학술논문

The initial oxidation of iron at 200/sup 0/C and 300/sup 0/C and the effect of surface sulfur
Document Type
Journal Article
Author
Source
Oxid. Met.; (United States); 16:1/2
Subject
36 MATERIALS SCIENCE
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY IRON
OXIDATION
AUGER ELECTRON SPECTROSCOPY
KINETICS
SULFUR
X-RAY EMISSION ANALYSIS
CHEMICAL ANALYSIS
CHEMICAL REACTIONS
ELECTRON SPECTROSCOPY
ELEMENTS
METALS
NONDESTRUCTIVE ANALYSIS
NONMETALS
SPECTROSCOPY
TRANSITION ELEMENTS 360105* -- Metals & Alloys-- Corrosion & Erosion
400201 -- Chemical & Physicochemical Properties
Language
English
Abstract
The growth of thin 0-200/sup 0/C has been studied as a function of time and oxygen partial pressure using proton- induced X-ray emission (PIXE) and Auger electron spectroscopy (AES). Oxidation was found to be initially retarded by sulfur which had segregated onto the iron surfaces during preoxidation annealing, but only if the iron surface contained the maximum or near-maximum sulfur coverage (ca. one-half monolayer). During and immediately following the oxygen- sulfur interaction, oxide buildup appeared to be limited by a surface reaction (adsorption, ionization, or dissociation). For most of the oxidation period, pressure-dependent logarithmic oxide growth was observed at 200/sup 0/C, and pressure-independent parabolic oxide growth at 300/sup 0/C. Interpretation of the data indicated that oxide growth at 200/sup 0/C may be limited by quantum mechanical tunneling of electronic species through the previously formed oxide film, and oxide growth at 300/sup 0/C may be limited by ionic diffusion through the previously formed oxided film. Comparison of AES and PIXE data indicated that oxide films formed at 200/sup 0/C were uniform in thickness over the surface of the metal, whereas films formed at 300/sup 0/C had relatively thin areas where sulfur had remained.