Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-19T11:59:35.365Z Has data issue: false hasContentIssue false

18 - Spark-induced breakdown spectroscopy: a description of an electrically generated LIBS-like process for elemental analysis of airborne particulates and solid samples

Published online by Cambridge University Press:  08 August 2009

Amy J. R. Hunter
Affiliation:
Physical Sciences Inc., USA
Lawrence G. Piper
Affiliation:
Physical Sciences Inc., USA
Andrzej W. Miziolek
Affiliation:
U.S. Army Research Laboratory, USA
Vincenzo Palleschi
Affiliation:
Istituto per I Processi Chimico-Fisici, Italy
Israel Schechter
Affiliation:
Technion - Israel Institute of Technology, Haifa
Get access

Summary

Introduction

Spark-induced breakdown spectroscopy (SIBS) is a plasma-based atomic emission analytical technique that draws from both traditional spark spectroscopy and laser-induced breakdown spectroscopy (LIBS). Like traditional spark spectroscopy, the plasma is formed electrically. Like LIBS, the sparks are generally made in ambient air and detection is timed to eliminate the initial very bright breakdown. SIBS has been applied to a variety of interesting and challenging analytical problems. This chapter describes the basic hardware required to perform SIBS analyses. Here we also present the application of SIBS to real-time monitoring of airborne microparticulate lead in workplace hygiene scenarios, and the use of SIBS as a field-screening analyzer for metal contamination in soils.

SIBS can be regarded as a “marriage” of two other pulsed plasma techniques for elemental analysis: laser-induced breakdown spectroscopy and traditional spark spectroscopy. The latter is generally performed upon conductive samples (metals) and currently is predominantly used in alloy analysis. The sample itself acts as the cathode, and an anode is brought very near to the surface. An electrical discharge is formed between the electrode and the sample and ablates some material while simultaneously creating a plasma. The ablated material from the sample is vaporized, atomized, and electronically excited in the plasma. Elemental components of the sample are identified by the presence of their persistent emission lines. This detection is performed either immediately after the plasma is created or after a delay to enable plasma cooling, and spectral simplification, to take place.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Barnes, R. M. (editor), Emission Spectroscopy (Stroudsburg, PA: Dowden, Hutchison & Ross, 1973)Google Scholar
Griem, H. R., Principles of Plasma Spectroscopy (Cambridge: Cambridge University Press, 1997)CrossRefGoogle Scholar
Hirsch, M. N. and Oskam, H. J. (editors), Gaseous Electronics, Volume 1: Electrical Discharges (New York: Academic Press, 1978)
Meek, J. M. and Craggs, J. D. (editors), Electrical Breakdown of Gases (New York: John Wiley and Sons, 1978)
Payling, R., Jones, D. G. and Bengtson, A. (editors), Glow Discharge Optical Emission Spectroscopy (Chichester: John Wiley and Sons, 1997)
Radziemski, L. J. and Cremers, D. A., Spectrochemical analysis using laser plasma excitation. In Laser Induced Plasmas and Applications, Radziemski, L. J. and Cremers, D. A. (editors), chapter 7 (New York: Marcel Dekker, 1989), p. 295
Berglund, R. N. and Liu, B. Y., Anal. Chem., 7 (1973), 147
Zynger, J. and Crouch, S. R., Appl. Spectrosc., 29 (1975), 244CrossRef
Hexavalent Chromium in Workplace Atmospheres (OSHA Method No. ID-215) (Salt Lake City, UT: OSHA, 1998)
Martin, M. and Cheng, M.-D., Appl. Spectrosc., 54 (2000), 1279CrossRef
Code of Federal Regulations, Title 40, Volume 17, Parts 266–299, 40CFR266, pp. 5–119, Standards for the Management of Specific Hazardous Wastes and Specific Types of Hazardous Waste Management Facilities, Revised as of July 1, 1997
US Environmental Protection Agency, Method 6200, Field Portable X-Ray Fluorescence Spectrometry for the Determination of Elemental Concentrations in Soil and Sediment, Revision 0, January 1998
US Environmental Protection Agency, Method 4500, Mercury in Soil by Immunoassay, Revision 0, January 1998
Fraser, M. E., Panagiotou, T., Hunter, A. J. R.et al., Plating and Surface Finishing, 87 (2000), 82
Eppler, A. S., Cremers, D. A., Hickmott, D. D., Ferris, M. J. and Koskelo, A. C., Appl. Spectrosc., 50 (1996), 1175CrossRef
Fisher, B. T., Johnsen, H. A., Buckley, S. G. and Hahn, D. W., Appl. Spectrosc., 55 (2001), 1312CrossRef

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×