Inhibition of Aluminum Alloy 2024 Corrosion by Vanadates: An In Situ Atomic Force Microscopy Scratching Investigation

CORROSION ◽  
2007 ◽  
Vol 63 (7) ◽  
pp. 672-688 ◽  
Author(s):  
M. Iannuzzi ◽  
G. S. Frankel

Abstract The morphology and kinetics of the localized corrosion of aluminum alloy (AA)2024-T3 (UNS A92024) at the open-circuit potential were investigated by in situ atomic force microscopy (AFM) scratching. The addition of metavanadate to chloride solutions resulted in outstanding corrosion inhibition. Samples exposed to 0.1 M sodium chloride (NaCl) with no inhibitor developed a trench-like attack at the periphery of large Al-Cu-Fe-Mn-(Si) intermetallic phases. The addition of dilute metavanadate markedly reduced the kinetics of the attack. In addition, most S-phase particles remained free of attack. Higher concentrations of metavanadate increased protection even further so that only high AFM tip forces could induce pitting corrosion. Corrosion attack was immediately observed when AA2024-T3 samples were exposed to chloride solutions containing orange decavanadates. The attack nucleated on the exposed surface but not under the AFM tip. The attack grew continuously, accompanied by gas evolution and formation of corrosion products. Optical inspection after the test indicated severe corrosion damage, confirming an overall poor performance of orange decavanadate solutions as corrosion inhibitors.

2005 ◽  
Vol 38 (2) ◽  
pp. 211-215 ◽  
Author(s):  
Yonggui Liao ◽  
Zhaohui Su ◽  
Xianggui Ye ◽  
Yunqi Li ◽  
Jichun You ◽  
...  

2019 ◽  
Vol 10 (29) ◽  
pp. 3933-3942 ◽  
Author(s):  
Joydeb Mandal ◽  
Rok Simic ◽  
Nicholas D. Spencer

SI-ATRP kinetics of acrylamide derivatives is studied in situ using a quartz crystal microbalance with dissipation (QCM-D). The effect of growth kinetics on polymer-brush dispersity have been examined using colloidal-probe atomic force microscopy.


Molecules ◽  
2019 ◽  
Vol 24 (10) ◽  
pp. 1895 ◽  
Author(s):  
Yong Joon Lee ◽  
Brandon L. Weeks

Kinetic thermal analysis was conducted using in situ atomic force microscopy (AFM) at a temperature range of 15–25 °C to calculate the activation energy of the sublimation of 2,4,6-trinitrotoluene (TNT) islands. The decay of different diameter ranges (600–1600 nm) of TNT islands was imaged at various temperatures isothermally such that an activation energy could be obtained. The activation energy of the sublimation of TNT increases as the diameter of islands increases. It was found that the coarsening and the sublimation rate of TNT islands can be determined by the local environment of the TNT surface. This result demonstrates that a diffusion model cannot be simply applied to “real world” systems for explaining the sublimation behavior and for estimating the coarsening of TNT.


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