects of research productivity. Also, institutional determinants were found to play a larger role, indicating the need for administrators to strive for a culture that is supportive of and an infrastructure that is conducive to their faculty’s research success. The authors use the field of hospitality and tourism management as a case study to develop a holistic and cohesive framework for knowledge worker productivity that can guide the evaluation, hiring, and development of researchers

Corrosion Inhibition of Aluminum Alloy 2024-T3 by Aqueous Vanadium Species

Nuclear magnetic resonance (NMR) measurements were made on aqueous vanadate solutions to characterize speciation as a function of pH and vanadate concentration. Additionally, potentiodynamic polarization measurements were carried out on Al alloy 2024-T3 in 50 mM NaCl solutions in which pH and vanadate concentration were systematically varied. Results showed that inhibition by vanadates occurred mainly in alkaline solutions where tetrahedrally coordinated vanadates, metavanadate and pyrovanadate, were abundant. Inhibition was not observed in solutions where octahedrally coordinated decavanadates predominated. Anodic inhibition, in the form of increased pitting potential, was observed in both aerated and deaerated solutions. In contrast, cathodic inhibition was observed only in aerated solutions acting primarily through the suppression of oxygen reduction. Energy-dispersive spectroscopy, used to collect chemical maps from aluminum coupons exposed to vanadate solutions, showed the suppression of Al_2CuMg particle dissolution compared to vanadate-free solutions. NMR measurements were also used to track changes in vanadate speciation with time, pH adjustment, and with exposure to metallic aluminum surfaces. NMR showed noninhibiting octahedrally coordinated decavanadates rapidly decompose into inhibiting tetrahedrally coordinated metavanadates and pyrovanadates after alkaline pH adjustment. While decomposition begins immediately upon pH adjustment, equilibrium may not be reached even after significant time periods

Dehydration-Induced Loss of Corrosion Protection Properties in Chromate Conversion Coatings on Aluminum Alloy 2024-T3

It is well known that chromate conversion coatings (CCCs) exhibit a prompt loss in corrosion resistance when exposed to moderately elevated temperatures (60-100°C). They also suffer a gradual loss in corrosion resistance due to ambient temperature exposure. To better understand the origins of losses in corrosion resistance, CCCs were formed on 99.99% Al, 1100 Al [Al-1.0(Fe, Si, Cu)], and 2024-T3 (Al-4.4Cu-1.5Mg-0.6Mn), exposed to elevated and ambient temperature exposures for various lengths of time, and characterized using several different methods. The Cr(VI):total Cr ratio in CCCs was estimated by analysis of data derived from X-ray absorption spectroscopy. Corrosion resistance was measured by electrochemical impedance spectroscopy. The evolution of shrinkage cracking was examined by environmental scanning electron microscopy. Cr(VI) leaching experiments were also carried out to characterize the effect of thermal exposure on Cr(VI) release. Thermal analysis and X-ray diffraction were conducted to characterize the temperature-dependent changes in CCCs. Results show that CCCs degrade in several distinct steps over the temperature range of 20 to 500°C. Our findings support the longstanding notion that dehydration is the root cause for losses in corrosion resistance due to aging at ambient and low temperatures (<150°C). Extended X-ray fine structure measurements indicate a shortening in Cr(III)-Cr(III) nearest neighbor distances upon dehydration. This is interpreted as a consolidation in the Cr(OH)_3 backbone of the CCC which leads to shrinkage cracking and immobilization of Cr(VI). This finding is important because it links older observations of the effects of aging and heating on CCCs to newer interpretations of CCC formation based on inorganic polymerization. Overall, these results reveal CCCs to be highly dynamic coatings with corrosion resistance properties that vary considerably in both the short term and long term