scholarly journals In Situ Preparation and Corrosion Resistance of a ZrO2 Film on a ZrB2 Ceramic

Coatings ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 455 ◽  
Author(s):  
Haitao Yang ◽  
Jian Zhang ◽  
Junguo Li ◽  
Qiang Shen ◽  
Lianmeng Zhang

ZrO2 films were in situ prepared using the anodic passivation of a ZrB2 ceramic in alkaline solutions. The composition and structure of the films were characterized using field-emission scanning electron microscopy (FE-SEM), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The corrosion resistances were evaluated in 0.1 M oxalate solution using the potentiodynamic polarization method (PDP) and the electrochemical impedance spectroscopy (EIS) technique. The results show that ZrO2 films can be prepared using anodization from −0.8 to 0.8 V standard hydrogen electrode (SHE) in 2–16 M NaOH solutions. During the anodization, the dehydration reaction of Zr(OH)4 to ZrO2 caused the volume shrinkage and tensile stress of the films. When the thickness of the films exceeded a critical value, the mud-cracking morphology occurred. The films without cracks exhibited the inhibition effect and provided effective corrosion protection in a 0.1 M H2C2O4 solution, which had a positive correlation with the film thickness. The film obtained when put in an 8 M NaOH solution (near the critical thickness) was found to significantly improve its corrosion resistance when put in a 0.1 M H2C2O4 solution by almost one order of magnitude compared with the bare ceramic.

Metals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1172
Author(s):  
Polina Metalnikov ◽  
Guy Ben-Hamu ◽  
Kwang Seon Shin ◽  
Amir Eliezer

Magnesium (Mg) alloys possess the lowest density among structural materials, and their application in the automotive and aircraft industries might enhance fuel efficiency. The mechanical properties can be improved by the addition of alloying elements. However, since Mg and its alloys are very susceptible to corrosion degradation, it is important to study the effect of these elements on the alloys’ corrosion behavior. In this study, 1 wt% of calcium (Ca) was added to wrought AM60 Mg alloy, and the electrochemical corrosion behavior of the alloys in alkaline solutions with and without Cl− ions was compared. The corrosion behavior was investigated by means of immersion tests, gravimetric measurements and potentiodynamic polarization (PDP); the characteristics of the oxide layer were studied by electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS). The addition of Ca resulted in precipitation of the ternary aluminum-rich (Mg-Al)2Ca phase. Scanning Kelvin probe force microscope (SKPFM) identified that this phase has a cathodic behavior relative to the α-Mg matrix; hence it can serve as additional sites for initiation of pitting corrosion. As a result, the corrosion resistance of wrought AM60 alloy with 1 wt% Ca addition deteriorated in a NaCl solution. However, in the absence of Cl− ions, alloying with Ca improves the corrosion resistance of wrought AM60 alloy due to the stabilization of the corrosion products layer. The effect of long-period immersion time on the corrosion behavior and alloy oxidation is discussed.


1970 ◽  
Vol 9 (9) ◽  
pp. 39-43
Author(s):  
Basu Ram Aryal ◽  
Jagadeesh Bhattarai

Simultaneous additions of tungsten, chromium and zirconium in the chromium- and zirconium-enriched sputter-deposited binary W-xCr and W-yZr are effective to improve the corrosion resistance property of the ternary amorphous W- xCr-yZr alloys after immersion for 240 h in 1 M NaOH solution open to air at 25°C. The corrosion rates of all the examined sputter-deposited (10-57)W-(18-42)Cr-(25-73)Zr alloys is higher than those of alloy-constituting elements (that is, tungsten, chromium and zirconium) in aggressive 1 M NaOH solution open to air at 25°C. The corrosion rates of all the examined sputter−deposited W–xCr–yZr alloys containing 10-57 at% tungsten, 18-42 at% chromium and 25-73 at% zirconium were in the range of 1.5-2.5 × 10−3 mm/y or lower which are more than two orders of magnitude lower than that of sputter-deposited tungsten and even about one order of magnitude lower than those of the sputter-deposited zirconium in 1 M NaOH solution. Keywords: Ternary W–Cr–Zr alloys; Amorphous; Corrosion rate; Open circuit potential; 1 M NaOH. DOI: http://dx.doi.org/10.3126/sw.v9i9.5516 SW 2011; 9(9): 39-43


2022 ◽  
Author(s):  
Xinchuang Zhang ◽  
Mei Wu ◽  
Bin Hou ◽  
Xuerui Niu ◽  
Hao Lu ◽  
...  

Abstract In this work, the N2O radicals in-situ treatment on gate region has been employed to improve device performance of recessed-gate AlGaN/GaN high-electron-mobility transistors (HEMTs). The samples after gate recess etching were treated by N2O radicals without physical bombardment. After in-situ treatment (IST) processing, the gate leakage currents decreased by more than one order of magnitude compared to the sample without IST. The fabricated HEMTs with the IST process show a low reverse gate current of 10-9 A/mm, high on/off current ratio of 108, and high fT×Lg of 13.44 GHz·μm. A transmission electron microscope (TEM) imaging illustrates an oxide layer with a thickness of 1.8 nm exists at the AlGaN surface. X-ray photoelectron spectroscopy (XPS) measurement shows that the content of the Al-O and Ga-O bonds elevated after IST, indicating that the Al-N and Ga-N bonds on the AlGaN surface were broken and meanwhile the Al-O and Ga-O bonds formed. The oxide formed by a chemical reaction between radicals and the surface of the AlGaN barrier layer is responsible for improved device characteristics.


2019 ◽  
Vol 26 (10) ◽  
pp. 1950080
Author(s):  
JIBO JIANG ◽  
HAOTIAN CHEN ◽  
LIYING ZHU ◽  
YAOXIN SUN ◽  
WEI QIAN ◽  
...  

Graphene oxide (GO) sheet and ultrasonic field (UF) were successfully employed to produce Ni–B/GO and UF–Ni–B/GO composite coatings on Q235 mild steel by electroless plating. The composite coatings’ structure and surface morphology were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Results showed that GO was successfully co-deposited in the Ni–B alloy. Moreover, UF–Ni–B/GO composite coatings have smoother surface and thicker cross-section than others. The microhardness and corrosion resistance of the sample coatings were determined using Vickers hardness tests, Tafel electrochemical tests and electrochemical impedance measurements (EIS) in 3.5[Formula: see text]wt.% NaCl solution to receive the effect of GO and ultrasonic. The findings indicated that UF–Ni–B/GO exhibited optimum hardness (856[Formula: see text]HV) and enhanced corrosion resistance (6.38 [Formula: see text][Formula: see text] over the Ni–B and Ni–B/GO coatings. Due to these interesting properties of the coating, it could be used as a protective material in the automotive and aerospace industries for parts of machines that were manipulated in high temperature and corrosive environments.


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


2011 ◽  
Vol 291-294 ◽  
pp. 65-71 ◽  
Author(s):  
Qing Jun Chen ◽  
Lin Li Hu ◽  
Xian Liang Zhou ◽  
Xiao Zhen Hua ◽  
Ying Jun Yang

The purpose of this study is to investigate the electrochemical properties of Fe44Cr16Mo16C18B6amorphous alloy coating fabricated using high velocity oxygen fuel (HVOF) technology in 2.0M HCl and NaOH solution at room temperature(25°C). Based on the potentiodynamic polarization curves and Electrochemical Impedance Spectroscopy(EIS) testing results of coating in aqueous solutions of HCl and NaOH, the corrosion resistance of Fe44Cr16Mo16C18B6amorphous alloy coating in HCl solution was superior to that in NaOH solution. The icorrwas 1.487×10-5A·cm-2in HClsolution and 1.107×10-4A·cm-2in NaOH solution, while the Rtreach to 5.789×104Ω·cm2and 9780Ω·cm2, respectively. On the other hand, these corrosion phenomenon could be better interpreted by R(Q(R(RQW)))(RL) and R(RL)(Q(R(CW))) equivalent circuit model, which were different from that of other Fe-based amorphous alloys in HCl and NaOH solution, respectively.


Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1029 ◽  
Author(s):  
Beatriz Martínez-Sánchez ◽  
Andrés Felipe Quintero-Jaime ◽  
Francisco Huerta ◽  
Diego Cazorla-Amorós ◽  
Emilia Morallón

In this study, the phosphonation of a polyaniline (PANI) backbone was achieved in an acid medium by electrochemical methods using aminophenylphosphonic (APPA) monomers. This was done through the electrochemical copolymerization of aniline with either 2- or 4-aminophenylphosphonic acid. Stable, electroactive polymers were obtained after the oxidation of the monomers up to 1.35 V (reversible hydrogen electrode, RHE). X-ray photoelectron spectroscopy (XPS) results revealed that the position of the phosphonic group in the aromatic ring of the monomer affected the amount of phosphorus incorporated into the copolymer. In addition, the redox transitions of the copolymers were examined by in situ Fourier-transform infrared (FTIR) spectroscopy, and it was concluded that their electroactive structures were analogous to those of PANI. From the APPA monomers it was possible to synthesize, in a controlled manner, polymeric materials with significant amounts of phosphorus in their structure through copolymerization with PANI.


Metals ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 950 ◽  
Author(s):  
Zequn Yu ◽  
Yuecheng Dong ◽  
Xin Li ◽  
Jingzhe Niu ◽  
Igor Alexandrov ◽  
...  

The aim of this study was to investigate the corrosion resistance of ultrafine-grained (UFG) Ti-6Al-7Nb fabricated by equal channel angular pressing (ECAP) and coarse-grained (CG) Ti- 6Al- 7Nb. The microstructure of each specimen was investigated by the electron backscattered diffraction (EBSD) method. The corrosion behavior of each specimen was determined by electrochemical measurement in Ringer’s solution. The surface corroded morphologies and oxide film formed on Ti-6Al-7Nb alloy after electrochemical measurement were investigated by scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). EBSD investigation shows that the grain size of UFG Ti-6Al-7Nb decreased to ~0.4 µm, accompanied by low angle grain boundaries (LAGBs) accounting for 39%. Potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) results indicated that UFG Ti-6Al-7Nb alloy possessed a better corrosion resistance. The surface corroded morphologies revealed many small and shallow corrosion pits, which can be attributed to the good compactness of the oxide film and a rapid self- repairing ability of the UFG Ti-6Al-7Nb alloy.


2020 ◽  
Vol ahead-of-print (ahead-of-print) ◽  
Author(s):  
Ming Liu ◽  
Jun Li ◽  
Danping Li ◽  
Lierui Zheng

Purpose At present, carbonated drinks such as cola are especially favored by the younger generation. But because of its acid, it often leads to tooth demineralization, resulting in “cola tooth”. However, the influence of cola on the corrosion resistance of passive film of TiA10 alloy restorative materials is rarely reported. The purpose of this study was to analysis the corrosion resistance, composition of the passive film of TA10 alloy in different concentrations of Cola. Design/methodology/approach The passive behavior of TA10 alloy in artificial saliva (AS) and Cola was studied by means of potentiodynamic polarization, electrochemical impedance spectroscopy, cyclic voltammetry, Mott-Schottky techniques and combined with X-ray photoelectron spectroscopy and Auger electron spectroscopy (AES) surface analysis. Findings With the increase of cola content, the self-corrosion current density of the alloy increases sharply, and the corrosion resistance of the passive film is the best in AS, while Rp in cola is reduced to half of that in AS. The thickness of the passive film in AS, AS +cola and cola is about 9.5 nm, 7.5 nm and 6 nm, respectively. The passive film in cola has more defects and the carrier density is 1.55 times as high as that in AS. Cola can weaken the formation process of the protected oxide, promote the formation of high valence Ti-oxides and increase the content of Mo-oxides in the passive film. Originality/value These results have important guiding significance for the safe use of the alloy in the complex oral environments.


2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Sheng-xue Yu ◽  
Rui-jun Zhang ◽  
Yong-fu Tang ◽  
Yan-ling Ma ◽  
Wen-chao Du

Nanostructured conversion coating of Al-Mg alloy was obtained via the surface treatment with zirconium titanium salt solution at 25°C for 10 min. The zirconium titanium salt solution is composed of tannic acid 1.00 g·L−1, K2ZrF60.75 g·L−1, NaF 1.25 g·L−1, MgSO41.0 g/L, and tetra-n-butyl titanate (TBT) 0.08 g·L−1. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectrum (FT-IR) were used to characterize the composition and structure of the obtained conversion coating. The morphology of the conversion coating was obtained by atomic force microscopy (AFM) and scanning electron microscopy (SEM). Results exhibit that the zirconium titanium salt conversion coating of Al-Mg alloy contains Ti, Zr, Al, F, O, Mg, C, Na, and so on. The conversion coating with nm level thickness is smooth, uniform, and compact. Corrosion resistance of conversion coating was evaluated in the 3.5 wt.% NaCl electrolyte through polarization curves and electrochemical impedance spectrum (EIS). Self-corrosion current density on the nanostructured conversion coating of Al-Mg alloy is9.7×10-8A·cm-2, which is only 2% of that on the untreated aluminum-magnesium alloy. This result indicates that the corrosion resistance of the conversion coating is improved markedly after chemical conversion treatment.


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