DOE-HDBK-1122-99 Module 1.13, Fundamental Academic Training Instructor's Guide Phase I; Module 1.13, Radiation Detector Theory
Functional areas: Radiological Training, Technician Training, Study Guide, Radiation Detector
In all aspects of radiological control, a knowledge of the characteristic and magnitude of the radiation field is essential in evaluating the degree of radiological hazard present. Radiation itself can not be detected directly. Because of this, radiation detection is accomplished by analysis of the effects produced by the radiation as it interacts in a material. Numerous different methods of accomplishing this analysis have been developed and implemented with varying degrees of success. Several of these have found extensive application in radiological control.
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Section 1
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Course Title: Radiological Control Technician
Module Title: Radiation Detector Theory
Module Number: 1.13
Objectives:
1.13.01 Identify the three fundamental laws associated with electrical charges.
1.13.02 Identify the definition of current, voltage and resistance and their respective
units.
1.13.03 Select the function of the detector and readout circuitry components in a
radiation measurement system.
1.13.04 Identify the parameters that affect the number of ion pairs collected in a gas-
filled detector.
1.13.05 Given a graph of the gas amplification curve, identify the regions of the curve.
1.13.06 Identify the characteristics of a detector operated in each of the useful regions
of the gas amplification curve.
1.13.07 Identify the definition of the following terms:
a. Resolving time
b. Dead time
c. Recovery time
1.13.08 Identify the methods employed with gas-filled detectors to discriminate
between various types of radiation and various radiation energies.
1.13.09 Identify how a scintillation detector and associated components operate to
detect and measure radiation.
1.13.10 Identify how neutron detectors detect neutrons and provide an electrical
signal.
1.13.11 Identify the principles of detection, advantages and disadvantages of a GeLi
detector and an HPGe detector.
INTRODUCTION
In all aspects of radiological control, a knowledge of the characteristic and magnitude of
the radiation field is essential in evaluating the degree of radiological hazard present.
Radiation itself can not be detected directly. Because of this, radiation detection is
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accomplished by analysis of the effects produced by the radiation as it interacts in a
material. Numerous different methods of accomplishing this analysis have been
developed and implemented with varying degrees of success. Several of these have found
extensive application in radiological control.
References
1. "Basic Radiation Protection Technology"; Gollnick, Daniel; Pacific Radiation
Press; 1983.
2. ANL-88-26 (1988) "Operational Health Physics Training"; Moe, Harold; Argonne
National Laboratory, Chicago.
3. "Radiation Detection and Measurement"; Knoll, Glenn F. John; Wiley & Sons;
1979.
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1.13.01 Identify the three fundamental laws associated with electrical charges.
Sources of Matter
Electrical theory is founded in the theory of the structure of matter. The term "matter" is
used to describe anything that has weight and occupies space. Matter exists in one of
three forms: liquid, solid, or gas, and it can be identified and measured. All matter is
composed of atoms.
Atoms are the key to understanding electricity because atoms contain electrically charged
particles. For example, the hydrogen atom contains one proton, which is positively
charged, and one electron, which is negatively charged.
All atoms contain protons and electrons. Protons are always located in the center of the
atom, an area called the nucleus. Electrons orbit around the nucleus. Protons are always
positively charged, and electrons are always negatively charged, but the value of each
charge is the same. In other words, if a proton has a charge of +1, then an electron has a
charge of -1.
Fundamental Laws for electrical charges:
Section 2
1. Opposite electrical charges of equal value cancel each other out.
2. Opposite electrical charges attract each other.
3. Like electrical charges repel each other.
A proton and electron cancel each other out because a +1 charge cancels out a -1 charge.
Therefore, when an atom contains an equal number of protons and electrons, the opposite
charges cancel each other out, making the atom electrical neutral.
Because opposite charges attract each other, an atom tends to retain its general structure.
The negatively charged electrons keep orbiting around the nucleus because they are
attracted to the positively charged protons. A particle that is orbiting around another
tends to move away from the second particle unless it is prevented from doing so. The
attraction between the electron and the nucleus keeps the electron in orbit around the
nucleus.
Movement of Electrons
Under certain circumstances, it is possible to remove some electrons from their orbits. A
source of energy is required to detach electrons from their orbits, and a steady supply of
energy is necessary to keep the detached electrons moving. The movement of electrons is
what the term electric current actually refers to. Materials in which the energy required
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to detach electrons from their orbits is low (such as copper and silver) readily conduct
electric current and are known as conductors. Materials in which the energy required to
detach electrons from their orbits is very high (such as air and paper) resist the flow of
electric current and are known as insulators.
Seven Sources of Energy
There are seven basic sources of energy that can be used to detach electrons from their
orbits and sustain electric current. They are (1) friction, (2) heat, (3) pressure, (4) light,
(5) chemical action, (6) magnetism, and (7) radiation. Friction, heat, pressure, and light
are used primarily in specialized applications. Chemical action and magnetism are more
commonly used to produce large amounts of electricity for general use.
Friction is the rubbing of one material against another. The rubbing causes electrons to
leave one material and move to the other. As the electrons are transferred, a positive
charge builds up on the material that is losing electrons, and a negative charge builds up
on the material that is gaining electrons. The type of electricity produced by friction is
called static electricity. Static electricity is more often a nuisance than a useful source of
electricity.
A thermocouple is a common example of an electrical device that uses heat as its source
of energy. The design of a thermocouple is based on the fact that heat will cause a small
amount of electricity to move across the junction of two dissimilar metals. Two metals
commonly used to make a thermocouple are copper and iron. Heat energy applied at the
junction of the wires causes electrons to leave the copper wire and move to the iron wire.
This movement of electrons is electric current, which can be measured. The amount of
current flow is related to the temperature at the junction of the wire.
Pressure can be applied to certain types of crystals to produce electricity. The
application of pressure to such crystals releases electrons from their orbits and thus causes
current to flow. Some types of pressure measuring devices make use of this effect.
Section 3
In some materials, light can cause atoms to release electrons. When this happens, current
flows through the material. This current, produced by what is called a photoelectric
effect, can be used to operate devices such as those that control the operation of street
lights. Daylight shining on special material in this type of device produces a small
current. The current operates a switch that shuts the light off in the morning. As long as
there is current through the switch, the light remains off. At nightfall, there is no light to
produce the current, so the light comes on.
Chemical action is one of the most common sources of energy used to produce
electricity. Certain types of chemical reactions create electricity by separating the
positive and negative charges in atoms. Batteries depend on chemical reactions to
produce electricity.
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1.13.02 Identify the definition of current, voltage and resistance and their respective units.
Magnetism is the major source of energy used to produce electricity in large quantities
because it is the most practical method. Generators use an effect of magnetism called
magnetic induction to produce electric current. Magnetic induction is the generation of
electric current in a conductor due to the relative motion between the conductor and a
magnetic field. For example, if a conductor is moved between the conductor and a
magnetic field. For example, if a conductor is moved between the poles of a magnet,
electrons will flow through the conductor.
Ionizing radiation can remove electrons from atoms and thereby create a flow of
electrons or current. This includes alpha, beta, and gamma radiation.
BASIC ELECTRICAL QUANTITIES
Current
Electrical current is the movement, or flow, of electrons past a given point in a
circuit. Current is measured in units called amperes. An ampere actually refers to the
rate of flow of electrons. One ampere is the flow of 6.24 x 1018 electrons past a given
point in 1 second (one coulomb/second).
There are two types of current: direct current and alternating current. Direct current (DC)
flows in only one direction. The flow of electrons in a DC circuit is similar to the flow of
water in a piping system. Alternating current (AC) reverses direction as it flows. The
electrons in an AC circuit flow back and forth continuously. Direct current is used to
explain most of the concepts in this unit because direct current is easier to illustrate and to
understand. In general, the concepts covered can be applied to alternating current as well,
with some minor variations, which will be noted when they are applicable.
Voltage
Voltage is the electrical potential difference that causes electrons to flow in a circuit.
Voltage is measured in units called volts. The voltage source in an electric circuit is
similar to the pump in a piping system. The voltage source pushes electrons through the
circuit in much the same way that the pump pushes water through the pipes. In industrial
facilities, two common sources of voltage are batteries and generators.
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Resistance
Resistance is the electrical quantity that opposes electron flow in a circuit.
Resistance is measured in units called ohms. An ohm is defined as the amount of
resistance that allows one ampere of current to flow in a circuit when there is one volt of
force pushing the current.
Section 4
All materials offer some resistance to current flow. The materials most often used in the
manufacture of electrical equipment are generally classified as either insulators or
conductors, depending on the amount of resistance they provide. Insulators offer a great
deal of resistance to current flow, while conductors offer very little resistance.
Ohm's Law
The relationship between current, voltage, and resistance was described by George Simon
Ohm in a form that is commonly referred to as Ohm's Law. Ohm's Law states that current
is equal to voltage divided by resistance. This law is often expressed using symbols for
each quantity. Using these symbols, Ohm's Law can be expressed as:
I �
E
R
where: I = current (A)
E = voltage (V)
R = resistance (Ω)
The form of Ohm's Law can be changed to show two other aspects of the relationship
between current, voltage, and resistance. The first of these is that voltage equals current
times resistance, or E = IR; and the second is that resistance equals voltage divided by
current, or R = E/I. Ohm's Law can be used in the appropriate form to determine one
quantity (current, voltage, or resistance) in an electrical circuit if the other two are known,
or to predict the effect that a change in one quantity will have on another.
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1.13.03 Select the function of the detector and readout circuitry components in a radiation
measurement system.
Detector
+
Amplifier
Reading Device
(Ammeter)
Battery
_
Power Source
Figure 1. Basic Radiation Measurement System
MEASUREMENT SYSTEMS
All radiation measurement systems consist of a detector and some sort of a readout
circuitry. A detector may be combined with appropriate circuitry to form an instrument,
or the detector and the readout may be separate (TLD + film, for example). (See
Figure 1)
Detector Function
In the detector, the incident radiation interacts with the detector material to
produce an observable effect, be it a chemical change or creation of an electrical
signal.
With a few exceptions, the effect caused by radiation incident on a detector is not
permanent.
In these detectors the effect is observed as it occurs and yields a signal in terms of events
per unit time. These detectors are typically used in association with rate meters,
instruments which read out in terms of cpm, mR/hr, etc.
The exceptions occur mostly in dosimetry instruments. In these detectors, the effects are
accumulated for analysis at a later time. Thus, instead of events per unit time, the
accumulated effect caused by all events is measured. These detectors are often classified
as integrating detectors.
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1.13.03 Select the function of the detector and readout circuitry components in a radiation
measurement system.
Detectors are characterized by the type of interaction which produces the effect and the
way in which the detector is operated.
Ionization Detectors
In ionization detectors, the incident radiation creates ion pairs in the detector. The
ionization media can be either gas (most common) or solid (semi-conductors). Gas filled
chambers can be operated as either ion chambers, proportional counters, or Geiger-
Mueller (GM) tubes. A typical solid ionization detector is a GeLi detector used in a
multichannel analyzer.
Excitation Detectors
Section 5
In excitation detectors, the incident radiation excites the atoms of the detector material.
The atoms give off the excess energy in the form of visible light. Thermoluminescent
dosimeters (TLD) and scintillation detectors fall in this category.
Chemical Detectors
In chemical detectors, the incident radiation causes ionization or excitation of the detector
media thereby causing chemical changes which can be analyzed. Film badges are an
example of a chemical detector.
Other Detectors
There are a number of detectors that don't use ionization, excitation, or chemical changes.
Examples are Cerenkov detectors, Activation foils, and Biological detectors.
Readout Circuitry
Readout circuitry measures and analyzes the produced effect and provides a usable
output indication.
There are two major categories of readouts. One is the rate meter, the other is the
counter. Within these categories, there can be numerous different circuit arrangements.
Rate meters are used with detectors that supply either an electric pulse or current. These
instruments provide an indication in terms of cpm, or mR/hr. Most radiological control
instruments with a meter indication are rate meters.
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guard ring
outer insulator
negative electrode (cathode)
positive electrode (anode)
fill gas
inner insulator
Figure 2. Basic Gas-filled Detector
Counters are used with detectors which supply a pulse. Each pulse is counted
individually. The output indication is in terms of total events, either counts or dose.
Most often, these counters are timer operated. Laboratory counters fall in this category.
Often, laboratory counters are called scalers. More complex electronic systems, such as
multi-channel analyzers and low background counting systems, are used to that provide
more detailed and specific data than simple scalers.
Detector Yield
As all detectors measure radiation as a function of its observed effects, a correlation must
be made between the effect and the incident radiation. For example, for all photons that
enter a detector, only 25% may create an output pulse. This detector would be said to
have a yield of 25%.
The less than 100% yield is caused by factors, such as size and shape of the detector; the
characteristics of the detector materials; the energy of the radiation; and the probability of
ionization for the radiation in the detector materials. The yield is concerned only with the
detector.
Note, however, that detector yield is only a factor in overall instrument response to
radiation. The position of the detector relative to the source, scatter, and self absorption
of the radiation by the source itself are some of the factors involved.
GAS FILLED DETECTORS
Basic Construction
Any contained
gas volume that
has a pair of
electrodes can serve as a gas filled ionization detector. The detector can be almost any
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shape or size but is usually cylindrical. The cylinder walls are usually used as one
electrode and an axial wire mounted in the center is used as the other electrode.
Insulators support the axial electrode. It should be noted that the size, shape, and
configuration is a function of the desired detector characteristics. (See Figure 2)
Section 6
The gas used in the detector can be almost any gaseous mixture that will ionize, including
air. Some ionization detectors, particularly ionization chambers use only air, while other
detectors use gas mixtures that ionize more readily to obtain the desired detector
response.
Basic Theory
A gaseous mixture in a normal undisturbed state has positive and negative charges which
are balanced such that no net charge is observed. When a particle or ray interacts with the
gas atoms or molecules (and in some gases, the detector materials), energy is added to the
gas and one or more electrons may be split off of the parent atom or molecule. The most
common process results in a single negatively charged electron, leaving behind a
positively charged atom. Together the negative electron and positive atom (minus one
electron) are called an ion-pair.
If left undisturbed, the negative ions can be collected by a positive ion and return to a
neutral state.
If a voltage potential is established across the two electrodes, electric fields are set up in
the gas volume between the electrons. In most detectors, the center electrode is positively
charged, and the shell of the detector is negatively charged. If an ion pair is created
between the electrodes, the electron will be attracted to the center electrode, while the
positively charged ion will be attracted to the detector shell. When either ion reaches the
electrode, electric currents are set up. Because of mass differences, the electron reaches
the electrode first. It takes up to 1,000 times longer for the positive ion to reach the side.
The amount of current flow is representative of the energy and number of radiation events
that caused ionization. The readout circuitry analyzes this current and provides an
indication of the amount of radiation that has been detected.
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1.13.04 Identify the parameters that affect the number of ion pairs collected in a gas-filled
detector.
Ion Pair Production
For a gas filled ionization detector to be of value for radiological control purposes, the
manner in which the response varies as a function of the energy, quantity, and type of
radiation must be known. Factors such as the size and shape of the detector, the
pressure and composition of the gas, the size of the voltage potential across the
electrodes, the material of construction, the type of radiation, the quantity of
radiation, and the energy of the radiation can all affect the response of the detector.
Detectors for a special purpose are designed to incorporate the optimum characteristics
necessary to obtain the desired response.
Type of Radiation
Each type of radiation has a specific probability of interaction with the detector media.
This probability varies with the energy of the incident radiation and the characteristics of
the detector gas. The probability of interaction is expressed in terms of specific
ionization with units of ion pairs per centimeter. A radiation with a high specific
ionization, such as alpha, will produce more ion pairs in each centimeter that it travels
than will a radiation with a low specific ionization such as gamma. In Table 1, note the
magnitude of the difference between the specific ionization for the three types of
radiation.
Energy of the Radiation
Section 7
Review of the data in Table 1 will reveal that, generally, the probability of interaction
between the incident particle radiation and the detector gas (and therefore the production
of ions) decreases with increasing radiation energy. In photon interactions, the overall
probability of interaction increases because of the increasing contribution of the pair
production reactions. As the energy of the particle radiation decreases, the probability of
interaction increases, not only in the gas, but also in the materials of construction. Low
energy radiations may be attenuated by the walls of the detector and not reach the gas
volume. Obviously, this must be accounted for in the design of the detector.
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Table 1. Specific Ionization In Air at STP.
Radiation Energy Ion pairs/cm
Alpha 3 MeV
6 MeV
55,000
40,000
Beta 0.5 MeV
1 MeV
3 MeV
110
92
77
Gamma 0.5 MeV
1 MeV
3 MeV
0.6
1.1
2.5
Quantity of Radiation
As the number of radiation events striking a detector increases, the overall probability of
an interaction occurring with the formation of an ion pair increases. In addition, the
number of ion pairs created increases and therefore detector response increases.
Detector Size
The probability of an interaction occurring between the incident radiation and a gas atom
increases as the number of atoms present increases. A larger detector volume offers more
"targets" for the incident radiation, resulting in a larger number of ion pairs. Since, each
radiation has a specific ionization in terms of ion pairs per centimeter, increasing the
detector size also increases the length of the path that the radiation traverses through the
detector. The longer the path, the larger the number of ion pairs.
Type of Detector Gas
The amount of energy expended in the creation of an ion pair is a function of the type of
radiation, the energy of the radiation, and the characteristics of the absorber (in this case,
the gas). This energy is referred to as the ionization potential, or W-Value, and is
expressed in units of electron volts per ion pair. Typical gases have W-Values of 25-50
eV, with an average of about 34 eV per ion pair.
Detector Gas Pressure
In the section on detector size, it was shown the probability of interaction increases with
detector size. In many cases, there is a practical limit to detector size. Instead of
increasing detector size to increase the number of "target" atoms, increasing the pressure
of the gas will accomplish the same goal. Gas under pressure has a higher density (more
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atoms per cm3) than a gas not under pressure, and therefore offers more targets, a higher
probability of interaction, and greater ion pair production. For example, increasing the
pressure of a typical gas to 100 psig increases the density by about 7 times.
Voltage Potential Across the Electrodes
Once the ion pair is created, it must be collected in order to produce an output pulse or
current flow from the detector. If left undisturbed, the ion pairs will recombine, and not
be collected. If a voltage potential is applied across the electrodes, a field is created in the
detectors, and the ion pairs will be accelerated towards the electrodes.
Section 8
The stronger the field, the stronger the acceleration. As the velocity of the electron
increases, the electron may cause one or more ionizations on its own. This process is
known as secondary ionization. The secondary ion pairs are accelerated towards the
electrode and collected, resulting in a stronger pulse than would have been created by the
ions from primary ionization.
Effect of Voltage Potential on the Detector Process
If the applied voltage potential is varied from 0 to a high value, and the pulse size
recorded, a response curve will be observed. For the purposes of discussion, this curve is
broken into six regions. The ion chamber region, the proportional region, and the Geiger-
Mueller region are useful for detector designs used in radiological control. Other regions
are not useful. In the recombination region, the applied voltage is insufficient to collect
all of the ion pairs before some of them recombine. In the limited proportional region,
neither the output current nor the number of output pulses are proportional to the
radiation level. Calibration is impossible. In the continuous discharge region, the voltage
is sufficient to cause arcing and breakdown of the detector gas.
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1.13.05 Given a graph of the gas amplification curve, identify the regions of the curve.
Figure 3. Six-region Curve for Gas-filled Detectors
1.13.06 Identify the characteristics of a detector operated in each of the useful regions of the
gas amplification curve.
Ion Chamber Detectors
As the voltage to the detector is increased, a point is reached at which essentially all of
the ions are collected before they can recombine. No secondary ionization or gas
amplification occurs. At this point, the output current of the detector will be at a
maximum for a given radiation intensity and will be proportional to that incident
radiation intensity. Also, the output current will be relatively independent of small
fluctuations in the power supply.
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The output of a gas-filled detector when 100% of the primary ion pairs are collected is
called the saturation current.
Advantages
• Output current is independent of detector operating voltage. Observe the flat region
of the curve in the ion chamber region. As a result, less regulated and thereby less
expensive and more portable power supplies can be used with ion chamber
instruments, and still offer a reasonably accurate response.
• Since the number of primary ion pairs is a function of the energy deposited in the
detector by the incident radiation, the ion chamber response is directly proportional
to the dose rate.
• Since exposure (x) is defined in terms of ionization of air by photons, an air-filled
ion chamber, when used for photon radiation, yields the true exposure rate.
Disadvantages
• Since only primary ion pairs created by each radiation event are collected, the
output currents are small. Independent current pulses large enough to measure are
not formed by each ionizing event. Instead, the total current output created by many
ionizing events is measured. Therefore, the sensitivity of a small ion chamber is
very poor because a few ionizing events per minute do not create sufficient currents
to be measured. A typical commercial portable ion chamber has a detector which
produces a current of about 2 E-14 amps per mR/hr.
Section 9
• Another consequence of the small output current is the effect humidity can have on
the instrument response. The electronics associated with the detector must have a
high impedance (approximately 1 E15 ohms) to measure currents this small. The
instrument incorporates insulators designed to maintain this high impedance. High
humidity conditions can cause the formation of condensation on those insulators.
(The resistance of relatively pure water is approximately 1 E7 ohms per centimeter.)
This condensation creates leakage paths which causes erroneous instrument
response.
• Since anything which changes the density of the gas affects the response, changes in
barometric pressure (or altitude) and/or ambient temperature can affect instrument
response in some cases. This is particularly the case with thin-walled chambers,
vented chambers, or chambers with windows. For instance, the response of a
typical commercial portable ion chamber instrument decreases by 2% for each
10 degree increase in temperature, or decreases by 2.3% for each inch of mercury
decrease in barometric pressure (4.6% per psig).
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Typical Applications
Portable survey instruments used for measuring dose rates are typically ion chamber
instruments. Ion chambers may also be used in several installed monitor systems such as
the Area Radiation Monitor Systems (ARMS) and the various Process Radiation
Monitors (PRMs).
Proportional Detectors
As the voltage on the detector is increased beyond the ion chamber region, the ions
created by primary ionization are accelerated by the electric field towards the electrode.
Unlike the ion chamber region, however, the primary ions gain enough energy in the
acceleration to produce secondary ionization pairs. These newly formed secondary ions
are also accelerated, causing additional ionizations. The large number of events, known
as an avalanche, creates a single, large electrical pulse.
In a proportional detector, the detector output is proportional to the total ionization
product in the detector. For a constant voltage, the ratio between the primary ionizations
and the total number of ions produced is a constant and is known as the Gas
Amplification Factor. The gas amplification factors for typical proportional detectors
range from a few hundred to about a million. Compare this with a Gas Amplification
Factor of only 1 for ion chamber detectors.
Since the gas amplification in a proportional detector is large, the output pulses are large
enough to be measured directly and individually. Since a single pulse is produced for
each incident radiation particle or photon, it is feasible to directly measure the number of
incident particles or photons which interacted with the detector. For this reason, a
proportional detector is often used as a "proportional counter" and is normally used in
instruments which read out in events per unit time, such as counts per minute. The total
current, which is a function of the number of the pulses and the pulse magnitude, could be
measured as is done with ion chamber detectors but this is only done in one type of
portable dose rate instrument.
As with the ion chamber detector, increasing radiation energy, or high specific ionization
radiations, will result in a larger pulse. Since we can measure the individual pulse, it is
possible to analyze both the rate of incidence and the energy or type of radiation with a
proportional counter. This allows for discrimination of different types of radiation or
different radiation energies by varying the high voltage (which affects the gas
amplification factor). When the voltage is increased, for example, the detectors output
also increases.
Section 10
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1.13.07 Identify the definition of the following terms:
a. Resolving time
b. Dead time
c. Recovery time
Resolving Time
After the ion avalanche occurs, it takes a finite time for the ions to be collected and for
the pulse to be generated. Similarly, it takes a finite period of time for the pulse to decay.
If another ionizing event occurs elsewhere in the detector during this period, another
avalanche may be initiated. When the ions reach the electrodes, they are collected along
with remaining ions from the first event. The resulting pulse may not be distinguishable
as two pulses by the associated electronics. The resulting reading will underestimate the
actual radiation field. The period of time between events, such that two distinguishable
pulses result, is known as resolving time. Resolving time is the total amount of time
from a measurable detector response before another pulse can be measured. In the
proportional region, the resolving time is short, usually in the range of 0.5 to 1 nano
seconds. This resolving time does not lead to problems at low count rates, but can result
in a considerable error at high count rates. It should be noted that usually the associated
electronics will have a resolving time longer than that of the detector.
Counter Construction
Proportional counters can be constructed using self-contained gas volumes or with
continuously cleaning gas volumes. The latter is usually called a gas flow proportional
counter. The detectors can also be constructed with the sample holder integral to the
detector, eliminating the need for a detector window.
• Cylindrical Counter - This configuration is typical of the proportional counters used
in portable survey instruments. The fill gas is commonly a hydrocarbon gas such as
P-10 (methane and argon), but other gases have been employed. For example, BF3
gas (boron trifluoride) is often used in detectors designed to count neutrons.
• Window 2π Gas Flow Hemispherical Counter - In this detector the gas volume is
replenished continuously, ensuring a constant supply of target atoms. (See Figure
4) P-10 is the most commonly used counting gas. The geometry of the detector is
such that, theoretically, almost 50% of the radiation's emitted from the source would
be available for detection. (The terms 2π and 4π refer to the number of steradians
around a point source in space. There are 2 steradians in a hemisphere, 4 in a
sphere.) In reality, the actual percentage may be somewhat higher due to
backscatter.
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Gas in Gas out
Detector
window
Sample slide
assembly
Sample holder
Sample
Anode
Figure 4. Basic 2π Proportional Detector w/ Window
• Windowless 2π Gas Flow Hemispherical Counter - This counter is similar to the
2π gas flow counter with the window. In fact, many of the gas flow proportional
counters commercially available can be converted between window and
windowless operation by a simple modification. In this counter, the source is
effectively within the detector. This allows for the counting of low energy or low
penetrating power radiation's which would have been stopped by the detector
window.
• 4π Gas Flow Spherical Counter - With this counter, the source material to be
analyzed is deposited on an extremely thin membrane. This membrane is then
positioned between the chamber halves, and the gas purge started. This detector
approaches the ideal 4π geometry. Because of the relative difficulty of use, this
counter finds little application at power stations.
Section 11
• Gas Flow, Flat - This is a commercially available alpha counter which is used in a
portable alpha survey instrument. The counting gas is propane.
Proportional Counter Advantages
• A proportional counter can be used to discriminate between the different types of
radiation.
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• A proportional counter output signal is larger and therefore a single ionizing event
can be recorded (good sensitivity).
• When measuring current output, a proportional detector is useful for dose rates
since the output signal is proportional to the energy deposited by ionization and
therefore proportional to the dose rate.
Proportional Counter Disadvantages
• A proportional counter is sensitive to high voltage changes because of the effect
on the gas amplification factor. As a result, more highly regulated power supplies
are necessary for proportional counters.
Typical Applications
Proportional counters find wide application in power stations. Gas flow proportional
counters are commonly used for alpha/or beta counting on laboratory samples.
Proportional counters are commonly used for neutron monitoring, from portable neutron
survey instruments to nuclear reactor neutron flux instruments.
Geiger-Mueller Detectors
As the voltage on the detector is increased beyond the proportional region, the detector
enters the limited proportional region. As mentioned before, this region is unusable for
radiological control purposes. In this region the small individual avalanches which occur
within the tube start to interfere with each other. This interference is unpredictable and
reduces the overall output signal.
As the voltage is increased further, the secondary ions are also accelerated to very high
velocities and gain sufficient energy to cause ionization themselves. These tertiary
ionizations spread rapidly throughout the tube causing an avalanche. The avalanche,
caused by a single ionization, results in a single very large pulse. The avalanche
continues until the fields created by the produced ions interfere with the field created by
the high voltage potential across the detector. When this occurs, the amount of
acceleration decreases preventing further secondary ionization and halting the avalanche.
The output pulse size is a function of the gas amplification which occurs. In a GM tube,
the gas amplification can range upwards from about 1 E8. Since the number of ions
eventually produced and collected have no relation to the initial incident ionizing event,
the pulse size is independent of radiation energy or specific ionization (a 0.1 MeV gamma
creates the same size pulse as a 0.5 MeV gamma). For this reason, GM tubes cannot
discriminate against different radiation types or radiation energies.
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Any radiation event with sufficient energy to create the first ion pair can create a large
pulse. For this reason, the GM detector is more sensitive than the ion chamber or
proportional counter.
A GM detector can also be avalanched by the small amount of energy released by a
positive ion when it is neutralized at the cathode. To prevent this undesirable occurrence,
a quenching gas is added to the counting gas. Thus, instead of causing ionization, this
excess energy is expended in dissociating the quenching gas molecules.
Dead Time and Recovery Time
Section 12
In the discussion on proportional counters, we found that if the ionizing events occurred
at too fast a rate, the output pulses created by these events may overlap, and as such
cannot be counted as individual pulses. Although the resulting pulse is larger, the two
pulses which caused it are approximately the same size (gas amplification remains
relatively constant). The time between incident events such that individually
distinguishable, measurable, pulses result is known as the resolving time. This time is
about 100-200 µsec.
In GM detectors, resolving time has greater impact on detector response. Resolving time
is the time from the initial measured pulse until another pulse can be measured by
the electronics. Resolving time is controlled by the electronics.
Dead time is the time from the initial pulse until another pulse can be produced by
the detector.
Recovery time is the time from the initial full size pulse to the next full size pulse
produced by the detector. The recovery time includes a smaller interval of time known
as the dead time. During the dead time, the detector can not respond to another ionizing
event. The dead time occurs because of the effect that the large number of positive ions
have on the voltage potential across the detector. In the recovery time, the detector can
respond, but because of a reduced gas amplification factor, the output pulses are too small
to measure. In most common day-to-day use, the resolving time is usually called the dead
time since for all practical purposes, the detector is "dead" until a pulse large enough to
trigger the electronics is created.
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Figure 5. Dead Time of a GM Detector
The following sequence of events should help to explain the processes involved in GM
detection.
• At time zero, the voltage potential across the detector is maximum. An incident
radiation causes ionization, resulting in an ion pair.
• These ion pairs are accelerated towards the center electrode, thereby gaining
energy.
• The primary ion pairs cause secondary ionization. The ion pairs created by the
secondary ionization begin to accelerate towards the center electrode, thereby
gaining energy. Since the potential is greatest near the center electrode, the bulk
of the ionization occurs near the center electrode.
• The secondary ion pairs cause additional ionization and ion pairs. These ion pairs
are accelerated and begin to cause ionization of their own. This process continues
and an avalanche occurs.
• The negative ions (electrons) are collected by the center electrode and form a
pulse. The positive ions form a cloud surrounding the center electrode. This ion
cloud reduces the voltage potential across the detector. With a reduced voltage
potential the gas amplification factor decreases such that secondary ionization
stops, thereby halting the avalanche.
The events described above occur very rapidly, in the range of a fraction of microsecond.
During this period the positive ion cloud is relatively stationary. The positive ion cloud is
the cause of both the dead time and recovery time. Continuing:
• The positive ion cloud starts to drift towards the shell of the detector.
• As the cloud drifts, the voltage potential starts to increase.
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Section 13
• After about a microsecond (typically) the voltage potential is high enough to
collect the electrons from another ionization should they occur. This is the end of
the dead time. If another event does occur, the pulse will be very small and
probably not measurable as the detector voltage is in the ion chamber region.
• As the ion cloud continues to drift, the voltage potential continues to increase and
gas amplification starts to occur. The detector is now in the proportional region.
An event which occurs now will result in a large pulse. Whether or not this pulse
is measured is a function of the input sensitivity of the electronic package.
• Eventually the gas amplification factor will increase to the point where an
avalanche can occur when the positive ions reach the detector shell and are
neutralized. At this point the detector has recovered and is ready for another
radiation event. This time is about µ100-300 sec in typical detectors.
• During neutralization, the positive ions may release photons which in themselves
could cause an avalanche if no quenching gas was present. Instead, the photons
react with the molecules of the quenching gas, thereby dissipating their energy.
The effect of the long resolving time in a GM detector is to reduce the ability of the
detector to measure high dose rates accurately. For example, with a 200 µsec resolving
time, a count rate of 10,000 cpm will be measured as 9,700 cpm, an error of 3%. At
100,000 cpm, the measured count rate will be 75,000, an error of 25%.
There is another effect in GM detectors that is related to resolving time. If the incident
radiation events occur at an extremely high rate, a string of small pulses will occur.
These pulses prevent the GM detector from completely recovering. Since a full size pulse
does not occur, the electronics will not indicate that any radiation is present.
GM Detector Construction
Although there is no technical reason why GM detectors cannot be operated as gas flow
detectors, this is not commonly done. Almost all GM detectors which are encountered in
radiological control work are cylindrical in construction.
Advantages of GM Detectors
• GM detectors are relatively independent of the pressure and temperature effects
which affect ion chamber detectors. This is because of the magnitude of the
output pulse.
• GM detectors require less highly regulated power supplies. This is because the
pulse repetition rate is measured and not the pulse height.
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• GM detectors are generally more sensitive to low energy and low intensity
radiations than are proportional or ion chamber detectors.
(There are exceptions.)
• GM detectors can be used with simpler electronics packages. The input
sensitivity of a typical GM survey instrument is 300-800 millivolt, while the input
sensitivity of a typical proportional survey instrument is 2 millivolt.
Disadvantages of GM Detectors
• GM detector response is not related to the energy deposited; therefore GM
detectors can not be used to directly measure true dose, as can be done with an ion
chamber instrument.
• GM detectors have a typically large recovery time. This limits their use in
extremely high radiation fields. Dead time in a GM detector can be reduced by
reducing the physical size of the detector. However, the smaller the detector, the
lower the sensitivity. For this reason, wide range GM survey instruments, such as
the Teletector or the E520, commonly have two GM detectors - one for the low
ranges, one for the high ranges.
Section 14
• GM detectors can not discriminate against different types of radiation (α, β, γ), nor
against various radiation energies. This is because the size of the GM avalanche
is independent of the primary ionization which created it.
Typical Applications
GM detectors are widely used in portable survey instruments at nuclear power facilities
due to their ruggedness and the simplicity of the associated electronics. GM detectors are
also used for personal monitoring for contamination (friskers), for process monitoring,
and for area radiation monitoring. In addition, GM detectors are often used for laboratory
counting when just a gross count is desired.
Comparison of the Various Radiation Detectors
When comparing the various detectors, one should keep in mind that exceptions are
possible, (e.g. a large, pressurized ion chamber may be more sensitive than a small GM
detector, even though, as a class, GM detectors are more sensitive than ion chambers.)
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1.13.08 Identify the methods employed with gas-filled detectors to discriminate between
various types of radiation and various radiation energies.
DISCRIMINATION
In the sections above, discrimination of radiation types and radiation energies was
introduced. Discrimination plays an important role in radiation measurement. In nuclear
power stations, "pure" radiation fields seldom exist. There is usually a combination of
gamma, neutron, beta, and sometimes alpha. These radiation types also exist at various
radiation energies.
In the complex radiation fields such as this, it becomes difficult to measure one radiation
in the presence of others - a detector that responds to alpha and beta radiation will often
also respond to gamma. Discrimination makes it possible to separate (to some extent) the
different radiation types or radiation energies.
Physical Discrimination
Shielding
Shielding is the most common method of discriminating against certain radiation types or
energies in radiation measurements. A thin metal window will stop the majority of alpha
particles. A thicker metal window will stop beta particles. Unfortunately, this process
only works by discriminating against lower energies or radiations with low penetrating
power. Gamma radiations cannot be shielded against without affecting response to beta
or alpha.
Shielding is sometimes used on GM detectors to obtain a smoother energy response
curve.
Detector Gas Fill
Each type of radiation has a specific ionization factor in a particular gas. In addition,
each different detector gas has a different response to various radiation energies. By
employing the most advantageous gas, a detector can be constructed that will have a
higher yield for a specific radiation type or radiation energy than it will for other radiation
types or energies.
A specific example of this is the use of BF3 gas in proportional detectors to measure
neutrons. In these detectors, the incident neutron fissions boron into lithium and an alpha
particle. This alpha particle has a much higher specific ionization than does a gamma
photon. The pulses created by neutrons are much larger than those created by gamma.
The electronics sort out the pulses by pulse height.
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1.13.09 Identify how a scintillation detector and associated components operate to detect and
measure radiation.
Section 15
Electronic Discrimination
In the previous sections, we found that in the ionization chamber and proportional
regions, the output pulse height was a function of the specific ionization of the radiation,
and the incident radiation energy. Because of the small pulse size, ion chambers are
usually not used for discrimination. Proportional counters are often used to discriminate
between radiations and sometimes between radiation energies. The proportional gas flow
counter used in counting rooms to measure alpha and/or beta sources is an example of
such an application.
Analyzing pulse heights is the primary method of electronic discrimination. Almost all
electronic packages used with radiation detectors have an adjustable input sensitivity
(often called discriminator level). By adjusting the input sensitivity to the desired value,
we can chose the minimum pulse height which will be measured. All pulses smaller than
this preselected pulse height will be rejected and not counted. For example, if we have
set the input sensitivity to measure only the large alpha pulses, the smaller beta or gamma
pulses will be ignored. The readout, then, will indicate only alpha radiation.
Some electronics packages also have an adjustable upper discriminator. In these circuits,
pulses that are too large will not be counted. The resulting band between the lower and
upper discriminators is called a window. Only pulses which fall within the window will
be counted. By changing the upper and lower discriminators, an unknown radiation field
or sample can be analyzed to determine which type of radiation or which energies of
radiation exist in the field or in the sample. This process is called pulse height analysis.
In proportional counters, it is common practice to leave the discriminators on one setting
and to vary the high voltage supply instead. As you remember, increasing the high
voltage, increases the gas amplification factor, which in turn increases pulse height, and
vice versa. Thus, alpha radiation would be measured at one voltage, alpha and beta at a
higher voltage (subtracting the alpha count from the alpha + beta count yields the beta
count).
SCINTILLATION DETECTORS
Scintillation detectors measure radiation by analyzing the effects of the excitation of the
detector material by the incident radiation. Scintillation is the process by which a
material emits light when excited. In a scintillation detector, this emitted light is
collected and measured to provide an indication of the amount of incident radiation.
Numerous materials scintillate - liquids, solids, and gases. A common example is a
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television picture tube. The coating on the screen is excited by the electron beam, and
emits light. A material which scintillates is commonly called a phosphor or a fluor. The
scintillations are commonly detected by a photomultiplier tube (PMT).
Scintillation Detector Components
Each scintillation detector is comprised of two major components, the phosphor or fluor,
and the photomultiplier tube. Various different phosphors and photomultiplier tubes are
available, and numerous combinations of these are possible. The combination chosen is
selected to achieve the desired response to radiation and other requirements of a particular
application.
Phosphors and Fluors
Section 16
There are four classes of phosphors of interest in field applications of scintillation:
organic crystals, organic liquids, inorganic crystals, and inorganic powders. The theory of
operation, use, and response of these phosphors varies. Each will be discussed
individually.
Organic Crystals
Organic crystal phosphors are normally aromatic hydrocarbons which contain benzene
rings. The most common organic crystal is anthracene. Anthracene offers a high response
to beta radiation and is commonly used in beta phosphors. The decay time (which is a
major part of scintillation resolving time) is on the order of 3 E-8 seconds.
Gamma photons do not interact often or create a large pulse from interactions in the low
density anthracene (1.25 g/cm3). Therefore, it is easy to detect only beta in the presence
of a mixed beta and gamma field.
In organic crystals, the incident radiation raises the molecules of the phosphor to a higher
energy state. Upon decay back to the ground state, these molecules emit light.
Organic Liquids
Organic liquid phosphors, usually called fluors, are comprised of organic material
suspended in an organic solvent. The organic material, usually called the solute, is the
scintillator. The solvent absorbs the radiation and transfers energy to the solute. The
mixture of solute and solvent is commonly called a "cocktail." Numerous mixtures are
available. These mixtures have a typical decay time of 2 - 8 E-9 seconds (0.002 - 0.008
µsec) and a density of 0.86 g/cm3.
The organic liquid fluor operates as follows: The incident radiation interacts with the
molecules of the solvent, exciting the molecules. By a process not well understood, the
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excited molecules transfer their energy to the molecules of the solute. The molecules of
the solute return to the ground state by emission of a light photon.
Inorganic Crystals
Inorganic crystals are comprised of inorganic salts, normally halides, which contain small
quantities of impurities, called activators. The most commonly used inorganic crystal
scintillator is sodium iodide, activated with thallium - commonly subscripted NaI(Tl).
NaI(Tl) crystals have a high density - 3.7 g/cm3, which allows for improved gamma
photon response. The decay time is about 3 E-7 seconds (0.3 µsec). NaI(Tl) has a high
response to beta particles; however, the need to hermetically seal a NaI(Tl) crystal to
prevent deterioration, limits the actual beta response.
Inorganic crystals operate as follows:
• An incident photon interacts with the crystal atoms (NaI) exciting the atom and
raising valence band electrons to the conductance band, leaving a "hole" in the
valence band.
• Some of these electrons and holes recombine to form an "exciton." The excitons,
free holes, and free electrons drift through the crystal.
• The impurity centers (T1) capture the excitons, free holes, and free electrons.
This capture raises the impurity center to an excited state.
• The impurity center will decay back to the ground state, and in doing so, emits a
light photon, which is proportional to the energy of the incident radiation.
Inorganic Powders
Zinc Sulfide activated with Silver (ZnS(Ag)) is an inorganic powder which is commonly
used as a phosphor in alpha scintillators. ZnS(Ag) scintillators have a high density, 4.1
g/cm3, and a relatively high response to beta and alpha radiation's. The response of this
scintillator to beta and gamma is minimized by the use of ZnS(Ag) as a thin film which is
within the alpha interaction range, but too thin for that of beta or gamma. ZnS(Ag) emits
two light photons one at 4-10 E-8 seconds (0.04 - 0.1 µsec), and another at 4-10 E-5
seconds (40 - 100 µsec).
Section 17
Inorganic powders operate with a mechanism similar to that of inorganic crystals.
Photomultiplier Tubes
The purpose of the photomultiplier tube is to detect the scintillations and to provide an
output signal proportional to the amount of scintillations. In doing this, photomultiplier
tubes can provide amplifications of 1 E6 and higher.
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Construction
Construction details vary from design to design, however, all photomultipliers have
typical components. These common components are: the photocathode, the dynode
assembly, an anode, voltage divider network, and shell. These components perform as
follows: (See Figure 6)
• Photocathode - made of an antimony - cesium composite. The purpose of the
photocathode is to convert the light photons to electrons (called photoelectrons).
• Dynode Assembly - A series of electrodes used to amplify the signal. Each
successive dynode has a higher voltage potential. The voltage gradient along the
tube accelerates the electrons towards the anode. This works as follows: the
photoelectron strikes the first dynode freeing one or more electrons. These
electrons are drawn towards the second dynode. At the second dynode each
electron frees one or more additional electrons. This process continues until the
electron cascade reaches the anode. Through this process, the initial
photoelectron is amplified, up to 106 times and higher. For an amplification of 106
an average of 4 electrons is freed by each incident electron reacting with each
dynode (10 dynodes - 410 � 106).
• Anode - The anode collects the electrons and generates an output pulse.
• Voltage Divider Network - Splits the high voltage supply into the various
potentials required by the dynodes.
• Shell - Supports the other components and seals the tube from stray light and stray
electric/magnetic fields.
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Figure 6. Photomultiplier Tube
Output
The photomultiplier tube provides an output pulse which is proportional to the incident
photons. The size of the pulse is a function of the energy of the light photon, and of the
electron multiplication. Varying the HV to the photomultiplier varies the pulse height.
It is possible for stray electrons to be amplified by the dynode, creating an output pulse
while no photon entered the tube. Those electrons can be spontaneously emitted from the
photocathode or by the dynodes themselves. This output signal is commonly called dark
current. Dark current increases with photomultiplier tube temperature, hence,
temperature changes may cause the detector to "drift."
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Applications of Scintillation Detectors
Inorganic Crystals - NaI(Tl)
NaI(Tl) scintillation detectors are commonly used in applications where high gamma
sensitivity and a high energy resolution is desired.
• The solid nature of the crystal "offers" more targets to a photon than does a GM
detector. For this reason, gamma scintillators typically have higher yields than
equivalently sized GM detectors.
Section 18
• The light output of the crystal is a function of the incident photon energy. The
output signal of the photomultiplier tube is a function of the light input, and
therefore is proportional to the energy of the incident radiation. This
characteristic allows scintillators to be used to perform pulse height analysis for
radiation energy. The NaI(Tl) scintillator has a higher energy resolution than a
proportional counter, allowing for more accurate energy determinations.
Resolution is the characteristic of a detector to be able to differentiate between
two close radiation energies. The higher the resolution, the closer the radiation
energies can be to each other and still be differentiated. It should be noted that
recent advances with semiconductor detectors have provided detectors with even
better resolution than NaI(Tl).
Liquid Scintillation Detectors
Crystal scintillation detectors such as NaI(Tl) have two limiting characteristics. The
crystals are 2π in nature; this fact lowers the possible efficiency of the detector. The
crystals need to be hermetically sealed. The materials used for sealing attenuate lower
energy radiation and both beta and alpha radiations.
Liquid scintillation units have been developed to remedy these situations for those
applications where it is desired to measure radiation of low energy or low penetrating
ability.
In liquid scintillation units, the fluor is mixed with the material to be analyzed (usually a
liquid). This vessel containing the fluor-sample mixture is then placed in a
photomultiplier tube array. (One or more PMTs may be used.)
In this manner, it is possible to analyze low energy beta emitters such as tritium (0.019
MeV) and/or carbon-14 (0.16 MeV), and to approximate 4π geometry.
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1.13.10 Identify how neutron detectors detect neutrons and provide an electrical signal.
Advantages of Scintillation Detectors
• Ability to discriminate between alpha, beta, gamma radiations and between
different radiation energies with a moderate resolution.
• (NaI(Tl)): High gamma sensitivity.
• (Liquid): Extremely low energy response.
• (ZnS(Ag): Most advantageous alpha detector.
Disadvantages
• (NaI(Tl)): No beta or alpha response, poor low energy gamma response.
• (Liquid): Relatively cumbersome. Solution is one time use only.
• Requires a regulated power supply for pulse height analysis.
• (NaI(Tl) and ZnS(Ag)): Detector is not a solid state device, needs to be handled
with care.
NEUTRON DETECTION
Because neutrons do not interact with material to form ions, they must be detected
indirectly. Several techniques are used.
Slow Neutron Detection
Boron Activation
When slow neutrons strike an atom of Boron-10, an alpha particle is emitted. This alpha
particle, in turn, produces ionizations which can be measured. A detector is lined with
Boron-10 or filled with Boron trifluoride, BF3, gas. These detectors are usually operated
in the ion chamber region or the proportional region. Boron activation is the most
commonly used method for slow neutron detection.
Photographic film can be made sensitive to slow neutrons by adding boron.
Fission Chambers
A slow neutron will cause an atom of U-235 to fission, with the two fission fragments
produced having a high kinetic energy and causing ionization to the material they pass
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Section 19
through. Thus, by coating one of the electrodes of an ionization chamber with a thin layer
of uranium enriched in U-235, a detector sensitive to slow neutrons is formed.
Scintillation
Scintillation detectors can be designed to detect slow neutrons by incorporating boron or
lithium in the scintillation crystal. The neutrons interact with the boron or lithium atoms
to produce an alpha particle, which then produces ionization and scintillation.
Slow Neutron Thermoluminescence
Thermoluminescent dosimeters can be designed to detect slow neutrons by incorporating
lithium-6 in the crystal.
Activation Foils
Various materials have the ability to absorb neutrons of a specific energy and become
radioactive through the radiative capture process. By measuring the radioactivity of thin
foils such as gold, silver or indium, we can determine the amount of neutrons to which
the foils were exposed. Commercially available criticality accident dosimeters often
utilize this method.
Fast Neutron Detection
Proton Recoil (Ion Chamber/Proportional)
When fast neutrons undergo elastic scatterings with hydrogen atoms, they frequently
strike the hydrogen atom with enough force to knock the proton nucleus away from the
orbiting electron. This energetic proton then produces ionization which can be measured.
Most devices for measuring fast neutrons use an ionization detector operated in either the
ion chamber or proportional region.
Thermalization (Slowing Down Fast Neutrons)
There are several methods for detecting slow neutrons, and few methods for detecting fast
neutrons. Therefore, one technique for measuring fast neutrons is to convert them to slow
neutrons, and then measure the slow neutrons. In this technique, a sheet of cadmium is
placed on the outside of the detector to absorb any slow neutrons which might be present.
A thickness of paraffin, or another good moderator, is placed under the cadmium to
convert the fast neutrons to slow ones. One of the slow neutron detectors is positioned
inside the paraffin to measure the slow neutrons, thereby measuring the original fast
neutrons.
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Commercial Application - Dose Rate Instrument
Neutrons are not detected with any degree of efficiency by common ion chambers, GM
tubes, or proportional counters. Any detection of neutrons by these detectors is due to
absorption of neutrons by detector materials or hydrogen recoil. The detection efficiency
can be increased by the utilization of materials with high neutron absorption cross
section. The basic material typically used is Boron. Boron can be used either as a coating
or as a gas, in the form of BF3. Boron, when it absorbs a neutron, emits an alpha particle
according to the following reaction:
10B + 1n �
7Li + α
The alpha particle causes ionization and gas amplification provides a usable electrical
signal. This reaction occurs only for thermal neutrons. Fast and intermediate neutrons
must be converted to thermal neutrons before they can be detected using Boron. Typical
thermalizing materials are paraffin and polyethylene.
Because of the energy dependence of neutron interaction, and the wide range of neutron
energies, the response curve of the detector is not linear. Attempts are made in design to
have the detector response curve approximate the quality factor versus energy curve by
placing a sphere or cylinder of polyethylene around the detector. (Polyethylene closely
approximates human tissue in composition.) Other techniques such as controlled loading
with cadmium, boron, or radially drilled holes are used to make the detector response
more equivalent to dose rate.
Section 20
The NBS released a table of the average flux to obtain 100 mrem/hr for various neutron
energies. (See Table 2) The goal of shield and detector design is to approximate this
relationship.
Table 2. Neutron Flux/Dose Relationship
Average Flux (n/cm2-sec)
Neutron Energy in MeV To obtain 1 mrem/hr
0.0001
0.02
0.1
1.0
2.5
5.0
7.5
10-30
268
200
110
32
8.0
7.2
6.8
4.0
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1.13.11 Identify the principles of detection, advantages and disadvantages of a GeLi detector
and an HPGe detector.
Valence
Band
Forbidden
Band
Conduction
Band
Conductor
(narrow gap)
Figure 7. Conductor
Valence
Band
Forbidden
Band
Conduction
Band
(wide gap)
Insulator
Figure 8. Insulator
Valence
Band
Forbidden
Band
Conduction
Band
(smaller gap)
Semiconductor
Figure 9. Semiconductor
e-
hole
Figure 10. Electron Hole
SEMICONDUCTOR DETECTORS
Principles of Semiconductor Detectors
In a crystal, the atoms are packed so tightly together that the energy
states of individual atoms are modified. This modification splits the
states into a number of closely spaced energy levels or bands. The
top most band (called the conduction band) has unfilled energy
levels. In a conducting solid, the group of "filled bands" is in direct
contact with the group of "unfilled bands," so electrons are easily
moved into the conduction band.
In a good insulator, there is a large enough gap between the group of
filled bands and the group of unfilled bands so that a large amount of
energy is required to move an electron to the conduction band.
A semiconductor has a smaller gap between the two groups of bands
so that under certain conditions, electrons can be moved to the con-
duction band. (For example, heating the material will move at least
some electrons to the conduction band.)
When an electron is moved to a higher band, that is, from valence
to conduction, a vacancy occurs in the band which it left. This
vacancy is called a hole.
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If a strong electric field is applied to the crystal, the electron in the conduction band
moves in accordance with the applied field. Similarly, in the group of filled bands, an
electron from a lower energy band moves up to fill the hole (vacancy) in the valence
band. The hole it leaves behind is filled by an electron from yet a lower energy band.
This process continues, so the net effect is that the hole appears to move down through
the energy bands in the filled group. Thus, the electron moves in one direction in the
unfilled group of bands, while the hole moves in the opposite direction in the filled group
of bands. This can be likened to a line of cars awaiting a toll booth, the toll booth being
the forbidden band. As a car leaves the "filled valence band" for the unfilled conductance
band, a hole is formed. The next car in line fills this hole, and creates a hole, and so on.
Consequently, the hole appears to move back through the line of cars.
Section 21
Any impurities in the crystalline structure can affect the conducting ability of the
crystalline solid. There are always some impurities in a semiconductor, no matter how
"pure" it is. However, in the fabrication of semiconductors, impurities are intentionally
added under controlled conditions. If the impurity added has an excess of outer electrons,
it is known as a donor impurity, because the "extra" electron can easily be raided or
donated to the conduction band. In effect the presence of this donor impurity decreases
the "gap" between the group of filled bands and the group of unfilled bands. Since
conduction occurs by the movement of a negative charge, the substance is known as an n-
type material. Similarly, if the impurity does not contain enough outer electrons, a
vacancy or hole exists. This hole can easily accept electrons from other energy levels in
the group of filled bands, and is called an acceptor substance. Although electrons move
to fill holes, as described above, the appearance is that the holes move in the opposite
direction. Since this impurity gives the appearance of positive holes moving, it is known
as a p-type material.
Since any crystalline material has some impurities in it, a given semiconductor will be an
n-type or a p-type depending on which concentration of impurity is higher. If the number
of n-type impurities is exactly equal to the number of p-type impurities, the crystalline
material is referred to as an "intrinsic semiconductor."
A semiconductor that has been "doped" with the proper amount of the correct type of
impurity to make the energy gap between the two groups of bands just right, makes a
good radiation detector. A charged particle loses energy by creating electron-hole pairs.
If the semiconductor is connected to an external electrical field, the collection of electron-
hole pairs can lead to an induced charge in the external circuit much as the collect of
electron-positive atom pairs (ion pairs) is used to measure radiation in an ion chamber.
Therefore, the semi-conductor detector relies on the collection of electron-hole pairs to
produce a usable electrical signal.
One disadvantage of the semiconductor "detector" is that the impurities, in addition to
controlling the size of the energy gap also act as traps. As electrons (or holes) move
through the crystalline material, they are attracted to the impurity areas or centers because
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JUNCTIONn p
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DEPLETION
REGION
Figure 11. n-p Junction
these impurity centers usually have a net charge. The carrier (electron or hole) may be
trapped for awhile at the impurity center and then released. As it begins to move again, it
may be trapped at another impurity center and then released again. If the electron or hole
is delayed long enough during transit through the crystal, it may not add to the electrical
output.
Thus, although the carrier is not actually lost, the net effect on readout is that it is lost.
Another disadvantage of the semiconductor detector is that the presence of impurities in
the crystal is hard to control to keep the energy gap where it is desired. A newer
technique, the junction counter, has been developed to overcome these disadvantages.
Section 22
In a semiconductor junction counter, an n-type substance is
united with a p-type substance. When the two are diffused
together to make a diffused junction, a depletion layer is
created between the two materials. (This depletion layer is
formed by the diffusion of electrons from the n-type material
into the p-type material and the diffusion of holes from the
p-type material into the n-type material.) This results in a
narrow region which is depleted of carriers and which
behaves like an insulator bounded by conducting electrodes. That is, a net charge on each
side of the depletion region impedes the further transfer of charge. This charge is positive
in the n-region and negative in the p-region. This barrier can be broken if we apply an
external voltage to the system and apply it with the proper bias. A "forward bias" is
applied when we connect the positive electrode to the p-region. In this case, the barrier
breaks down and electrons flow across the junction. However, if we apply a "reverse
bias" (negative electrode connected to the p-region), the barrier height is increased and
the depleted region is extended.
A further advancement in junction counters is the p-n type. This counter has an intrinsic
region between the n and p surface layers. (An intrinsic semiconductor was discussed
earlier and is effectively a pure semiconductor.) The presence of an intrinsic region
effectively creates a thicker depletion area. A Ge(Li) detector is an example of this type
of detector.
Lithium (an n-type material) is diffused into p-type germanium. The n-p junction that
results is put under reverse bias, and the temperature of the material is raised. Under
these conditions, the lithium ions drift through the germanium, balancing n and p material
and forming an intrinsic region.
The heat and bias are removed and the crystal cooled quickly to liquid nitrogen
temperatures. This intrinsic region serves as the region in which interactions can take
place. The intrinsic region can be thought of as a built-in depletion region.
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Due to the large size of the depletion region and the reduced mobility of the electrons and
holes due to the depressed temperature, a high charge is necessary to cause conduction.
The charge is chosen high enough to collect ion pairs, but low enough to prevent noise.
Due to the increased stopping power of germanium over air at -321 oF the energy required
to create an ion pair is only 2.96 eV compared to 33.7 eV for air. This means that by
theory, a germanium detector will respond to any radiation that will create ion pairs. In
actuality, however, the response to radiations other than gamma is limited by the
materials surrounding the detector, material necessary to maintain temperature. Another
consideration limiting response is the geometry of the crystal. The most efficient response
occurs when the interaction takes place in the center of the intrinsic region, this can only
occur for gamma.
Radiation interacts with atoms in the intrinsic region to produce electron hole pairs. The
presence of ion pairs in the depletion region causes current flow. This is similar to a
transistor, in that instead of inducing charges in the center section (the base in a
transistor) by a battery or an other source, the charge is induced by the creation of ion
pairs. Since it is not necessary for the ion produced to reach the p and n region to be
collected, as in a gas filled chamber, the response is faster.
Section 23
Since the number of ion pairs produced is a function of the incident energy, and the
resulting current is a function of the amount of ion pairs, Ge(Li) response is in terms of
energy.
GeLi Systems
A typical Ge(Li) detector system consists of a vacuum enclosed Ge(Li) crystal which is
coaxial in shape and attached to a copper cold finger through an agate insulator. The
crystal is under a vacuum to prevent frost forming on the crystal, and damage caused by
impurities in the air. The cold finger is immersed in liquid nitrogen in a dewar.
The crystal is subject to failure should its temperature be raised to room temperature due
to lithium ion drift and increased electron noise.
Advantages of Ge(Li) Detectors
GeLi detectors offer an advantage of high resolution (i.e. the ability to differentiate
between closely adjacent gamma photopeaks. It can resolve the 3 photopeaks of 95Zr/Nb
whereas this would appear as 1 photopeak with NaI(Tl) detectors.
GeLi also has a short response time and a more linear energy response than NaI(Tl).
Small size crystals offer the best resolution but the efficiency of detection is lowered.
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Disadvantages of Ge(Li) Detectors
GeLi systems can only be used for gamma photon detection. A cryogenic (liquid
nitrogen) system is required to cool the detector and this adds to the initial cost as well as
a continuing operation cost.
Because detectors are presently limited to less than 100-300 cc in size, the efficiency of
counting is low compared to NaI. Counting times in excess of 1,000 minutes are
necessary for environmental samples.
Intrinsic Germanium Detectors
One of the major disadvantages of GeLi detectors is the requirement that the crystal must
always be kept cooled by liquid nitrogen. If the detector is ever allowed to reach room
temperature, the lithium ions will drift and an effective intrinsic/depletion region (the area
of electron-hole pair formation) will no longer exist. The detector can be returned to the
manufacturer for redrifting, but the process is expensive and time consuming. The
detector may be less efficient than before the redrifting. The bulky size of the liquid
nitrogen dewar also places limitations on the uses of a GeLi detector. A semiconductor
detector that could be operated and/or stored at room temperature would have advantages
for use in installed effluent monitors or portable units.
Principles of Operation
In natural germanium of normal purity, the depletion region is only a few millimeters
thick. The crystal is, in effect, a conductor due to the impurities in the crystal. Resistance
is very low in the crystal, and detected electron flow (noise) may be caused by conditions
other than radiation (e.g., heat). As a result, the natural crystal is virtually useless for
radiation detection.
The use of the lithium drifting process in GeLi detectors creates an artificial
depletion/intrinsic zone of 10-15 mm. The GeLi detector is a semiconductor. The
resistance is greater than the resistance for a natural germanium crystal, and by applying
the correct voltage to the crystal, most non-radiation events that induce electron flow can
be eliminated. GeLi detectors are used in radiation detection; however, the crystal must
be maintained at the temperature of liquid nitrogen to maintain the depletion/intrinsic
zone.
Section 24
If an extremely pure germanium crystal is created, the crystal's resistance will be
sufficiently big so that a depletion region of 10mm can be obtained by using a reverse
bias voltage, instead of drifting lithium through the germanium as is done in GeLi
detectors. This pure germanium crystal would have, like GeLi crystals, semiconductor
properties, and by applying the correct voltage could be used to collect electrons induced
by radiation. Recently, processes for creating germanium in a very high state of purity
have been developed. This, in turn, has led to the development of a semiconductor that
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can be stored at room temperature. The pure germanium crystals are usually called
"intrinsic germanium" or "high purity germanium" (abbreviated HPGe) detectors. HPGe
crystals are perhaps the most highly purified material that has even been produced.
Note that in the above paragraph it was stated that the HPGe crystals could be stored at
room temperature. This is because HPGe crystals are not lithium drifted. However, there
was no mention of operating detectors with the crystals at room temperature. In order to
reduce unwanted detector noise (caused by reduced resistance at room temperature) the
detector must be operated at the temperature of liquid nitrogen. Experience has shown
that the crystals can be cycled between room and cold temperatures without damage.
Most manufacturers, however, recommend that the detectors be continuously maintained
at liquid nitrogen temperatures if possible.
Advantages of HPGe's
HPGe's offer high resolution as an advantage. Additionally, the dewar used for storing
the liquid nitrogen coolant for HPGe detectors can be smaller than the dewar used for
GeLi detectors. HPGe detectors are more portable. The main advantage is that should
the detector be allowed to rise to room temperature (with no voltage applied) the detector
need only be returned to and stabilized at liquid nitrogen temperatures to be used.
Disadvantages of HPGe's
Even though the dewar is smaller for the HPGe detector they still require liquid nitrogen
cooling and tend to be fairly expensive.
CONDENSER R-METER AND CHAMBER
Method of Detection
The condenser chamber is an integrating, air wall tissue equivalent ionization chamber
used to measure exposure to X or gamma radiation. The chamber generally consists of a
Bakelite shell, coated on the inner surface with graphite to make it conducting, and an
insulated central electrode. The chamber is mounted at one end of a shielded stem
containing a solid dielectric storage condenser. The chambers vary is size and shape
depending on their exposure range. The smaller the chamber volume the higher the
exposure it is capable of measuring.
The Condenser R-Meter performs two functions. It applies a charge to the chamber and,
after exposure, serves as a read-out device to determine the amount of exposure. It
contains a line-operated d.c. power supply, which provides a charging voltage of
approximately 500 volts. The read-out device is a string electrometer. Functionally, this
is a d.c. voltmeter with infinite input resistance. It is a descendant of the gold leaf
electroscope which was used as a detector in the early days of radiation physics. Instead
of a gold leaf, this instrument uses a platinum coated quartz fiber, bent into a horseshoe
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shape and soldered at each end to a horseshoe shaped support. When a charge is applied
to the fiber support and a nearby deflecting electrode, the fiber is attracted toward the
electrode to an extent proportional to the applied charge. A small light bulb casts a
shadow of the fiber on a scale, which is observed through an optical system. In operation,
the chamber is connected to the charger-reader, the charging switch is rotated to "charge"
and the electrometer is adjusted to zero on the scale. This puts a full charge on the
chamber, which can then be disconnected and placed wherever exposure is to be
measured. After the exposure, the chamber is again plugged into the charger-reader and
the residual charge is read. Since the loss of charge is proportional to the exposure, the
scale can be calibrated in roentgens.
The Condenser R-Meter is a secondary standard. It must be calibrated against a primary
standard, the free-air chamber. The Condenser R-Meter, in turn, can be used to calibrate
other survey instruments. The protective cap must always be on the chamber when the
exposure is made.
Range
Condenser chambers vary in size. The total exposure a chamber measures decreases as
the chamber volume increases. Chambers are generally available which enable us to
cover exposure ranges from several mR up to 250 R.
Energy Response
Condenser chambers vary in wall material and thickness as well as in size. The choice of
wall material and thickness off-sets the energy dependence of the chambers.
Use
The condenser chambers are generally used to calibrate X and gamma radiation sources,
and for making surveys of X-ray equipment. Condenser chambers may also be used to
measure neutron radiation. Some chambers are boron lined and measure the ionization
from the alpha particles emitted in the boron-thermal neutron reaction. Other chambers
are made of tissue equivalent material to measure the absorbed dose of any ionizing
radiation.
Module Number: 1.13