Cation profiling of passive films on stainless steel formed in sulphuric and acetic acid by deconvolution of angle-resolved X-ray photoelectron spectra

被引:23
作者
Hogstrom, Jonas [1 ]
Fredriksson, Wendy [1 ]
Edstrom, Kristina [1 ]
Bjorefors, Fredrik [1 ]
Nyholm, Leif [1 ]
Olsson, Claes-Olof A. [1 ]
机构
[1] Uppsala Univ, Angstrom Lab, Dept Chem Angstrom, S-75121 Uppsala, Sweden
关键词
XPS; Stainless steel; Passive films; Deconvolution; Cation distribution; Ion solubility; QUARTZ-CRYSTAL MICROBALANCE; CR-MO ALLOYS; SURFACE-COMPOSITION; DEPTH PROFILES; IRON(III) HYDROLYSIS; XPS; LAYERS; BEHAVIOR; ESCA; POLARIZATION;
D O I
10.1016/j.apsusc.2013.07.158
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An approach for determining depth gradients of metal-ion concentrations in passive films on stainless steel using angle-resolved X-ray photoelectron spectroscopy (ARXPS) is described. The iterative method, which is based on analyses of the oxidised metal peaks, provides increased precision and hence allows faster ARXPS measurements to be carried out. The method was used to determine the concentration depth profiles for molybdenum, iron and chromium in passive films on 316L/EN 1.4432 stainless steel samples oxidised in 0.5 M H2SO4 and acetic acid diluted with 0.02 M Na2B4O7 center dot 10H(2)O and 1 M H2O, respectively. The molybdenum concentration in the film is pin-pointed to the oxide/metal interface and the films also contained an iron-ion-enriched surface layer and a chromium-ion-dominated middle layer. Although films of similar composition and thickness (i.e., about 2 nm) were formed in the two electrolytes, the corrosion currents were found to be three orders of magnitude larger in the acetic acid solution. The differences in the layer composition, found for the two electrolytes as well as different oxidation conditions, can be explained based on the oxidation potentials of the metals and the dissolution rates of the different metal ions. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:700 / 714
页数:15
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