An oxidation mechanism map for tungsten

2022 ◽  
Vol 209 ◽  
pp. 114373
Author(s):  
Dóra Nagy ◽  
Samuel A. Humphry-Baker
Keyword(s):  
2009 ◽  
Vol 24 (4) ◽  
pp. 821-826
Author(s):  
Hui-Yi TANG ◽  
De-Gui ZHU ◽  
Bo LIU ◽  
Hong-Liang SUN

1997 ◽  
Vol 36 (10) ◽  
pp. 37-44 ◽  
Author(s):  
Eduardo Torres ◽  
Raunel Tinoco ◽  
Rafael Vazquez-Duhalt

Lignin peroxidase, cytochrome c and haemoglobin were tested for oxidation of polycyclic aromatic hydrocarbon (PAH) in the presence of hydrogen peroxide. The reaction mixture Contained water-miscible organic solvents in order to reduce the mass transfer limitation of hydrophobic substrates. The reaction products from all three haemoproteins were mainly quinones, suggesting the same oxidation mechanism for the three biocatalysts. The haeme prosthetic group must have located in a protein environment for it to catalyze these reactions, and only certain types of protein environment are able to induce this type of haemebased catalytic activity. The solvent hydrophobicity is a factor affecting the biocatalysis in organic media. Substrate partitioning between the active site (haeme) and the bulk solvent is the main factor of the biocatalytic behaviour in organic solvent mixtures. Site-directed mutagenesis of yeast cytochrome c significantly altered the kinetic behaviour of the protein. The Gly82;Thr 102 variant was 10 times more active and showed a catalytic efficiency 10-fold greater than the wild-type iso-1-cytochrome c. These results suggest that it is possible to design a new biocatalyst for environmental purposes.


1982 ◽  
Vol 47 (10) ◽  
pp. 2746-2748 ◽  
Author(s):  
Miroslav Matrka ◽  
Jana Pípalová

Oxidation of Trypan Blue with cerium(IV) ion in acid medium gives arenediazonium cation similar to the oxidation product of N,N-dimethyl-4-aminoazobenzene. Quantitative evaluation of the arenediazonium salt formed has been carried out spectrophotometrically after previous C-azo coupling with 2-naphthol.


2021 ◽  
Vol 180 ◽  
pp. 109197
Author(s):  
Chunyu Guo ◽  
Enhui Wang ◽  
Shuize Wang ◽  
Xinmei Hou ◽  
Zhijun He ◽  
...  

2020 ◽  
Vol 124 (29) ◽  
pp. 16149-16158
Author(s):  
Osamu Kobayashi ◽  
Kunihiro Noda ◽  
Naohiko Ikuma ◽  
Dai Shiota ◽  
Takayoshi Ishimoto ◽  
...  

2021 ◽  
Vol 40 (1) ◽  
pp. 53-65
Author(s):  
Li Sun ◽  
Weiping Yan

Abstract More attention has been paid to the exfoliation of oxide scale on high-temperature heating surface of utility boiler. The oxidation mechanism of HCM12A steel in supercritical water is proposed and the growth of oxide film is simulated. The duplex scale contains an outer magnetite layer and an inner Cr-rich spinel layer. According to the data of Backhaus and Töpfer, the diffusion coefficient values of iron in magnetite layer are discussed and the function of R V, R I {R}_{\text{I}} for oxygen activity can be used for calculation of iron diffusion coefficients in Cr-rich spinel layer. Based on Wagner’s oxidation theory, the oxidation rate constants of HCM12A are calculated at 500 and 600°C in supercritical water, compared with experimental data of the relevant literatures. The oxygen activities at the interfaces of alloy/Cr-rich spinel oxide and magnetite/supercritical water are estimated. The simulation results of weight gain are matched with the test data. The iron diffusion mechanisms inside the magnetite layer and the Cr-rich spinel layer are analyzed. The iron diffusion coefficient at the interface of Cr-rich spinel/magnetite is discontinuous, while the oxygen activity is continuous in the whole double layer. The thickness of oxide scale on inner tube walls of the final superheater coils (T91) of a 600 MW supercritical boiler is calculated by using the calculation method provided by the paper. The modeling results, the measured data, and the calculation results by the method are compared. Accurate calculation of the thickness of the inner and outer oxide scales can provide a necessary basis for predicting the stress and exfoliation of oxide scales.


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