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80
Advantages
60 1. Economy
2. Wide temperature spans
40
3. Simple
20 Disadvantages
1. Lower sensitivity
0
0 2 4 6 8 10 12 14 16 2. Susceptible to absorption errors due to
WAVELENGTH (MICROMETERS) sight path conditions
Fig. 1 Water Vapor Transmission Characteristics
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RATIO THERMOMETERS
A ratio thermometer measures radiated energy in
two narrow bands and calculates the ratio of the
two energies. This ratio is a temperature-depen-
M67 dent function. The temperature measurement is
Fig. 2 A Modern Infrared Thermometer not primarily dependent on the energy in the two
bands, only on the ratio of the two energies.
Therefore, any influence that affects the amount
BAND-PASS THERMOMETERS of energy in each band by the same percentage
Band-pass thermometers were initially derived has no effect on the temperature indication.
from simple, broadband thermometers. Lens, Changes in target size have no effect. If the emis-
window, or filter characteristics were selected to sivity of the target is the same at both wave-
view only a selected portion of the spectrum. The lengths, the indicated temperature is not changed
5 ±0.2µm band-pass was used to measure glass by changes in emissivity. Unfortunately, this con-
surface temperature because glass emits strongly dition is not fulfilled by all oxidizable materials.
in this region, but poorly below or immediately For other materials, the ratio techniques may
above this band. However, an 8-14µm band-pass reduce or eliminate changes in indicated temper-
can be used to measure glass surface if the glass ature caused by changes in surface finish. The
has surroundings cooler than itself. The 8-14µm ratio technique may reduce the effect of energy-
band is also preferred for low temperature, absorbing materials such as particulates or C02
general-purpose use because energy in this band between the target and the thermometer, if the
is not attenuated by atmospheric moisture. percentage of absorption is the same at each
wavelength.
RATIO:
NARROW BAND THERMOMETERS
Advantages
Narrow band thermometers operate over a
narrow range of wavelengths. The spectral 1. Less sensitive to varying target size or
response of many narrow band thermometers is intermittent blockage of sight path by
smoke, particles, etc.
determined by the optical filter used. Such
narrow band thermometers are used as general- Disadvantages
purpose instruments over the temperature range 1. Higher cost
of interest. For example, a thermometer using a 2. Need to know ratio of emissivity in the
silicon cell detector will have a response that two wavebands of measurement.
peaks at 0.9µm. The upper limit of usefulness is
3. Sensitive to changes in ratio of
about 1.1µm. Such a thermometer can only be emissivities
used at temperatures above 600°C (1100°F).
Other narrow band thermometers utilize filters to
restrict response to a selected wavelength to meet
OPTICAL PYROMETERS
the needs of a particular application. Some Although optical pyrometers are no longer manu-
examples are: factured in significant numbers, there are proba-
bly hundreds of thousands in everyday use, and
Wavelength-µm Application
they are sufficiently unique in design and use to
0.65 Accurate measurement of high warrant a separate discussion.
temperature objects in the open
An optical pyrometer measures the radiation from
3.43 ± 0.2 Thin film, polyethylene-type the target in a narrow band of visible
plastics wavelengths, centered at about 0.65 µm in the
red/yellow portion of the spectrum. The most
3.86 To measure through
commonly used optical pyrometers are manually
products of combustion
operated. The operator sights the pyrometer on
the target. At the same time he can see in the
NARROW BAND: eyepiece the image of an internal tungsten lamp
Advantages filament.
1. High accuracy even when emissivity The operator matches the filament color to the
unknown or varying, if short wavelength target by varying the
units chosen. For measuring in the open current through the
2. Selected wave-bands for looking at or filament with a
through glass, plastics and flames. rheostat, and when
Disadvantages the target image and
the tungsten fila-
1. Narrow temperature spans ment image are the
2. Difficult to select optimum unit to meet same color, the tar- M90
all criteria. get temperature can
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be read from a scale on the rheostat knob. When receives, and radiates more thermal radiation for
the target and filament colors are the same, the fil- all wavelength intervals than any other mass of
ament image apparently vanishes, so these the same area and temperature.
pyrometers have also been called disappearing
filament pyrometers.
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102
WIEN-PLANCK LAW
The Wien-Planck Law expresses the radiation 300 K
10
emitted per unit area of a blackbody as a function
of wavelength, λ , and temperature, T.
JλT dλ = C1λ-5(∋ C /λΤ – 1)–1dλ
2 1
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NON-BLACKBODY RADIATION
The blackbody is an ideal concept. Real objects Thus, for any opaque body the emittance (e)
do not emit radiation as blackbodies, but at some equals the absorbance (a).
lower rate. The ratio of the energy radiated by a If the object is translucent, like some plastics or
body to that radiated by a blackbody at the same glass, some of the energy incident on the object
temperature is emittance (e), a number less than will be transmitted through the object. Therefore,
1. If the body is opaque, the emittance (e) is in general, t is transmittance, and
related to the reflectance (r) of the body by:
e+r+t=1
e + r = 1 or e = 1 – r
For most materials, e, r, and t are functions of
To understand that this must be true, consider an wavelength.
opaque object at temperature T, which is at equi-
librium with its surroundings. This means that Fig. 5 illustrates the variation in emittance with
temperature T is not changing. Nearby bodies wavelength for some materials. In general, the
radiate energy according to their temperatures, emittance of metals is highest at short wave-
some of which reaches the object. Some energy lengths. The emittance of ceramics is highest at
is reflected by the object. The remainder is long wavelengths.
absorbed. But the object is also emitting radia- Because emittance is wavelength-dependent and
tion proportional to its temperature, T. If the tem- the amount of energy radiated at each wavelength
perature is not changing, then the absorbed radi- depends on temperature, the apparent emittance,
ation must be balanced by the emitted radiation. also referred to as emissivity, of a material
If the emitted energy is greater than the absorbed depends on the temperature at which it was
energy, the object will cool. If the object absorbs determined, at the wavelengths at which the mea-
more than it emits, the temperature will increase. surement is taken.
1.0
PYREX
Total Spectral 0.65-1.0µm
Aluminum 0.8 SILICON
Unoxidized 0.02 – 0.15 0.05 – 0.25
Lightly oxidized 0.1 – 0.2 0.2 – 0.3 SAPPHIRE
0.6
EMISSIVITY
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objective mirror
eyepiece
lens
detector (b)
detector
beam splitting prism housing
(c) Fig. 7 The Arrangement of One Type of Industrial Infrared Thermometer
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receives radiation through a small opening in the tors, this release of charge is measured as a
reflector. The radiation multiply reflected change in resistance. In photovoltaic detectors,
between the mirror and the target appears to the such as silicon, germanium, and indium anti-
detector to be from a blackbody. A commercial monide, the release of a charge produces a volt-
thermometer using this principle can read the age output.
temperature of targets with emittance as low as
The release of electrons and “holes” in photo-
0.6 without correction. The reflector must be
conductive and photovoltaic detectors requires
placed close to the surface being measured to
that arriving photons have a minimum energy that
exclude extraneous radiation and prevent radia-
depends on the molecular structure of the detec-
tion losses.
tor material. Thus, all photon detectors have a
maximum wavelength (minimum photon energy)
ELEMENTS OF beyond which they do not respond. The peak
INFRARED THERMOMETERS response is usually at a wavelength a little shorter
than the cutoff wavelength.
The selection of a detector and optical elements
for an IRT is normally the concern of the ther- The approximate peak response wavelengths of
mometer vendor who balances out the conflicting some photon detectors are:
elements of cost, accuracy, speed of response, Material Wavelength, µm
and usable temperature range. The user should Silicon 0.9
be aware of how the selection of detectors and Germanium 1.7
optical elements influences the range of wave- Lead sulfide 2.5
lengths over which a thermometer responds. Indium arsenide 3.0
When applying an IRT to the measurement of Indium antimonide 6.0
products in the presence of atmospheric absorp-
tion or reflections from other objects, or when try- Pyroelectric detectors respond to changes in
ing to measure the temperature of materials such received radiation with a changing surface charge.
as glass or plastics, the spectral response of an IRT Because it responds to changes in incoming radia-
will determine whether a usable temperature tion, the detector need not reach thermal equilib-
measurement is possible. rium when the target temperature changes.
However, the incoming radiation must be
chopped, and the detector signal cannot be uti-
DETECTORS lized directly. The detector changes can be
Detectors for IRTs are of three types: thermal, likened to a change in charge of a capacitor, which
photon, and pyroelectric. Thermal detectors must be read with high impedance circuitry.
reach an equilibrium temperature proportional to Pyroelectric detectors bear a radiation-absorbent
the temperature of the target. The detector output coating, so they can have a spectral response as
is then interpreted as target temperature. The broad as thermal detectors, or, by selecting the
most common thermal detectors today are ther- characteristics of the coating, a more restricted
mopiles and thermistor bolometers. response.
A thermopile consists of one or more minute ther-
mocouples connected in series. The output, as OPTICAL SYSTEMS
from any thermocouple, is a DC millivoltage.
Thermopiles may be manufactured from thin The optical system of an IRT may be composed of
strips of metal or, more commonly, vacuum lenses or mirrors or combinations of both. In gen-
deposited on a substrate. Usually, both eral, the reflectivity of mirrors is not significantly
thermopiles and bolometers are blackened with dependent on wavelength over the range of
carbon black or wavelengths used for industrial temperature
other broadband
absorbing material Refractive Cut-off Mechanical &
so that they respond Material Index Wavelength - µm Chemical Stability Remarks
to radiation through- Glass 1.5 2.8 Excellent Excellent transmission
out the entire spec- in the visible.
Fused Silica 1.4 4.0 Excellent Excellent transmission
trum, thus the com- in the visible.
mon term, broad- Calcium Fluoride 1.4 10.0 Good Good visible transmission.
band detectors. Relatively high
chromatic aberration.
Photon detectors Arsenic trisulfide 2.35 12.0 Good Low transmission
respond to incident in the visible. Low
radiation by releas- chromatic aberration.
ing electric charges. Zinc Sulfide 2.25 14.0 Good Very low transmission
in the visible.
In lead sulfide and
Polyethylene — 20.0 Poor Sometimes used as
lead selenide photo- window. Easily distorted
conductive detec- or crazed by heat
Table 3. Properties of Lens and Window Materials
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measurement. Therefore, mirror systems do not only if the image in the focal plane is large rela-
determine the spectral response of the pyrometer. tive to the lens, and the focal plane is many lens
A mirror system must usually be protected from diameters from the lens, will the actual field of
dirt and physical damage by a window. The char- view be given by the angle θ. The actual FOV is
acteristics of the window, and those of the detec- always larger.
tor, determine the band of wavelengths over
Most thermometers have images in the focal
which the thermometer responds.
plane that are the same diameter as the lens or
Mirror systems have been common mainly in smaller, so the statement of an angular FOV is not
fixed focus optical systems. To vary the focus of sufficient definition. Therefore, diagrams or
an optical system requires that at least one ele- tables are usually used to define the FOV. In
ment be movable. Providing for this motion in practice, any statement of the FOV is only an
mirror systems is often more complicated than in approximation because of spherical and chromat-
lens systems. The selection of lens and window ic aberration in the optics. Spherical aberration
materials is always a compromise between the is caused by the fact that rays hitting the lens
optical and physical properties of the material remote from its axis are bent more than rays pass-
and the desired wavelength response of the ing the lens near its axis. A circular field stop is
pyrometer. The properties of some typical lens therefore imaged as a circle with a fuzzy halo
and window materials are given in Table 3. around it. Mirrors also have spherical aberration.
Chromatic aberration occurs because the refrac-
FIELD OF VIEW tive index of optical materials changes with wave-
length. At shorter wavelengths the refractive
The field of view (FOV) of an IRT is a statement of index is lower, and rays exiting are bent more and
the size of the target at a specified distance from focus nearer the lens. Rays of longer wavelengths
the thermometer. This may be stated in the form are focused farther from the lens. The image of a
of a diagram, a table of target sizes versus dis- field stop over a band of wavelengths is therefore
tance, sometimes simply as the target size at the a fuzzy image.
focal plane and the distance to the focal plane, or
as an angular FOV. Other and generally smaller contributions to
fuzziness of the FOV are scattering of rays of light
by imperfections in the optical material and
reflections from the internal parts of the IRT.
Good quality materials minimize the former
cause. Roughening and blackening of interior
surfaces to reduce reflections reduce the latter
effect.
There are no standards at present for stating the
FOV of IRTs. Some manufacturers state an FOV
that includes the effects of aberrations; others do
not. In practice, it is preferable to select an FOV
which is smaller in diameter than the target, but
if the target and the FOV diameters are almost the
Fig. 9 The Field of View of a Perfect Infrared Thermometer same size, it may be advisable to determine the
FOV experimentally as follows:
Sight the IRT on a target that gives a steady, uni-
If the output of an IRT is to be the same as its form source of radiation. At the focal plane, inter-
calibrated output, the target must fill the FOV. If pose a series of apertures of different diameter
the target fills the FOV at any distance from the between the IRT and the target, and plot the out-
thermometer, the output will be the calibrated put of the IRT against the aperture area. For aper-
output, or nearly so, as discussed below. The ture areas less than the nominal target area, the
image of the field stop in the focal plane in most output of the IRT should increase directly propor-
thermometers is larger than the diameter of the tional to aperture area. Above the nominal target
field stop. θ is the angular FOV. Between the area the output should increase only a small
aperture stop and the focal plane, the FOV is amount with further increases in aperture area.
determined by the stop diameter and the image
diameter. A perfect IRT would show no increase, but no
such IRT exists. Increases of a few tenths of a per-
Lines drawn from the extremities of the image to cent in output for each doubling of the aperture
the extremities of the aperture stop enclose the area indicate that the nominal field of view takes
FOV. Beyond the focal plane the field of view is into account the effects of aberrations. If these
determined by rays extending from the extremi- are not taken into account, the IRT may show a
ties of the aperture stop through the extremities of significant increase in output as the viewable tar-
the image in the focal plane. Fig. 9 shows that get area is increased above the nominal value.
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••
detectors, a spherical
•••
••••••••
blackbody calibration infrared temperature-measuring instruments peri-
source makes the best odically submitting transfer standards to the
design compromise; it
includes the smallest national standards organization for calibration
•• possible practical aper- against a primary standard. The transfer standard
Aperture •• •• ture, preferably with a may be a resistance thermometer, thermocouple,
tube
•••••••• tube extension.
infrared thermometer, or variable-temperature
•••••••
Castable ceramic Heating
blackbody source. Once
• • • the measurement
uncertainty of the transfer standard has been
••
refractory material
•••
elements
••••••••
established and documented, it is used as a com-
parator for checking other transfer standards or for
over the target surface, accurate temperature checking working standards. Its calibration
••
control, fast stabilization at a new temperature integrity is maintained by special manufacturing
••
••
setting, long-term temperature stability, and, of methods and careful storage and use. The reality
••••••••
course, the highest emissivity over the prescribed of this classic calibration traceability protocol is
spectral band. Other considerations that may that the time needed and the cost involved for
••••••••••• •• enter into the design are aperture acceptance
•••
angle, overall size, portability, power consump-
national standards organizations to carry out this
work usually is prohibitive for most intending
•••
tion, and the need for remote control and data participants, due to the standards organizations’
•• •••••••••• acquisition.
CALIBRATION TRACEABILITY
•••••••••••• The most common application for blackbody
••••••••••• •• ••• Heating elements
•••
••••••••••••
••••sources
•• is the calibration of radiometers and Castable ceramic
infrared thermometers. Because these devices are
•• ••••••••••• refractory material
••••••
•••••••••••• emissivity dependent—that is, their measurement
•••••••••••• Cylindrical cavity Blackbody
accuracy is related to the infrared emitting prop- cavity
erty of the target of interest—the only way to ••••••••••••
••••••••••••
determine measurement uncertainty with a high ••••••••
Refractory
• • • • • •• • • ••• •• level of assurance is to calibrate against a source
•••••••••
Blackbody Heating
••••••
•••
••••••••
••••• of known emissivity and temperature. This then
raises the question of how to be assured that the
••
calibration source is accurate, and superficially
••••••••••••
•• ••••••••••••
Conical cavity
surface elements
• • • •
••••••••• ••• this would seem to lead into a realm of doubt that
••••••••••••• •••••••••••••
••••••••••
has no end, other than in crippling paranoia.
Fortunately, the Calibration Traceability protocol
• • •••
••••
••
••••••••
saves the intending user from this fate. ••• • •
•••••••••• ••
•••••••••••••
Calibration traceability is based on a hierarchy of
calibration standards, with the national standard Inverted conical cavity
at the top of the accountability tree. National
standards organizations such as the National FIGURE 2. To address needs such as portablility, small size, ruggedness, rapid and
frequent source temperature change, and wide temperature range capabilities, black-
Institute of Standards and Technology (NIST) in body calibration standards incorporate nonspherical cavity configurations.
the USA and the National Physical Laboratories in
the United Kingdom possess three primary types
of radiometric calibration sources; fixed-tempera- limited physical resources and budgets.
ture, freezing-point blackbody sources; variable-
temperature blackbody sources; and tungsten-
TOOLS FOR CALIBRATION STANDARDS
strip lamp sources.
The increasing demand for calibration traceabili-
More important in terms of their status as custodi-
ty brought on by a high-technology environment
ans of primary temperature standards, national
and the pervasiveness of quality-assurance
standards organizations are able to use radiomet-
programs in manufacturing has coincided with
ric measurement instruments that are capable of
the commercial development of freezing-point
higher accuracy than could be practicably
blackbody calibration sources, high-performance
achieved for working instruments in the field.
variable-temperature blackbody calibration
This is due partly to the design and partly to being
sources, and tungsten-strip lamp systems. These
able to operate them in a closely controlled
devices have enabled private-sector organizations
environment. In hierarchical terms, NIST’s stan-
to provide calibration assurance to a level that is
dards are referred to as “Primary Standards.” All
close enough to national standards for most users
other calibration standards are referred to as
and more than adequate for quality-assurance
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programs such as ISO 9000. Private-sector cali- ence tables for lamp current versus temperature.
bration laboratories usually cater to in-house The source has a current limiter to control the rate
needs, but some of these laboratories also offer of lamp current change and thereby extend lamp
the service commercially to outside customers. life. Now, more-easily used higher-emissivity car-
bon-tube sources are available, which may dis-
The assurance that the commercial calibration
place the tungsten-strip lamp as a calibration
laboratories can offer the user of radiometric sen-
method.
sors is derived largely from the freezing-point
blackbody calibration sources. These sources
provide fixed-point, primary calibration standards
for the checking of transfer standards at discrete
temperatures from 29.76°C to 1084.62°C.
The freezing-point calibration source principle of
operation is based on the temperature arrest
phenomenon, which occurs when a molten sub-
stance changes to a solid. During the cooling
curve arrest period, the substance remains at a
predictable temperature for several minutes and
then continues to cool. In the case of high-purity
FIGURE 4. For calibrating thermal imaging systems or mapping
metallic elements, the predictability of the arrest and surveillance equipment, or for long-path spectrophotometers,
temperature is very precise and thus can be used a calibration source requires a large target area. Source (on the
as a primary temperature calibration standard. right) area is 305mm square; the controller is on the left.
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realization of the Gold freezing point, 1337.33K, when the target diameter is such that the energy
the metal is first completely melted by setting the collected is equal to 98% of the energy that
controller temperature approximately 20K above would be collected for an infinitely large target.
the freezing temperature at 1357K. To insure that In this way the FOV is experimentally determined
the metal is completely molten, the furnace is to be ~140:1. In the experiments reported in this
kept at this temperature for approximately 30 paper the target distance is approximately 50cm
minutes. Then the temperature controller is set to and therefore the target size is 3.6mm. Since the
1327K, ~10K below the freezing point. The tem- target size is about 40% smaller than the cavity
perature of the freezing metal is then recorded as aperture, 6mm, negligible errors in temperature
a function of time by using a 960nm narrow band determination due to radiation originating from
radiometer as described in the next section. outside the cavity aperture are expected.
λT 2 Φ
D
δT = 14388 1n
(Φ) ( ) (1)
0.6
The undeviated light proceeds toward a 960nm,
0.4
11nm FWHM, interference filter, F. The distance
TEMPERATURE VARIATION (K)
from the back side of the objective lens to the fil- 0.3
ter varies according to the target distance from
0.1
~130mm to ~155mm. After passing through the
FREEZING PLATEAU
filter, the light proceeds ~8mm to a 0.79mm aper- 0.0
ture that is placed approximately 1mm in front of
-0.1
the active area of a 1mm diameter Silicon photo-
diode, D. The silicon photodiode is operated in -0.3
the photovoltaic mode. The current from the pho-
-0.4
todiode is measured by a Keithley 485 precision SUPERCOOL
picoammeter and is then inputted in the form of a -0.6
0 2 4 6 8 10 12
voltage to a Fluke 8842A voltmeter. The Fluke TIME (MIN)
meter has a precision of 5 digits in the voltage
range of interest. This results in a resolution of FIGURE 3. Typical Au freezing curve obtained with the NBR at 960nm,
approximately 5.6mK near the Gold freezing
point. The output of the Fluke is then sent to a The purity of the freezing metal is of extreme
computerized data acquisition system. importance in fixed point thermometry. The addi-
The field of view (FOV) of the radiometer is tion of small amounts of impurity atoms to an oth-
defined as the target distance to diameter ratio erwise pure substance alters the freezing point of
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the pure substance.5,6 Depending upon the ratio of we are ignoring temperature gradients across the
the solid solubility of the impurity to its liquid sol- freezing metal.
ubility, the equilibrium freezing point of a sub-
TABLE 1.
stance is either elevated or depressed. This Freezing-Point Depression of Au
change in the freezing point will manifest itself Resulting from the Impurity Content
through a sloping freezing plateau.7 In other Mass Freezing Point
words, the formation of the first solid after nucle- Impurity Fraction (ppm) Change (mK)
ation will occur at a temperature different from Ag 0.1 –0.2
the temperature at which the last solid is formed. Ca 0.1 –0.6
It should be cautioned, however, that a sloping Fe 0.1 –0.4
Mg 0.3 –2.8
plateau may also be due to the spatial variations
Si 0.1 –0.8
in the distribution of the emitted radiation at dif- Ti 0.5 +2.4
ferent times during the freeze and the melt.8 In the –2.4mK Total change
experiments on Gold, there is no evidence of a
slope on the steady state freezing plateau. It must
be kept in mind, however, that since the resolu- The radiometric method described in this paper,
tion is limited to 5.6mK the effect of impurities on however, relies on the cavity temperature and not
the Gold freezing point cannot be ruled out. The on the temperature at the solid-liquid interface
freezing point change due to the impurity content within the crucible. Since the graphite walls of
must therefore be considered. As a first attempt at the cavity have a finite thickness and a relatively
estimating the change in the freezing point, the small thermal conductivity, there will be a tem-
slope of the binary alloy phase diagrams in the perature drop across the wall from the freezing
vicinity of the zero impurity concentration is metal to the inside of the cavity. The temperature
used.9 However, this analysis is not possible in the drop across the cavity walls is estimated by con-
case of phase diagrams in which the equilibrium sidering the thermal conduction power from the
solidus curve has a very large slope and hence solid-liquid interface to the inside of the graphite
cannot be resolved from the diagram. As a result, cavity and the radiation power loss from the cav-
the Clausius-Clapeyron equation10 is examined in ity to the environment. The heat transfer rate from
determining the freezing point depressions. the freezing metal across the graphite crucible
Comparison between the depressions obtained base is given by
from the phase diagrams with those obtained (TAu – Tcavity)
from this equation shows that the latter predicts qc = κA
freezing point depressions that are at most half as ∆X (3)
much as the depressions extrapolated from the
phase diagrams. Hence, the Clausius-Clapeyron where TAu is the temperature of the freezing metal,
equation is used in determining the freezing point Tcavity is the temperature inside the cavity, A is the
depressions. The Clausius-Clapeyron equation for area of the crucible base, κ is the thermal con-
an ideal dilute binary solution, assuming negligi- ductivity of the graphite at TAu and ∆X is the wall
ble solid solubility of the impurity, is given by thickness. If the crucible base is not contained
within a cavity, and the only loss mechanism for
∆T ≅ RT 1n(NA)
2
the surface is radiation, then the power inputted
Lf (2) from the freezing metal qc would be radiated by
the surface to the ambient. The radiated power qr
where ∆T is the freezing point depression, T is the is given by
freezing temperature of the pure substance, NA is
the mole fraction of the pure substance, R is the qr = ∋wallσA (Tcavity4 – Tambient4)
universal gas constant and Lf is the heat of fusion (4)
of the pure substance. Given the mass fraction of
the impurities, as provided by the manufacturer,
the freezing point depression due to each impuri- where ∋ wall is the graphite emissivity and σ is the
ty is calculated independently of the others. Stefan-Boltzmann constant. However, if the base
Adding the contribution from each impurity, a is surrounded by a wall (cavity), the radiated
total freezing point depression of 2.4mK is calcu- power becomes
lated, as detailed in Table 1. The freezing point ∋
elevation due to Titanium is estimated from the qr = (1 - cavity) ∋ wallσ A (Tcavity4 – Tambient4)
phase diagrams. By making the conservative (1 - ∋ wall)
assumption that the calculated value is half that of (5)
the true value, a worst case freezing point depres-
sion of 6mK is estimated. Therefore, the tempera- where ∋ cavity is the cavity emissivity. Equating
ture of the solid-liquid interface within the cru- Equations 3 and 5, we obtain an approximate
cible is estimated to be 1337.324K. It is further solution for the temperature drop across the
assumed that the temperature of the solid-liquid graphite wall:
(1 - ∋ cavity) ∆X ∋ wallσ (Tcavity4 – Tambient4)
interface is the temperature that is immediately in (TAu – Tcavity) =
contact with the graphite crucible. In other words, (1 - ∋ wall) κ
(6)
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It is clear from equation 6 that as the cavity emis- It was shown above that using a Au FPBB, a
sivity approaches 1, the temperature drop across narrow band radiometer (NBR) at 960nm can be
the wall approaches zero. An approximate calibrated to an accuracy of (-0.17 ± 0.02)K. It
method is used to calculate the apparent emissiv- should be noted, however, that this is not the total
ity of the graphite cavity11 to be 0.99925, using a accuracy that would be obtained in the calibra-
graphite emissivity of 0.833 (Ref. 12) and not con- tion of a NBR since other factors, such as the lin-
sidering the enhancing effect of the conical end of earity of the detector and the size of source effect,
the cylindrical cavity. However, less than ideal would also contribute to the calibration error.13
conditions are assumed and the cavity emissivity An approximate relation between the calibration
is estimated to be 0.999. This emissivity is 0.1% error of the NBR and the uncertainty in the tem-
better than the apparent emissivity in the absence perature of the FPBB sources is given by:
of the aperture (lid) on the cylindrical cavity.
δTa δTβ δTa
Consequently the estimated cavity emissivity can
be confidently assumed to be not higher than the
true cavity emissivity. Hence, for calculating the
[
1n rm
δT ≅ T 2 T 2 + 1n rs
a
( )( +
Tβ2 Ta2 )]
temperature drop across the cavity wall, using (8)
equation 6, the worst case conditions
are assumed: ∋ cavity = 0.999, ∋ wall = 0.833, where Ta , Tβ , δTa , δTβ are the temperatures and
∆X =0.27cm, κ = (0.54 ± 0.03)W/cmK, and the associated uncertainties of the a and the β
TAu=1337.324K. For the ambient temperature FPBB sources, T is the measured temperature, rm
298K is assumed; however, it can readily be is the ratio of the flux at T to that at Ta and rs is the
observed, from equation 6, that the effect of the ratio of the flux at Ta to that at Tβ. It can be noted
ambient temperature on the temperature drop is from equation 8 that the error increases quadrati-
negligible and for all practical purposes that cally with temperature and in direct proportion to
term may be dropped. Inserting all of the above the errors and the uncertainties associated with
parameters in equation 6, we obtain Tcavity = the FPBB sources. Consequently, an accurate
(1337.280 ± 0.002)K. By adding the ±0.023K knowledge of the temperature of the FPBBs is
noise in quadrature to Tcavity we obtain Tcavity = extremely important since they are used for estab-
(1337.280 ± 0.023)K. lishing the effective wavelengths of the NBRs as
well as serving as pivotal points of calibration.
A radiometer viewing the cavity, however,
assumes that the cavity emissivity is 1, and as a In both industry and research institutions, increas-
result outputs an apparent temperature Ta given ingly accurate non-contact temperature measure-
by: ments are demanded. Thus, the uncertainty of
1 1 λ these measurements has to be established through
∋
Ta = Tcavity – 14388 1n( cavity ) an accurate means for calibrating infrared ther-
(7) mometers, radiometers, imaging pyrometers,
spectrographic analyzers, and related non-con-
Inserting Tcavity = (1337.280 ± 0.023)K, tact instruments. The FPBB source is a useful and
λ=0.960µm, and ∋ cavity = 0.999 in equation 7, we compact primary standard for calibrating such
obtain Ta = (1337.1610.023)K. Therefore, using instruments, either directly or indirectly through
the Gold FPBB source, the total accuracy in cali- the use of VTBB sources.
brating a narrow band radiometer at 0.960µm is
(-0.17 ± 0.02)K.
References:
1. J. C. Richmond and D. P. DeWitt, eds., Applications of Radiation Thermometry (American
CONCLUSION Society for Testing and Materials, Philadelphia, 1985).
2. H. Preston-Thomas, “The International Temperature Scale of 1990 (ITS-90),” Metrologia
Using the freezing point blackbody (FPBB) 27, 3-10 (1990).
3. F. Sakuma and S. Hattori, “A practical-type fixed point blackbody furnace,” in
sources, high quality transfer standard radiome- Temperature, Its Measurement and Control in Science and Industry, J. F. Schooley, ed.
ters may be calibrated. For example, assuming (American Institute of Physics, New York, 1982), Vol. 5 pp. 535-539.
4. J. Fischer and H. J. Jung, “Determination of the thermodynamic temperatures of the freez-
that the effective wavelength of the transfer stan- ing points of silver and gold by near-infrared pyrometry.” Metrologia 26, 245-252 (1989).
dard radiometer does not vary with temperature, 5. M. C. Flemings, Solidification Processing (McGraw-Hill, New York, 1974).
one can use any two FPBB sources to obtain the 6. L. S. Darken and R. W. Gurry, Physical Chemistry of Metals (McGraw-Hill, New York,
1953), Chaps. 10–12, pp. 235-325.
mean-effective wavelength of the radiometer. 7. E. H. McLaren, “The freezing points of high purity metals as precision temperature stan-
Then the radiance temperature of any variable dards,” in Temperature, Its Measurement and Control in Science and Industry, C. M.
Herzfeld, ed. (Reinhold, New York, 1962), Vol. 3, pp. 185-198.
temperature blackbody (VTBB) source may be 8. K. D. Mielenz, R. D. Saunders, Jr., and J. B. Shumaker, “Spectroradiometric determination
easily determined by dividing the flux from it to of the freezing temperature of gold,” J. Res. Natl. Inst. Stand. Technol. 95, 49-67 (1990).
9. H. Baker, ed., American Society of Metals Handbook, Alloy Phase Diagrams (ASM
the flux from a FPBB source and using Planck’s Materials Park, Ohio, 1992), Vol. 3, pp. 2:65-2:79.
law. Hence, using transfer standard radiometers, 10. O. Kubaschewski and C. B. Alcock, Metallurgical Thermo-Chemistry (Pergamon, New
York, 1979), Chap. 1, p. 45.
radiance temperature is routinely transferred to 11. T. J. Quinn, “The calculation of the emissivity of cylindrical cavities giving near blackbody
VTBB sources, which are in turn used for the cal- radiation,” Br. J. Appl. Phys. 18, 1105-1113 (1967).
ibration of non-contact thermometers. In this way 12. Y. S. Touloukian and D. P. DeWitt, eds., Thermal Radiative Properties, Nonmetallic Solids
(IFI/Plenum, New York, 1972), Vol. 8, pp. 44-50.
a hierarchy of calibration standards has been 13. T. Ricolfi and M. Battuello, “Precision infrared thermometer for the temperature interval
established that is used in practical radiometric 232°C - 1085°C,” in Temperature, Its Measurement and Control in Science and Industry,
J. F. Schooley, ed. (American Institute of Physics, New York, 1992), Vol. 6, Part 2, pp. 797-
sensor calibration. 800.
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