J.M Hu
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J.X. Wu
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H.M Meng
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YR. Zhu
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D.B. Sun and D.J. Yang(Beijing Corrosion and Protection Center
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Open Laboratory of Corrosion
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Erosion and Surface Technology
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University of Science and Technology Beijing
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Beijing 100083
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China)
金属学报(英文版)
Titanium based IrO2 +Ta2O5 oxide anodes with different compositions and pyrolysis temperatures were prepared by termodecompoisition method. By using X-ray diffraction (XRD), the structure and texture coefficient of the coatings, TC(hkl), of IrO2 rutile crystal have been tested. It showed that, the crystallization processes of IrO2 and Ta2O5 in xIrO2 +(100-x) Ta2 O5 (x is in mol%) films affected and confined each other.In the mixed system, IrO2 rutile phase existed as a solid solution with Ta, and attained the maximum solubility when x=70mol%, i.e. for the coating of 70% IrO2 +Ta2O5.For the coatings of low iridium content or at low preparing tem pemture, (110) and (101) pwtered orientations were dominant. However, preferred growth of IrO2 weakened with increasing either iridium content or temperature. Three typical surface morphologies were observed by using scanning electron tnicroscopy(SEM). The crystallite size of the mixed oxide coatings were finest for the the film of 70%IrO2 +30%Ta2O5,and decreased with the pyrolysis tempemture. As the results of the finest crystallite segregating on sudece and the maxitnum solid solubility of Ir and Ta component in deposits, the coatings with the composition of 70%IrO2 +Ta2O5 prepared at 450℃ presented the mdrimutn electrocatalgtic activitg for O2 evolution in 0. 5M H2SO4 solution.UP to 550℃, Ti base suffered to oxidation resulting in decreasing anode conductivity,therefore, coatings performed a low activity.
关键词:
titanium based coating anode
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J.M. Hu
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H.M. Meng
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D.B. Sun
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S.J. Zhang
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J.X. Wu and D.J. Yang Beijing Corrosion and Protection Center
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Open Laboratory of Corrosion
,
Erosion and Surface Technology
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University of Science and Technology Beijing
,
Beijing 100083
,
China
金属学报(英文版)
Service life of two different oxide anodes in phenolsulfonic acid (PSA) solution was investigated by accelerated electrolysis. The durability of Ti/IrO_2+Ta_2 O_5 anode increased by the addition of SnO_2 in the mixed oxides. The degradation mechanisms of Ti/IrO_2+ Ta_2 O_5 and Ti/IrO_2 +Ta_2 O_5 +SnO+2 anodes were different. It was shown from the observation of scanning electron microscopy (SEM) and the electrochcmical measurement that, the deactivation of Ti/IrO_2 + Ta_2 O_5 anode was due to the build-up of an organic film on surface. The growth of the covered film on surface was restricted by addition of SnO_2, which resulted in increasing of the service life of anodes. The over-potential for oxygen evolution on Ti/IrO_2 +Ta_2 O_5 electrode increased after doping SnO_2, and the intermediate products of PSA building-up on the surface was much more rapidly oxidized. Meanwhile, a certain part of the surface oxide deposit entered into the solution leading to loss of oxides, which resulted in degradation of Ti/IroO_2 + Ta_2 O_5 anode containing SnO_2 component.
关键词:
metal oxide anode
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Corrosion Science
The early stages of the evolution of atmospheric corrosion of carbon steels exposed in both a laboratory simulated and a natural atmosphere environment in Shenyang have been observed by in situ scanning electron microscopy. In the case of laboratory cyclic wet-dry tests, even though the chloride content level is very low, filiform corrosion is initiated in the early stage. The filiform corrosion grows in random directions, forming a network of ridges. White nodules nucleate and grow on the ridges during continued corrosion and eventually connect with each other to form the initial corrosion scale. Pits were also found on the surface beneath corrosion products. In the case of a natural atmospheric environment, both filiform corrosion and other localized corrosion, such as pitting and inter-granular attack take place in the initial stage. It is obvious that there is variety of localized corrosion in the initial stage of atmospheric corrosion. (C) 2007 Elsevier Ltd. All rights reserved.
关键词:
steel;atmospheric corrosion;initial stage;localized corrosion;in-situ;iron;electrolyte;thickness
Materials Chemistry and Physics
The corrosion behaviour of CortenA weathering steel has been investigated using a laboratory accelerated test that involved cyclic wet/dry conditions in Qinghai salt lake water diluted 30 times The characteristics of the rust layers on tested samples were observed by SEM and EPMA analyzed by IRS and XRD and studied by polarization and EIS measurements The weight loss was almost linear indicating that the rust layer had no retarding effect on the corrosion process The crystalline components of the rust layers consisted primarily of beta-FeOOH magnetite (Fe(3)O(4)) and gamma-FeOOH As the corrosion proceeded the amount of beta-FeOOH decreased while that of magnetite and gamma-FeOOH increased XRD EDAX and EPMA indicated that the complex corrosion products magnesioferrite (MgFe(2)O(4)) and iowaite (Mg(4)Fe(OH)(8)OCl 4H(2)O) probably existed in the rust layer in which case they will have had an important Influence on the protectiveness of the rust layer The results of electrochemical measurements showed that the rust layer exhibited high reduction reactivity which facilitated the corrosion of weathering steel in the wetting process The large rust capacitance and small rust resistance indicated that the rust layer had a loose and porous structure which provided poor protection (c) 2010 Elsevier B V All rights reserved
关键词:
Elements;Corrosion test;Electrochemical techniques;Electron probe;low-alloy steels;atmospheric corrosion;carbon-steel;electrochemical;impedance;room-temperature;rust layers;iron;mechanism;products;environment
Surface & Coatings Technology
Using a halide-activated pack-cementation method but at a temperature (600 degrees C) noticeably lower than normal, an eta-Fe(2)Al(5) coating and two delta-Ni(2)Al(3) coatings with and without dispersions of CeO(2) nanoparticles were developed respectively on a low-carbon steel and the steel pretreated with an electrodeposited film of Ni or Ni-CeO(2). The erosion-corrosion (E-C) performance of the three aluminide coatings during 100 h exposure at similar to 600 degrees C in a coal-firing laboratory-scale fluidized-bed combustor (FBC) was investigated, by mounting the aluminized samples onto a rig which maintained rotation for accelerating the relative impacting speed of flying solid particles (mainly SiO(2) bed materials). The eta-Fe(2)Al(5) and the CeO(2)-free delta-Ni(2)Al(3) coatings experienced an unacceptable recession rate. Compared to the two CeO(2)-free aluminide coatings, the CeO(2)-dispersed delta-Ni(2)Al(3) coating offered profoundly improved E-C resistance, because the latter coating was not only strengthened by the CeO(2) dispersion and grain refinement, it also could grow a more adherent alumina scale. (C) 2011 Elsevier B.V. All rights reserved.
关键词:
Erosion-corrosion;CeO(2)-dispersion-strengthening;Aluminizing coating;Grain refinement;Hardening;Reactive element effect;oxidation resistance;reactive elements;alloy-steels;water-vapor;power-plant;nickel;combustion;mechanisms;additions;behavior
F.Lu
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Q.P.Zhong
金属学报(英文版)
Galvanic compatibility between graphite epoxy composite materials (GECM) and LY12CZ aluminum alloy was evaluated in different atmospheric corrosion environ-ments and by laboratory electrochemical measurements.Open circuit potential elec-trochemical measurements showed a relatively large potemtial difference about 1 volt between the GECM and LY12CZ aluminum alloy,and this difference provided the driving force for galvanic corrosion of the LY12CZ aluminum alloy as an anode. Having been exposed for 1,3or 5years in Beijing,Tuandao and Wanning station,GECM/LY12CZ couples showed significant losses of strength and elongation.Protec-tive coatings and non-conductive barriers breaking the galvanic corrosion circuit were evaluated under the same atmospheric corrosive conditions.Epoxy primer paint,glass cloth barriers and LY12CZ anodizing were effective in glvanic corrosion control for GECM/LY12CZ couples.
关键词:
galvanic corrosion
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XIAO Kui
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DONG Chaofang
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LI Xiaogang
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WANG Fuming
钢铁研究学报(英文版)
The formation and development of corrosion products on carbon steel surface during the initial stage of atmospheric corrosion in a laboratory simulated environment have been studied by scanning electron microscopy (SEM) and Raman spectroscopy. The results showed that two different shapes of corrosion products, that is, ring and chain, were formed in the initial stage of corrosion. MnS clusters were found in the nuclei of corrosion products at the active local corrosion sites. The ringshaped products were composed of lepidocrocite (γFeOOH) and maghemite (γFe2O3) transformed from lepidocrocite. The chaintype products were goethite (αFeOOH). A formation mechanism of the corrosion products is proposed.
关键词:
atmospheric corrosion;corrosion product;carbon steel
Y.Z. Luo
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D.Y. Yu
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Z.M. Xu
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Y. Luo
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G.T. Qi and J.L. Yang Departent of Chemistry
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Huazhong University of Science and Technology
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Wuhan 430074
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China
金属学报(英文版)
The corrosion behaviors of different material in the condensate water from the natural gas purifying station were studied by laboratory tests, field tests and measurements of polarization curve. The results showed that hot dipping aluminum steel had a good corrosion resistance to the accompanying gas of crude oil and condensate water in the natural gas purifying station.
关键词:
condencate water
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