Published February 28, 2005 | Version v1
Journal article

Analysis of painted steel by a hand-held X-ray fluorescence spectrometer

  • 1. Department of Materials Science and Engineering, Kyoto University, Sakyo-ku, Kyoto 606-8501 (Japan) and Forensic Science Laboratory, Kyoto Pref. Police H.Q., Kamigyo-ku, Kyoto 602-8550 (Japan)
  • 2. Rigaku Corporation Niton Project, 4-14-4 Sendagaya, Shibuya-ku, Tokyo 151-0051 (Japan)
  • 3. Rigaku Corporation, 3-9-2 Matsubara-cho, Akishima-shi, Tokyo 196-8666 (Japan)
  • 4. Department of Materials Science and Engineering, Kyoto University, Sakyo-ku, Kyoto 606-8501 (Japan)

Description

Steel with a paint layer was analyzed with a hand-held X-ray fluorescence spectrometer. When the 0.5 mm thick paint layer was composed mainly of light elements, alloying elements in steel such as Fe, Cr, Ni, W, and Mo were easily detected. 0.2% Mo in steel was detectable even if the paint contained Ti or Fe as a main element. The signal intensity of each element in steel decreased exponentially when the paint thickness increased, and the degree of decrease depended on the X-ray energy. Therefore the peak intensity for non-painted steel could be calculated from the paint thickness. The paint thickness was estimated from the intensity ratio Fe Kβ/Kα or W Lβ/Lα. When a paint of Ti (0.07-0.49 mm thick) was used, the peak intensities of the Fe Kα, Cr Kα, Ni Kα, and Mo Kα lines for non-painted steel were estimated by using the intensity ratio Fe Kβ/Kα, with errors of less than 30%. The content of each element in steel is estimated when the fluorescent X-rays are detectable by analysis of painted steel without removing the paint layer. On-site screening of painted steel can be performed on the basis of the alloy composition estimated by analysis with a hand-held XRF spectrometer

Additional details

Identifiers

DOI
10.1016/j.sab.2004.12.010;
PII
S0584-8547(05)00003-0;

Publishing Information

Journal Title
Spectrochimica Acta. Part B, Atomic Spectroscopy
Journal Volume
60
Journal Issue
2
Journal Page Range
p. 249-252
ISSN
0584-8547
CODEN
SAASBH

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.