Empirical APFs
This menu allows the user to selectively load empirical APFs (Area Peak Factors) from a supplied ASCII file (compound APFs) or data entry (specified APFs). Specified APFs are discussed elsewhere.
A powerful feature in Probe for EPMA allows the user to select an Area-Peak-Factor (APF) correction for use in correcting x-ray intensities for peak shift and shape changes between the standard and the unknown. This can occur especially with Kα lines of the light elements such as oxygen, nitrogen, carbon and boron. With these elements, differences in the bond energies between say TiC and SiC will produce significantly different peak shapes resulting in systematic errors in the analysis of these materials when only the peak x-ray intensities are used.
For example, when analyzing oxygen and using MgO or Fe2O3 as an oxygen standard, analyses of SiO2 will produce errors up to about 4.5%. This effect is independent of the matrix correction and can be corrected for only by the use of the appropriate APFs.
The APF concept was proposed by Bastin and Heijligers (Bastin and Heijligers, 1986) to provide a simple correction scheme for this effect. It basically requires measuring the ratio of the peak intensity to the integrated intensity between a primary standard and a number of secondary standards on the light element spectrometer used. The wavelength scan feature in Probe for EPMA can be used to acquire the peak shape profiles. After correcting for background and removal of extraneous peaks from interfering lines (requires use of an off-line peak stripping program), the APF can be calculated. The calculation of the APF factor is shown below :
Where
:
is the
integrated intensity of the secondary standard (unknown)
is the peak intensity of the primary standard
is the
peak intensity of the secondary standard (unknown)
is the integrated intensity of the primary standard
The peak shape and shift of light element peaks can be easily demonstrated using MgO and SiO2 standard samples. First select a suitable layered dispersive element (LDE) analyzing crystal for oxygen Kα analysis. Tune the spectrometer using the MgO standard and acquire a standard sample for MgO. Assign MgO as the calibration standard for oxygen. Then move to the SiO2 standard and acquire another quantitative standard sample on the SiO2 sample. Note that the analysis of SiO2 using MgO as a calibration standard will result in a low total for the SiO2, somewhere around 96-97 %. This is not an error in the mass absorption coefficient (MAC), and no attempt should be made to correct this problem by entering an arbitrary MAC value.
Instead, the proper APF correction will need to be applied as shown below. Although the values below are relative to Fe2O3, you will note that the APF for MgO is 1.000, which means that these correction factors apply equally well relative to MgO. In the Oxygen Area Peak Factor table below you will note that oxygen in the presence of SiO2 needs to be corrected by a factor of 1.0444 when MgO or Fe2O3 is used as a calibration standard. After entering this APF correction factor for the oxygen channel and re-analyzing, note that the total is now close to 100 %.
It is very important to note that the APF values selected or entered are always measured relative to some standard sample. For example, if measuring C Kα and using Fe3C as the primary standard for carbon, then any C Kα APF values used must be those measured relative to Fe3C. For the same reason, if using APF values for a particular (light) element and one decides to re-assign the standard for that element, the APF values for that element must also be changed to reflect the standard re-assignment. See the section above for information on re-calculating the APF values relative to another standard.
For the above reason it is usually most efficient to simply always use the same standard for each light element analyzed. Typically (in order to utilize the APF values in the supplied EMPAPF.DAT file) these will be :
- Oxygen : MgO or Fe2O3
- Nitrogen : AlN
- Carbon : Fe3C
- Boron : B metal
Note: The specified APF correction in Probe for EPMA Xtreme will also allow the user to enter empirical APF values in each run at the bottom of the Element dialog from the Elements/Cations button in the Analyze! window and is a separate correction from the compound APF correction being discussed here.
The user may enter one or more APF factors for each emitting element although they are generally applied to soft x-ray lines. Note however that even S Kα exhibits peak shift and shape changes when comparing sulfide and sulfate peaks and there is well documented shifts and peak shape changes for Si Kα and Al Kα from metallic to oxides or silicate compounds. The APF for each absorber will be summed according to its weight fraction in the composition and applied to the emitting element counts during the ZAF or Phi-Rho-Z iteration.
If it is desired to correct a complete unknown for peak shape changes, simply perform a wavelength scan on the standard being used for the light element emitter (oxygen, carbon, etc.) and also on the unknown. Calculate the APF using the expression above and then from the Analytical | Empirical APFs menu, enter the same APF for all absorbers in the unknown. The program will then sum the APFs which will be the same as the single measured APF. Note that this APF may only apply to a single composition. One can perform additional wavelength scans on other samples to confirm this however. Alternatively one can enter the single empirical APF in the APF field in the Elements/Cations dialog as described above.
The APF correction values are defined in the EMPAPF.DAT file in the Probe for EPMA program data directory (usually C: \ProgramData\Probe Software\Probe for EPMA). The file contains some 50 or 60 values that may or may not be applicable, depending on the analyzing crystals and standards available. The user may edit the file using any ASCII text editor such as NotePad or TextPad to insert their own measurements. Be careful to avoid adding any <tab> characters when editing the file (use space or comma delimited values only). Note that the elements may be in any order although they have been sorted to facilitate editing.
The format of the EMPAPF.DAT file is shown below :
"b" "ka" "c" 1.02 "B4C/B/STE"
"b" "ka" "n" 1.2 "BN/B/STE"
"b" "ka" "al" 1.12 "AlB2/B/STE"
"b" "ka" "al" 1.01 "AlB12/B/STE"
"b" "ka" "si" 1 "SiB3/B/STE"
"b" "ka" "si" .92 "SiB6/B/STE"
"b" "ka" "ti" .75 "TiB/B/STE"
"b" "ka" "ti" .88 "TiB2/B/STE"
"b" "ka" "v" 1 "VB2/B/STE"
"b" "ka" "cr" .9 "CrB/B/STE"
"b" "ka" "cr" 1.1 "CrB2/B/STE"
"b" "ka" "fe" 1.1 "FeB/B/STE"
"b" "ka" "fe" 1.25 "Fe2B/B/STE"
"b" "ka" "co" 1.2 "CoB/B/STE"
"b" "ka" "co" 1.02 "Co2B/B/STE"
"b" "ka" "ni" 1.2 "NiB/B/STE"
"b" "ka" "ni" 1.06 "Ni2B/B/STE"
"b" "ka" "ni" .98 "Ni3B/B/STE"
"b" "ka" "zr" .8 "ZrB2/B/STE"
"b" "ka" "nb" .8 "NbB/B/STE"
"b" "ka" "nb" .9 "NbB2/B/STE"
"b" "ka" "mo" .94 "MoB/B/STE"
"b" "ka" "la" .9 "LaB6/B/STE"
"b" "ka" "ta" .88 "TaB/B/STE"
"b" "ka" "ta" 1.1 "TaB2/B/STE"
"b" "ka" "w" .98 "WB/B/STE"
"b" "ka" "u" 1.04 "UB4/B/STE"
"c" "ka" "b" 1.01 "B4C/Fe3C/WSi/59.8"
"c" "ka" "si" .933 "SiC/Fe3C/WSi/59.8"
"c" "ka" "ti" .868 "TiC/Fe3C/WSi/59.8"
"c" "ka" "v" .873 "V2C/Fe3C/WSi/59.8"
"c" "ka" "v" .873 "VC/Fe3C/WSi/59.8"
"c" "ka" "cr" .8 "Cr7C3/Fe3C/STE"
"c" "ka" "cr" .83 "Cr3C2/Fe3C/STE"
"c" "ka" "cr" .8 "Cr23C6/Fe3C/STE"
"c" "ka" "zr" .88 "ZrC/Fe3C/WSi/59.8"
"c" "ka" "nb" .79 "NbC/Fe3C/STE"
"c" "ka" "mo" .82 "Mo2C/Fe3C/STE"
"c" "ka" "hf" .83 "HfC/Fe3C/STE"
"c" "ka" "ta" .96 "TaC/Fe3C/STE"
"c" "ka" "w" .97 "WC/Fe3C/STE"
"c" "ka" "w" 1.02 "W2C/Fe3C/STE"
"n" "ka" "si" 1.103 "Si3N4/AlN/WSi/59.8"
"n" "ka" "ti" .997 "TiN/AlN/WSi/59.8"
"n" "ka" "v" 1.0226 "VN/AlN/WSi/59.8"
"n" "ka" "cr" 1.018 "Cr2N/AlN/WSi/59.8"
"n" "ka" "fe" 1.012 "Fe2N/AlN/WSi/59.8"
"n" "ka" "zr" .9952 "ZrN/AlN/WSi/59.8"
"n" "ka" "hf" 1.002 "HfN/AlN/WSi/59.8"
"o" "ka" "b" 1.0628 "B6O/Fe2O3/WSi/59.8"
"o" "ka" "mg" 1 "MgO/Fe2O3/WSi/59.8"
"o" "ka" "al" 1.0213 "Al2O3/Fe2O3/WSi/59.8"
"o" "ka" "si" 1.0444 "SiO2/Fe2O3/WSi/59.8"
"o" "ka" "ti" .9796 "TiO2/Fe2O3/WSi/59.8"
"o" "ka" "cr" .993 "Cr2O3/Fe2O3/WSi/59.8"
"o" "ka" "mn" 1.0121 "MnO/Fe2O3/WSi/59.8"
"o" "ka" "fe" .9962 "Fe3O4/Fe2O3/WSi/59.8"
"o" "ka" "co" 1.0133 "CoO/Fe2O3/WSi/59.8"
"o" "ka" "ni" 1.0153 "NiO/Fe2O3/WSi/59.8"
"o" "ka" "cu" .9946 "Cu2O/Fe2O3/WSi/59.8"
"o" "ka" "cu" .9943 "CuO/Fe2O3/WSi/59.8"
"o" "ka" "zn" .9837 "ZnO/Fe2O3/WSi/59.8"
"o" "ka" "ga" 1 "Ga2O3/Fe2O3/WSi/59.8"
"o" "ka" "zr" .9823 "Y3Fe5O12/Fe2O3/WSi/59.8"
The first column (in the example is "b" for Boron) is the atomic symbol of the emitting element. The second column ("ka" in the example equals Kα) is the x-ray line of the emitter. The third column is the atomic symbol of the absorber element. The fourth column is the actual area peak factor (APF) that has been experimentally measured. The last parameter is a string that contains the conditions under which the APF was measured. For example, the comment "B4C/B/STE" indicates that the peak and integrated intensities for the APF were measured on a B4C (boron carbide) sample, relative to a B (elemental Boron) primary standard, using a Pb Stearate analyzer. The reason that this information is needed is because the APF is a relative measurement (to a standard) and the value is dependent on the resolution (crystal type) used. If a LDE (layered dispersive element) analyzer is used, the 2d of the analyzer should be indicated also as seen in the example file above.
The first and third columns (emitting atomic symbol and absorber atomic symbol) must be valid element symbols. The second column (x-ray line) must be "ka", "kb", "la", "lb", "ma" or "mb". All element and x-ray symbols must be enclosed in double quotes. The fourth column (APF value) must be a real number greater than 0.0. The comment string must be enclosed in double quotes.
These values can then be loaded from the Analytical | Empirical APFs menu item in Probe for EPMA. Note that the comments listed after each APF value can be used to indicate the experimental conditions under which the APF was measured. For consistency sake, the formula of the compound measured is listed first, then the primary reference standard used and finally the analyzing crystal type (and 2d spacing if desired) used. Edit the EMPAPF.DAT file in the Probe for EPMA directory to add additional APFs from your own measurements.
The following is a short listing of some typical APFs taken from Bastin and Heijligers (1986). Because the factors are spectrometer and crystal dependent these should be used as a guide only.
Oxygen Area Peak Factors (APF)