Evolution of Oxide Film of T91 Steel in Water Vapor Atmosphere at 750 °C

2013 ◽  
Vol 81 (3-4) ◽  
pp. 383-392 ◽  
Author(s):  
Guangming Liu ◽  
Caifu Wang ◽  
Fei Yu ◽  
Jihong Tian
2014 ◽  
Vol 670-671 ◽  
pp. 74-81 ◽  
Author(s):  
Anusara Srisrual ◽  
Jean Pierre Petit ◽  
Yves Wouters ◽  
Alain Galerie

Nickel based alloys are well considered materials for uses in high temperature applications. Inconel 690 is the one of outstanding candidate with the superior properties. The aim of this report is to present the influence of water vapor on thermal oxide film. Inconel 690 was oxidized under dry and wet atmosphere at 900°C for 30 hours. The oxidized samples were characterized by SEM/EDS, Raman spectroscopy, and photoelectrochemical technique. The results illustrated that typical thermal oxides grown on alloy composed of Cr, Fe, Ni, in forms of Cr2O3, NiFe2O4, NiCr2O4, Fe2O3, Fe2–xCrxO3and/or solid solution of NiFe2O4−NiCr2O4. The presence of water vapor affected on oxide morphology, its stoichiometry, and also semiconducting behavior. Oxide film grown under water vapor atmosphere show the homogeneity. Water vapor promoted the predominated oxide of Cr2O3with n−type semiconducting. Moreover the characterization revealed the effect of surface orientation on oxidation mechanism in case of sample which oxidized in oxygen atmosphere.


2021 ◽  
Vol 27 (S1) ◽  
pp. 2102-2103
Author(s):  
Boyi Qu ◽  
Klaus van Benthem

Metals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1021
Author(s):  
Mauro Andres Cerra Florez ◽  
Gemma Fargas Ribas ◽  
Jorge Luiz Cardoso ◽  
Antonio Manuel Mateo García ◽  
Joan Josep Roa Rovira ◽  
...  

Aging heat treatments in maraging steels are fundamental to achieve the excellent mechanical properties required in several industries, i.e., nuclear, automotive, etc. In this research, samples of maraging 300 alloy were aged using a novel procedure that combines different steps with two atmospheres (nitrogen and water vapor) for several hours. The oxidized surface layer was chemical, microstructural and micromechanically characterized. Due to the thermodynamic and kinetic conditions, these gases reacted and change the surface chemistry of this steel producing a thin iron-based oxide layer of a homogeneous thickness of around 500 nm. Within the aforementioned information, porosity and other microstructural defects showed a non-homogeneous oxide, mainly constituted by magnetite, nickel ferrite, cobalt ferrite, and a small amount of hematite in the more external parts of the oxide layer. In this sense, from a chemical point of view, the heat treatment under specific atmosphere allows to induce a thin magnetic layer in a mixture of iron, nickel, and cobalt spinel ferrites. On the other hand, the oxide layer presents an adhesive force 99 mN value that shows the capability for being used for tribological applications under sliding contact tests.


2018 ◽  
Vol 136 ◽  
pp. 362-366 ◽  
Author(s):  
Kazunari Katayama ◽  
Haruaki Sakagawa ◽  
Tsuyoshi Hoshino ◽  
Satoshi Fukada

1998 ◽  
Vol 106 (1235) ◽  
pp. 731-733 ◽  
Author(s):  
Toshihiko SAKAI ◽  
Kazutaka TAKIZAWA ◽  
Akira NAGATOMI ◽  
Takashi WATANABE ◽  
Naofumi MORITA ◽  
...  

2011 ◽  
Vol 295-297 ◽  
pp. 693-699
Author(s):  
Zhi Wu Wang ◽  
Yan Lei ◽  
Wei Wang

Discrete mass gain method is adopted to determine the oxidation kinetic behaviors of 2Cr12NiMoWV steel in water vapor at 540°C and 17.5 MPa. Results indicate that the kinetic curve of the oxidation experiences a dramatic turning where the oxidation has lasted 20h, namely, the oxidation is faster than before the oxidation point of 20h, then oxidation rate is greatly reduced;, and after the oxidation has lasted for 300h, its reaction is inhibited to enter into a relatively stable period. The test analysis of oxide film under scanning electronic microscopy and electronic probe microanalyser shows that the formation process of the oxide film is as follows: needle-like oxide nuclei → short-strip oxide → fine equiaxed crystal grains → large equiaxed crystal grains or columnar crystal particles. The alloying elements involved in oxidation represent the law as follows: Fe, Mo and Si react with vapor at the initial stage of oxidation reaction to form Mo and Si-contained Fe-rich oxide. As the oxidation reaction proceeds, Cr gathered at the interface between the surface oxide film and the matrix, is internally oxidized. The Mo, Si and Cr in the surface oxide will be continuously volatilized with the occurrence of oxidation reaction.


1999 ◽  
Vol 14 (9) ◽  
pp. 3552-3558 ◽  
Author(s):  
P. Torri

Oxidation of sputter-deposited nanocrystalline Mo–Si–N (MoSi2.2N2.5) coatings in oxygen–water vapor atmosphere has been studied in the temperature range 400–850 °C. In addition, the oxidation properties of nanolayered Mo–Si–N/SiC coatings at 700 °C were studied and compared to those of single-layer coatings of both components. No pest disintegration was observed in Mo–Si–N up to 200 h of oxidation. A preexponential rate constant of (3.7 ± 0.5) × 109 (1015 atoms/cm2)2/h and activation energy 1.03 ± 0.02 eV were determined from an Arrhenius plot for parabolic oxygen buildup on Mo–Si–N. Up to 20% less oxygen was detected in the oxidized nanolayered coatings compared to either of the components as a single layer, indicating an improvement in oxidation resistance.


2009 ◽  
Vol 16 (4) ◽  
pp. 535-540 ◽  
Author(s):  
Du-qing Zhang ◽  
Guang-ming Liu ◽  
Guo-qun Zhao ◽  
Yan-jin Guan

2004 ◽  
Vol 151 (5) ◽  
pp. A774 ◽  
Author(s):  
E. Djurado ◽  
F. Boulc’h ◽  
L. Dessemond ◽  
N. Rosman ◽  
M. Mermoux

2021 ◽  
Author(s):  
Ya Cheng ◽  
Jianping Chen ◽  
Huiqing Guo ◽  
Yanqiu Lei ◽  
Fenrong Liu

Abstract The desulfurization mechanisms of thiophene and 2-methyl thiophene were investigated by the density functional theory (DFT) during pyrolysis under water vapor atmosphere. All possible reaction pathways of these desulfurization mechanisms were explored at M06-2X/6-311g (d) level. The Multwfn3.0 and VMD1.9.2 programs were used to analyze weak interactions between thiophene compounds and H2O molecule. It can be seen that hydrogen bonds can be formed in the reactions of thiophene sulfurs and H2O. Since H2O molecule can decompose at higher temperature and generate free radicals, such as·H and·OH,, the desulfurization mechanisms of thiophene and 2-methyl thiophene with free radicals need to be further considered. The reaction energy barriers (∆G≠) and reaction energies (∆GP) of thiophene and 2-methyl thiophene with H2O molecule (g) or free radicals (·H and·OH) have been stimulated and calculated in detail. Based on the transition state theory (TST), the rate constants corresponding to these elementary reactions are also calculated, meanwhile the speed and spontaneity of every reaction can be obtained from the aspect of kinetics. Theoretically, it is found that H2O (g) directly attacking C-S bonds of thiophene and 2-methyl thiophene cannot easily generate COS and H2S even at 1200 K in terms of thermodynamics and kinetics. If the desulfurization mechanisms of thiophenes are investigated by free radicals mechanisms under steam atmosphere, their initial energy barriers needing to be overcome significantly reduce. Therefore, desulfurization mechanisms of thiophenes and H2O (g) are the most possibly dominated by radical reactions at higher temperatures and H2S is mainly generated.


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