Study of properties of surface layer of iron-cobalt catalysts for synthesis of ammonia by x-ray photoelectron spectroscopy (XPES) method

1985 ◽  
Vol 20 (5) ◽  
pp. 585-587
Author(s):  
V. K. Yatsimirskii ◽  
A. I. Senkevich ◽  
E. V. Ishchenko
Coatings ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 380 ◽  
Author(s):  
Klodian Xhanari ◽  
Matjaž Finšgar

The corrosion inhibition effect of five azole compounds on the corrosion of an AA6082 aluminium alloy in 5 wt.% NaCl solution at 25 and 50 °C was investigated using weight loss and electrochemical measurements. Only 2-mercaptobenzothiazole (MBT) showed a corrosion inhibition effect at both temperatures and was further studied in detail, including with the addition of potassium iodide as a possible intensifier. Surface analysis of the MBT surface layer was performed by means of attenuated total reflectance Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and time-of-flight secondary ion mass spectrometry techniques. The hydrophobicity of the MBT surface layer was also investigated.


1989 ◽  
Vol 169 ◽  
Author(s):  
S.C. Han ◽  
D.Z. Liu ◽  
X.M. Xie ◽  
Z.L. Wu ◽  
G.C. Huth

AbstractAuger electron spectroscopy (AES) and core‐level x‐ray photoelectron spectroscopy (XPS) have been used to study the compositional and electronic‐state variations from the contaminated surface layer to the inner region of YBa2Cu3Ox and Bi2(Sr,Ca)n+1Cun02n+4 compounds. The results showed that the carbon‐rich contamination layer in BSCCO is thin and easier to be removed by Ar+ sputtering, indicating a much more stable surface than that of YBCO. This layer is oxygen deficient and contains higher Cu2+ satellites ( 2p3d9 final states) than in the bulk materials. Line‐shape analysis suggests three‐Gaussian features for both Cu 2p3/2 and O Is lines. The 529 eV signal is observed in both YBCO and BSCCO O Is spectra.


2012 ◽  
Vol 66 (5) ◽  
pp. 510-518 ◽  
Author(s):  
Paul J. Burke ◽  
Zeynel Bayindir ◽  
Georges J. Kipouros

Magnesium (Mg) and its alloys are attractive for use in automotive and aerospace applications because of their low density and good mechanical properties. However, difficulty in forming magnesium and the limited number of available commercial alloys limit their use. Powder metallurgy may be a suitable solution for forming near-net-shape parts. However, sintering pure magnesium presents difficulties due to surface film that forms on the magnesium powder particles. The present work investigates the composition of the surface film that forms on the surface of pure magnesium powders exposed to atmospheric conditions and on pure magnesium powders after compaction under uniaxial pressing at a pressure of 500 MPa and sintering under argon at 600 °C for 40 minutes. Initially, focused ion beam microscopy was utilized to determine the thickness of the surface layer of the magnesium powder and found it to be ∼10 nm. The X-ray photoelectron analysis of the green magnesium sample prior to sintering confirmed the presence of MgO, MgCO3·3H2O, and Mg(OH)2 in the surface layer of the powder with a core of pure magnesium. The outer portion of the surface layer was found to contain MgCO3·3H2O and Mg(OH)2, while the inner portion of the layer is primarily MgO. After sintering, the MgCO3·3H2O was found to be almost completely absent, and the amount of Mg(OH)2 was also decreased significantly. This is postulated to occur by decomposition of the compounds to MgO and gases during the high temperature of sintering. An increase in the MgO content after sintering supports this theory.


2002 ◽  
Vol 757 ◽  
Author(s):  
Katherine L. Smith ◽  
Zhaoming Zhang ◽  
Peter McGlinn ◽  
Darren Attard ◽  
Huijing Li ◽  
...  

ABSTRACTPolished tiles (7×7×2 mm3) of Nd-bearing zirconolite were fabricated and then some were irradiated on both large faces with 3 MeV or 2 MeV Au2+ ions (total fluence of ≥ 1 × 1015 ions/cm2) in order to render the zirconolite amorphous and so simulate displacement damage caused by alpha decay. Both the irradiated and non-irradiated tiles were then subjected to static dissolution tests in 0.01M nitric solution (pH2) at 90 C, for periods of 0–1, 1–7, 7–14 and 14–28 days. It was found that radiation damage did not affect the dissolution rate of zirconolite as indicated by the elemental leach rates of Nd, Ti, Ca and Al. The results of solution analyses are consistent with those obtained from X-ray Photoelectron Spectroscopy (XPS) in that the Ca, Nd, Ti and Al concentrations in the top surface layer (< 5 nm) all decreased with respect to that of Zr after dissolution testing, and the leached surface composition of the non-irradiated zirconolite is very similar to that of the two irradiated specimens. The implications of these results are discussed in the context of previous work.


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