X-rays are one of the main diagnostical tools in medicine

since its discovery by Wilhelm Roentgen in 1895.

Current estimates show that there are approximately 650

medical and dental X-ray examinations per 1000 patients per year.

X-rays are produced when high energetic electrons

interact with matter.

The kinetic energy of the electrons is converted into

electromagnetic energy by atomic interactions (see chapter 7.1.)
 The X-ray tube provides an environment for X-ray production
via bremsstrahlimg and characteristic radiation mechanisms.

The classical X-ray tube requires:

electron source

electron acceleration potential

target for X-ray production

 The intensity of the electron beam determines the intensity
of the X-ray radiation. The electron energy determines the shape of
the bremsstrahlungs spectrum, in particular the endpoint of the
spectrum. Low energy X-rays are absorbed in the tube material.
 The X-ray energy determines also the emission of
characteristic lines from the target material.
The major components of the modern X-ray tube are:

cathode (electron source)

anode (acceleration potential)

rotor/stator (target device)

glass/metal envelope (vacuum tube)

The figure shows a modern X-ray tube and housing assembly.

Typical operation conditions are:

Acceleration Voltage: 20 to 150 kV

Electron Current: 1 to 5 mA (for continuous operation)

Electron Current: 0.1 to 1.0 A (for short exposures)

 The cathode consists of:

a. a spiral of heated low resistance R tungsten wire (filament) for

electron emission. Wire is heated by filament current I = U / R.
( U  10 V, I  3-6 A )
Electrons are released by thermionic emission, the
electron current is determined by the temperature which depends
on the wire current. The electron current is approximately 5 to 10
times less than the wire current.

b. a focusing cup with a negative bias voltage applied to focus the

electron distribution.
 The anode is the target electrode and is maintained at a positive
potential difference Va with respect to the cathode. Electrons are therefore
accelerated towards the anode: E = wVa
Upon impact, energy loss of electrons takes place by scattering and
excitation processes, producing heat, electromagnetic radiation and X-rays.

 0.5% of the electron energy is converted into X-rays.

 Because of the relatively low X-ray production efficiency,
most of the released energy comes in form of heat:

heat generation is a major limitation for X-ray machines

high melting point material with high X-ray output

tungsten (high melting point) good overall radiative emission

molybdenum (high melting points) high emission of characteristic X-rays
 The two major anode configurations are:

The stationary anode is the classical configuration,

tungsten target for X-ray production and copper block as heat sink
 The rotating anode is a tungsten disc, large rotating surface
area warrants heat distribution, radiative heat loss (thermally
decoupled from motor to avoid overheating of the shaft)
 The anode angle is defined as the angle of the target
surface to the central axis of the X-ray tube.

The focal spot size is the anode area that is hit by the
electrons.

The anode angle q determines the effective focal spot size:

effective focal length = focal length • sinq

The angle q also determines the X-ray field size coverage. For
small angles the X-ray field extension is limited due to absorption and
attenuation effects of X-ray photons parallel to the anode surface.
 Typical angles are: q = T to 20°.

A small angle in close distance is recommended for

small spot coverage, a large angle is necessary for large
area coverage.
 The X-rays pass through a tube window (with low X-ray
absorption) perpendicular to the electron beam.

Usually the low energy component of the X-ray spectrum

does not provide any information because it is completely absorbed in
the body tissue of the patient. It does however contribute significantly
to the absorbed dose of the patient which excess the acceptable dose
limit.

These lower energies are therefore filtered out by aluminum

or copper absorbers of various thickness.
 The minimum thickness d depends on the maximum
operating potential of the X-ray tube but is typically d  2.5 mm for
Va  100 kV

The intensity drops exponentially with the thickness d:

with eff as material dependent absorption coefficient.

 The absorption coefficient is determined in terms of
the Half-Value Layer HVL which is the thickness of a material
necessary to reduce the intensity to 50% of its original value.

The solution yields:

 Graph showing how the intensity of an x-ray beam
is reduced by an absorber whose linear absorption
coefficient is  = 0.10 cm1.
 The spectral distribution of the X-rays can be defined by
the appropriate choice of filters.

The filter material depends on the energy range of the

original X-ray distribution!
 The influence of different filter combinations for a 200 kV
X-ray spectrum is shown in the figure.
 The X-ray beam size is limited by a collimator system, the
collimators are lead for complete absorption.
Collimator design allows to optimize the point exposure!
 The size of the collimator (object size) determines the
geometric "unsharpness" (blurring) of the image.

The blurring B in the image is given by:

where a is the effective size of the collimator of the

X-ray tube and m is the image magnification:

The resulting geometric unsharpeness Ug is defined:

Additional unsharpeness can be caused by the image

receptor (grain size, resolution of the film, etc) and by movement of
the object (restless person).
 For general radiography purposes the geometric
unsharpeness dominates the other components

Therefore the unsharpeness will increase with increasing

magnification. To keep magnification small (close to m=1) requires
the image receptor to be as close as possible to the patient and the
focus patient distance to be large.

Typical conditions are:

a  1mm 110cm
m= =1.1
d1  1 m 100cm
d2  10 cm

 1 
Ug =1mm   1-  =0.091mm
 1.1
 For a close dental X-ray shot the conditions are:

a  1mm 6cm
m= =1.2
d1  5 cm 5cm
d2  1 cm

 1 
Ug =1mm   1-  =0.167mm
 1.2 
 The radiographic image of the X-ray exposure is
determined by the interaction of the X-rays which are transmitted
through the patient with a photon detector (film, camera etc.)
 Primary X-ray photons have passed through the patient
without interaction, they carry useful information.

They give a measure for the probability that a photon pass through
the patient without interaction which is a function of the body tissue
attenuation coefficients.

Secondary photons result from interaction inside the patient, they

are usually deflected from their original direction and carry therefore only
little information. They create background noise which degrades the
contrast of the image.

Scattered photons are often absorbed in grids between the patient

and the image receptor.
 The two dimensional image I(x, y) of the three dimensional
distribution of the X-ray attenuating body tissue of the patient can be
described as a function of the initial photon intensity N of energy E,
the energy absorption efficiency of the image receptor (E) (film) and
the attenuation coefficients  which have to be considered along the
photon path in z-direction.

with S(E) as distribution of the scattered secondary X-ray photons.

The expression can be simplified to:

with R as the ratio of secondary to primary radiation.

 As higher the attenuation coefficient, as larger absorption,
as lower the final intensity of the image.

For bone tissue the attenuation coefficient is considerably larger

than for soft body tissue, therefore increased absorption.
The quality of the image can be assessed by a few physical parameters:

radiographic contrast

noise and dose

CONTRAST OF THE IMAGE

Consider that you want to image clearly a target tissue of thickness x

with an attenuation coefficient 2 inside the body of thickness t with a lower soft
body tissue attenuation coefficient 1
 The contrast C of the target tissue volume is defined
in terms of the image distribution function I1 and I2:

I1 gives the energy absorbed outside the target tissue

I2 gives the energy absorbed inside the target volume.

Approximating for an X-ray energy E:

 The expression can be simplified to:

The contrast depends mainly on the difference of attenuation coefficients

1 and 2 as well as on the ratio of scattered to primary X-ray photons.

As higher the ratio R (the number of scattered photons), as lower the contrast.

Therefore it is important to understand and to reduce secondary

scattered photon intensity to minimize R.
The number of scattered photons depends on several parameters:

X-ray field size; an increase in field size increases R 3.5

Thickness of radiated volume (increase is roughly proportional

with thickness due to increase in scattering events)

X-ray energy dependence - decrease of scatter with increasing energy

 To reduce the number of secondary scattered photons a
led grid is typically between object and image receptor. Because
scattered photons will not meet the grid at normal incidence, they
will be absorbed by the grid stripes.
 NOISE AND DOSE

Even if the imaging system may have high contrast the noise
level may prevent identification of the object.

Two major noise components are:

statistical fluctuations in the number of X-ray photons

fluctuations in the receptor and display system

 The first component of the noise is called quantum noise can usually
be reduced by increasing the number of photons used to form an image.

This however will increase the dose absorbed by the patient which
should be minimized.

What is the minimum surface dose required on a body of

thickness t to see a contrast C for an object of size x over an area A
against a background of pure quantum noise?

The signal to be detect is:

The image noise in an area A results from a statistical Poisson process

and can be derived as:
This yields for the signal to noise ratio SNR:

An object becomes detectable if the SNR exceeds a threshold value of:

At these conditions the number of incident photons N for the patient can
be calculated to:
 The absorbed dose D for the patient is determined by the
number of photons per area N, the mass energy absorption coefficient
for tissue (), and the photon energy E:

The minimum dose required to visualize a fixed object increases with

the fourth power of the object size.

For a fixed dose and contrast there is a minimum object size which
can be visualized.