Intrinsic Diffusivities Ratio Analysis in Double Multiphase Systems

2021 ◽  
Vol 413 ◽  
pp. 47-64
Author(s):  
Mykhaylo V. Yarmolenko

Our investigations show that electrochemical corrosion of copper is faster than electrochemical corrosion of aluminium at temperatures below 100°C. Literature data analysis shows that the Al atoms diffuse faster than the Cu atoms at temperatures higher than 475°C, Al rich intermetallic compounds (IMCs) are formed faster in the Cu-Al system, and the Kirkendall plane shifts toward the Al side. Electrochemical corrosion occurs due to electric current and due to diffusion. An electronic devise working time, for example, depends on initial copper cover thickness on aluminium wire, connected to the electronic devise, temperature, and volume and dislocation pipe diffusion coefficients, so copper, iron, and aluminium electrochemical corrosion rates are investigated experimentally at room temperature and at temperature 100°C. Intrinsic diffusivities ratios of copper and aluminium at different temperatures and diffusion activation energies in the Cu-Al system are calculated by proposed here methods using literature experimental data. Dislocation pipe and volume diffusion activation energies of pure iron are calculated separately by earlier proposed method using literature experimental data. Aluminium dissolved into NaCl solution as the Al3+ ions at room temperature and at temperature 100°C, iron dissolved into NaCl solution as the Fe2+ (not Fe3+) ions at room temperature and at temperature 100°C, copper dissolved into NaCl solution as the Cu+ ions at room temperature and as the Cu+ and the Cu2+ ions at temperature 100°C. It is found experimentally that copper corrosion is higher than aluminium corrosion, and ratio of electrochemical corrosion rates, kCu/kAl>1, decreases with temperature increasing, although iron electrochemical corrosion rate does not depend on temperature below 100°C. It is obvious, because the melting point of iron is more higher than the melting point of copper or aluminium. It is calculated that the copper electrochemical corrosion rate is approximately equal to aluminium electrochemical corrosion at temperature about 300°C, so copper can dissolve into NaCl solution mostly as the Cu2+ ions at temperature about 300°C. The ratio of intrinsic diffusivities, DCu/DAl<1, increases with temperature increasing, and the intrinsic diffusivity of aluminium could be approximately equal to the intrinsic diffusivity of copper at temperature about 460oC. Intrinsic diffusivities ratios in the Cu-Zn system at temperature 400°C and in the Cu-Sn system at temperatures from 190°C to 250°C are analyzed theoretically using literature experimental data. Diffusion activation energies and pre-exponential coefficients for the Cu-Sn system are calculated combining literature experimental results.

Author(s):  
Mykhaylo Viktorovych Yarmolenko

Our investigations show that electrochemical corrosion of copper is faster than electrochemical corrosion of aluminium at temperatures below 100oC. Literature data analysis shows that the Al atoms diffuse faster than the Cu atoms at temperatures higher than 475oC, Al rich intermetallic compounds (IMCs) are formed faster in the Cu-Al system, and the Kirkendall plane shifts toward Al side. Electrochemical corrosion occurs due to electric current and due to diffusion. An electronic devise working time, for example, depends on initial copper cover thickness on aluminium wire, connected to the electronic devise, temperature, and volume and dislocation pipe diffusion coefficients, so copper, iron, and aluminium electrochemical corrosion rates are investigated experimentally at room temperature and at temperature 100oC. Intrinsic diffusivities ratios of copper and aluminium at different temperatures and diffusion activation energies in the Cu-Al system are calculated by proposed here methods using literature experimental data. Dislocation pipe and volume diffusion activation energies of pure iron are calculated separately by earlier proposed method using literature experimental data. Aluminium dissolved into NaCl solution as the Al3+ ions at room temperature and at temperature 100oC, iron dissolved into NaCl solution as the Fe2+ (not Fe3+) ions at room temperature and at temperature 100oC, copper dissolved into NaCl solution as the Cu+ ions at room temperature and as the Cu+ and the Cu2+ ions at temperature 100oC. It is founded experimentally that copper corrosion is higher than aluminium corrosion, and ratio of electrochemical corrosion rates, kCu/kAl&gt;1, decreases with temperature increasing, although iron electrochemical corrosion rate doesn’t depend on temperature below 100oC. It is obvious, because melting point of iron is more higher then melting point of copper or aluminium. It is calculated that copper electrochemical corrosion rate is approximately equal to aluminium electrochemical corrosion at temperature about 300oC, so copper can dissolve into NaCl solution mostly as the Cu2+ ions at temperature about 300oC. Ratio of intrinsic diffusivities, DCu/DAl &lt;1, increases with temperature increasing, and intrinsic diffusivity of aluminium could be approximately equal to intrinsic diffusivity of copper at temperature about 460oC.


2021 ◽  
Author(s):  
Mykhaylo Viktorovych Yarmolenko

Our investigations show that electrochemical corrosion of copper is faster than electrochemical corrosion of aluminium at temperatures below 100°C. Literature data analysis shows that the Al atoms diffuse faster than the Cu atoms at temperatures higher than 475°C, Al-rich intermetallic compounds (IMCs) are formed faster in the Cu-Al system, and the Kirkendall plane shifts towards the Al side. Electrochemical corrosion occurs due to electric current and diffusion. An electronic device working time, for example, depends on the initial copper cover thickness on the aluminium wire, connected to the electronic device, temperature, and volume and dislocation pipe diffusion coefficients, so copper, iron, and aluminium electrochemical corrosion rates are investigated experimentally at room temperature and at temperature 100°C. Intrinsic diffusivities ratios of copper and aluminium at different temperatures and diffusion activation energies in the Cu-Al system are calculated by the proposed methods here using literature experimental data. Dislocation pipe and volume diffusion activation energies of pure iron are calculated separately by earlier proposed methods using literature experimental data. Aluminium dissolved into NaCl solution as the Al3+ ions at room temperature and at temperature 100°C, iron dissolved into NaCl solution as the Fe2+ (not Fe3+) ions at room temperature and at temperature 100°C, copper dissolved into NaCl solution as the Cu+ ions at room temperature, and as the Cu+ and the Cu2+ ions at temperature 100°C. It is found experimentally that copper corrosion is higher than aluminium corrosion, and the ratio of electrochemical corrosion rates, kCu/kAl > 1, decreases with temperature increasing, although iron electrochemical corrosion rate does not depend on temperature below 100°C. It is obvious because the melting point of iron is higher than the melting point of copper or aluminium. It is calculated that copper electrochemical corrosion rate is approximately equal to aluminium electrochemical corrosion at a temperature of about 300°C, so the copper can dissolve into NaCl solution mostly as the Cu2+ ions at a temperature of about 300°C. The ratio of intrinsic diffusivities, DCu/DAl < 1, increases with temperature increasing, and intrinsic diffusivity of aluminium could be approximately equal to intrinsic diffusivity of copper at a temperature of about 460°C.


2012 ◽  
Vol 326-328 ◽  
pp. 255-260 ◽  
Author(s):  
Andrzej Kiełbus ◽  
Tomasz Rzychoń ◽  
Joanna Michalska ◽  
Michal Stopyra

In this paper, the corrosion resistance of two sand-casting creep resistant magnesium alloys Mg-9Al-1.5Ca-0.3Sr and Mg-9Al-2.2Ca-0.8Sr in the salt environment has been investigated. Specimens of each alloy has been immersed in 3.5% NaCl solution at room temperature and successively taken out after 1, 2, 4, 5 and 9 days. After immersion test, the microstructure and the appearances of the corroded structure were examined. The corrosion rates of both investigated alloys increased lineally with increasing the exposure time in both solutions. Mg-9Al-1.5Ca-0.3Sr alloy exhibits the higher corrosion rate during the immersion test than Mg-9Al-2.2Ca-0.8Sr. The corrosion layer of both alloys consists of MgO, MgOH and phases containing Cl, Na, Al and Ca. The increase of Ca content in the Mg-9Al-2.2Ca-0.8Sr alloy improved the corrosion resistance due to the formation of the reticular (Mg,Al)2Ca phase, which acted as an effective barrier against corrosion.


2014 ◽  
Vol 998-999 ◽  
pp. 43-46
Author(s):  
Jun Chen ◽  
Quan An Li ◽  
Xing Yuan Zhang

The corrosion behavior of AZ81 magnesium alloy with the LPC addition has been investigated in this paper. The results show that with the addition of 1-5% LPC, the microstructure of AZ81 magnesium alloy is remarkably refined, and the spotted, high-melting point phase Al-RE intermetallic compounds is found in the alloy. The corrosion behavior of AZ81 alloy decreases firstly and then increases sharply with the increase of LPC addition. When the content of LPC is 2.5%, AZ81 magnesium alloy shows the lowest corrosion rate. The corrosion rates in 3.5%NaCl solution are always higher than those in 0.5%NaCl solution. The corrosion products from the surface are mainly composed of Mg (OH) 2 compositions.


2002 ◽  
Vol 67 (11) ◽  
pp. 777-782 ◽  
Author(s):  
Dragutin Drazic ◽  
Jovan Popic

By combining electrochemical corrosion rate measurements and spectrophotometric analysis of the electrolyte it was shown that at room temperature chromium dissolves in deaerated 0.1M Na2SO4 + H2SO4 (pH1) solution as Cr(II) and Cr(III) ions in he ratio Cr(II):Cr(III)?7:1. This process was stable over 4h without any detectable change. The total corrosion rate of chromium calculated from the analytical data is about 12 times higher, than that determined electrochemically by cathodic Tafel line extrapolation to the corrosion potential. This finding was confirmed by applying the weight-loss method for the determination of the corrosion rate. This enormous difference between these experimentally determined corrosion rates can be explained by the rather fast, "anomalous" dissolution process proposed by Kolotyrkin and coworkers (chemical reaction of Cr with H2O molecules) occurring simultaneously with the electrochemical corrosion process.


1970 ◽  
Vol 25 ◽  
pp. 53-61
Author(s):  
Minu Basnet ◽  
Jagadeesh Bhattarai

The corrosion behavior of the sputter-deposited nanocrystalline W-Cr alloys wasstudied in 0.5 M NaCl and alkaline 1 M NaOH solutions at 25°C, open to air usingimmersion tests and electrochemical measurements. Chromium metal acts synergisticallywith tungsten in enhancing the corrosion resistance of the sputter-deposited W-Cr alloys soas to show higher corrosion resistance than those of alloy-constituting elements in both 0.5M NaCl and 1 M NaOH solutions. In particular, the nanocrystalline W-Cr alloys containing25-91 at% chromium showed about one order of magnitude lower corrosion rates (that is,about 1-2 × 10-3 mm.y-1) than those of tungsten and chromium metals even for prolongedimmersion in 0.5 M NaCl solution at 25°C. On the other hand, the corrosion rate of thesputter-deposited W-Cr alloys containing 25-75 at % chromium was decreased significantlywith increasing chromium content and showed lowest corrosion rates (that is, 1.5-2.0 × 10-3 mm.y-1) after immersed for prolonged immersion in 1 M NaOH solution. The corrosion ratesof these nanocrystalline W-(25-75)Cr alloys are nearly two orders of magnitude lower thanthat of tungsten and more than one order of magnitude lower corrosion rate than that ofsputter-deposited chromium metal in 1 M NaOH solution. The corrosion-resistant of all theexamined sputter-deposited W-Cr alloys in 0.5 M NaCl solution is higher than in alkaline 1M NaOH solution at 25°C. Open circuit potentials of all the examined W-Cr alloys areshifted to more noble direction with increasing the chromium content in the alloys afterimmersion for 72 h in both 0.5 M NaCl and 1 M NaOH solutions at 25°C, open to air.Keywords: Sputter deposition, nanocrystalline W-Cr alloys, corrosion test, electrochemicalmeasurement, NaCl and NaOH solutions.DOI:  10.3126/jncs.v25i0.3300Journal of Nepal Chemical Society Volume 25, 2010 pp 53-61


2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
D. Elango ◽  
A. Daniel Das ◽  
S. P. Kumaresh Babu ◽  
S. Natarajan ◽  
A. Yeshitla

In this present research, the coatings of SA209-T1 using high velocity oxygen fuel were employed for the application of boiler tubes. Due to the adaptation of corrosion easy in boiler material, the research of those properties is significant because of its criticality and functionality during the service time. A right coating was found and applied on the SA209-T1 surface against corrosive environments. Good corrosion resistance is achieved by WC-flyash coatings applied on SA209-T1 substrate. The 90% WC-10% flyash coatings were found to be more protective followed by SA209-T1 steel. WC-flyash covering was tracked down so that the covering is compelling to secure the SA209-T1 steel substrate. It is reasoned that the arrangement of NiO, Cr2O3, CoO, and NiCr2O4 could add to the advancement of consumption opposition in coatings. The steel of uncoated endured erosion as extraordinary stripping and spalling of the scale, which could be because of the development of Fe2O3 oxide scale unprotectively. This paper reveals the performance, applications, and development of 90wt.% WC and 10wt.% fly ash through HVOF coating in SA209-T1 for electrochemical corrosion studies at room temperature.


2019 ◽  
Vol 9 (9) ◽  
pp. 1092-1099
Author(s):  
Fenghong Cao ◽  
Chang Chen ◽  
Zhenyu Wang

The corrosion characteristics and corrosion mechanism of the extruded ZK80 alloy with different states soaking in 3.5% NaCl solution at room temperature were analyzed via OM, SEM, EDS, XRD and static weightlessness method and other experimental analysis methods. The results show that when the aging temperature is constant, and the corrosion rate decreases with the lengthen of aging time, while when the corrosion time is constant, the corrosion rate increases with the increase in aging time. Appropriate aging treatment not only refines the grain of the alloy, but also precipitates the Mg–Zn phase which can effectively prevent the corrosion process and improve the anti-corrosion properties of the alloy. The main corrosion characteristics of the alloy are filamentary corrosion and pitting corrosion.


2014 ◽  
Vol 953-954 ◽  
pp. 1492-1495
Author(s):  
Ping Li

The corrosion rates of rebar HRB400 in 0.5 wt.% NaCl solution were measured, and the mechanical properties before and after corrosion were tested. The results showed that, with the increase of corrosion time, the corrosion rate of rebar HRB400 increases and the corrosion becomes heavier. Meanwhile, the yield strength and tensile strength decrease, but the elongation decreases at first and then increases.


2019 ◽  
Vol 11 (1) ◽  
pp. 26-32 ◽  
Author(s):  
Muhammad Sohail ◽  
Fayaz Hussain ◽  
Ali Dad Chandio ◽  
Maryam Sheikh

Corrosion is one of the major problems of mild steels in acidic medium. This can be minimized by the application of corrosion inhibitors, however; the most of inhibitors are toxic in nature. Therefore inhibitors from green sources are highly desirable to maintain the sustainability of the environmental system. Consequently, in this study ginger was selected; its juice extracted mechanically and used as an inhibitor. The different concentrations of ginger extract such as 0.25ml, 0.5ml, 0.75ml and 1ml were mixed in 0.1 M HCl solution to record the effect of inhibitor on corrosion rate at room temperature and at an elevated temperature of 50ᵒC. Electrochemical linear polarization resistance (LPR) tests were carried out to determine the corrosion rates at both temperatures with different additions of the inhibitor respectively. The LPR test uses three electrodes, first electrode of AISI 1019 (mild steel), second electrode is standard electrode of saturated calomel while the third electrode consists of graphite, which is called counter electrode, to measure potential difference. The whole assembly was dipped in the solution having varying concentration of inhibitors. The corrosion rate was found to be higher in the absence of ginger- extract. Conversely, the corrosion rate was dramatically reduced more prominently at 50oC but was less effective at Troom; with the trace-additions of ginger-inhibitor. So this research would be the good contribution to overcome the deterioration of mild steel and increase its life at ambient temperatures, by using economically available environmentally-friendly organic compound specially the use of locally available raw material should be focused.


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