Electron probe micro-analyzer (EPMA)
What is Electron probe micro-analyzer (EPMA)
- imaging modes such as secondary-electron imaging (SEI), back-scattered electron imaging (BSE), and cathodoluminescence imaging (CL),
- acquiring 2D element maps,
- acquiring compositional information by energy-dispersive spectroscopy (EDS) and wavelength-dispersive spectroscopy (WDS),
- analyzing crystal-lattice preferred orientations (EBSD).
Fundamental Principles of Electron probe micro-analyzer (EPMA)
Electron probe micro-analyzer (EPMA) Instrumentation - How Does It Work?
EPMA consists of four major components, from top to bottom:
- An electron source, commonly a W-filament cathode referred to as a "gun."
- A series of electromagnetic lenses located in the column of the instrument, used to condense and focus the electron beam emanating from the source; this comprises the electron optics and operates in an analogous way to light optics.
- A sample chamber, with movable sample stage (X-Y-Z), that is under a vacuum to prevent gas and vapor molecules from interfering with the electron beam on its way to the sample; a light microscope allows for direct optical observation of the sample.
- A variety of detectors arranged around the sample chamber that are used to collect x-rays and electrons emitted from the sample.
- Quantitative EPMA analysis is the most commonly used method for chemical analysis of geological materials at small scales.
- In most cases, EPMA is chosen in cases where individual phases need to be analyzed (e.g., igneous and metamorphic minerals), or where the material is of small size or valuable for other reasons (e.g., experimental run product, sedimentary cement, volcanic glass, matrix of a meteorite, archeological artifacts such as ceramic glazes and tools).
- In some cases, it is possible to determine a U-Th age of a mineral such as monazite without measuring isotopic ratios.
- EPMA is also widely used for analysis of synthetic materials such as optical wafers, thin films, microcircuits, semi-conductors, and superconducting ceramics.
Strengths and Limitations of Electron probe micro-analyzer (EPMA)?
- An electron probe is essentially the same instrument as an SEM, but differs in that it is equipped with a range of crystal spectrometers that enable quantitative chemical analysis (WDS) at high sensitivity.
- An electron probe is the primary tool for chemical analysis of solid materials at small spatial scales (as small as 1-2 micron diameter); hence, the user can analyze even minute single phases (e.g., minerals) in a material (e.g., rock) with "spot" analyses.
- Spot chemical analyses can be obtained in situ, which allows the user to detect even small compositional variations within textural context or within chemically zoned materials.
- Electron probes commonly have an array of imaging detectors (SEI, BSE, and CL) that allow the investigator to generate images of the surface and internal compositional structures that help with analyses.
- Although electron probes have the ability to analyze for almost all elements, they are unable to detect the lightest elements (H, He and Li); as a result, for example, the "water" in hydrous minerals cannot be analyzed.
- Some elements generate x-rays with overlapping peak positions (by both energy and wavelength) that must be separated.
- Microprobe analyses are reported as oxides of elements, not as cations; therefore, cation proportions and mineral formulae must be recalculated following stoichiometric rules.
- Probe analysis also cannot distinguish between the different valence states of Fe, so the ferric/ferrous ratio cannot be determined and must be evaluated by other techniques (see Mossbauer
User's Guide - Sample Collection and Preparation
- Nearly any solid material can be analyzed. In most cases, samples are prepared as standard-size 27 x 46 mm rectangular sections, or in 1-inch round disks. Rectangular sections of rock or similar materials are most often prepared as 30-micron-thick sections without cover slips. Alternatively, 1-inch cores can be polished. Chips or grains can be mounted in epoxy disks, then polished half way through to expose a cross-section of the material.
- The most critical step prior to analysis is giving the sample a fine polish so that surface imperfections do not interfere with electron-sample interactions. This is particularly important for samples containing minerals with different hardnesses; polishing should yield a flat surface of uniform smoothness.
- Most silicate minerals are electrical insulators. Directing an electron beam at the sample can lead to electrical charging of the sample, which must be dissipated. Prior to analysis, samples are typically coated with a thin film of a conducting material (carbon, gold and aluminum are most common) by means of evaporative deposition. Once samples are placed in a holder, the coated sample surface must be put in electrical contact with the holder (typically done with a conductive paint or tape). Choice of coating depends on the type of analysis to be done; for example, most EPMA chemical analysis is done on samples coated by C, which is thin and light enough that interference with the electron beam and emitted X-rays is minimal.
- Samples are loaded into the sample chamber via a vacuum interlock and mounted on the sample stage. The sample chamber is then pumped to obtain a high vacuum.
- To begin a microprobe session, suitable analytical conditions must be selected, such as accelerating voltage and electron beam current, and the electron beam must be properly focused. If quantitative analyses are planned, the instrument first must be standardized for the elements desired.
Data Collection, Results and Presentation
Modern microprobes make it possible to collect large datasets of "spot" analyses of minerals with a high degree of accuracy and efficiency. Examples of typical applications include determination of compositional variations in zoned minerals (that can be related to elemental mapping), or multiple analyses of mineral parageneses for the purposes of geothermobarometry. Data output (after standardization, and numerous data correction procedures such as background substraction and a variety of 'matrix' corrections) is typically a data table of weight percent of the simple oxides that comprise each mineral. An example of qualitative data tables can be seen in the Results section of the WDS module. These compositional data can then be recalculated as mineral structural formulae based on stoichiometric principles.
The following literature can be used to further explore Electron probe micro-analyzer (EPMA)
- Reed, S. J. B., 1993, Electron Microprobe Analysis (2nd Ed.), Cambridge University Press.
- Reed, S. J. B., 1995, Electron Microprobe Microanalysis, in Philip J Potts, John F. w. Bowles, Stephen J. B. Reed, and Mark R. Cave (eds), Microprobe Techniques in the Earth Sciences, The Mineralogical Society Series, vol 6., p. 49-90.
- Reed, S. J. B., 2005, Electron Microprobe Analysis and Scanning Electron Microscopy in Geology (2nd Ed.), Cambridge University Press.
- Goldstein, J. I., Newbury, D. E., Echlin, P., Joy, D.C., Lyman, C. E., Lifshin, E., Sawyer, L. C., and Michael, J.R., 2003, Scanning Electron Microscopy and X-Ray Microanalysis: A text for biologists, materials scientists, and geologists (3rd Ed.), Plenum Press
For more information about Electron probe micro-analyzer (EPMA) follow the links below.
- Electron Microrobe Labs in the USA and Canada compiled by Dr. Stephen C. Kuehn (Concord University)
- University of Minnesota Electron Microprobe Lab - a comprehensive overall resource on EPMA lab instrumentation and sample preparation
- University of Massachusetts-Amherst Probe Lab - also a good site with particular emphasis on geochronological applications of EPMA
- Electron Microprobe–Dave Waters, Oxford University
- Compilation of Microprobe Labs in the US and Canada by Stephen Kuehn, Concord University, W VA.
Teaching Activities and Resources
Teaching activities, labs, and resources pertaining to Electron probe micro-analyzer (EPMA).
- Extending Mineralogy by Electron Microprobe Analysis (Goodge, 2003) is a lab module that shows how microprobe analysis can be integrated in the learning environment. It uses EDS, BSE and WDS techniques to help make connections between mineralogy and petrology. It can be done with an in-house SEM or EPMA, via remote teleconnection to another lab, or even entirely on paper.
- Working with Electron Microprobe Data from a High Pressure Experiment (Schwab, 2004) is a problem set in which students use electron microprobe analyses of a peridotite partial melting experiment to determine mineral formulas, calculate unit cell content, plot results on a classification diagram, and use a geothermometer.
- Zoned Plagioclase Exercise (Smith, 2003) allows students to become familiar with the various types of zoning found to occur in plagioclase feldspars, recognize and identify the various zoning types, and interpret the petrogenesis of the various zoning types from optical and microprobe data.