Journal articles on the topic 'High temperature oxidation'

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1

WANG, RUZHUAN, WEIGUO LI, and DAINING FANG. "A THERMO-DAMAGE STRENGTH MODEL FOR THE SiC-DEPLETED LAYER OF ULTRA-HIGH-TEMPERATURE CERAMICS ON HIGH TEMPERATURE OXIDATION." International Journal of Applied Mechanics 05, no. 03 (September 2013): 1350026. http://dx.doi.org/10.1142/s1758825113500269.

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At high temperatures above 1650°C, the SiC -depleted layer of ultra-high-temperature ceramics which has high porosity appears during the oxidation process. In this present paper, based on the studies of the oxidative mechanisms and the fracture mechanisms of ultra-high-temperature ceramics under normal and high temperatures, a thermo-damage strength model for the SiC -depleted layer on high temperature oxidation was proposed. Using the model, the phase transformation, microstructure development and fracture performance in the SiC -depleted layer on high temperature oxidation were studied in detail. The study showed that the porosity is mainly related to the oxidation of SiC . And while the SiC is substantially completely oxidized, only a very small part of matrix is oxidized. The fracture strength of the SiC -depleted layer degrades seriously during the high temperature oxidation process. And the bigger the initial volume fraction of SiC , the lower the fracture strength of the SiC -depleted layer is. This layer may become the origin of failure of material, thus the further researches should be undertaken to improve the oxidation behavior for the ultra-high-temperature ceramics in a wider temperature range.
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2

Tuchida, K., K. Wathanyu, Chiraporn Auechalitanukul, and S. Surinphong. "High Temperature Performance of TiAlON Thin Films." Advanced Materials Research 622-623 (December 2012): 690–94. http://dx.doi.org/10.4028/www.scientific.net/amr.622-623.690.

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In this paper, the thermal oxidation behavior, adhesion and tribological properties of TiAlON films coated on hastelloyX substrate, typically used for fuel nozzle in gas turbine engine application, have been studied. The uncoated and coated samples were heated to different temperatures, i.e. 950, 1050 and 1150 °C in the controlled atmosphere. The surface appearance, microstructure, chemical composition and adhesion of films were investigated. The thermal oxidations were observed in all testing conditions showing thicker oxide film at higher temperature. However, spalling of oxide scales was found in hastelloyX and TiAlON coated at 1150°C suggesting the maximum working temperature of < 1150 °C. The critical loads corresponding to the full delamination of the thermal oxidation coated specimens were found to be higher than the non-thermal oxidation specimens. The effect of thermal oxidation on damage patterns during scratch tests, i.e. less chipping and cracking for thermal oxidation specimen, were also observed. The tribological properties were also investigated under different load under room temperature and 600 and 1000°C. The results suggested significant improvement in wear resistance of coated sample especially at low load at all temperatures.
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3

Yoshimura, Masahiro, Jun-ichiro Kase, and Shigeyuki Sōmiya. "Oxidation of SiC powder by high-temperature, high-pressure H2O." Journal of Materials Research 1, no. 1 (February 1986): 100–103. http://dx.doi.org/10.1557/jmr.1986.0100.

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The reaction between SiC powder and H2O has been studied at 400°–800 °C under 10 and 100 MPa. Silicon carbide reacted with H2O to yield amorphous SiO2 and CH4 by the reaction SiC + 2H2O→SiO2 + CH4 above 500 °C. Cristobalite and tridymite crystallized from amorphous silica after the almost complete oxidation of SiC above 700 °C. The oxidation rate, as calculated from the weight gain, increased with temperature and pressure. The Arrhenius plotting of the reaction rate based on a Jander-type model gave apparent activation energies of 167–194 kJ/mol. Contrasted with oxidation in oxidative atmosphere, oxidation in H2O is characterized by the diffusion of H2O and CH4 in an amorphous silica layer where the diffusion seemed to be rate determining. Present results suggest that the oxidation of SiC includes the diffusion process of H2O in silica layers when atmospheres contain water vapor.
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4

Wen, You-Hai. "High Temperature Oxidation Modeling." ECS Meeting Abstracts MA2020-02, no. 9 (November 23, 2020): 1173. http://dx.doi.org/10.1149/ma2020-0291173mtgabs.

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5

Warnatz, Jürgen. "Hydrocarbon oxidation high-temperature chemistry." Pure and Applied Chemistry 72, no. 11 (January 1, 2000): 2101–10. http://dx.doi.org/10.1351/pac200072112101.

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The exact knowledge of hydrocarbon oxidation kinetics is very important due to the fact that this process is involved in many technological processes: combustion in engines and furnaces, flame synthesis of materials, partial oxidation processes in chemical technology, catalytic combustion, and exhaust gas treatment, etc. An overview is given on the present state of the art with respect to kinetic data on gas-phase and (shortly) surface oxidation of hydrocarbons. Furthermore, some applications are described in the areas mentioned above. Examples for the importance of the gas-phase oxidation of hydrocarbons are ignition and combustion in engines and furnaces and partial oxidation processes in industrial chemical reactors. In many applications, both gas-phase and surface chemistry are taking place. Examples here are flame generation of diamonds and syngas generation.
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6

Coker, Eric N., Burl Donaldson, Walter Gill, Nadir Yilmaz, and Francisco M. Vigil. "The Isothermal Oxidation of High-Purity Aluminum at High Temperature." Applied Sciences 13, no. 1 (December 24, 2022): 229. http://dx.doi.org/10.3390/app13010229.

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The isothermal oxidation in air of high purity aluminum sheet was studied as a function of temperature using Thermogravimetric Analysis simultaneously with Differential Scanning Calorimetry (TGA/DSC). The rates and extents of oxidation were found to be non-linear functions of the temperature, in agreement with the literature. Between 650 °C and 750 °C very little oxidation took place; at 850 °C oxidation occurred after an induction period, while at 950 °C oxidation occurred without an induction period. At oxidation temperatures between 1050 °C and 1150 °C rapid passivation of the surface of the aluminum occurred, while at 1250 °C and above, an initial rapid mass increase was observed, followed by a more gradual increase in mass. The initial rapid increase in mass was accompanied by a significant exotherm, which was quantified by DSC. At temperatures of 1050 °C and above the specimen coalesced into a spheroidal particle, whereas at lower temperatures the original morphology was retained due to the cohesive strength of the native oxide layer. Cross-sections of oxidized specimens were characterized by scanning electron microscopy (SEM); the observed alumina skin thicknesses correlated qualitatively with the observed mass increases. Interrogation of the surface of an oxidized spheroidal particle by SEM showed a fractured alumina shell around a partially hollow core of aluminum which appeared to have grain boundaries.
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7

Ariharan, S., Manis Hazra, and Kantesh Balani. "High-temperature oxidation of graphite." Nanomaterials and Energy 7, no. 2 (December 2018): 37–43. http://dx.doi.org/10.1680/jnaen.18.00008.

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8

AMANO, Tadaaki, Masako SATO, Daisuke DOI, Masayuki HASHIMOTO, and Akira OKUBO. "High-temperature oxidation of Cr2S3." Journal of Advanced Science 11, no. 1 (1999): 26–27. http://dx.doi.org/10.2978/jsas.11.26.

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9

NARITA, Toshio. "High Temperature Oxidation and Coating." Journal of The Surface Finishing Society of Japan 64, no. 4 (2013): 229–34. http://dx.doi.org/10.4139/sfj.64.229.

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10

Belousov, Valerii V., and A. A. Klimashin. "High-temperature oxidation of copper." Russian Chemical Reviews 82, no. 3 (March 31, 2013): 273–88. http://dx.doi.org/10.1070/rc2013v082n03abeh004343.

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11

Voitovich, R. F. "High-temperature oxidation of materials." Powder Metallurgy and Metal Ceramics 34, no. 7-8 (1996): 441–45. http://dx.doi.org/10.1007/bf00559437.

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12

Lee, C. C., and P. Shen. "High temperature oxidation of Ni2AlTi." Journal of Materials Science 24, no. 10 (October 1989): 3707–11. http://dx.doi.org/10.1007/bf02385760.

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13

Paljević, M. "High-temperature oxidation of ZrAl." Journal of the Less Common Metals 138, no. 1 (March 1988): 107–11. http://dx.doi.org/10.1016/0022-5088(88)90240-8.

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14

Carol, L. A., and G. S. Mann. "High-temperature oxidation of rhodium." Oxidation of Metals 34, no. 1-2 (August 1990): 1–12. http://dx.doi.org/10.1007/bf00664336.

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15

Evans, H. E., and M. P. Taylor. "Oxidation of high-temperature coatings." Proceedings of the Institution of Mechanical Engineers, Part G: Journal of Aerospace Engineering 220, no. 1 (January 2006): 1–10. http://dx.doi.org/10.1177/095441000622000101.

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16

Sharif, A. A. "High-temperature oxidation of MoSi2." Journal of Materials Science 45, no. 4 (February 2010): 865–70. http://dx.doi.org/10.1007/s10853-009-4012-8.

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17

Matthews, S., and Ian W. M. Brown. "High temperature oxidation of Al4C3." Corrosion Science 173 (August 2020): 108793. http://dx.doi.org/10.1016/j.corsci.2020.108793.

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18

Burcat, Alexander, and Krishnan Radhakrishnan. "High temperature oxidation of propene." Combustion and Flame 60, no. 2 (May 1985): 157–69. http://dx.doi.org/10.1016/0010-2180(85)90004-5.

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19

Sequeira, C. A. C. "ChemInform Abstract: High-Temperature Oxidation." ChemInform 42, no. 39 (September 1, 2011): no. http://dx.doi.org/10.1002/chin.201139245.

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20

Jiang, Ji Chao, and Xiu Yan Luo. "High Temperature Oxidation Behaviour of AlCuTiFeNiCr High-Entropy Alloy." Advanced Materials Research 652-654 (January 2013): 1115–18. http://dx.doi.org/10.4028/www.scientific.net/amr.652-654.1115.

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The oxidation behaviour of AlCuTiFeNiCr high-entropy alloy with was studied at 850 oC in atmosphere. The oxide layer of long-term oxidation behavior were examined using optical, X-ray powder diffraction (XRD) with the aid of scanning electron microscopy (SEM) equipped with an energy dispersive X-ray analysis (EDX). The oxidation kinetics follows a parabolic rate law. The oxidation rate decreases gradually as the oxidation proceeds.
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21

Zeng, Tao, Dai Ning Fang, Xia Mei Lu, and Fei Fei Zhou. "Fracture Strength of Ultra-High Temperature Ceramics." Key Engineering Materials 368-372 (February 2008): 1785–87. http://dx.doi.org/10.4028/www.scientific.net/kem.368-372.1785.

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This paper presents a theoretical model to predict the fracture strength of ultra-high temperature ceramics (UHTCs). According to different mechanisms, the environmental temperature is divided into four ranges. Effects of temperature and oxidation on the fracture strength of UHTCs are investigated in each temperature range. The results show that oxidation plays an important role in enhancing the fracture strength of UHTCs at high temperatures.
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22

Sivaramakrishnan, R., R. S. Tranter, and K. Brezinsky. "High-pressure, high-temperature oxidation of toluene." Combustion and Flame 139, no. 4 (December 2004): 340–50. http://dx.doi.org/10.1016/j.combustflame.2004.09.006.

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23

Guo, Pengjia, Shengqiang Ma, Ming Jiao, Ping Lv, Jiandong Xing, Liujie Xu, and Zhifu Huang. "Effect of Chromium on Microstructure and Oxidation Wear Behavior of High-Boron High-Speed Steel at Elevated Temperatures." Materials 15, no. 2 (January 12, 2022): 557. http://dx.doi.org/10.3390/ma15020557.

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In order to investigate the effect of Cr content on the microstructures and oxidation wear properties of high-boron high-speed steel (HBHSS), so as to explore oxidation wear resistant materials (e.g., hot rollers), a scanning electron microscope, an X-ray diffractometer, an electron probe X-ray microanalysis and an oxidation wear test at elevated temperatures were employed to investigate worn surfaces and worn layers. The results showed that the addition of Cr resulted in the transformation of martensite into ferrite and pearlite, while the size of the grid morphology of borides in HBHSSs was refined. After oxidation wear, oxide scales were formed and the high-temperature oxidation wear resistance of HBHSSs was gradually improved with increased additions of Cr. Meanwhile, an interaction between temperature and load in HBHSSs during oxidation wear occurred, and the temperature had more influence on the oxidation wear properties of HBHSSs. SEM observations indicated that a uniform and compact oxide film of HBHSSs in the worn surface at elevated temperatures was generated on the worn surface, and the addition of Cr also reduced the thickness of oxides and inhibited the spallation of worn layers, which was attributed to improvements in microhardness and oxidation resistance of the matrix in HBHSSs. A synergistic effect of temperature and load in HBHSSs with various Cr additions may dominate the oxidation wear process and the formation and spallation of oxide films.
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24

Zufman, V. Yu, S. V. Shevtsov, A. I. Ogarkov, I. A. Kovalev, K. B. Kuznetsov, A. A. Ashmarin, N. A. Ovsyannikov, et al. "High-temperature oxidation of nickel using oxidative constructing approach." Inorganic Materials: Applied Research 8, no. 2 (March 2017): 344–47. http://dx.doi.org/10.1134/s2075113317020253.

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25

Zufman, V. Yu, S. V. Shevtsov, A. I. Ogarkov, I. A. Kovalev, K. B. Kuznetsov, A. A. Ashmarin, N. A. Ovsyannikov, et al. "High-temperature iron oxidation within the oxidative development approach." Inorganic Materials: Applied Research 8, no. 5 (September 2017): 772–75. http://dx.doi.org/10.1134/s2075113317050306.

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26

Pochiraju, K. V., and G. P. Tandon. "Modeling Thermo-Oxidative Layer Growth in High-Temperature Resins." Journal of Engineering Materials and Technology 128, no. 1 (August 1, 2005): 107–16. http://dx.doi.org/10.1115/1.2128427.

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This paper describes modeling of degradation behavior of high-temperature polymers under thermo-oxidative aging conditions. Thermo-oxidative aging is simulated with a diffusion-reaction model in which temperature, oxygen concentration, and weight-loss effects are considered. A parametric reaction model based on a mechanistic view of the reaction is used for simulating reaction-rate dependence on the oxygen availability in the polymer. Macroscopic weight-loss measurements are used to determine the reaction and polymer consumption parameters. The diffusion-reaction partial differential equation system is solved using Runge-Kutta methods. Simulations illustrating oxidative layer growth in a high-temperature PMR-15 polyimide resin system under isothermal conditions are presented and correlated with experimental observations of oxidation layer growth. Finally, parametric studies are conducted to examine the sensitivity of material parameters in predicting oxidation development.
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27

Wang, Junfeng, Qiaobai He, Guanqi Liu, Qi Zhang, Guotan Liu, Zhihao Huang, Xiaoshuo Zhu, and Yudong Fu. "High-Temperature Oxidation Behavior of AlTiNiCuCox High-Entropy Alloys." Materials 14, no. 18 (September 15, 2021): 5319. http://dx.doi.org/10.3390/ma14185319.

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In this study, the high-temperature oxidation behavior of a series of AlTiNiCuCox high-entropy alloys (HEAs) was explored. The AlTiNiCuCox (x = 0.5, 0.75, 1.0, 1.25, 1.5) series HEAs were prepared using a vacuum induction melting furnace, in which three kinds of AlTiNiCuCox (x = 0.5, 1.0, 1.5) alloys with different Co contents were oxidized at 800 °C for 100 h, and their oxidation kinetic curves were determined. The microstructure, morphology, structure, and phase composition of the oxide film surface and cross-sectional layers of AlTiNiCuCox series HEAs were analyzed using scanning electron microscopy (SEM), energy-dispersive spectrometry (EDS), and X-ray diffraction (XRD). The influence of Co content on the high-temperature oxidation resistance of the HEAs was discussed, and the oxidation mechanism was summarized. The results indicate that, at 800 °C, the AlTiNiCuCox (x = 0.5, 1.0, 1.5) series HEAs had dense oxide films and certain high-temperature oxidation resistance. With increasing Co content, the high-temperature oxidation resistance of the alloys also increased. With increasing time at high temperature, there was a significant increase in the contents of oxide species and Ti on the oxide film surface. In the process of high-temperature oxidation of AlTiNiCuCox series HEAs, the interfacial reaction, in which metal elements and oxygen in the alloy form ions through direct contact reaction, initially dominated, then the diffusion process gradually became the dominant oxidation factor as ions diffused and were transported in the oxide film.
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28

Zhu, EN, Dianxiu Xia, Qing Han, Peidun Chen, Xuelin Wang, Zhiheng Liu, and Kun Jiang. "High Temperature Oxidation Behavior of 439 Ferritic Stainless Steel at Different Temperatures." Journal of Physics: Conference Series 2541, no. 1 (July 1, 2023): 012053. http://dx.doi.org/10.1088/1742-6596/2541/1/012053.

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Abstract In recent years, due to the installation of selective catalytic reduction (Selective Catalytic Reduction, hereinafter referred to as SCR) devices, high temperature oxidation failure has occurred frequently in automobile exhaust systems. To explore its high temperature failure mechanism, this paper takes 439 ferritic stainless steel which is often used in automobile exhaust pipes as an example and uses XRD, SEM, and EDS experimental methods to study its oxidation behavior at 700 °C, 800 °C and 900 °C. The results show that the oxide layer becomes thicker and the failure degree increases with the increase of the working temperature of 439 stainless steel. The oxidation products at different temperatures are different. When the oxidation temperature is 700 °C, the phase structure of the oxide layer on the surface of the sample is Cr2O3 and Fe2O3, and the oxide layer is dense and uniform. As the temperature rises to 800 °C, the surface oxidation products are sintered together, and the needle-like Fe2O3 structure appears on the oxide film. When the oxidation temperature rises to 900 °C, the oxide layer appears inner and outer layers, the outer layer is Fe2O3 shell structure, the inner layer is generated FeO, Fe2O3, and other iron oxides, and oxidation is very serious. At the junction of the oxide layer and the substrate, there are particles such as SiO2, TiO2, Fe2Nb in the substrate, which has a positive effect on the high temperature oxidation.
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29

Park, Soon Yong, Poonam Yadav, and Dong Bok Lee. "High Temperature Oxidation Behavior of High Strength Steel Plates." Defect and Diffusion Forum 369 (July 2016): 83–88. http://dx.doi.org/10.4028/www.scientific.net/ddf.369.83.

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Three kinds of high-strength steel plates containing (less than 0.07%, or 0.024%, or 0.057%)-Si were oxidized at 700-900 °C isothermally and cyclically in atmospheric air, and their oxidation behavior was compared. The composition of the steels significantly affected the scaling rates, thickness, and adherence of the formed scales. The most important element in terms of oxidation was Si because Si affected the oxidation rates and scale adherence much. Silicon formed quite slowly a growing SiO2–containing scale around the scale/matrix interface. In the Si-deficient steel, quite thick oxide scales formed, and their adherence was poor. An optimum amount of Si was necessary in order to decrease the oxidation rate, and improve the scale adherence.
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30

Belzunce, F. J., V. Higuera, and S. Poveda. "Oxidación a alta temperatura de recubrimientos de CoNiCrAlY." Boletín de la Sociedad Española de Cerámica y Vidrio 39, no. 3 (June 30, 2000): 333–36. http://dx.doi.org/10.3989/cyv.2000.v39.i3.851.

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31

Zulnuraini, Zahraa, and Noraziana Parimin. "Performance of Fe-33Ni-18Cr Alloy at High Temperature Oxidation." Materials Science Forum 1010 (September 2020): 65–70. http://dx.doi.org/10.4028/www.scientific.net/msf.1010.65.

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This paper investigates the performance of Fe-33Ni-18Cr alloy at high temperature oxidation. The samples were isothermally oxidized at three different oxidation temperatures, namely, 600 °C, 800 °C and 1000 °C for 150 hours. This alloy was ground by using several grits of SiC paper as well as weighed by using analytical balance and measured by using Vernier caliper before oxidation test. The characterization was carried out using scanning electron microscope (SEM) equipped with energy dispersive x-ray (EDX) and x-ray diffraction (XRD). The results show that, the higher oxidation temperatures, the weight gain of the samples were increase. Sample of 1000 °C indicate more weight gain compared to samples oxidized at 600 °C and 800 °C. The kinetic of oxidation of all samples followed the parabolic rate law. The surface morphology of oxide scale at lower temperature is thin and form a continuous layer, while at high temperature, the oxide scale develops thick layer with angular oxide particles.
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32

Colson, J. C., and J. P. Larpin. "High-Temperature Oxidation of Stainless Steels." MRS Bulletin 19, no. 10 (October 1994): 23–25. http://dx.doi.org/10.1557/s088376940004817x.

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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.
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33

Lee, Dong Bok, and Y. D. Jang. "High Temperature Oxidation of Ti39.4Al10V Alloy." Materials Science Forum 449-452 (March 2004): 813–16. http://dx.doi.org/10.4028/www.scientific.net/msf.449-452.813.

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Alloys of Ti39.4Al10V (at.%) that consisted mainly of ordered β-Ti, γ-TiAl and α2-Ti3Al phases were oxidized at 700, 800, 900, and 1000oC in air. The oxide scales formed consisted largely of an outermost, thin TiO2 layer, an outer, thin Al2O3 layer, and an inner, very thick (TiO2+Al2O3) mixed layer. Vanadium, which was uniformly distributed throughout the oxide scale, harmfully decreased oxidation resistance, and made thick, nonadherent scales owing to the formation of low melting compounds of V-oxides. The oxidation progressed via the outward diffusion of Ti, Al and V ions, and the concurrent inward transport of oxygen.
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34

NANRI, Hayato, Tsuyoshi ATAKA, Nobuyuki TAKEUCHI, Shingo ISHIDA, Koji WATANABE, and Mitsuru WAKAMATSU. "High Temperature Oxidation of .BETA.-SiC." Journal of the Society of Materials Science, Japan 43, no. 493 (1994): 1360–65. http://dx.doi.org/10.2472/jsms.43.1360.

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35

Mevrel, R. "Cyclic oxidation of high-temperature alloys." Materials Science and Technology 3, no. 7 (July 1987): 531–35. http://dx.doi.org/10.1080/02670836.1987.11782264.

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36

Muinonen, M., G. Plascencia, and T. Utigard. "High Temperature Oxidation of Bessemer Matte." Canadian Metallurgical Quarterly 49, no. 3 (July 2010): 249–54. http://dx.doi.org/10.1179/cmq.2010.49.3.249.

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37

Rose, Volker, Vitali Podgursky, Ioan Costina, René Franchy, and Harald Ibach. "High temperature oxidation of CoAl(100)." Surface Science 577, no. 2-3 (March 2005): 139–50. http://dx.doi.org/10.1016/j.susc.2004.12.028.

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38

Takada, Takehiko, and Yuji Kimura. "Evaluation of High Temperature Oxidation Characteristics." Transactions of the Japan Society of Mechanical Engineers Series A 60, no. 578 (1994): 2342–49. http://dx.doi.org/10.1299/kikaia.60.2342.

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39

Lavrenko, V. A., and A. F. Alexeev. "High-temperature oxidation of boron nitride." Ceramics International 12, no. 1 (January 1986): 25–31. http://dx.doi.org/10.1016/s0272-8842(86)80006-2.

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40

Frank, P., J. Herzler, Th Just, and C. Wahl. "High-temperature reactions of phenyl oxidation." Symposium (International) on Combustion 25, no. 1 (January 1994): 833–40. http://dx.doi.org/10.1016/s0082-0784(06)80717-4.

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41

Brezinsky, K., E. J. Burke, and I. Glassman. "The high temperature oxidation of butadiene." Symposium (International) on Combustion 20, no. 1 (January 1985): 613–22. http://dx.doi.org/10.1016/s0082-0784(85)80550-6.

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42

Stander, P. P., and C. P. J. Van Vuuren. "The high temperature oxidation of FeV2O4." Thermochimica Acta 157, no. 2 (January 1990): 347–55. http://dx.doi.org/10.1016/0040-6031(90)80036-x.

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43

Moon, Jae-Jin, Deug-Joong Kim, and Dong-Bok Lee. "High temperature oxidation of chromium nitrides." Metals and Materials International 8, no. 2 (April 2002): 211–14. http://dx.doi.org/10.1007/bf03027020.

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44

Doychak, Joseph, and Toni Grobstein. "The oxidation of high-temperature intermetallics." JOM 41, no. 10 (October 1989): 30–31. http://dx.doi.org/10.1007/bf03220358.

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45

El Majid, Z., and M. Lambertin. "High temperature oxidation of aluminide coatings." Materials Science and Engineering 87 (March 1987): 205–10. http://dx.doi.org/10.1016/0025-5416(87)90380-6.

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Maruyama, Toshio. "High Temperature Oxidation of Metals (1)." Zairyo-to-Kankyo 44, no. 6 (1995): 370. http://dx.doi.org/10.3323/jcorr1991.44.370.

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Maruyama, Toshio. "High Temperature Oxidation of Metals (3)." Zairyo-to-Kankyo 45, no. 8 (1996): 495–98. http://dx.doi.org/10.3323/jcorr1991.45.495.

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HOMMA, Teiichi. "Initial stages of high temperature oxidation." Hyomen Kagaku 9, no. 9 (1988): 684–89. http://dx.doi.org/10.1380/jsssj.9.684.

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Slepterev, Artem A., Valerii S. Salnikov, Pavel G. Tsyrulnikov, Aleksandr S. Noskov, Viktor N. Tomilov, Nataliya A. Chumakova, and Andrey N. Zagoruiko. "Homogeneous high-temperature oxidation of methane." Reaction Kinetics and Catalysis Letters 91, no. 2 (August 12, 2007): 273–82. http://dx.doi.org/10.1007/s11144-007-5158-5.

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Nikonorov, E. M., T. E. Rogozhina, T. I. Nazarova, and M. V. Kuznetsova. "High-temperature oxidation of isoparaffinic oil." Chemistry and Technology of Fuels and Oils 21, no. 4 (April 1985): 198–200. http://dx.doi.org/10.1007/bf00723296.

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