scholarly journals Driving electrochemical corrosion of implanted CoCrMo metal via oscillatory electric fields without mechanical wear

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Thomas S. Welles ◽  
Jeongmin Ahn

AbstractDecades of research have been dedicated to understanding the corrosion mechanisms of metal based implanted prosthetics utilized in modern surgical procedures. Focused primarily on mechanically driven wear, current fretting and crevice corrosion investigations have yet to precisely replicate the complex chemical composition of corrosion products recovered from patients’ periprosthetic tissue. This work specifically targets the creation of corrosion products at the metal on metal junction utilized in modular hip prosthetics. Moreover, this manuscript serves as an initial investigation into the potential interaction between implanted CoCrMo metal alloy and low amplitude electrical oscillation, similar in magnitude to those which may develop from ambient electromagnetic radiation. It is believed that introduction of such an electrical oscillation may be able to initiate electrochemical reactions between the metal and surrounding fluid, forming the precursor to secondary wear particles, without mechanically eroding the metal’s natural passivation layer. Here, we show that a low magnitude electrical oscillation (≤ 200 mV) in the megahertz frequency (106 Hz) range is capable of initiating corrosion on implanted CoCrMo without the addition of mechanical wear. Specifically, a 50 MHz, 200 mVpp sine wave generates corrosion products comprising of Cr, P, Ca, O, and C, which is consistent with previous literature on the analysis of failed hip prosthetics. These findings demonstrate that mechanical wear may not be required to initiate the production of chemically complex corrosion products.

2019 ◽  
Vol 39 (4) ◽  
pp. 1496-1506 ◽  
Author(s):  
Lei Guo ◽  
Chenglong Zhang ◽  
Qing He ◽  
Zhihua Li ◽  
Jianxing Yu ◽  
...  

2013 ◽  
Vol 842 ◽  
pp. 104-109
Author(s):  
Yan Zou ◽  
Qiang Bai ◽  
Jia Wang ◽  
Wei Wang ◽  
Xiang Feng Kong

The galvanic and potential distributions of carbon steel immersed in seawater were studied by wire beam electrode (WBE) technique. Results indicated that the corrosion of carbon steel in seawater tended to local corrosion. With immersion time increasing, local corrosion was more and more serious. During the initial immersion period, the top of the coupon near the water surface was main cathode. With the corrosion extended, corrosion products gradually gathered on the surface of the carbon steel. Potential differences between cathode and anode gradually became small. Cathode and anode redistributed on the surface of carbon steel. At last, the top and the bottom were cathode while the middle was anode. The areas of anode first increased and then decreased. The areas of cathode were in contrast.


CORROSION ◽  
1975 ◽  
Vol 31 (6) ◽  
pp. 192-197
Author(s):  
L. S. SU ◽  
E. SHEPPARD

Abstract The complex corrosion mechanisms for pressurized aqueous solutions in contact with various aerosol containers were studied electrochemically. A pressurized corrosion cell consisting of an aerosol container serving as the working electrode, a platinum rod serving as a hybrid reference-counter electrode, and the pressurized liquids as the electrolyte was designed and fabricated. The correlation of the results between two accelerated electrochemical corrosion tests, namely the galvanostatic polarization test and a 24-hour accelerated constant polarization potential test, and a 10-week storage test, was excellent. It was found that the addition of 0.1%disodium phosphate (DSP) to the aqueous solutions pressurized with a 10% isobutane-propane propellent blend changed the color of the systems to colorless, produced an electrodeposition of colloidal particles, and shifted the site of the crevice corrosion from the bulk-stagnant interface towards the stagnant area. Three distinct and characteristic zones of the polarization potential responses were observed during the anodic galvanostatic polarization measurements, and their mechanisms are discussed.


2010 ◽  
Vol 152-153 ◽  
pp. 353-356
Author(s):  
Peng Zhang ◽  
Gang Chen ◽  
Bin Guo ◽  
Shu Kang Cheng

The current research explores the effect of alternating magnetic field on corrosion rate and products compositions of 45 steel, by use of electrochemical test, scanning electron microscopy (SEM) and X-ray diffraction (XRD). The calculated inhibition efficiency of the alternating magnetic field based on electrochemical corrosion rate is up to 16.66%. Electrochemical corrosion morphology and surface products were also discussed. The surface of specimen is uniform and compact in magnetized sea water relation to that in 3.5% NaCl solution and sea water. The corrosion products of 45 steel in sea water are FeCl2•4H2O, Fe(OH)3 and FeOOH. However, the corrosion products of 45 steel in magnetized sea water are FeOOH, Fe3O4 and FeCl3•6H2O chiefly.


1980 ◽  
Vol 35 (11-12) ◽  
pp. 1081-1085 ◽  
Author(s):  
Peter Scheurich ◽  
Ulrich Zimmermann ◽  
Maja Mischel ◽  
Ingolf Lamprecht

Abstract Human red blood cells suspended in a slightly hypotonic solution of low electric conductivity were exposed to an inhomogeneous and alternating electric field (sine wave, 30 V peak-to-peak value, electrode distance 120 μm, 0.5 to 2 MHz). Due to the dielectrophoretic effect the cells align parallel to the field lines under the formation of pearl chains. At high voltages (10 V amplitude) membrane fusion is observed between the adhered red blood cells in the pearl chains, whereby the chains become attached to the electrodes. In contrast to the pearl chains observed at voltages of up to 5 V amplitude the resulting fused and uniform aggregates which exhibit no recognisable individual cells under the light microscope, remain stable, even after the alternating electric field has been switched off or after haemolysis in response to osmotic shock. The fused aggregates are highly elastic. If the field strength of the applied alternating electric field is further increased they are stretched in the direction of the opposite electrode. Frequently, bridges are formed between the two electrodes. The uniform bridges remain stable for some time even in the absence of an electric field. The possibility of cell fusion and its initiation by electrical breakdown of the cell membranes are discussed.


The work was carried on biomedical implants and the selection of correct methods for corrosion studies and study of the corrosion products, electrochemical methods are used to determine the metal and alloys corrosion rate and to characterize the corrosion damage. Microscopy and spectroscopy studies are used for characterization and determination of thickness and nature of the corrosion products.


Author(s):  
R.D. Apostolova ◽  
◽  
E.M. Shembel

The article presents some new results of the studies of corrosion processes in lithium battery systems with non-aqueous electrolytes. The following processes are considered: electrochemical corrosion of positive and negative electrodes, corrosion of structural materials, and electrochemical and chemical decomposition of non-aqueous electrolytes, which occurs simultaneously with the main electrochemical process. The main attention is paid to the role of corrosion processes on current collectors of current sources. Corrosion processes on aluminum current collector and stainless steel current collector for positive electrodes of lithium batteries are particularly considered. An important role of corrosion in the degradation of the lithium battery is emphasized. Case studies on corrosion in positive electrodes and lithium electrode are mentioned. Considerable attention is paid to the contact corrosion in aircraft, with an emphasis on the need for further studies of this process. The proposed corrosion mechanisms are considered.


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