FLIR Systems FLIRT5590 Infrared Camera User Manual Part 4

FLIR Systems AB Infrared Camera Part 4

User Manual Part 4

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28
Application examples
28.3 Oxidized socket
28.3.1
General
Depending on the type of socket and the environment in which the socket is installed, oxides may occur on the socket's contact surfaces. These oxides can lead to locally increased resistance when the socket is loaded, which can be seen in an infrared image
as local temperature increase.
A socket’s construction may differ dramatically from one manufacturer to another. For
this reason, different faults in a socket can lead to the same typical appearance in an infrared image.
Local temperature increase can also result from improper contact between a wire and
socket, or from difference in load.
28.3.2
Figure
The image below shows a series of fuses where one fuse has a raised temperature on
the contact surfaces against the fuse holder. Because of the fuse holder’s blank metal,
the temperature increase is not visible there, while it is visible on the fuse’s ceramic
material.
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Application examples
28.4 Insulation deficiencies
28.4.1
General
Insulation deficiencies may result from insulation losing volume over the course of time
and thereby not entirely filling the cavity in a frame wall.
An infrared camera allows you to see these insulation deficiencies because they either
have a different heat conduction property than sections with correctly installed insulation,
and/or show the area where air is penetrating the frame of the building.
When you are inspecting a building, the temperature difference between the inside and
outside should be at least 10°C (18°F). Studs, water pipes, concrete columns, and similar components may resemble an insulation deficiency in an infrared image. Minor differences may also occur naturally.
28.4.2
Figure
In the image below, insulation in the roof framing is lacking. Due to the absence of insulation, air has forced its way into the roof structure, which thus takes on a different characteristic appearance in the infrared image.
28.5 Draft
28.5.1
General
Draft can be found under baseboards, around door and window casings, and above ceiling trim. This type of draft is often possible to see with an infrared camera, as a cooler
airstream cools down the surrounding surface.
When you are investigating draft in a house, there should be sub-atmospheric pressure
in the house. Close all doors, windows, and ventilation ducts, and allow the kitchen fan
to run for a while before you take the infrared images.
An infrared image of draft often shows a typical stream pattern. You can see this stream
pattern clearly in the picture below.
Also keep in mind that drafts can be concealed by heat from floor heating circuits.
28.5.2
Figure
The image below shows a ceiling hatch where faulty installation has resulted in a strong
draft.
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Application examples
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About FLIR Systems
FLIR Systems was established in 1978 to pioneer the development of high-performance
infrared imaging systems, and is the world leader in the design, manufacture, and marketing of thermal imaging systems for a wide variety of commercial, industrial, and government applications. Today, FLIR Systems embraces five major companies with
outstanding achievements in infrared technology since 1958—the Swedish AGEMA Infrared Systems (formerly AGA Infrared Systems), the three United States companies Indigo Systems, FSI, and Inframetrics, and the French company Cedip.
Since 2007, FLIR Systems has acquired several companies with world-leading expertise
in sensor technologies:
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•
•
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•
•
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•
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•
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•
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Extech Instruments (2007)
Ifara Tecnologías (2008)
Salvador Imaging (2009)
OmniTech Partners (2009)
Directed Perception (2009)
Raymarine (2010)
ICx Technologies (2010)
TackTick Marine Digital Instruments (2011)
Aerius Photonics (2011)
Lorex Technology (2012)
Traficon (2012)
MARSS (2013)
DigitalOptics micro-optics business (2013)
DVTEL (2015)
Point Grey Research (2016)
Prox Dynamics (2016)
Figure 29.1 Patent documents from the early 1960s
FLIR Systems has three manufacturing plants in the United States (Portland, OR, Boston,
MA, Santa Barbara, CA) and one in Sweden (Stockholm). Since 2007 there is also a
manufacturing plant in Tallinn, Estonia. Direct sales offices in Belgium, Brazil, China,
France, Germany, Great Britain, Hong Kong, Italy, Japan, Korea, Sweden, and the USA
—together with a worldwide network of agents and distributors—support our international customer base.
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About FLIR Systems
FLIR Systems is at the forefront of innovation in the infrared camera industry. We anticipate market demand by constantly improving our existing cameras and developing new
ones. The company has set milestones in product design and development such as the
introduction of the first battery-operated portable camera for industrial inspections, and
the first uncooled infrared camera, to mention just two innovations.
Figure 29.2 1969: Thermovision Model 661. The
camera weighed approximately 25 kg (55 lb.), the
oscilloscope 20 kg (44 lb.), and the tripod 15 kg
(33 lb.). The operator also needed a 220 VAC
generator set, and a 10 L (2.6 US gallon) jar with
liquid nitrogen. To the left of the oscilloscope the
Polaroid attachment (6 kg (13 lb.)) can be seen.
Figure 29.3 2015: FLIR One, an accessory to
iPhone and Android mobile phones. Weight: 90 g
(3.2 oz.).
FLIR Systems manufactures all vital mechanical and electronic components of the camera systems itself. From detector design and manufacturing, to lenses and system electronics, to final testing and calibration, all production steps are carried out and
supervised by our own engineers. The in-depth expertise of these infrared specialists ensures the accuracy and reliability of all vital components that are assembled into your infrared camera.
29.1 More than just an infrared camera
At FLIR Systems we recognize that our job is to go beyond just producing the best infrared camera systems. We are committed to enabling all users of our infrared camera systems to work more productively by providing them with the most powerful camera–
software combination. Especially tailored software for predictive maintenance, R & D,
and process monitoring is developed in-house. Most software is available in a wide variety of languages.
We support all our infrared cameras with a wide variety of accessories to adapt your
equipment to the most demanding infrared applications.
29.2 Sharing our knowledge
Although our cameras are designed to be very user-friendly, there is a lot more to thermography than just knowing how to handle a camera. Therefore, FLIR Systems has
founded the Infrared Training Center (ITC), a separate business unit, that provides certified training courses. Attending one of the ITC courses will give you a truly hands-on
learning experience.
The staff of the ITC are also there to provide you with any application support you may
need in putting infrared theory into practice.
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About FLIR Systems
29.3 Supporting our customers
FLIR Systems operates a worldwide service network to keep your camera running at all
times. If you discover a problem with your camera, local service centers have all the
equipment and expertise to solve it within the shortest possible time. Therefore, there is
no need to send your camera to the other side of the world or to talk to someone who
does not speak your language.
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Terms, laws, and definitions
Term
Definition
Absorption and emission2
The capacity or ability of an object to absorb incident radiated energy is always the same as the capacity to emit its
own energy as radiation
Apparent temperature
uncompensated reading from an infrared instrument, containing all radiation incident on the instrument, regardless of
its sources3
Color palette
assigns different colors to indicate specific levels of apparent
temperature. Palettes can provide high or low contrast, depending on the colors used in them
Conduction
direct transfer of thermal energy from molecule to molecule,
caused by collisions between the molecules
Convection
heat transfer mode where a fluid is brought into motion, either by gravity or another force, thereby transferring heat
from one place to another
Diagnostics
examination of symptoms and syndromes to determine the
nature of faults or failures4
Direction of heat transfer5
Heat will spontaneously flow from hotter to colder, thereby
transferring thermal energy from one place to another6
Emissivity
ratio of the power radiated by real bodies to the power that is
radiated by a blackbody at the same temperature and at the
same wavelength7
Energy conservation8
The sum of the total energy contents in a closed system is
constant
Exitant radiation
radiation that leaves the surface of an object, regardless of
its original sources
Heat
thermal energy that is transferred between two objects (systems) due to their difference in temperature
Heat transfer rate9
The heat transfer rate under steady state conditions is directly proportional to the thermal conductivity of the object,
the cross-sectional area of the object through which the heat
flows, and the temperature difference between the two ends
of the object. It is inversely proportional to the length, or
thickness, of the object10
Incident radiation
radiation that strikes an object from its surroundings
IR thermography
process of acquisition and analysis of thermal information
from non-contact thermal imaging devices
Isotherm
replaces certain colors in the scale with a contrasting color. It
marks an interval of equal apparent temperature11
Qualitative thermography
thermography that relies on the analysis of thermal patterns
to reveal the existence of and to locate the position of
anomalies12
Quantitative thermography
thermography that uses temperature measurement to determine the seriousness of an anomaly, in order to establish repair priorities12
2. Kirchhoff’s law of thermal radiation.
3. Based on ISO 18434-1:2008 (en).
4. Based on ISO 13372:2004 (en).
5. 2nd law of thermodynamics.
6. This is a consequence of the 2nd law of thermodynamics, the law itself is more complicated.
7. Based on ISO 16714-3:2016 (en).
8. 1st law of thermodynamics.
9. Fourier’s law.
10. This is the one-dimensional form of Fourier’s law, valid for steady-state conditions.
11. Based on ISO 18434-1:2008 (en)
12. Based on ISO 10878-2013 (en).
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Terms, laws, and definitions
Term
Definition
Radiative heat transfer
Heat transfer by the emission and absorption of thermal
radiation
Reflected apparent temperature
apparent temperature of the environment that is reflected by
the target into the IR camera13
Spatial resolution
ability of an IR camera to resolve small objects or details
Temperature
measure of the average kinetic energy of the molecules and
atoms that make up the substance
Thermal energy
total kinetic energy of the molecules that make up the
object14
Thermal gradient
gradual change in temperature over distance13
Thermal tuning
process of putting the colors of the image on the object of
analysis, in order to maximize contrast
13. Based on ISO 16714-3:2016 (en).
14. Thermal energy is part of the internal energy of an object.
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Thermographic measurement
techniques
31.1 Introduction
An infrared camera measures and images the emitted infrared radiation from an object.
The fact that radiation is a function of object surface temperature makes it possible for
the camera to calculate and display this temperature.
However, the radiation measured by the camera does not only depend on the temperature of the object but is also a function of the emissivity. Radiation also originates from
the surroundings and is reflected in the object. The radiation from the object and the reflected radiation will also be influenced by the absorption of the atmosphere.
To measure temperature accurately, it is therefore necessary to compensate for the effects of a number of different radiation sources. This is done on-line automatically by the
camera. The following object parameters must, however, be supplied for the camera:
•
•
•
•
•
The emissivity of the object
The reflected apparent temperature
The distance between the object and the camera
The relative humidity
Temperature of the atmosphere
31.2 Emissivity
The most important object parameter to set correctly is the emissivity which, in short, is a
measure of how much radiation is emitted from the object, compared to that from a perfect blackbody of the same temperature.
Normally, object materials and surface treatments exhibit emissivity ranging from approximately 0.1 to 0.95. A highly polished (mirror) surface falls below 0.1, while an oxidized
or painted surface has a higher emissivity. Oil-based paint, regardless of color in the visible spectrum, has an emissivity over 0.9 in the infrared. Human skin exhibits an emissivity 0.97 to 0.98.
Non-oxidized metals represent an extreme case of perfect opacity and high reflexivity,
which does not vary greatly with wavelength. Consequently, the emissivity of metals is
low – only increasing with temperature. For non-metals, emissivity tends to be high, and
decreases with temperature.
31.2.1
31.2.1.1
Finding the emissivity of a sample
Step 1: Determining reflected apparent temperature
Use one of the following two methods to determine reflected apparent temperature:
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Thermographic measurement techniques
31.2.1.1.1
Method 1: Direct method
Follow this procedure:
1. Look for possible reflection sources, considering that the incident angle = reflection
angle (a = b).
Figure 31.1 1 = Reflection source
2. If the reflection source is a spot source, modify the source by obstructing it using a
piece if cardboard.
Figure 31.2 1 = Reflection source
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Thermographic measurement techniques
3. Measure the radiation intensity (= apparent temperature) from the reflection source
using the following settings:
• Emissivity: 1.0
• Dobj: 0
You can measure the radiation intensity using one of the following two methods:
Figure 31.3 1 = Reflection source
Figure 31.4 1 = Reflection source
You can not use a thermocouple to measure reflected apparent temperature, because a
thermocouple measures temperature, but apparent temperatrure is radiation intensity.
31.2.1.1.2
Method 2: Reflector method
Follow this procedure:
1. Crumble up a large piece of aluminum foil.
2. Uncrumble the aluminum foil and attach it to a piece of cardboard of the same size.
3. Put the piece of cardboard in front of the object you want to measure. Make sure that
the side with aluminum foil points to the camera.
4. Set the emissivity to 1.0.
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Thermographic measurement techniques
5. Measure the apparent temperature of the aluminum foil and write it down. The foil is
considered a perfect reflector, so its apparent temperature equals the reflected apparent temperature from the surroundings.
Figure 31.5 Measuring the apparent temperature of the aluminum foil.
31.2.1.2
Step 2: Determining the emissivity
Follow this procedure:
1. Select a place to put the sample.
2. Determine and set reflected apparent temperature according to the previous
procedure.
3. Put a piece of electrical tape with known high emissivity on the sample.
4. Heat the sample at least 20 K above room temperature. Heating must be reasonably
even.
5. Focus and auto-adjust the camera, and freeze the image.
6. Adjust Level and Span for best image brightness and contrast.
7. Set emissivity to that of the tape (usually 0.97).
8. Measure the temperature of the tape using one of the following measurement
functions:
• Isotherm (helps you to determine both the temperature and how evenly you have
heated the sample)
• Spot (simpler)
• Box Avg (good for surfaces with varying emissivity).
9. Write down the temperature.
10. Move your measurement function to the sample surface.
11. Change the emissivity setting until you read the same temperature as your previous
measurement.
12. Write down the emissivity.
Note
• Avoid forced convection
• Look for a thermally stable surrounding that will not generate spot reflections
• Use high quality tape that you know is not transparent, and has a high emissivity you
are certain of
• This method assumes that the temperature of your tape and the sample surface are
the same. If they are not, your emissivity measurement will be wrong.
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31.3 Reflected apparent temperature
This parameter is used to compensate for the radiation reflected in the object. If the
emissivity is low and the object temperature relatively far from that of the reflected it will
be important to set and compensate for the reflected apparent temperature correctly.
31.4 Distance
The distance is the distance between the object and the front lens of the camera. This
parameter is used to compensate for the following two facts:
• That radiation from the target is absorbed by the atmosphere between the object and
the camera.
• That radiation from the atmosphere itself is detected by the camera.
31.5 Relative humidity
The camera can also compensate for the fact that the transmittance is also dependent
on the relative humidity of the atmosphere. To do this set the relative humidity to the correct value. For short distances and normal humidity the relative humidity can normally be
left at a default value of 50%.
31.6 Other parameters
In addition, some cameras and analysis programs from FLIR Systems allow you to compensate for the following parameters:
• Atmospheric temperature – i.e. the temperature of the atmosphere between the camera and the target
• External optics temperature – i.e. the temperature of any external lenses or windows
used in front of the camera
• External optics transmittance – i.e. the transmission of any external lenses or windows
used in front of the camera
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History of infrared technology
Before the year 1800, the existence of the infrared portion of the electromagnetic spectrum wasn't even suspected. The original significance of the infrared spectrum, or simply
‘the infrared’ as it is often called, as a form of heat radiation is perhaps less obvious today than it was at the time of its discovery by Herschel in 1800.
Figure 32.1 Sir William Herschel (1738–1822)
The discovery was made accidentally during the search for a new optical material. Sir
William Herschel – Royal Astronomer to King George III of England, and already famous
for his discovery of the planet Uranus – was searching for an optical filter material to reduce the brightness of the sun’s image in telescopes during solar observations. While
testing different samples of colored glass which gave similar reductions in brightness he
was intrigued to find that some of the samples passed very little of the sun’s heat, while
others passed so much heat that he risked eye damage after only a few seconds’
observation.
Herschel was soon convinced of the necessity of setting up a systematic experiment,
with the objective of finding a single material that would give the desired reduction in
brightness as well as the maximum reduction in heat. He began the experiment by actually repeating Newton’s prism experiment, but looking for the heating effect rather than
the visual distribution of intensity in the spectrum. He first blackened the bulb of a sensitive mercury-in-glass thermometer with ink, and with this as his radiation detector he proceeded to test the heating effect of the various colors of the spectrum formed on the top
of a table by passing sunlight through a glass prism. Other thermometers, placed outside
the sun’s rays, served as controls.
As the blackened thermometer was moved slowly along the colors of the spectrum, the
temperature readings showed a steady increase from the violet end to the red end. This
was not entirely unexpected, since the Italian researcher, Landriani, in a similar experiment in 1777 had observed much the same effect. It was Herschel, however, who was
the first to recognize that there must be a point where the heating effect reaches a maximum, and that measurements confined to the visible portion of the spectrum failed to locate this point.
Figure 32.2 Marsilio Landriani (1746–1815)
Moving the thermometer into the dark region beyond the red end of the spectrum, Herschel confirmed that the heating continued to increase. The maximum point, when he
found it, lay well beyond the red end – in what is known today as the ‘infrared
wavelengths’.
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History of infrared technology
When Herschel revealed his discovery, he referred to this new portion of the electromagnetic spectrum as the ‘thermometrical spectrum’. The radiation itself he sometimes referred to as ‘dark heat’, or simply ‘the invisible rays’. Ironically, and contrary to popular
opinion, it wasn't Herschel who originated the term ‘infrared’. The word only began to appear in print around 75 years later, and it is still unclear who should receive credit as the
originator.
Herschel’s use of glass in the prism of his original experiment led to some early controversies with his contemporaries about the actual existence of the infrared wavelengths.
Different investigators, in attempting to confirm his work, used various types of glass indiscriminately, having different transparencies in the infrared. Through his later experiments, Herschel was aware of the limited transparency of glass to the newly-discovered
thermal radiation, and he was forced to conclude that optics for the infrared would probably be doomed to the use of reflective elements exclusively (i.e. plane and curved mirrors). Fortunately, this proved to be true only until 1830, when the Italian investigator,
Melloni, made his great discovery that naturally occurring rock salt (NaCl) – which was
available in large enough natural crystals to be made into lenses and prisms – is remarkably transparent to the infrared. The result was that rock salt became the principal infrared optical material, and remained so for the next hundred years, until the art of synthetic
crystal growing was mastered in the 1930’s.
Figure 32.3 Macedonio Melloni (1798–1854)
Thermometers, as radiation detectors, remained unchallenged until 1829, the year Nobili
invented the thermocouple. (Herschel’s own thermometer could be read to 0.2 °C
(0.036 °F), and later models were able to be read to 0.05 °C (0.09 °F)). Then a breakthrough occurred; Melloni connected a number of thermocouples in series to form the
first thermopile. The new device was at least 40 times as sensitive as the best thermometer of the day for detecting heat radiation – capable of detecting the heat from a person
standing three meters away.
The first so-called ‘heat-picture’ became possible in 1840, the result of work by Sir John
Herschel, son of the discoverer of the infrared and a famous astronomer in his own right.
Based upon the differential evaporation of a thin film of oil when exposed to a heat pattern focused upon it, the thermal image could be seen by reflected light where the interference effects of the oil film made the image visible to the eye. Sir John also managed
to obtain a primitive record of the thermal image on paper, which he called a
‘thermograph’.
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History of infrared technology
Figure 32.4 Samuel P. Langley (1834–1906)
The improvement of infrared-detector sensitivity progressed slowly. Another major breakthrough, made by Langley in 1880, was the invention of the bolometer. This consisted of
a thin blackened strip of platinum connected in one arm of a Wheatstone bridge circuit
upon which the infrared radiation was focused and to which a sensitive galvanometer responded. This instrument is said to have been able to detect the heat from a cow at a
distance of 400 meters.
An English scientist, Sir James Dewar, first introduced the use of liquefied gases as cooling agents (such as liquid nitrogen with a temperature of –196°C (–320.8°F)) in low temperature research. In 1892 he invented a unique vacuum insulating container in which it
is possible to store liquefied gases for entire days. The common ‘thermos bottle’, used
for storing hot and cold drinks, is based upon his invention.
Between the years 1900 and 1920, the inventors of the world ‘discovered’ the infrared.
Many patents were issued for devices to detect personnel, artillery, aircraft, ships – and
even icebergs. The first operating systems, in the modern sense, began to be developed
during the 1914–18 war, when both sides had research programs devoted to the military
exploitation of the infrared. These programs included experimental systems for enemy
intrusion/detection, remote temperature sensing, secure communications, and ‘flying torpedo’ guidance. An infrared search system tested during this period was able to detect
an approaching airplane at a distance of 1.5 km (0.94 miles), or a person more than 300
meters (984 ft.) away.
The most sensitive systems up to this time were all based upon variations of the bolometer idea, but the period between the two wars saw the development of two revolutionary
new infrared detectors: the image converter and the photon detector. At first, the image
converter received the greatest attention by the military, because it enabled an observer
for the first time in history to literally ‘see in the dark’. However, the sensitivity of the image converter was limited to the near infrared wavelengths, and the most interesting military targets (i.e. enemy soldiers) had to be illuminated by infrared search beams. Since
this involved the risk of giving away the observer’s position to a similarly-equipped enemy
observer, it is understandable that military interest in the image converter eventually
faded.
The tactical military disadvantages of so-called 'active’ (i.e. search beam-equipped) thermal imaging systems provided impetus following the 1939–45 war for extensive secret
military infrared-research programs into the possibilities of developing ‘passive’ (no
search beam) systems around the extremely sensitive photon detector. During this period, military secrecy regulations completely prevented disclosure of the status of infraredimaging technology. This secrecy only began to be lifted in the middle of the 1950’s, and
from that time adequate thermal-imaging devices finally began to be available to civilian
science and industry.
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Theory of thermography
33.1 Introduction
The subjects of infrared radiation and the related technique of thermography are still new
to many who will use an infrared camera. In this section the theory behind thermography
will be given.
33.2 The electromagnetic spectrum
The electromagnetic spectrum is divided arbitrarily into a number of wavelength regions,
called bands, distinguished by the methods used to produce and detect the radiation.
There is no fundamental difference between radiation in the different bands of the electromagnetic spectrum. They are all governed by the same laws and the only differences
are those due to differences in wavelength.
Figure 33.1 The electromagnetic spectrum. 1: X-ray; 2: UV; 3: Visible; 4: IR; 5: Microwaves; 6:
Radiowaves.
Thermography makes use of the infrared spectral band. At the short-wavelength end the
boundary lies at the limit of visual perception, in the deep red. At the long-wavelength
end it merges with the microwave radio wavelengths, in the millimeter range.
The infrared band is often further subdivided into four smaller bands, the boundaries of
which are also arbitrarily chosen. They include: the near infrared (0.75–3 μm), the middle
infrared (3–6 μm), the far infrared (6–15 μm) and the extreme infrared (15–100 μm).
Although the wavelengths are given in μm (micrometers), other units are often still used
to measure wavelength in this spectral region, e.g. nanometer (nm) and Ångström (Å).
The relationships between the different wavelength measurements is:
33.3 Blackbody radiation
A blackbody is defined as an object which absorbs all radiation that impinges on it at any
wavelength. The apparent misnomer black relating to an object emitting radiation is explained by Kirchhoff’s Law (after Gustav Robert Kirchhoff, 1824–1887), which states that
a body capable of absorbing all radiation at any wavelength is equally capable in the
emission of radiation.
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Theory of thermography
Figure 33.2 Gustav Robert Kirchhoff (1824–1887)
The construction of a blackbody source is, in principle, very simple. The radiation characteristics of an aperture in an isotherm cavity made of an opaque absorbing material represents almost exactly the properties of a blackbody. A practical application of the
principle to the construction of a perfect absorber of radiation consists of a box that is
light tight except for an aperture in one of the sides. Any radiation which then enters the
hole is scattered and absorbed by repeated reflections so only an infinitesimal fraction
can possibly escape. The blackness which is obtained at the aperture is nearly equal to
a blackbody and almost perfect for all wavelengths.
By providing such an isothermal cavity with a suitable heater it becomes what is termed
a cavity radiator. An isothermal cavity heated to a uniform temperature generates blackbody radiation, the characteristics of which are determined solely by the temperature of
the cavity. Such cavity radiators are commonly used as sources of radiation in temperature reference standards in the laboratory for calibrating thermographic instruments,
such as a FLIR Systems camera for example.
If the temperature of blackbody radiation increases to more than 525°C (977°F), the
source begins to be visible so that it appears to the eye no longer black. This is the incipient red heat temperature of the radiator, which then becomes orange or yellow as the
temperature increases further. In fact, the definition of the so-called color temperature of
an object is the temperature to which a blackbody would have to be heated to have the
same appearance.
Now consider three expressions that describe the radiation emitted from a blackbody.
33.3.1
Planck’s law
Figure 33.3 Max Planck (1858–1947)
Max Planck (1858–1947) was able to describe the spectral distribution of the radiation
from a blackbody by means of the following formula:
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Theory of thermography
where:
Wλb
Blackbody spectral radiant emittance at wavelength λ.
Velocity of light = 3 × 108 m/s
Planck’s constant = 6.6 × 10-34 Joule sec.
Boltzmann’s constant = 1.4 × 10-23 Joule/K.
Absolute temperature (K) of a blackbody.
λ
Wavelength (μm).
Note The factor 10-6 is used since spectral emittance in the curves is expressed in
Watt/m2, μm.
Planck’s formula, when plotted graphically for various temperatures, produces a family of
curves. Following any particular Planck curve, the spectral emittance is zero at λ = 0,
then increases rapidly to a maximum at a wavelength λmax and after passing it approaches zero again at very long wavelengths. The higher the temperature, the shorter
the wavelength at which maximum occurs.
Figure 33.4 Blackbody spectral radiant emittance according to Planck’s law, plotted for various absolute
temperatures. 1: Spectral radiant emittance (W/cm2 × 103(μm)); 2: Wavelength (μm)
33.3.2
Wien’s displacement law
By differentiating Planck’s formula with respect to λ, and finding the maximum, we have:
This is Wien’s formula (after Wilhelm Wien, 1864–1928), which expresses mathematically the common observation that colors vary from red to orange or yellow as the temperature of a thermal radiator increases. The wavelength of the color is the same as the
wavelength calculated for λmax. A good approximation of the value of λmax for a given
blackbody temperature is obtained by applying the rule-of-thumb 3 000/T μm. Thus, a
very hot star such as Sirius (11 000 K), emitting bluish-white light, radiates with the peak
of spectral radiant emittance occurring within the invisible ultraviolet spectrum, at wavelength 0.27 μm.
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Figure 33.5 Wilhelm Wien (1864–1928)
The sun (approx. 6 000 K) emits yellow light, peaking at about 0.5 μm in the middle of
the visible light spectrum.
At room temperature (300 K) the peak of radiant emittance lies at 9.7 μm, in the far infrared, while at the temperature of liquid nitrogen (77 K) the maximum of the almost insignificant amount of radiant emittance occurs at 38 μm, in the extreme infrared wavelengths.
Figure 33.6 Planckian curves plotted on semi-log scales from 100 K to 1000 K. The dotted line represents
the locus of maximum radiant emittance at each temperature as described by Wien's displacement law. 1:
Spectral radiant emittance (W/cm2 (μm)); 2: Wavelength (μm).
33.3.3
Stefan-Boltzmann's law
By integrating Planck’s formula from λ = 0 to λ = ∞, we obtain the total radiant emittance
(Wb) of a blackbody:
This is the Stefan-Boltzmann formula (after Josef Stefan, 1835–1893, and Ludwig Boltzmann, 1844–1906), which states that the total emissive power of a blackbody is proportional to the fourth power of its absolute temperature. Graphically, Wb represents the
area below the Planck curve for a particular temperature. It can be shown that the radiant
emittance in the interval λ = 0 to λmax is only 25% of the total, which represents about the
amount of the sun’s radiation which lies inside the visible light spectrum.
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Figure 33.7 Josef Stefan (1835–1893), and Ludwig Boltzmann (1844–1906)
Using the Stefan-Boltzmann formula to calculate the power radiated by the human body,
at a temperature of 300 K and an external surface area of approx. 2 m2, we obtain 1 kW.
This power loss could not be sustained if it were not for the compensating absorption of
radiation from surrounding surfaces, at room temperatures which do not vary too drastically from the temperature of the body – or, of course, the addition of clothing.
33.3.4
Non-blackbody emitters
So far, only blackbody radiators and blackbody radiation have been discussed. However,
real objects almost never comply with these laws over an extended wavelength region –
although they may approach the blackbody behavior in certain spectral intervals. For example, a certain type of white paint may appear perfectly white in the visible light spectrum, but becomes distinctly gray at about 2 μm, and beyond 3 μm it is almost black.
There are three processes which can occur that prevent a real object from acting like a
blackbody: a fraction of the incident radiation α may be absorbed, a fraction ρ may be reflected, and a fraction τ may be transmitted. Since all of these factors are more or less
wavelength dependent, the subscript λ is used to imply the spectral dependence of their
definitions. Thus:
• The spectral absorptance αλ= the ratio of the spectral radiant power absorbed by an
object to that incident upon it.
• The spectral reflectance ρλ = the ratio of the spectral radiant power reflected by an object to that incident upon it.
• The spectral transmittance τλ = the ratio of the spectral radiant power transmitted
through an object to that incident upon it.
The sum of these three factors must always add up to the whole at any wavelength, so
we have the relation:
For opaque materials τλ = 0 and the relation simplifies to:
Another factor, called the emissivity, is required to describe the fraction ε of the radiant
emittance of a blackbody produced by an object at a specific temperature. Thus, we
have the definition:
The spectral emissivity ελ= the ratio of the spectral radiant power from an object to that
from a blackbody at the same temperature and wavelength.
Expressed mathematically, this can be written as the ratio of the spectral emittance of
the object to that of a blackbody as follows:
Generally speaking, there are three types of radiation source, distinguished by the ways
in which the spectral emittance of each varies with wavelength.
• A blackbody, for which ελ = ε = 1
• A graybody, for which ελ = ε = constant less than 1
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• A selective radiator, for which ε varies with wavelength
According to Kirchhoff’s law, for any material the spectral emissivity and spectral absorptance of a body are equal at any specified temperature and wavelength. That is:
From this we obtain, for an opaque material (since αλ + ρλ = 1):
For highly polished materials ελ approaches zero, so that for a perfectly reflecting material (i.e. a perfect mirror) we have:
For a graybody radiator, the Stefan-Boltzmann formula becomes:
This states that the total emissive power of a graybody is the same as a blackbody at the
same temperature reduced in proportion to the value of ε from the graybody.
Figure 33.8 Spectral radiant emittance of three types of radiators. 1: Spectral radiant emittance; 2: Wavelength; 3: Blackbody; 4: Selective radiator; 5: Graybody.
Figure 33.9 Spectral emissivity of three types of radiators. 1: Spectral emissivity; 2: Wavelength; 3: Blackbody; 4: Graybody; 5: Selective radiator.
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33.4 Infrared semi-transparent materials
Consider now a non-metallic, semi-transparent body – let us say, in the form of a thick flat
plate of plastic material. When the plate is heated, radiation generated within its volume
must work its way toward the surfaces through the material in which it is partially absorbed. Moreover, when it arrives at the surface, some of it is reflected back into the interior. The back-reflected radiation is again partially absorbed, but some of it arrives at the
other surface, through which most of it escapes; part of it is reflected back again.
Although the progressive reflections become weaker and weaker they must all be added
up when the total emittance of the plate is sought. When the resulting geometrical series
is summed, the effective emissivity of a semi-transparent plate is obtained as:
When the plate becomes opaque this formula is reduced to the single formula:
This last relation is a particularly convenient one, because it is often easier to measure
reflectance than to measure emissivity directly.
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The measurement formula
As already mentioned, when viewing an object, the camera receives radiation not only
from the object itself. It also collects radiation from the surroundings reflected via the object surface. Both these radiation contributions become attenuated to some extent by the
atmosphere in the measurement path. To this comes a third radiation contribution from
the atmosphere itself.
This description of the measurement situation, as illustrated in the figure below, is so far
a fairly true description of the real conditions. What has been neglected could for instance be sun light scattering in the atmosphere or stray radiation from intense radiation
sources outside the field of view. Such disturbances are difficult to quantify, however, in
most cases they are fortunately small enough to be neglected. In case they are not negligible, the measurement configuration is likely to be such that the risk for disturbance is
obvious, at least to a trained operator. It is then his responsibility to modify the measurement situation to avoid the disturbance e.g. by changing the viewing direction, shielding
off intense radiation sources etc.
Accepting the description above, we can use the figure below to derive a formula for the
calculation of the object temperature from the calibrated camera output.
Figure 34.1 A schematic representation of the general thermographic measurement situation.1: Surroundings; 2: Object; 3: Atmosphere; 4: Camera
Assume that the received radiation power W from a blackbody source of temperature
Tsource on short distance generates a camera output signal Usource that is proportional to
the power input (power linear camera). We can then write (Equation 1):
or, with simplified notation:
where C is a constant.
Should the source be a graybody with emittance ε, the received radiation would consequently be εWsource.
We are now ready to write the three collected radiation power terms:
1. Emission from the object = ετWobj, where ε is the emittance of the object and τ is the
transmittance of the atmosphere. The object temperature is Tobj.
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2. Reflected emission from ambient sources = (1 – ε)τWrefl, where (1 – ε) is the reflectance of the object. The ambient sources have the temperature Trefl.
It has here been assumed that the temperature Trefl is the same for all emitting surfaces within the halfsphere seen from a point on the object surface. This is of course
sometimes a simplification of the true situation. It is, however, a necessary simplification in order to derive a workable formula, and Trefl can – at least theoretically – be given a value that represents an efficient temperature of a complex surrounding.
Note also that we have assumed that the emittance for the surroundings = 1. This is
correct in accordance with Kirchhoff’s law: All radiation impinging on the surrounding
surfaces will eventually be absorbed by the same surfaces. Thus the emittance = 1.
(Note though that the latest discussion requires the complete sphere around the object to be considered.)
3. Emission from the atmosphere = (1 – τ)τWatm, where (1 – τ) is the emittance of the atmosphere. The temperature of the atmosphere is Tatm.
The total received radiation power can now be written (Equation 2):
We multiply each term by the constant C of Equation 1 and replace the CW products by
the corresponding U according to the same equation, and get (Equation 3):
Solve Equation 3 for Uobj (Equation 4):
This is the general measurement formula used in all the FLIR Systems thermographic
equipment. The voltages of the formula are:
Table 34.1 Voltages
Uobj
Calculated camera output voltage for a blackbody of temperature
Tobj i.e. a voltage that can be directly converted into true requested
object temperature.
Utot
Measured camera output voltage for the actual case.
Urefl
Theoretical camera output voltage for a blackbody of temperature
Trefl according to the calibration.
Uatm
Theoretical camera output voltage for a blackbody of temperature
Tatm according to the calibration.
The operator has to supply a number of parameter values for the calculation:
•
•
•
•
•
the object emittance ε,
the relative humidity,
Tatm
object distance (Dobj)
the (effective) temperature of the object surroundings, or the reflected ambient temperature Trefl, and
• the temperature of the atmosphere Tatm
This task could sometimes be a heavy burden for the operator since there are normally
no easy ways to find accurate values of emittance and atmospheric transmittance for the
actual case. The two temperatures are normally less of a problem provided the surroundings do not contain large and intense radiation sources.
A natural question in this connection is: How important is it to know the right values of
these parameters? It could though be of interest to get a feeling for this problem already
here by looking into some different measurement cases and compare the relative
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magnitudes of the three radiation terms. This will give indications about when it is important to use correct values of which parameters.
The figures below illustrates the relative magnitudes of the three radiation contributions
for three different object temperatures, two emittances, and two spectral ranges: SW and
LW. Remaining parameters have the following fixed values:
• τ = 0.88
• Trefl = +20°C (+68°F)
• Tatm = +20°C (+68°F)
It is obvious that measurement of low object temperatures are more critical than measuring high temperatures since the ‘disturbing’ radiation sources are relatively much stronger in the first case. Should also the object emittance be low, the situation would be still
more difficult.
We have finally to answer a question about the importance of being allowed to use the
calibration curve above the highest calibration point, what we call extrapolation. Imagine
that we in a certain case measure Utot = 4.5 volts. The highest calibration point for the
camera was in the order of 4.1 volts, a value unknown to the operator. Thus, even if the
object happened to be a blackbody, i.e. Uobj = Utot, we are actually performing extrapolation of the calibration curve when converting 4.5 volts into temperature.
Let us now assume that the object is not black, it has an emittance of 0.75, and the transmittance is 0.92. We also assume that the two second terms of Equation 4 amount to 0.5
volts together. Computation of Uobj by means of Equation 4 then results in Uobj = 4.5 /
0.75 / 0.92 – 0.5 = 6.0. This is a rather extreme extrapolation, particularly when considering that the video amplifier might limit the output to 5 volts! Note, though, that the application of the calibration curve is a theoretical procedure where no electronic or other
limitations exist. We trust that if there had been no signal limitations in the camera, and if
it had been calibrated far beyond 5 volts, the resulting curve would have been very much
the same as our real curve extrapolated beyond 4.1 volts, provided the calibration algorithm is based on radiation physics, like the FLIR Systems algorithm. Of course there
must be a limit to such extrapolations.
Figure 34.2 Relative magnitudes of radiation sources under varying measurement conditions (SW camera). 1: Object temperature; 2: Emittance; Obj: Object radiation; Refl: Reflected radiation; Atm: atmosphere radiation. Fixed parameters: τ = 0.88; Trefl = 20°C (+68°F); Tatm = 20°C (+68°F).
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Figure 34.3 Relative magnitudes of radiation sources under varying measurement conditions (LW camera). 1: Object temperature; 2: Emittance; Obj: Object radiation; Refl: Reflected radiation; Atm: atmosphere radiation. Fixed parameters: τ = 0.88; Trefl = 20°C (+68°F); Tatm = 20°C (+68°F).
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Emissivity tables
This section presents a compilation of emissivity data from the infrared literature and
measurements made by FLIR Systems.
35.1 References
1. Mikaél A. Bramson: Infrared Radiation, A Handbook for Applications, Plenum press,
N.Y.
2. William L. Wolfe, George J. Zissis: The Infrared Handbook, Office of Naval Research,
Department of Navy, Washington, D.C.
3. Madding, R. P.: Thermographic Instruments and systems. Madison, Wisconsin: University of Wisconsin – Extension, Department of Engineering and Applied Science.
4. William L. Wolfe: Handbook of Military Infrared Technology, Office of Naval Research,
Department of Navy, Washington, D.C.
5. Jones, Smith, Probert: External thermography of buildings..., Proc. of the Society of
Photo-Optical Instrumentation Engineers, vol.110, Industrial and Civil Applications of
Infrared Technology, June 1977 London.
6. Paljak, Pettersson: Thermography of Buildings, Swedish Building Research Institute,
Stockholm 1972.
7. Vlcek, J: Determination of emissivity with imaging radiometers and some emissivities
at λ = 5 µm. Photogrammetric Engineering and Remote Sensing.
8. Kern: Evaluation of infrared emission of clouds and ground as measured by weather
satellites, Defence Documentation Center, AD 617 417.
9. Öhman, Claes: Emittansmätningar med AGEMA E-Box. Teknisk rapport, AGEMA
1999. (Emittance measurements using AGEMA E-Box. Technical report, AGEMA
1999.)
10. Matteï, S., Tang-Kwor, E: Emissivity measurements for Nextel Velvet coating 811-21
between –36°C AND 82°C.
11. Lohrengel & Todtenhaupt (1996)
12. ITC Technical publication 32.
13. ITC Technical publication 29.
14. Schuster, Norbert and Kolobrodov, Valentin G. Infrarotthermographie. Berlin: WileyVCH, 2000.
Note The emissivity values in the table below are recorded using a shortwave (SW)
camera. The values should be regarded as recommendations only and used with
caution.
35.2 Tables
Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference
3M type 35
Vinyl electrical
tape (several
colors)
< 80
LW
≈ 0.96
13
3M type 88
Black vinyl electrical tape
< 105
LW
≈ 0.96
13
3M type 88
Black vinyl electrical tape
< 105
MW
< 0.96
13
3M type Super 33
Black vinyl electrical tape
< 80
LW
≈ 0.96
13
Aluminum
anodized sheet
100
0.55
Aluminum
anodized, black,
dull
70
SW
0.67
Aluminum
anodized, black,
dull
70
LW
0.95
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Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Aluminum
anodized, light
gray, dull
70
SW
0.61
Aluminum
anodized, light
gray, dull
70
LW
0.97
Aluminum
as received, plate
100
0.09
Aluminum
as received,
sheet
100
0.09
Aluminum
cast, blast
cleaned
70
SW
0.47
Aluminum
cast, blast
cleaned
70
LW
0.46
Aluminum
dipped in HNO3,
plate
100
0.05
Aluminum
foil
27
10 µm
0.04
Aluminum
foil
27
3 µm
0.09
Aluminum
oxidized, strongly
50–500
0.2–0.3
Aluminum
polished
50–100
0.04–0.06
Aluminum
polished plate
100
0.05
Aluminum
polished, sheet
100
0.05
Aluminum
rough surface
20–50
0.06–0.07
Aluminum
roughened
27
10 µm
0.18
Aluminum
roughened
27
3 µm
0.28
Aluminum
sheet, 4 samples
differently
scratched
70
SW
0.05–0.08
Aluminum
sheet, 4 samples
differently
scratched
70
LW
0.03–0.06
Aluminum
vacuum
deposited
20
0.04
Aluminum
weathered,
heavily
17
SW
0.83–0.94
20
0.60
Aluminum bronze
Aluminum
hydroxide
powder
0.28
Aluminum oxide
activated, powder
0.46
Aluminum oxide
pure, powder
(alumina)
0.16
Asbestos
board
0.96
Asbestos
fabric
0.78
Asbestos
floor tile
35
SW
0.94
Asbestos
paper
40–400
0.93–0.95
Asbestos
powder
0.40–0.60
Asbestos
slate
20
0.96
LLW
0.967
Asphalt paving
20
Brass
dull, tarnished
20–350
0.22
Brass
oxidized
100
0.61
Brass
oxidized
70
SW
0.04–0.09
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Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Brass
oxidized
70
LW
0.03–0.07
Brass
oxidized at 600°C
200–600
0.59–0.61
Brass
polished
200
0.03
Brass
polished, highly
100
0.03
Brass
rubbed with 80grit emery
20
0.20
Brass
sheet, rolled
20
0.06
Brass
sheet, worked
with emery
20
0.2
Brick
alumina
17
SW
0.68
Brick
common
17
SW
0.86–0.81
Brick
Dinas silica,
glazed, rough
1100
0.85
Brick
Dinas silica,
refractory
1000
0.66
Brick
Dinas silica, unglazed, rough
1000
0.80
Brick
firebrick
17
SW
0.68
Brick
fireclay
1000
0.75
Brick
fireclay
1200
0.59
Brick
fireclay
20
0.85
Brick
masonry
35
SW
0.94
Brick
masonry,
plastered
20
0.94
Brick
red, common
20
0.93
Brick
red, rough
20
0.88–0.93
Brick
refractory,
corundum
1000
0.46
Brick
refractory,
magnesite
1000–1300
0.38
Brick
refractory,
strongly radiating
500–1000
0.8–0.9
Brick
refractory, weakly
radiating
500–1000
0.65–0.75
Brick
silica, 95% SiO2
1230
0.66
Brick
sillimanite, 33%
SiO2, 64% Al2O3
1500
0.29
Brick
waterproof
17
SW
0.87
Bronze
phosphor bronze
70
SW
0.08
Bronze
phosphor bronze
70
LW
0.06
Bronze
polished
50
0.1
Bronze
porous, rough
50–150
0.55
Bronze
powder
0.76–0.80
Carbon
candle soot
0.95
Carbon
charcoal powder
0.96
Carbon
graphite powder
0.97
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Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Carbon
graphite, filed
surface
20
0.98
Carbon
lampblack
20–400
0.95–0.97
Chipboard
untreated
20
SW
0.90
Chromium
polished
50
0.10
Chromium
polished
500–1000
0.28–0.38
Clay
fired
70
0.91
Cloth
black
20
0.98
20
0.92
Concrete
Concrete
dry
36
SW
0.95
Concrete
rough
17
SW
0.97
Concrete
walkway
LLW
0.974
Copper
commercial,
burnished
20
0.07
Copper
electrolytic, carefully polished
80
0.018
Copper
electrolytic,
polished
–34
0.006
Copper
molten
1100–1300
0.13–0.15
Copper
oxidized
50
0.6–0.7
Copper
oxidized to
blackness
0.88
Copper
oxidized, black
27
0.78
Copper
oxidized, heavily
20
0.78
Copper
polished
50–100
0.02
Copper
polished
100
0.03
Copper
polished,
commercial
27
0.03
Copper
polished,
mechanical
22
0.015
Copper
pure, carefully
prepared surface
22
0.008
Copper
scraped
27
0.07
Copper dioxide
powder
0.84
Copper oxide
red, powder
0.70
0.89
80
0.85
20
0.9
Ebonite
Emery
coarse
Enamel
Enamel
lacquer
20
0.85–0.95
Fiber board
hard, untreated
20
SW
0.85
Fiber board
masonite
70
SW
0.75
Fiber board
masonite
70
LW
0.88
Fiber board
particle board
70
SW
0.77
Fiber board
particle board
70
LW
0.89
Fiber board
porous, untreated
20
SW
0.85
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Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Glass pane (float
glass)
non-coated
20
LW
0.97
14
Gold
polished
130
0.018
Gold
polished, carefully
200–600
0.02–0.03
Gold
polished, highly
100
0.02
Granite
polished
20
LLW
0.849
Granite
rough
21
LLW
0.879
Granite
rough, 4 different
samples
70
SW
0.95–0.97
Granite
rough, 4 different
samples
70
LW
0.77–0.87
20
0.8–0.9
Gypsum
Ice: See Water
Iron and steel
cold rolled
70
SW
0.20
Iron and steel
cold rolled
70
LW
0.09
Iron and steel
covered with red
rust
20
0.61–0.85
Iron and steel
electrolytic
100
0.05
Iron and steel
electrolytic
22
0.05
Iron and steel
electrolytic
260
0.07
Iron and steel
electrolytic, carefully polished
175–225
0.05–0.06
Iron and steel
freshly worked
with emery
20
0.24
Iron and steel
ground sheet
950–1100
0.55–0.61
Iron and steel
heavily rusted
sheet
20
0.69
Iron and steel
hot rolled
130
0.60
Iron and steel
hot rolled
20
0.77
Iron and steel
oxidized
100
0.74
Iron and steel
oxidized
100
0.74
Iron and steel
oxidized
1227
0.89
Iron and steel
oxidized
125–525
0.78–0.82
Iron and steel
oxidized
200
0.79
Iron and steel
oxidized
200–600
0.80
Iron and steel
oxidized strongly
50
0.88
Iron and steel
oxidized strongly
500
0.98
Iron and steel
polished
100
0.07
Iron and steel
polished
400–1000
0.14–0.38
Iron and steel
polished sheet
750–1050
0.52–0.56
Iron and steel
rolled sheet
50
0.56
Iron and steel
rolled, freshly
20
0.24
Iron and steel
rough, plane
surface
50
0.95–0.98
Iron and steel
rusted red, sheet
22
0.69
Iron and steel
rusted, heavily
17
SW
0.96
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Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Iron and steel
rusty, red
20
0.69
Iron and steel
shiny oxide layer,
sheet,
20
0.82
Iron and steel
shiny, etched
150
0.16
Iron and steel
wrought, carefully
polished
40–250
0.28
Iron galvanized
heavily oxidized
70
SW
0.64
Iron galvanized
heavily oxidized
70
LW
0.85
Iron galvanized
sheet
92
0.07
Iron galvanized
sheet, burnished
30
0.23
Iron galvanized
sheet, oxidized
20
0.28
Iron tinned
sheet
24
0.064
Iron, cast
casting
50
0.81
Iron, cast
ingots
1000
0.95
Iron, cast
liquid
1300
0.28
Iron, cast
machined
800–1000
0.60–0.70
Iron, cast
oxidized
100
0.64
Iron, cast
oxidized
260
0.66
Iron, cast
oxidized
38
0.63
Iron, cast
oxidized
538
0.76
Iron, cast
oxidized at 600°C
200–600
0.64–0.78
Iron, cast
polished
200
0.21
Iron, cast
polished
38
0.21
Iron, cast
polished
40
0.21
Iron, cast
unworked
900–1100
0.87–0.95
Krylon Ultra-flat
black 1602
Flat black
Room temperature up to 175
LW
≈ 0.96
12
Krylon Ultra-flat
black 1602
Flat black
Room temperature up to 175
MW
≈ 0.97
12
Lacquer
3 colors sprayed
on Aluminum
70
SW
0.50–0.53
Lacquer
3 colors sprayed
on Aluminum
70
LW
0.92–0.94
Lacquer
Aluminum on
rough surface
20
0.4
Lacquer
bakelite
80
0.83
Lacquer
black, dull
40–100
0.96–0.98
Lacquer
black, matte
100
0.97
Lacquer
black, shiny,
sprayed on iron
20
0.87
Lacquer
heat–resistant
100
0.92
Lacquer
white
100
0.92
Lacquer
white
40–100
0.8–0.95
Lead
oxidized at 200°C
200
0.63
Lead
oxidized, gray
20
0.28
#T559880; r. AL/45866/46124; en-US
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35
Emissivity tables
Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Lead
oxidized, gray
22
0.28
Lead
shiny
250
0.08
Lead
unoxidized,
polished
100
0.05
100
0.93
100
0.93
0.75–0.80
Lead red
Lead red, powder
Leather
tanned
Lime
0.3–0.4
Magnesium
22
0.07
Magnesium
260
0.13
538
0.18
20
0.07
0.86
1500–2200
0.19–0.26
600–1000
0.08–0.13
700–2500
0.1–0.3
17
SW
0.87
Magnesium
Magnesium
polished
Magnesium
powder
Molybdenum
Molybdenum
Molybdenum
filament
Mortar
Mortar
dry
36
SW
0.94
Nextel Velvet
811-21 Black
Flat black
–60–150
LW
> 0.97
10 and
11
Nichrome
rolled
700
0.25
Nichrome
sandblasted
700
0.70
Nichrome
wire, clean
50
0.65
Nichrome
wire, clean
500–1000
0.71–0.79
Nichrome
wire, oxidized
50–500
0.95–0.98
Nickel
bright matte
122
0.041
Nickel
commercially
pure, polished
100
0.045
Nickel
commercially
pure, polished
200–400
0.07–0.09
Nickel
electrolytic
22
0.04
Nickel
electrolytic
260
0.07
Nickel
electrolytic
38
0.06
Nickel
electrolytic
538
0.10
Nickel
electroplated on
iron, polished
22
0.045
Nickel
electroplated on
iron, unpolished
20
0.11–0.40
Nickel
electroplated on
iron, unpolished
22
0.11
Nickel
electroplated,
polished
20
0.05
Nickel
oxidized
1227
0.85
Nickel
oxidized
200
0.37
Nickel
oxidized
227
0.37
#T559880; r. AL/45866/46124; en-US
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35
Emissivity tables
Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Nickel
oxidized at 600°C
200–600
0.37–0.48
Nickel
polished
122
0.045
Nickel
wire
200–1000
0.1–0.2
1000–1250
0.75–0.86
Nickel oxide
Nickel oxide
500–650
0.52–0.59
Oil, lubricating
0.025 mm film
20
0.27
Oil, lubricating
0.050 mm film
20
0.46
Oil, lubricating
0.125 mm film
20
0.72
Oil, lubricating
film on Ni base:
Ni base only
20
0.05
Oil, lubricating
thick coating
20
0.82
Paint
8 different colors
and qualities
70
SW
0.88–0.96
Paint
8 different colors
and qualities
70
LW
0.92–0.94
Paint
Aluminum, various ages
50–100
0.27–0.67
Paint
cadmium yellow
0.28–0.33
Paint
chrome green
0.65–0.70
Paint
cobalt blue
0.7–0.8
Paint
oil
17
SW
0.87
Paint
oil based, average of 16 colors
100
0.94
Paint
oil, black flat
20
SW
0.94
Paint
oil, black gloss
20
SW
0.92
Paint
oil, gray flat
20
SW
0.97
Paint
oil, gray gloss
20
SW
0.96
Paint
oil, various colors
100
0.92–0.96
Paint
plastic, black
20
SW
0.95
Paint
plastic, white
20
SW
0.84
Paper
4 different colors
70
SW
0.68–0.74
Paper
4 different colors
70
LW
0.92–0.94
Paper
black
0.90
Paper
black, dull
0.94
Paper
black, dull
70
SW
0.86
Paper
black, dull
70
LW
0.89
Paper
blue, dark
0.84
Paper
coated with black
lacquer
0.93
Paper
green
0.85
Paper
red
0.76
Paper
white
20
0.7–0.9
Paper
white bond
20
0.93
Paper
white, 3 different
glosses
70
SW
0.76–0.78
#T559880; r. AL/45866/46124; en-US
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35
Emissivity tables
Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Paper
white, 3 different
glosses
70
LW
0.88–0.90
Paper
yellow
0.72
17
SW
0.86
Plaster
plasterboard,
untreated
20
SW
0.90
Plaster
rough coat
20
0.91
Plastic
glass fibre laminate (printed circ.
board)
70
SW
0.94
Plastic
glass fibre laminate (printed circ.
board)
70
LW
0.91
Plastic
polyurethane isolation board
70
LW
0.55
Plastic
polyurethane isolation board
70
SW
0.29
Plastic
PVC, plastic floor,
dull, structured
70
SW
0.94
Plastic
PVC, plastic floor,
dull, structured
70
LW
0.93
Platinum
100
0.05
Platinum
1000–1500
0.14–0.18
Platinum
1094
0.18
Platinum
17
0.016
Platinum
22
0.03
Platinum
260
0.06
Platinum
538
0.10
Plaster
Platinum
pure, polished
200–600
0.05–0.10
Platinum
ribbon
900–1100
0.12–0.17
Platinum
wire
1400
0.18
Platinum
wire
500–1000
0.10–0.16
Platinum
wire
50–200
0.06–0.07
Porcelain
glazed
20
0.92
Porcelain
white, shiny
0.70–0.75
Rubber
hard
20
0.95
Rubber
soft, gray, rough
20
0.95
Sand
Sand
0.60
20
0.90
Sandstone
polished
19
LLW
0.909
Sandstone
rough
19
LLW
0.935
Silver
polished
100
0.03
Silver
pure, polished
200–600
0.02–0.03
Skin
human
32
0.98
Slag
boiler
0–100
0.97–0.93
Slag
boiler
1400–1800
0.69–0.67
Slag
boiler
200–500
0.89–0.78
#T559880; r. AL/45866/46124; en-US
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35
Emissivity tables
Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Slag
boiler
600–1200
0.76–0.70
Soil
dry
20
0.92
Soil
saturated with
water
20
0.95
Stainless steel
alloy, 8% Ni, 18%
Cr
500
0.35
Stainless steel
rolled
700
0.45
Stainless steel
sandblasted
700
0.70
Stainless steel
sheet, polished
70
SW
0.18
Stainless steel
sheet, polished
70
LW
0.14
Stainless steel
sheet, untreated,
somewhat
scratched
70
SW
0.30
Stainless steel
sheet, untreated,
somewhat
scratched
70
LW
0.28
Stainless steel
type 18-8, buffed
20
0.16
Stainless steel
type 18-8, oxidized at 800°C
60
0.85
Stucco
rough, lime
10–90
0.91
Styrofoam
insulation
37
SW
0.60
0.79–0.84
Tar
paper
20
0.91–0.93
Tile
glazed
17
SW
0.94
Tin
burnished
20–50
0.04–0.06
Tin
tin–plated sheet
iron
100
0.07
Titanium
oxidized at 540°C
1000
0.60
Titanium
oxidized at 540°C
200
0.40
Titanium
oxidized at 540°C
500
0.50
Titanium
polished
1000
0.36
Titanium
polished
200
0.15
Titanium
polished
500
0.20
Tungsten
1500–2200
0.24–0.31
Tungsten
200
0.05
Tungsten
600–1000
0.1–0.16
Snow: See Water
Tar
Tungsten
filament
3300
0.39
Varnish
flat
20
SW
0.93
Varnish
on oak parquet
floor
70
SW
0.90
Varnish
on oak parquet
floor
70
LW
0.90–0.93
Wallpaper
slight pattern,
light gray
20
SW
0.85
Wallpaper
slight pattern, red
20
SW
0.90
Water
distilled
20
0.96
#T559880; r. AL/45866/46124; en-US
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35
Emissivity tables
Table 35.1 T: Total spectrum; SW: 2–5 µm; LW: 8–14 µm, LLW: 6.5–20 µm; 1: Material; 2: Specification;
3:Temperature in °C; 4: Spectrum; 5: Emissivity: 6:Reference (continued)
Water
frost crystals
–10
0.98
Water
ice, covered with
heavy frost
0.98
Water
ice, smooth
0.97
Water
ice, smooth
–10
0.96
Water
layer >0.1 mm
thick
0–100
0.95–0.98
Water
snow
0.8
Water
snow
–10
0.85
Wood
17
SW
0.98
Wood
19
LLW
0.962
0.5–0.7
Wood
ground
Wood
pine, 4 different
samples
70
SW
0.67–0.75
Wood
pine, 4 different
samples
70
LW
0.81–0.89
Wood
planed
20
0.8–0.9
Wood
planed oak
20
0.90
Wood
planed oak
70
SW
0.77
Wood
planed oak
70
LW
0.88
Wood
plywood, smooth,
dry
36
SW
0.82
Wood
plywood,
untreated
20
SW
0.83
Wood
white, damp
20
0.7–0.8
Zinc
oxidized at 400°C
400
0.11
Zinc
oxidized surface
1000–1200
0.50–0.60
Zinc
polished
200–300
0.04–0.05
Zinc
sheet
50
0.20
#T559880; r. AL/45866/46124; en-US
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#T559880; r. AL/45866/46124; en-US
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LOEF (List Of Effective Files)
T501011.xml; en-US; AL; 45866; 2017-10-18
T505552.xml; en-US; 9599; 2013-11-05
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T505013.xml; en-US; 39689; 2017-01-25
T505652.xml; en-US; 39869; 2017-01-31
T505192.xml; en-US; 39872; 2017-01-31
T505193.xml; en-US; 39571; 2017-01-20
T505194.xml; en-US; 39872; 2017-01-31
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Website
last
page
http://www.flir.com
Customer support
http://support.flir.com
Copyright
© 2017, FLIR Systems, Inc. All rights reserved worldwide.
Disclaimer
Specifications subject to change without further notice. Models and accessories subject to regional market considerations. License procedures may apply.
Products described herein may be subject to US Export Regulations. Please refer to exportquestions@flir.com with any questions.
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T559880
AL
45866
46124
en-US
2017-10-18
2017-10-31

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Language                        : en-us
Flir Scms Spath                 : 140
Flir Scms Xtitle                : Applies to: T600, T600bx, T610, T620, T620bx, T630, T630sc, T640, T640bx, T650sc, T660.
Flir Scms Type                  : 
Flir Scms Title                 : Manual: FLIR T6xx series
Flir Scms Swver                 : 
Flir Scms Snappl                : 
Flir Scms Release               : AL
Flir Scms Publno                : T559880
Flir Scms Pnappl                : Applies to: 55903-1015, 55903-0922, 55903-1016, 55903-1022, 55903-1007, 55903-1008, 55903-1017, 55903-1522, 55903-2823, 55903-2822, 55903-2923, 55903-2922, 55903-8022, 55903-3922, 55903-4022, 55903-5023, 55903-5022, 55903-5125, 55903-5122, 55903-5123, 55903-5124, 55903-5223, 55903-5222, 55903-5623, 55903-5622, 55903-5723, 55903-5722, 55903-5823, 55903-5822, 55904-6222, 55904-6322, 55904-6422, 55904-8023, 55904-8123, 55904- 8124, 55904-8223, 55904-6823, 55904-6822, 55904-6925, 55904-6922, 55904-6923, 55904-6924, 55904-7023, 55904-7022, 55904-7423, 55904-7422, 55904-7523, 55904-7522, 55904-7623, 55904-7622, 55904-7723, 55904-7823, 55904-7824, 55904-7825, 55904-7923, 55904-8423, 55904-8422, 55904-8523, 55904-8522, 55904-8524, 55904-8525, 55904-8623, 55904-8622.
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Author                          : Copyright 2017, FLIR Systems, Inc. All rights reserved worldwide.
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