scholarly journals Effect of SiO2 Dispersion on Chlorine-Induced High-Temperature Corrosion of High-Velocity Air-Fuel Sprayed NiCrMo Coating

CORROSION ◽  
10.5006/2802 ◽  
2018 ◽  
Vol 74 (9) ◽  
pp. 984-1000 ◽  
Author(s):  
Esmaeil Sadeghi ◽  
Nicolaie Markocsan ◽  
Tanvir Hussain ◽  
Matti Huhtakangas ◽  
Shrikant Joshi

NiCrMo coatings with and without dispersed SiO2 were deposited using high-velocity air-fuel technique. Thermogravimetric experiments were conducted in 5% O2 + 500 vppm HCl + N2 with and without a KCl deposit at 600°C for up to 168 h. The SiO2-containing coating showed lower weight change as a result of formation of a protective and adherent Cr-rich oxide scale. SiO2 decelerated short-circuit diffusion of Cr3+ through scale’s defects, e.g., vacancies, and promoted the selective oxidation of Cr to form the protective Cr-rich oxide scale. Furthermore, the presence of SiO2 led to less subsurface depletion of Cr in the coating, and accordingly less corrosion of the substrate. The formed corrosion product on the SiO2-free coating was highly porous, non-adherent, and thick.


Author(s):  
L. P. Lemaire ◽  
D. E. Fornwalt ◽  
F. S. Pettit ◽  
B. H. Kear

Oxidation resistant alloys depend on the formation of a continuous layer of protective oxide scale during the oxidation process. The initial stages of oxidation of multi-component alloys can be quite complex, since numerous metal oxides can be formed. For oxidation resistance, the composition is adjusted so that selective oxidation occurs of that element whose oxide affords the most protection. Ideally, the protective oxide scale should be i) structurally perfect, so as to avoid short-circuit diffusion paths, and ii) strongly adherent to the alloy substrate, which minimizes spalling in response to thermal cycling. Small concentrations (∼ 0.1%) of certain reactive elements, such as yttrium, markedly improve the adherence of oxide scales in many alloy systems.



MRS Bulletin ◽  
1994 ◽  
Vol 19 (10) ◽  
pp. 23-25 ◽  
Author(s):  
J.C. Colson ◽  
J.P. Larpin

The first stainless steels, mainly low carbon chromium-iron alloys, have been known since the beginning of this century. These steels show good resistance against wet corrosion and high-temperature corrosion. This article focuses on high-temperature corrosion, with emphasis on gaseous sulfidizing and oxidizing environments. The discussion is limited to these two gases since corrosion involving halogen-and/or carbon-containing gases involves other specific processes. The behavior of binary and ternary alloys will be successively examined, then the role of minor elements will be considered.Fundamental Mechanisms of High-Temperature Corrosion of Stainless SteelUsually, a dry corrosion process results in the formation of corrosion products, giving a simple or complex oxide or sulfide scale on a metallic substrate, separating it from the aggressive gaseous environment and, consequently, acting as a protective barrier. Scale growth is controlled by the conductivity of the reaction products which are solid electrolytes. Generally, the mechanism of scale growth is governed by outward cation or inward anion diffusion processes. This is the basis of the model originally put forward by Wagner for a single metal and subsequently developed for alloys, and particularly, for stainless steels. This one-way point-defect diffusion process is responsible for the observed parabolic scaling kinetics characterized by a parabolic rate constant kp. This model is well described in the literature.In the case of stainless steels, formation of a protective scale is required; this is possible if the oxide or sulfide products have a low diffusivity to cations or anions due to a low density of point defects in the crystal lattice. The protective characteristics of the corrosion products may be experimentally determined by measurement of their electrical conductivity, although the scales should also be effective against short-circuit transport of ions, atoms, or molecules. The best barriers consist of oxides, such as Al2O3, SiO2, and Cr2O3.



2006 ◽  
Vol 15-17 ◽  
pp. 398-403
Author(s):  
Jee Hoon Choi ◽  
Dong Bok Lee

L12-type Al65.5Ti24.4Cr10.1 alloys were prepared by induction melting followed by thermomechanical treatment. Corrosion tests were performed between 1173 and 1373 K in a flowing Ar-1% SO2 atmosphere for up to 150 hr. The corrosion proceeded mainly via the oxidation reaction. The oxide scale was primarily composed of Al2O3, together with a small amount of TiO2 that appeared mainly in the lower part of the oxide scale during the latter stages of corrosion. The formation of the highly stoichiometric, slowly growing alumina scale on the surface significantly improved the corrosion resistance of the alloys. Neither internal corrosion products nor sulfides were detected.



2011 ◽  
Vol 311-313 ◽  
pp. 1555-1558
Author(s):  
Chia Chieh Wei ◽  
Chaur Jeng Wang ◽  
Horng Yih Liou ◽  
Kuo Ming Chen

Co-firing of biomass and coal has drawn many attentions because it can reduce the amount of CO2 release of the coal power plant/incinerator. However, the higher amount of sulfur, chlorine, potassium and calcium in biomass could lead to a more serious corrosion. In this study, the high-temperature corrosion of Fe-Cr-Mo alloy at 400 °C to 600 °C in co-firing of biomass and coal was performed. The results show that the weight change of specimen tested in co-firing of biomass and coal is 1.7 to 2.4 times of that for specimen tested in dry air. Also, the weight change of specimen tested in co-firing increased with the tested temperature and time increased. For the specimen tested in co-firing with different ratio of biomass/coal, the weight change of specimen increased with the ratio of biomass/coal increased.



CORROSION ◽  
1959 ◽  
Vol 15 (1) ◽  
pp. 23-24 ◽  
Author(s):  
V. H. TROUTNER

Abstract The corrosion product films formed on aluminum in aqueous environments at high temperatures have been examined with the electron microscope. A technique is described for the preparation of electron microscope replicas of the surface of the corrosion product films adjacent to the metal. Electron micrographs are shown of corrosion product films formed during various stages of corrosion in high purity water, and in corrosion inhibited systems. Corrosion inhibition was found to be assocated with different crystalline structures of the corrosion product films. 2.3.6



CORROSION ◽  
1974 ◽  
Vol 30 (4) ◽  
pp. 131-138 ◽  
Author(s):  
RICHARD F. REISING ◽  
DOUGLAS P. KRAUSE

Abstract Gas turbine engines are susceptible to high temperature corrosion which is enhanced by marine atmospheres. This high temperature corrosion is also known as sulfidation because it is believed that the formation of metal sulfides from sulfur containing substances is essential. An understanding of the corrosion mechanisms involved is necessary in seeking methods of eliminating the problem, and the initial step in formulating mechanisms is to identify the chemical reactions involved. Corrosion product characterization is essential for this identification. Characterization of the corrosion products from the nickel-sodium sulfate-air system at temperatures near 1000 C (1832 F) suggests that the sodium sulfate acts as a flux rather than as a chemical reactant. Some of the techniques used to characterize the corrosion products are discussed.



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