ATTENTION: This site is down for maintenance in read-only mode.

The following is an abstract for the selected article. A PDF download of the full text of this article is available here. Members may download full texts at no charge. Non-members may be charged a small fee for certain articles.

Quantitative Simultaneous Elemental Determinations in Alloys Using Laser-Induced Breakdown Spectroscopy (LIBS) in an Ultra-High Vacuum

Volume 48, Number 1 (Jan. 1994) Page 58-64

Thiem, T.L.; Salter, R.H.; Gardner, J.A.; Lee, Y.I.; Sneddon, J.

Laser-induced breakdown spectroscopy (LIBS) in an ultra-high vacuum is used in simultaneous quantitative elemental analysis of NIST transition metal alloy samples. A plasma is formed by focusing a Nd:YAG laser onto the sample's surface inside a vacuum chamber. UV-visible emission from excited species is monitored with the use of an optical multichannel analyzer (OMA). Linear calibration curves are shown for the elements (percent composition) Al (0.2-1.2%), Cu (0.021-0.49%), Fe (4.5-51.0%), Ni (30.8-80.3%), and Zn (6-12.8%) with the use of nonresonant lines. Detection limits (signal-to-noise = 3) vary with sample composition complexity from 0.0001% for Ni in a simple copper alloy (SRM 1111) to 0.16% for Al in a complex granular sample (SRM 349a). Absolute detection limits are estimated to be in the 20-200 μg/g range for the elements of interest. Simultaneous mass spectra were taken by sweeping the magnetic field of a mass spectrometer. Preliminary results showed the magnet could not be swept fast enough for multielement analysis. The use of a position-sensitive ion detection system is proposed.