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Introduction to XRF

Introduction to
X-Ray
Fluorescence
Analysis

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Introduction to XRF

DR. HARSH MOHAN


DEPARTMENT OF PHYSICS
M.L.N. COLLEGE
YAMUNA NAGAR
(HARYANA

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Introduction to XRF

Electromagnetic Radiation
1014Hz - 1015Hz
1Hz - 1kHz 1kHz - 1014Hz 1015Hz - 1021Hz
Extra-Low Radio Microwave Infrared Ultraviolet X-Rays,
Frequency
(ELF) Visible Light Gamma Rays

Low energy High energy

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Introduction to XRF

Theory
 A source X-ray strikes an
inner shell electron. If at
high enough energy (above
absorption edge of
element), it is ejected it
from the atom.

 Higher energy electrons


cascade to fill vacancy,
giving off characteristic
fluorescent X-rays.

 For elemental analysis of


Na - U.

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Introduction to XRF

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Introduction to XRF

How can we create core holes?


•X-rays, Electrons, Ions which
have higher energy than the core
electron ionization energies.

•Electrons and ions produces many


peaks with multiple excitations. X-
ray excitation is preferable.

•Now, X-ray fluorescence analysis


by X-ray excitation is a standard
technique for trace element
analysis

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Introduction to XRF

The Hardware

• Sources
• Optics
• Filters & Targets
• Detectors

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Introduction to XRF

Sources
•X-Ray Tubes

•Radioisotopes

•Other Sources
–Scanning Electron Microscopes
–Synchrotrons
–Positron and other particle beams

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Introduction to XRF

X-Ray Tubes
•X-ray tubes work on the principle:
• Accelerating electrons in an electrical field
and decelerating them in a suitable anode
material.
•The region of the electron beam in which
this takes place must be evacuated in order
to prevent collisions with gas molecules.
• Hence there is a vacuum within the
housing
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Introduction to XRF

X-Ray Tubes
•The technical means of achieving this is
to apply high voltage between a heated
cathode (e.g. a filament) and a suitable
anode material.
• Electrons emanate from the heated
cathode material and are accelerated
towards the anode by the applied high
voltage

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Introduction to XRF

X-Ray Tubes
• They strike the anode material and lose their
energy through deceleration.
• Only a small proportion of their energy loss
(approx.1-2%, depending on the anode material)
is radiated in the form of X-rays.
•The greatest amount of energy contributes to
heating up the anode material.
• Consequently the anode has to be cooled which
is achieved by connection to a water-cooling
system.

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Introduction to XRF

X-Ray Tubes
•The proportion of the electron energy loss
emitted in the form of an X-ray can be between
zero and the maximum energy that the electron
has acquired as a result of the acceleration in the
electrical field
•The X-rays escape from the housing at a
special point that is particularly transparent
with a thin beryllium window

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Introduction to XRF

Side Window X-Ray Tube

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Introduction to XRF

Side Window X-Ray Tube


•In side-window tubes, a negative high voltage is
applied to the cathode.

•The electrons emanate from the heated cathode


and are accelerated in the direction of the anode.

•The anode is set on zero voltage and


thus has no difference in potential to the
surrounding housing material and the laterally
mounted beryllium exit window

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Introduction to XRF

Side Window X-Ray Tube


• For physical reasons, a proportion of the electrons
are always scattered on the surface of the anode.

• The extent to which these backscattering electrons


arise depends, among other factors, on the anode
material and can be as much as 40%.

•In the side-window tube, these backscattering


electrons contribute to the heating up of the
surrounding material, especially the exit window.

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Introduction to XRF

Side Window X-Ray Tube


•As a consequence, the exit window must withstand
high levels of thermal stress and cannot be selected with
just any thickness.
•The minimum usable thickness of a beryllium window
for side-window tubes is 300 μ m.
•This causes an excessively high absorption of the low-
energy characteristic L radiation of the anode material in
the exit window .
•Thus a restriction of the excitation of lighter elements
in a sample.

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Introduction to XRF

End Window X-Ray Tube

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Introduction to XRF

End Window X-Ray Tube


•The distinguishing feature of the end-window tubes is that
the anode has a positive high voltage and the beryllium exit
window is located on the front end of the housing
•The cathode is set around the anode in a ring (annular
cathode) and is set at zero voltage. The electrons emanate
from the heated cathode and are accelerated towards the
electrical field lines on the anode.
•Due to the fact that there is a difference in potential between
the positively charged anode and the surrounding material,
including the beryllium window, the backscattering electrons
are guided back to the anode and thus do not contribute to the
rise in the exit window’s temperature.
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Introduction to XRF

End Window X-Ray Tube


•The beryllium window remains “cold” and can therefore be
thinner than in side-window tubes. Windows are used with a
thickness of 125 μm and 75 μm.
• This provides a prerequisite for exciting light elements with
the characteristic L radiation of the anode material (e.g.
rhodium).
•Due to the high voltage applied, non-conductive, de ionized
water must be used for cooling. Instruments with end-window
tubes are therefore equipped with a closed, internal circulation
system containing deionized water that cools the tube head as
well.

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Introduction to XRF

Duane–Hunt law
•The Duane–Hunt law, named after the
American physicists William Duane and
Franklin Hunt

• It gives the maximum frequency of X-


rays that can be emitted by
Bremsstrahlung in an X-ray tube by
accelerating electrons through an
excitation voltage V into a metal target.
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Introduction to XRF

Duane–Hunt law
•In an X-ray tube, electrons are accelerated in a vacuum by
an electric field and shot into a piece of metal called the
"target". X-rays are emitted as the electrons slow down
(decelerate) in the metal.

• The output spectrum consists of a continuous spectrum of


X-rays, with additional sharp peaks at certain energies

•The continuous spectrum is due to bremsstrahlung, while


the sharp peaks are characteristic X-rays associated with
the atoms in the target.

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Introduction to XRF

Bremsstrahlung X-Rays and Characteristic X-Rays

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Introduction to XRF

Duane–Hunt law
•The maximum frequency νmax is given by

which corresponds to a minimum wavelength

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Introduction to XRF

Duane–Hunt law

where h is Planck's constant, e is the charge of the


electron, and c is the speed of light. This can also be
written as:

The process of X-ray emission by incoming electrons is


also known as the inverse photoelectric effect.

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Introduction to XRF
X-ray tube emission

Ee = E’e + hν
Continuum Spectra: Results from
Collisions between the electrons and the At λ o, E’e = 0
atoms of target materials
hν 0 = hc/λ o = Ve

V: accelerating voltage
e: charge on e-
λ 0 = 12,398/V
Duane-Hunt Law
•Independent of material
•Related to acceleration
λ0
voltage  E
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Introduction to XRF
Line spectra is possible!

From electron transitions


involving inner shells

•Atomic number>23
λ0
λ0
L •2 line series K and L ,
E K> EL
Atomic number < 23 ,K
only
Line Spectrum of a Molybdenum target
A minimum acceleration voltage required for each element increases
with atomic number

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Radioisotopes
Isotope Fe-55 Cm-244 Cd-109 Am-241 Co-57

Energy (keV) 5.9 14.3, 22, 88 59.5 122


18.3
Elements (K- Al – V Ti-Br Fe-Mo Ru-Er Ba - U
lines)
Elements (L- Br-I I- Pb Yb-Pu None none
lines)

 While isotopes have fallen out of favor they are still useful for
many gauging applications.

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Introduction to XRF

Other Sources
Several other radiation sources are capable of
exciting material to produce x-ray fluorescence
suitable for material analysis.

Scanning Electron Microscopes (SEM) – Electron beams excite the


sample and produce x-rays. Many SEM’s are equipped with an EDX
detector for performing elemental analysis
Synchotrons - These bright light sources are suitable for research
and very sophisticated XRF analysis.
 Positrons and other Particle Beams – All high energy particles
beams ionize materials such that they give off x-rays. PIXE is the
most common particle beam technique after SEM.

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Source Modifiers
Several Devices are used to modify the shape
or intensity of the source spectrum or the
beam shape
 Source Filters
 Secondary Targets
 Polarizing Targets
 Collimators
 Focusing Optics

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Source Filters
Filters perform one of two functions
–Background Reduction
–Improved Fluorescence

Source Filter

Detector

X-Ray
Source

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Filter Transmission Curve


Titanium Filter transmission curve
%
T Absorption
R Edge
A Low energy x-rays
N are absorbed Very high energy
S x-rays are transmitted
M
I
T
T X-rays above the absorption
E
D
edge energy are absorbed

ENERGY
Ti Cr
The transmission curve shows the parts of the source
spectrum are transmitted and those that are absorbed

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Filter Fluorescence Method


With Zn Source filter Target peak

Continuum
Radiation

ENERGY (keV) Fe
Region

The filter fluorescence method decreases the background and


improves the fluorescence yield without requiring huge amounts of
extra power.

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Filter Absorption Method


Target peak

With Ti Source filter


Continuum
Radiation

ENERGY (keV) Fe
Region
The filter absorption Method decreases the background while
maintaining similar excitation efficiency.

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Secondary Targets
Improved Fluorescence and lower background
The characteristic fluorescence of the custom line
source is used to excite the sample, with the
lowest possible background intensity.

It requires almost 100x the flux of filter methods


but gives superior results.

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Secondary Targets
Sample

Detector
X-Ray Tube

Secondary Target
A. The x-ray tube excites the secondary target
B. The Secondary target fluoresces and excites the
sample
C. The detector detects x-rays from the sample

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Secondary Target Method


With Zn Secondary
Target
Tube
Target
peak
Continuum
Radiation

ENERGY (keV) Fe
Region

Secondary Targets produce a more monochromatic


source peak with lower background than with filters

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Secondary Target Vs Filter

Comparison of optimized direct-filtered excitation with secondary


target excitation for minor elements in Ni-200

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Polarizing Target Theory


a) X-ray are partially polarized whenever they scatter off a
surface
b) If the sample and polarizer are oriented perpendicular to
each other and the x-ray tube is not perpendicular to the
target, x-rays from the tube will not reach the detector.
c) There are three type of Polarization Targets:
– Barkla Scattering Targets - They scatter all source energies
to reduce background at the detector.
– Secondary Targets - They fluoresce while scattering the
source x-rays and perform similarly to other secondary
targets.
– Diffractive Targets - They are designed to scatter specific
energies more efficiently in order to produce a stronger peak
at that energy.

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Collimators
Collimators are usually circular or a slit and restrict the size or
shape of the source beam for exciting small areas in either
EDXRF or uXRF instruments. They may rely on internal
Bragg reflection for improved efficiency.

Sample

Collimator sizes range from 12


microns to several mm
Tube

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Focusing Optics
Because simple collimation blocks unwanted x-rays
it is a highly inefficient method. Focusing optics like
polycapillary devices and other Kumakhov lens
devices were developed so that the beam could be
redirected and focused on a small spot. Less than 75
um spot sizes are regularly achieved.

Bragg reflection
inside a Capillary
Source Detector

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Detectors
• Si(Li)
• PIN Diode
• Silicon Drift Detectors
• Proportional Counters
• Scintillation Detectors

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Detector Principles
A detector is composed of a non-conducting or semi-conducting
material between two charged electrodes.
X-ray radiation ionizes the detector material causing it to become
conductive, momentarily.
The newly freed electrons are accelerated toward the detector
anode to produce an output pulse.
In ionized semiconductor produces electron-hole pairs, the
number of pairs produced is proportional to the X-ray photon
energy
E
n=
e

where : n = number of electron-hole pairs produced


E = X-ray photon energy
e = 3.8ev for Si at LN2 temperatures

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Si(Li) Detector
FET
Window

Super-Cooled Cryostat

Dewar
filled with
Si(Li) LN2
Pre-Amplifier
crystal

Cooling: LN2 or Peltier


Window: Beryllium or Polymer
Counts Rates: 3,000 – 50,000 cps
Resolution: 120-170 eV at Mn K-alpha
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Si(Li) Cross Section

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PIN Diode Detector

Cooling: Thermoelectrically cooled (Peltier)


Window: Beryllium
Count Rates: 3,000 – 20,000 cps
Resolution: 170-240 eV at Mn k-alpha
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Silicon Drift Detector- SDD

Packaging: Similar to PIN Detector


Cooling: Peltier
Count Rates; 10,000 – 300,000 cps
Resolution: 140-180 eV at Mn K-alpha
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Proportional Counter
Window

Anode Filament

Fill Gases: Neon, Argon, Xenon, Krypton


Pressure: 0.5- 2 ATM
Windows: Be or Polymer
Sealed or Gas Flow Versions
Count Rates EDX: 10,000-40,000 cps WDX: 1,000,000+
Resolution: 500-1000+ eV

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Scintillation Detector
PMT (Photo-multiplier tube)
Sodium Iodide Disk Electronics

Window: Be or Al Connector
Count Rates: 10,000 to 1,000,000+ cps
Resolution: >1000 eV

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Spectral Comparison - Au

Si(Li) Detector Si PIN Diode Detector


10 vs. 14 Karat 10 vs. 14 Karat
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Polymer Detector Windows

♦ Optional thin polymer windows compared


to a standard beryllium windows
♦ Affords 10x improvement in the MDL for sodium (Na)

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Detector Filters
Filters are positioned between the sample and
detector in some EDXRF and NDXRF systems
to filter out unwanted x-ray peaks.
Sample

Detector Filter

Detector

X-Ray
Source

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Detector Filter Transmission


Niobium Filter Transmission and Absorption
% EOI is transmitted
T
R
A Low energy x-rays
N are absorbed Very high energy
S Absorption x-rays are transmitted
M Edge
I
T
T X-rays above the absorption
E
D
edge energy are absorbed

ENERGY
S Cl
A niobium filter absorbs Cl and other higher energy
source x-rays while letting S x-rays pass. A detector
filter can significantly improve detection limits.
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Filter Vs. No Filter


Detector filters can dramatically improve the element of interest
intensity, while decreasing the background, but requires 4-10 times
more source flux. They are best used with large area detectors that
normally do not require much power.

Unfiltered Tube
target, Cl, and Ar
Interference Peak

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Ross Vs. Hull Filters


 The previous slide was
an example of the Hull
or simple filter method.

 The Ross method


illustrated here for Cl
analysis uses intensities
through two filters, one
transmitting, one
absorbing, and the
difference is correlated
to concentration. This is
an NDXRF method
since detector resolution
is not important.

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Wavelength Dispersive XRF


Wavelength Dispersive XRF relies on a diffractive device
such as crystal or multilayer to isolate a peak, since the
diffracted wavelength is much more intense than other
wavelengths that scatter of the device.
Sample

Detector

Collimators

X-Ray
Source
Diffraction Device

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Diffraction
The two most common diffraction devices used in WDX
instruments are the crystal and multilayer. Both work
according to the following formula.
nλ = 2d × sinθ

n = integer
d = crystal lattice or
multilayer spacing
θ = The incident angle
λ = wavelength Atoms

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Multilayers
While the crystal spacing is based on the natural atomic
spacing at a given orientation the multilayer uses a
series of thin film layers of dissimilar elements to do
the same thing.
Modern multilayers
are more efficient
than crystals and can
be optimized for
specific elements.

Often used for low Z


elements.

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Soller Collimators
Soller and similar types of collimators are used to
prevent beam divergence. The are used in WDXRF to
restrict the angles that are allowed to strike the
diffraction device, thus improving the effective
resolution.

Sample

Crystal

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Cooling and Temperature Control


Many WDXRF Instruments use:

•X-Ray Tube Coolers, and

•Thermostatically controlled instrument coolers

The diffraction technique is relatively inefficient and WDX


detectors can operate at much higher count rates, so WDX
Instruments are typically operated at much higher power
than direct excitation EDXRF systems. Diffraction devices
are also temperature sensitive.

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Chamber Atmosphere
Sample and hardware chambers of any XRF instrument may be
filled with air, but because air absorbs low energy x-rays from
elements particularly below Ca, Z=20, and Argon sometimes
interferes with measurements purges are often used. The two
most common purge methods are:

Vacuum - For use with solids or pressed pellets

Helium - For use with liquids or powdered materials

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Changers and Spinners


Other commonly available sample handling
features are sample changers or spinners.

Automatic sample changers are usually of the circular or


XYZ stage variety and may have hold 6 to 100+ samples

Sample Spinners are used to average out surface features


and particle size affects possibly over a larger total surface
area.

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Typical PIN Detector Instrument

This configuration is most commonly used in higher


end benchtop EDXRF Instruments.

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Typical Si(Li) Detector Instrument

This has been historically the most common laboratory


grade EDXRF configuration.

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Energy Dispersive
Electronics
Fluorescence generates a current in the detector. In a detector
intended for energy dispersive XRF, the height of the pulse produced is
proportional to the energy of the respective incoming X-ray.

Signal to Electronics
Element
A
Element
B
Element
DETECTOR
C
Element
D

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Multi-Channel Analyser
• Detector current pulses are translated into counts (counts per
second, “CPS”).
• Pulses are segregated into channels according to energy via
the MCA (Multi-Channel Analyser).

Intensity
(# of CPS
per Channel)
Channels, Energy
Signal from Detector

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WDXRF Pulse Processing


 The WDX method uses the diffraction device and
collimators to obtain good resolution, so The
detector does not need to be capable of energy
discrimination. This simplifies the pulse processing.

 It also means that spectral processing is simplified


since intensity subtraction is fundamentally an
exercise in background subtraction.

Note: Some energy discrimination is useful since it allows for rejection of low
energy noise and pulses from unwanted higher energy x-rays.

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How to analyze X-Ray Fluorescence
Wavelength-dispersive vs. energy-dispersive
Energy-dispersive Wavelength-dispersive

electronic 2dsinθ=λ
signal Energy
processing
crystal
MCA
solar-slit solar-slit

semiconduct
or/
superconduct gas/scintillation
or detector
detector

Energy
Introduction to XRF

From Energy-dispersive to Wavelength-dispersive


Spectrometer
To further upgrade signal to background ratio
Energy-dispersive TXRF Wavelength-dispersive TXRF

Si(Li)
Scintillator
Detector Analyzing detector
Crystal
(Johansson)

X-ray X-
Sample Sample
ray
Substrate Substrate

Advantages
Large solid angle (High detection efficiency)Collecting Advantages
whole XRF spectra simultaneously
High energy-resolution
Disadvantage
Good signal to background ratio
s
Low energy-resolution
Disadvantage
Limitation of counting-rate
s
Scattering background Low detection-efficiency

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Evaluating Spectra
In addition to elemental peaks, other peaks
appear in the spectra:
• K & L Spectral Peaks
• Rayleigh Scatter Peaks
• Compton Scatter Peaks
• Escape Peaks
• Sum Peaks
• Bremstrahlung

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K & L Spectral Lines


L beta

 K - alpha lines: L shell e-


L alpha
transition to fill vacancy in K
shell. Most frequent
K beta transition, hence most intense
peak.
 K - beta lines: M shell e-
K alpha
transitions to fill vacancy in K
shell.

K Shell  L - alpha lines: M shell e-


transition to fill vacancy in L
L Shell
shell.
M Shell
 L - beta lines: N shell e-
N Shell transition to fill vacancy in L
shell.

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K & L Spectral Peaks

K-Lines

L-lines

Rh X-ray Tube
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Scatter

Some of the source X-


rays strike the sample
Sample
and are scattered back
at the detector.

Sometimes called
“backscatter”

Detector Source

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Rayleigh Scatter
• X-rays from the X-ray tube or
target strike atom without
promoting fluorescence.
• Energy is not lost in collision. (EI =
EO)
• They appear as a source peak in
spectra.
• AKA - “Elastic” Scatter
EO

EI

Rh X-ray Tube

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Compton Scatter
• X-rays from the X-ray tube or
target strike atom without
promoting fluorescence.
• Energy is lost in collision. (EI >
EO)
• Compton scatter appears as a
source peak in spectra, slightly
less in energy than Rayleigh
Scatter.
• AKA - “Inelastic” Scatter
EO

EI

Rh X-ray Tube

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Sum Peaks
 2 photons strike the detector at the same
time.
 The fluorescence is captured by the
detector, recognized as 1 photon twice
its normal energy.
 A peak appears in spectra, at: 2 X
(Element keV).

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Escape Peaks

• X-rays strike the sample and


promote elemental fluorescence.
• Some Si fluorescence at the
surface of the detector escapes,
and is not collected by the
detector.
• The result is a peak that appears
in spectrum, at: Element keV - Si
keV (1.74 keV).

1.74 keV

Rh X-ray Tube

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Brehmstrahlung

Brehmstrahlung (or Continuum) Radiation:


German for “breaking radiation”, noise that appears in
the spectra due to deceleration of electrons as they strike
the anode of the X-ray tube.

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Interferences

Spectral Interferences

Environmental Interferences

Matrix Interferences

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Spectral Interferences
220 eV Resolution • Spectral interferences are peaks
140 eV Resolution in the spectrum that overlap the
spectral peak (region of interest)
of the element to be analyzed.

• Examples:
– K & L line Overlap - S & Mo, Cl
& Rh, As & Pb
– Adjacent Element Overlap - Al
& Si, S & Cl, K & Ca...

• Resolution of detector
determines extent of overlap.

Adjacent Element Overlap

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Environmental Interferences
Al Analyzed with Si Target
• Light elements (Na - Cl) emit
Air Environment weak X-rays, easily attenuated by
He Environment air.
• Solution:
– Purge instrument with He
(less dense than air = less
attenuation).
– Evacuate air from analysis
chamber via a vacuum pump.
• Either of these solutions also
eliminate interference from Ar
(spectral overlap to Cl). Argon
(Ar) is a component of air.

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Matrix Interferences
Absorption/Enhancement Effects
• Absorption: Any element can absorb or scatter
the fluorescence of the element of interest.
• Enhancement: Characteristic x-rays of one
element excite another element in the sample,
enhancing its signal.

Influence Coefficients, sometimes called alpha


corrections are used to mathematically correct for
Matrix Interferences

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Absorption-Enhancement Affects
Sample
Red = Fe, absorbed
Blue = Ca, enhanced

Source X-ray

X-Ray Captured
by the detector.

 Incoming source X-ray fluoresces Fe.


 Fe fluorescence is sufficient in energy to fluoresce Ca.
 Ca is detected, Fe is not. Response is proportional to concentrations of
each element.

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Software
• Qualitative Analysis
• Semi-Quantitative Analysis (SLFP, NBS-
GSC.)
• Quantitative Analysis (Multiple intensity
Extraction and Regression methods)

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Qualitative Scan Peak ID


Automated Peak identification programs are a useful
qualitative examination tool

Element Tags

 This spectrum also contrasts the resolution of a PIN diode detector


with a proportional counter to illustrate the importance of detector
resolution with regard to qualitative analysis.

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Semi-Quantitative Analysis
• The algorithm computes both the
SLFP intensity to concentration relationship
Standardless Fundamental and the absorption affects
Parameters
• Results are typically within 10 - 20 %
of actual values.

FP (with Standards)  The concentration to intensity


NBS-GSC, NRLXRF, Uni-Quant, relationship is determined with
TurboQuant, etc… standards, while the FP handles the
absorption affects.

• Results are usually within 5 - 10 %


of actual values

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Quantitative Analysis
XRF is a reference method,
standards are required for
quantitative results.

Standards are analysed,


Concentration

intensities obtained, and a


calibration plot is generated
(intensities vs. concentration).

XRF instruments compare the


spectral intensities of unknown
Intensity samples to those of known
standards.

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Standards
 Standards (such as certified reference materials) are
required for Quantitative Analysis.
 Standard concentrations should be known to a better
degree of precision and accuracy than is required for
the analysis.
 Standards should be of the same matrix as samples to be
analyzed.
 Number of standards required for a purely empirical
method, N=(E+1)2, N=# of standards, E=# of Elements.
 Standards should vary independently in concentration
when empirical absorption corrections are used.

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Introduction to XRF

Sample Preparation
Powders:
Grinding (<400 mesh if possible) can minimise scatter affects due to particle size.
Additionally, grinding insures that the measurement is more representative of the entire
sample, vs. the surface of the sample.
Pressing (hydraulically or manually) compacts more of the sample into the analysis
area, and ensures uniform density and better reproducibility..
Solids:
Orient surface patterns in same manner so as minimise scatter affects.
Polishing surfaces will also minimise scatter affects.
Flat samples are optimal for quantitative results.
Liquids:
Samples should be fresh when analysed and analysed with short analysis time - if sample
is evaporative.
Sample should not stratify during analysis.
Sample should not contain precipitants/solids, analysis could show settling trends with
time.

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

ADVANTAGES AND
DISADVANTAGES
Advantages of X-Ray Spectrometry

* Simple spectra
* Spectral positions are almost independent of the chemical
state of the analyte
* Minimal sample preparation
* It is non-destructive

* Applicable over a wide range of concentrations

* Good precision and accuracy


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Introduction to XRF
Disadvantages of X-Ray Spectrometry

* X-ray penetration of the sample is limited to the top 0.01 -


0.1 mm layer

* Light elements (below 22Ti) have very limited sensitivity


although C is possible on new instruments

* Inter element (MATRIX) effects may be substantial and


require computer correction

* Limits of detection are only modest

* Instrumentation is fairly expensive

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Introduction to XRF

XRF Applications

XRF analyze almost all chemical elements and application


includes –
􀃆 Mineral, ceramic, cement, rock composition

􀃆 S, Cl & Pb in petroleum products

􀃆 Additives to polymers & paints

􀃆 Alloy identification for ferrous & non-ferrous materials

􀃆 Trace metals in alloys & solutions

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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Introduction to XRF

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