Microprocessors, instrumentation and control

Charles J. Fraser , ... (Sections iii.5.i–iii.v.eight), in Mechanical Engineer'due south Reference Book (Twelfth Edition), 1994

3.5.eight.5 Radiation thermometers

Radiations thermometers (which were formerly known equally pyrometers) are not based on whatsoever change of property with temperature only use the electromagnetic radiation from a body to be measured. Every bit the body warms up, the total radiations it emits increases apace (with the fourth power of the absolute temperature) and the spectral distribution shifts to shorter wavelengths. The temperature can thus be determined past measuring the radiations, and there is the clear advantage that all the detecting equipment is remote from the hot trunk. Limitations to the technique are that it is more hard to mensurate lower temperatures, where the energy emitted is much less, and that the emissivity of the radiating surface comes into the equation also as its temperature.

In this blazon of thermometer the radiation is focused on a detector. A lens may exist used for this purpose (it must be made of a cloth that transmits the advisable radiation) or sometimes a mirror to give complete spectral coverage. A thermopile, consisting of a number of thermoelectric junctions connected in series to increase their output, may be used as detector. Alternatively a pyroelectric device may be employed; in this, charges are liberated as the temperature changes. These latter devices do not answer to steady-state signals, so the radiations must be 'chopped', which is usually effected by having a segmented disc rotating in its path. The semiconductor photodiode is another detector that is sometimes used at shorter wavelengths.

Surface emissivity is much less important when the radiations to be measured has emerged from a 'window' in a hollow body. This makes the technique particularly applicable to furnaces. Dependence on emissivity is besides reduced in the arrangement shown in Figure three.79. If the reflectivity of the hemi-spherical mirror in that location approaches unity, the effective emissivity of the surface likewise tends to unity, though with this set-up the advantage of having all equipment remote from the hot surface is, of form, sacrificed.

Figure 3.79. Arrangement to reduce emissivity dependence

Sometimes the measurement is of full radiation, sometimes of that inside a detail ring of wavelengths, which are called from considerations of detector sensitivity and material manual. Shorter wavelengths are appropriate for hotter bodies, longer for colder. By working in the far material transmission. Shorter wavelengths are appropriate for hotter bodies, longer for colder. Past working in the far infrared (at xxx μm wavelength) temperatures every bit low as −50°C accept been measured, just applications are much more than common up from 50 to 100 G higher.

When, as is often the case, radiations thermometers are used in dusty atmospheres, an air purge will be desirable to keep the front end optical surface clean. In some designs, the detector is kept further outside a hostile environment by using optical fibres equally links.

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Temperature Measurement

C. Hagart-Alexander , in Instrumentation Reference Book (Fourth Edition), 2010

21.6.ii.iii Optical (Disappearing Filament) Thermometer

Optical radiation thermometers provide a uncomplicated and authentic means for measuring temperatures in the range 600°C to 3,000°C. Since their operation requires the eye and judgment of an operator, they are not suitable for recording or control purposes. Nonetheless, they provide an effective way of making spot measurements and for calibration of full radiation thermometers.

In construction an optical radiation thermometer is similar to a telescope. Nonetheless, a tungsten filament lamp is placed at the focus of the objective lens. Effigy 21.56 shows the optical organization of an optical radiation thermometer. To use the instrument, the point at which the temperature is required to be known is viewed through the musical instrument. The current through the lamp filament is adapted so that the filament disappears in the epitome. Figure 21.57 shows how the filament looks in the eyepiece confronting the groundwork of the object, furnace, or whatever is to have its temperature measured. At (a) the current through the filament is too loftier and it looks brilliant against the lite from the furnace; at (c) the current is too low; at (b) the filament is at the aforementioned temperature as the background. The temperature of the filament is known from its electrical resistance. Temperature readout is achieved either past a meter measuring the current through the filament or past temperature calibrations on the control resistor regulating the current through the lamp. The filter in the eyepiece shown in Figure 21.56 passes low-cal at a wavelength around 0.65 μm.

Figure 21.56. Optical system of disappearing filament thermometer.

FIGURE 21.57. Appearance of image in optical thermometer.

Lamps for optical thermometers are not normally operated at temperatures much in excess of 1,500°C. To extend the range of the instrument across this temperature, a neutral filter of known transmission cistron can exist placed in the calorie-free path earlier the lamp. The measurement accuracy of an optical thermometer is typically ±five°C between 800°C and 1,300°C and ±x°C between 1,300°C and 2,000°C.

Corrections for Nonblack-Body Conditions

Like the total radiation thermometer, the optical thermometer is afflicted past the emissivity of the radiations source and by whatsoever absorption of radiation, which may occur between the radiation source and the instrument.

The spectral emissivity of brilliant metal surfaces at 0.65 μm is greater than the total emissivity ε, representing the boilerplate emissivity over all wavelengths. The correction required for the departure from black-body weather is therefore less than in the case of full radiation thermometers.

Due to the fact that a given change of temperature produces a much larger alter in radiant energy at 0.65 μm than produced in the average of radiant energy overall wavelengths, the readings of an optical radiation thermometer require smaller corrections than for a total radiation instrument.

The relationship between the apparent temperature T a and the true temperature T is given past Equation (21.41) which is based on Wien's law,

(21.41) one T 1 T a = λ log x ε λ 6245

where λ is the wavelength in micrometers (usually 0.65 μm) and ελ is the spectral emissivity at wavelength λ.

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Experimental techniques

Yanqiu Huang , ... Zhixiang Cao , in Industrial Ventilation Blueprint Guidebook (Second Edition), 2021

four.three.5.4 Infrared thermometers

At that place are several types of optical thermometers: total radiation pyrometers, effulgence pyrometers, two-color pyrometers, and IR radiation thermometers ( DeWitt, 1988; Richmond, 1984). The measurement range and applications of these instruments differ from each other. The main principle is the same: The measurement is based on observing the electromagnetic radiation emitted by the surface or gas. Every bit a issue, the 2d common feature is the noncontact-type measurement, where the measurement is carried out at a distance from the object without touching it with a probe. Unlike pyrometer-blazon instruments are used for high temperatures, covering the range betwixt 300°C and 6000°C. In ventilation applications the relevant temperatures are, however, considerably lower. For this reason only the IR radiations thermometer is of interest.

In the IR thermometer, long-wave radiations is focused on the detector with a lens or mirror system. Lenses must be fabricated of a glass capable of not absorbing as well much radiation. The detector, which converts the radiations to an electrical signal, tin can exist a thermal detector such equally a thermopile, a photovoltaic detector, or a photomultiplier. The focusing system tin can be connected to the detector through an optical fiber, which gives flexibility in placing the different parts of the instrument. The detector signal is amplified and treated to give a proper output for the display.

The measurement range is dependent on the instrument but can embrace the range –50°C to +500°C. The accuracy is not equally high as the best contact thermometers. One reason for this is that the emissivity of the surface has an effect on the measurement effect, and an emissivity correction is necessary for most instruments. The positive features are noncontact measurement and very fast dynamics, which enable a rapid browse of surface temperatures from a altitude; this is convenient when carrying out, for example, thermal comfort measurements.

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EXPERIMENTAL TECHNIQUES

KAI SIREN , ... PETER 5. NIELSEN , in Industrial Ventilation Pattern Guidebook, 2001

12.iii.5.four Infrared Thermometers 14 , 15

There are several types of optical thermometers: total radiation pyrometers, brightness pyrometers, two-color pyrometers, and infrared radiation thermometers. The measurement range and applications of these instruments differ from each other. The principal principle is the same: The measurement is based on observing the electromagnetic radiation emitted by the surface or gas. Equally a upshot, the second mutual feature is the noncontact-type measurement, where the measurement is carried out at a distance from the object without touching information technology with a probe. Different pyrometer-type instruments are used for high temperatures, covering the range between 300 and 6000 °C. In ventilation applications the relevant temperatures are, yet, considerably, lower. For this reason only the infrared radiation thermometer is of interest.

In the infrared thermometer, long-moving ridge radiation is focused on the detector with a lens or mirror arrangement. Lenses must be made of a glass capable of not absorbing too much radiation. The detector, which converts the radiations to an electrical signal, tin be a thermal detector such as a thermopile, a photovoltaic detector, or a photomultiplier. The focusing system can be continued to the detector through an optical cobweb, which gives flexibility in placing the dissimilar parts of the musical instrument. The detector point is amplified and treated to give a proper output for the display.

The measurement range is dependent on the instrument simply tin can cover the range −fifty to +500 °C. The accuracy is not as high as the all-time contact thermometers. One reason for this is that the emissivity of the surface has an result on the measurement result, and an emissivity correction is necessary for most instruments. The positive features are noncontact measurement and very fast dynamics, which enable a rapid scan of surface temperatures from a distance; this is convenient when conveying out, for example, thermal comfort measurements.

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Temperature and Ways of Measuring It

Miroslav Dramićanin , in Luminescence Thermometry, 2018

2.4 The international temperature scale and the provisional low temperature scale

A common temperature calibration was needed to grant meaningful comparisons of temperature measurements fabricated by unlike people. The International Temperature Scale (ITS-xc), adopted in 1989 past the International Committee for Weights and Measures (CIPM), covers the temperature range from 0.65 K to the highest temperature measurable by practical implementation of the Planck radiation constabulary using monochromatic radiation. The Provisional Low Temperature Calibration (PLTS-2000), adopted by CIPM in 2000, covers the temperature range from 0.ix mK to one K. Since ITS-90 and PLTS-2000 differ in their overlapping range (from 0.65 to 2 K), a new iii He vapor force per unit area scale (PTB-2006) was adopted. This scale passes into the ITS-90 in a higher place ii K, and into the PLTS-2000 below ane One thousand. These internationally agreed temperature scales are approximations of the thermodynamic temperature scale and are used for defining international Kelvin temperatures (symbols T 90 or T 2000) and international Celsius temperatures (symbol t 90 or t 2000). The relation between T 90 (T 2000) and t 90 (t 2000) is the aforementioned as that of their thermodynamic counterparts: t ninety (or t 2000) [°C] =T ninety (or T 2000) [K] − 273.15.

The ITS-90 assigns temperature values, which take been adamant by principal thermometry, to a series of highly reproducible states of thing (temperature stock-still points or defining points), postulates interpolating or extrapolating instruments for a specific subrange of temperature, and defines any required interpolating or extrapolating equations [vi]. ITS-ninety specifies 16 temperature stock-still points (defining points) which cover a temperature range from 13.8033 to 1357.77 Yard. Temperature fixed points are well-defined and reproducible states of matter to which precise values of temperature can be assigned. These are listed in Table 2.1 with their designated temperatures. For practical reasons, 1 should be aware of a set of secondary reference points which comprehend a temperature range from 0.85 (the superconductive transition of zinc) to 3687 K (the melting point of tungsten). The listing of selected secondary reference points can exist found in [11].

Table two.1. Temperature Fixed Points (Defining Points) of the ITS-90

Equilibrium land T 90 (M) t ninety (°C)
Triple point of hydrogen 13.8033 −259.3467
Boiling point of hydrogen at a pressure of 33,321.three Pa 17.035 −256.115
Boiling bespeak of hydrogen at a pressure of 101,292 Pa xx.27 −252.88
Triple point of neon 24.5561 −248.5939
Triple point of oxygen 54.3584 −218.7916
Triple point of argon 83.8058 −189.3442
Triple signal of mercury 234.3156 −38.8344
Triple point of water 273.16 0.01
Melting point of gallium 302.9146 29.7646
Freezing point of indium 429.7485 156.5985
Freezing point of tin 505.078 231.928
Freezing indicate of zinc 692.677 419.527
Freezing point of aluminum 933.473 660.323
Freezing point of silver 1234.93 961.78
Freezing signal of gilt 1337.33 1064.18
Freezing point of copper 1357.77 1084.62

To define temperature in 5 ranges, the ITS-90 requires helium vapor pressure thermometers, helium gas thermometers, standard platinum resistance thermometers, and monochromatic radiations thermometers, as follows (see Fig. ii.ii):

Figure 2.2. Temperature stock-still points and thermometers of the International Temperature Scale (ITS-90).

1.

0.65–5 K defined in terms of the vapour pressures of 3He and 4He,

2.

3–24.5561 K using a constant volume helium gas thermometer,

iii.

13.8033–273.16 K using a platinum resistance thermometer,

4.

273.fifteen–1234.93 K using a platinum resistance thermometer, and

5.

1234.94 K and above using a monochromatic radiation thermometer.

The PLTS-2000 uses the melting pressure of iiiHe to provide the footing for temperature measurement. The guidance on the applied methods by which the melting pressures tin exist measured is beyond the scope of this book. However, a prissy presentation of the topic tin can be establish in [12].

Both ITS-ninety and PLTS-2000 are not only important as an internationally accepted approximation to thermodynamic temperature, merely also because they define procedures, fixed points, and thermometer specifications required in order to establish temperature scales. Traceability of all applied temperature measurements ought to be established, developed, and maintained towards ITS-90 or PLTS-2000.

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Temperature measurement

Alan Due south. Morris , Reza Langari , in Measurement and Instrumentation (3rd Edition), 2021

14.xiv.1 Reference instruments and special calibration equipment

The principal reference standard musical instrument for calibration at the top of the calibration chain is a helium gas thermometer, a platinum RTD, or a narrow-band radiation thermometer according to the temperature range of the instrument existence calibrated, as simply explained at the end of the concluding section. Nonetheless, at lower levels inside the calibration chain, almost any instrument from the list of instrument classes given in Department 14.1 might be used for workplace calibration duties under detail circumstances. Where involved in such duties, of course, the instrument used would be 1 of high accuracy that was reserved solely for scale duties. The list of instruments suitable for workplace-level calibration therefore includes mercury-in-glass thermometers, base of operations metal thermocouples (Type K), noble metal thermocouples (Types B, R, and S), platinum RTDs, and radiation pyrometers. Yet, a subset of this list is usually preferred for most calibration operations. Up to 950°C, the platinum RTD is oftentimes used every bit a reference standard. Higher up that temperature up to nearly 1750°C, a Type Southward (platinum/rhodium-platinum) thermocouple is usually employed. Type K (chromel-alumel) thermocouples are likewise used as an alternative reference standard for temperature scale up to 1000°C.

Although no special types of instrument are needed for temperature calibration, the temperature of the environment within which 1 instrument is compared with another has to be carefully controlled. This requires purposely designed equipment, which is available commercially from a number of manufacturers.

To calibrate all temperature transducers other than radiation thermometers in a higher place a temperature of xx°C, a furnace consisting of an electrically heated ceramic tube is unremarkably used. The temperature of such a furnace can typically exist controlled within limits of ±2°C over the range of twenty°C to 1600°C.

Below 20°C, a stirred water bath is used to provide a abiding reference temperature, and the aforementioned equipment tin be used for temperatures up to 100°C. Similar stirred liquid baths containing oil or salts (potassium/sodium nitrate mixtures) can be used to provide reference temperatures up to 600°C.

To calibrate radiation thermometers, a radiation source that approximates equally closely every bit possible the behavior of a black body is required. The actual value of the emissivity of the source must be measured past a surface pyrometer. Some form of optical bench is too required so that instruments being calibrated can be held firmly and aligned accurately.

The simplest form of radiations source is a hot plate heated by an electrical chemical element. The temperature of such devices can be controlled within limits of ±1°C over the range of 0°C to 650°C and the typical emissivity of the plate surface is 0.85. Type R noble metal thermocouples embedded in the plate are normally used every bit the reference instrument.

A blackbody cavity provides a heat source with much amend emissivity. This can be constructed in various alternative forms co-ordinate to the temperature range of the radiations thermometers to be calibrated, although a common feature is a blackened conical cavity with a cone angle of about xv degrees.

To calibrate low-temperature radiation pyrometers (measuring temperatures in the range of twenty–200°C), the blackbody cavity is maintained at a constant temperature (±0.v°C) past immersing it in a liquid bath. The typical emissivity of a cavity heated in this way is 0.995. Water is suitable for the bath in the temperature range of 20–90°C and a silicone fluid is suitable for the range of 80–200°C. Inside these temperature ranges, a mercury-in-glass thermometer is commonly used equally the standard reference calibration instrument, although a platinum RTD is used when improve accuracy is required.

Another form of blackbody cavity is ane lined with a refractory material and heated by an electrical element. This gives a typical emissivity of 0.998 and is used to calibrate radiation pyrometers at college temperatures. Within the range of 200–1200°C, temperatures can be controlled within limits of ±0.five°C and a Type R thermocouple is generally used as the reference musical instrument. At the higher range of 600–1600°C, temperatures can be controlled within limits of ±ane°C and a Blazon B thermocouple (30% rhodium-platinum/6% rhodium-platinum) is normally used as the reference instrument. As an alternative to thermocouples, radiation thermometers can also exist used as a standard within ±0.v°C over the temperature range of 400–1250°C.

To provide reference temperatures in a higher place 1600°C, a carbon cavity furnace is used. This consists of a graphite tube with a conical radiations crenel at its end. Temperatures up to 2600°C can be maintained with an accuracy of ±5°C. Narrow-band radiation thermometers are used equally the reference standard instrument.

The equipment mentioned in the paragraphs above merely provides an environs in which radiation thermometers can be calibrated against some other reference standard instrument. To obtain an absolute reference standard of temperature, a fixed-bespeak blackbody furnace is used. This has a radiation cavity consisting of a conical-ended cylinder that contains a crucible of 99.999% pure metal. If the temperature of the metal is monitored as it is heated at a constant rate, an arrest period is observed at the melting signal of the metal when the temperature ceases to rise for a brusk interval. Thus, the melting point, and hence the temperature respective to the output reading of the monitoring instrument at that instant, are defined exactly. Measurement uncertainty is on the order of ±0.3°C. The list of metals and their melting points was presented earlier at the outset of Section fourteen.14.

In the scale of radiations thermometers, knowledge of the emissivity of the hot plate or blackbody furnace used as the radiations source is essential. This is measured past special types of surface pyrometer. Such instruments incorporate a hemispherical, gilded-plated surface supported on a telescopic arm that allows information technology to be put into contact with the hot surface. The radiations emitted from a minor pigsty in the hemisphere is contained of the surface emissivity of the measured torso and is equal to that which would exist emitted by the torso if its emissivity value were 100. This radiations is measured by a thermopile with its common cold junction at a controlled temperature. A black hemisphere is also provided with the instrument, which can be inserted to cover the gold surface. This allows the instrument to measure the normal radiation emission from the hot body and then allows the surface emissivity to be calculated by comparison the two radiations measurements.

Inside this list of special equipment, mention must also be made of standard tungsten strip lamps, which are used to provide constant known temperatures in the calibration of optical pyrometers. The various versions of these provide a range of standard temperatures between 800°C and 2300°C to an accuracy of ±ii°C.

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Melt spinning

Yasuhiro Murase , Akihiko Nagai , in Avant-garde Fiber Spinning Technology, 1994

ii.3.ii Fiber construction formation in the spinline

At which bespeak in the spinline will the fiber construction be formed in the instance of ultra-high-speed spinning such as at 10000   m/min? Figure ii.29 shows the filament temperature in the spinline measured by a non-contact type infra-red radiations thermometer. The filament temperature decreases linearly down to a point 100  cm below the spinneret at spinning speeds of 4000   m/min and 8000   m/min. The filament temperature further decreases monotonically almost to the have-up in the example of a speed of 4000   grand/min. At a spinning speed of 8000   m/min, the filament temperature drops abruptly by thinning when the necking takes identify. The temperature drop becomes slower when necking is completed and and then a temperature rise is observed for 20   cm downstream. In Fig. 2.thirty, the observed cooling curve is compared with the calculated cooling curve for a spinning speed of 8000   m/min. The filament temperature was calculated from the following equation by assuming that no crystallization would take place. The ambient temperature was set to 150   °C for x   cm below the spinneret, and 20   °C elsewhere.

2.29. Change of filament temperature in spinline at 4000   yard/min and 8000   m/min. 17

two.30. Calculated and measured filament temperatures in spinline. 17

[2.6] Nu = h D / k a = 0.42 R e 0.334 1 + 8 v y / v 2 0.167

[two.seven] W C p d T / d 10 = π D h T T a

Here W denotes the polymer output, Cp the specific heat of polymer, T the filament temperature, Ta the ambience temperature, D the filament bore, Nu the Nusselt number, ka the thermal conductivity, h the heat transfer coefficient, Re the Reynolds number, 5 the filament velocity and vy the velocity of cooling air ventilated vertically.

The calculated temperature agreed well with the observed filament temperature until necking was completed, as seen from Fig. 2.30. The observed filament temperature deviated from the calculated value downstream from this bespeak. This discrepancy is probably due to crystallization which is not considered in the model adding. The exotherm at crystallization caused a slight temperature rise by compensating for the cooling of the filament.

Figures 2.31 and 2.32 show the changes of the filament bore, the spinning stress and the birefringence ∆due north in the spinline at spinning speeds of 4000   thousand/min and 8000   m/min. At a spinning speed of 4000   m/min, ∆north increases gradually from the betoken where the filament diameter and the filament velocity are 60   μm and 2000   m/min, respectively, and saturates at the completion of filament thinning.

2.31. Change of characteristic properties in spinline at 4000   m/min. 17

2.32. Change of characteristic properties in spin line at 8000   one thousand/min. 17

At a spinning speed of 8000   thou/min, ∆n increases quickly from the spot where the necking terminates. The filament bore and the filament velocity at this spot are 35   μm and 5500   grand/min, respectively. The spinning stress at this spot is 108 dyne/cm2, which is plenty to promote chain orientation. ∆n so increases from 0.04 (at the spot where the necking terminates) to 0.11 for fifteen   cm downstream. The filament temperature rises in accordance with this rapid increase of ∆northward, and crystallization gain.

The wide-angle X-ray diffraction pattern reveals only an baggy halo from the filament sampled at a point 8   cm upstream from the neck. The minor spots from crystallites appear First at the completion of necking. Distinct crystallite spots are observed from the filament sampled at a point seven   cm downstream from the cease of necking, and the crystallites are well grown at a indicate 16   cm downstream from the cease of necking. The results indicate that the crystallization starts at the end of necking and progresses rapidly for 20   cm downstream. This ways that a loftier spinning stress is exerted to promote rapid orientation-induced crystallization and the fiber structure is established within a curt period after the necking is completed.

This thinning procedure and the subsequent structure formation are schematically shown past Ishizaki et al. x and Ichara et al. 5 as in Fig. two.33. When a polymer melt is extruded from the spinneret at a spinning speed of 10000   m/min, information technology yields to decrease the elongational viscosity and necking develops speedily at a wearisome filament velocity of 300   thou/min because the remainder between the cohesive strength and the spinning stress is disturbed. Molecular orientation progresses mainly at the filament surface, and ∆n increases to 0.03 with the completion of necking. Then the aromatic rings get stacked to grade crystallite nuclei, and the crystallites abound rapidly for several cm downstream. Although this procedure penetrates gradually from the yarn surface to the inside, the crystal growth is then rapid that many microvoids are generated in the non-crystallized area such as between and within fibrils. Since the spinning stress concentrates on the surface, the molecular orientation will not ameliorate in the central part of filament where the baggy structure is frozen-in. The progress of this structure formation is shown schematically in Fig. 2.33.

2.33. Model of fiber structure formation (from lohara et al. 5 and Ishizaki et al. 10

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PC-based data conquering

Dipali Bansal , in Real-Time Data Conquering in Human Physiology, 2021

2.ii.i.5 Thermal sensors

Body surface and deep tissue core temperature is another important physiological parameter to establish the physical well-being of human systems. A variety of sensor devices measure temperature from the skin, oral cavities, rectum, or urinary bladder as per prevailing concrete conditions and medical advice. Such thermometers use transducers, based on semiconductors, thermocouples, infrared sensors, optical fibers, quartz crystal temperature sensors, etc. Abnormal pare temperatures can exist a effect of irregular blood apportionment or excessive heat generation in adjacent tissues. Arterial claret regulates the temperature of tissues that accept loftier metabolic action. Authentic observations of temperature are vital equally certain targeted therapies such as thermotherapy or hyperthermia for cancer prison cell devastation require precise measurement of tissue temperature.

Temperature sensors are role of catheters, probes, or needles, etc. or may be used directly for measurements. Thermistors are metallic-based sintered oxides of cobalt, iron, nickel, copper, or manganese temperature sensors having negative temperature coefficients. These sensors are extremely sensitive compared to conventional platinum probes and hence are suitable for body temperature measurement especially achieving higher resolution in minor temperature range. Thermocouples are used for local temperature measurement in the shape of needles, catheters, and insulated wires. Typically, a thermocouple provides an electromotive force in a closed loop having ii junctions of different metals at dissimilar temperatures, ofttimes referred to as Seebeck Effect. Diodes and transistors with p–n junction are used as temperature sensors as a pn junction displays skilful linear temperature characteristics at constant forward-bias current. Crystal resonators such as quartz crystal resonators are also used for temperature measurement as the frequency of resonation exhibits about linear temperature coefficient beyond a big temperature range.

Temperature measurement is carried out by both noncontact and contact measurement techniques based on the clinical needs and the instrument involved. Noncontact temperature measurement is achieved by utilizing the radiation heat transfer such equally infrared radiation thermometers. Microwave-based radiometers can be used for deep tissue measurement and imaging. Infrared radiation thermometer detects the thermal radiations emitted by the man torso or object surface respective to the far-infrared region. Infrared thermometers also simultaneously receive ambient radiations as reflected from the body surface. Thermal detectors and photon detectors are two types of infrared detectors. Thermal detectors measure out temperature based on the incident forcefulness of radiation and report it as rise of temperature. They operate at room temperature and are wavelength independent. Photon detectors are comparatively very sensitive and quick in output, but the sensitivity is dependent on the wavelength. These need to be cooled equally incident photon excites a semiconductor for an electrical output. Noncontact blazon tympanic thermometer is a very handy instrument working on the principle of capturing infrared radiation reflected by the tympanic membrane in the ear. The probe is housed every bit a part of the handheld thermometer which is directed slightly in the external auditory canal. The measurement process is very helpful in infants, intensive care units, and in anesthetic patients, especially as it hardly requires a few seconds for obtaining the core body temperatures. Information technology is non a continuous process for temperature measurement and is contradicted in patients with obstructions in ears such as a foreign trunk, wet, pus formation, blood, or cerebrospinal fluids.

Contact-type temperature measurement clearly requires the probe to be in physical affect with the surface or medium for measurements. Clinical glass mercury thermometer is the most commonly used instrument for body temperature for decades considering of its simplicity, reliability, cost, and ease of handling. However, it is not suitable for continuous monitoring which is pertinent in patients during anesthesia or in duress. Some pertinent solutions for core body temperature measurements use indwelling probes for rectal, bladder, or esophageal measurements.

Rectal temperature probes are inserted few centimeters into the anal sphincter. These are flexible probes with a thermistor on the tip for temperature measurement. Rectal temperature measurement is considered to be gilt standard in infants or noncooperative patients beneath the age of 4 years. It may not be suitable in infants below 2–3 months of age to avoid rectal perforation. Rectal temperatures indicate peripheral blood flow status and hence are considered to be an of import parameter. Information technology is also sometimes avoided with patients under anesthesia as the rectal temperature takes some time to stabilize and lags behind the changes in core body temperature say if measured from esophagus. Esophageal temperature measurements are preferred to be washed shut to heart levels to avoid interference from tracheal air past inserting flexible probes through the oral cavity or through the nose preferably for patients under anesthesia under postoperative care. It gives a very genuine assessment of core body temperature on a continuous ground. Bladder temperature measurement is an automated choice in patients who necessarily demand a urinary catheter owing to problems related to irregular urine catamenia, enlarged prostrate requiring intervention, etc. This technique relieves the need for an additional probe to be inserted either intravenously or orally as the patient is already under severe trauma.

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2D woven fabric composites under fatigue loading of different types and in different environmental conditions

One thousand. Kawai , in Fatigue of Textile Composites, 2015

eight.v.four Consequence of frequency

Loading frequency is considered to accept a significant influence on the sensitivity to fatigue for the carbon fabric composite, probing the effect of self-generated heating and intrinsic rate-dependence (Curtis, Moore, Slater, & Zahlan, 1988; Sun et al., 1979). Figure 8.22 shows the alter in the surface temperature of specimens during fatigue loading (10 Hz, RT) for different fiber orientations; the surface temperature of the specimen was measured with an infrared radiation thermometer (PM133A, YOKOGAWA). The surface temperature of specimens increased rapidly in the intermediate range of fatigue life (∼x 4), and the increment in surface temperature was larger than twenty   °C, similar to the observation by Pandita et al. (2001). The magnitude of the alter in surface temperature depends on the fiber orientation besides every bit the maximum fatigue stress. It is worth noting that the range of fatigue life in which the surface temperature of the specimen raises rapidly corresponded apparently to the range in which the off-centrality fatigue strength reduces rapidly.

Figure eight.22. Rise in temperature of specimen surface for various fiber orientations during room temperature fatigue testing at 10   Hz.

Kawai and Taniguchi (2006).

Off-axis fatigue tests with a depression frequency of ii   Hz were additionally performed at room temperature for the fiber orientations θ  =   fifteen°, 30°, 45°. Comparison betwixt the rises in surface temperature of specimens during the fatigue loading at 2 and 10   Hz is shown in Effigy 8.23 for a representative cobweb orientation θ  =   30°, demonstrating that the temperature increment is suppressed in the case of the lower frequency. Effigy 8.24 shows the off-axis fatigue data at ii   Hz for all the tested fiber orientations θ  =   15°, 30°, 45°, together with the on-centrality fatigue data at x   Hz. The off-axis Southward–Due north relationships at 2   Hz are almost linear over the range of fatigue life up to 106 cycles, in contrast to the S-shaped off-centrality S–Northward curves at ten   Hz. Unlike the tendency at 10 Hz, no rapid reduction in off-axis fatigue strength appeared in the intermediate range of fatigue life (∼10iv) for the fatigue loading at ii   Hz. The change in shape of off-centrality S–Northward curves from an S-shape to a directly line indicates that fatigue life is extended at a lower frequency for an identical magnitude of fatigue load. Apparently, the decreased sensitivity to fatigue was brought about by suppressing the increase in specimen temperature. Another important point is that the off-centrality Southward–Due north relationships at 2   Hz are near parallel to the on-centrality S–N relationships at x   Hz over the tested range of fatigue cycles.

Figure 8.23. Comparison betwixt the rises in temperature of specimen surface for θ  =   xxx° during room temperature fatigue testing at 2 and 10   Hz.

Kawai and Taniguchi (2006).

Effigy viii.24. S–N relationships σ max−2Due north f for diverse fiber orientations at room temperature (R  =   0.ane, f  =   2   Hz).

Kawai and Taniguchi (2006).

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Doping and semiconductor characterizations

Shinya Ohmagari , ... Julien Pernot , in Power Electronics Device Applications of Diamond Semiconductors, 2018

2.2.4.2 Upshot of off angles of diamond substrates

Considerable progress has been made in heavily doping phosphorus donors [23,25], with a strategy shift to make it more conductive, particularly, by using a hopping conduction [28] that emerges above [P]/[C]>1020  cm3; still, in that location remains the challenge to reach much college electrical conductivity optimizing P-doped diamond growth weather condition including substrate misorientation angles.

In the present study, phosphorus-doped homoepitaxial diamond films were grown on two vicinal {1   1   1}-diamond substrates (hereafter referred to as sample 1 and sample ii) by microwave plasma CVD [29], where a self-designed reactor was used [xxx]. Different misorientation angles of 0.3°≤ |θ mis| ≤ 5.viii° toward a [ 1 ¯ 2 ane ¯ ] misorientation vector a mis at plus θ mis or [ 1 2 ¯ i ] at minus θ mis, defined equally shown in Fig. 2.ii.13A and B, were provided on i surface of the substrate, resulting in a wedge shape on the lateral confront (Fig. 2.2.13B). The source gas was a mixture of hydrogen (H2, a purity of ix   N), methane (CH4, half-dozen   North), and phosphine diluted with hydrogen (PHiii/H2=1000   ppm, vi   N); the total gas period rate and the pressure were k   sccm and 100   Torr, respectively. The concentration ratios of CH4/H2 (0.05%) and PHthree/CH4 (104  ppm) were adjusted through mass menstruation controllers. The substrate temperature of ca. 930°C was maintained during the growth time of 2   h by a microwave input power of ca. 310 Westward and monitored using a radiations thermometer.

Figure 2.2.13. Schematic drawings showing (A) a definition of off angle of substrate and (B) multiple off angled substrate prepared for this experiment.

Source: Reprinted from Appl. Phys. Lett. 109 (18) (2016) 182102, with permission from AIP Publishing LLC.

Fig. 2.2.14 nowadays images obtained using a three-dimensional laser-scanning microscope of the as-grown surface over a 30×thirty   µmii expanse (sample 1) with the arithmetic mean roughness along the a mis, R a. Two flat surfaces below ca. 10   nm resolution in laser microscopy were obtained at −0.5° and 0.three°. When θ mis >1.4°, the development of dislocation growth due to a loftier-concentration phosphorus doping became observable from the growth hillocks when the film thickness T f increased (see Fig. 2.two.14 for T f). The different T f originated from the incremental growth rate with increasing θ mis—as we demonstrate later. Although earlier studies with (ca. 5×10xvi  cm−3 [31]) and without phosphorus doping [32] conspicuously showed step-menses growth on vicinal substrates with θ mis > 2°, our results point that footstep-flow growth occurs primarily in every θ mis. Information technology also shows that smoothen surfaces of up to ca. 0.four   µm can be obtained even when highly doped ([P]/[C] ~ten20  cm−3 in the solid stage).

Figure 2.2.14. Surface morphologies of phosphorus doped diamond thin films grown on each off angled area.

Source: Reprinted from Appl. Phys. Lett. 109 (eighteen) (2016) 182102, with permission from AIP Publishing LLC.

Secondary ion mass spectrometry revealed that the phosphorus incorporation concentration in the diamond lattice, C p=[P]/[C], increased with off angles θ mis decrease, as shown in Fig. 2.two.15A. Maximum values of 9.six×tenxix  cm−3 (sample 1) and 8.0×1019  cm−3 (sample 2) were obtained at the smallest θ mis. The incorporation efficiency is 5.iv% at |θ mis|=0.3° (sample 1) and four.6% at |θ mis|=0.5° (sample 2), as shown in the correct axis of Fig. 2.two.15A. The efficiency at the minimal |θ mis| is 7.6 (sample 1) and ii.5 (sample 2) times college than that at θ mis > five.v° and improved by an order of magnitude compared with previous studies [23,25] where like C p values were obtained. In contrast to the tendency of C p, the growth rate R g decreases with off angles θ mis decrease (Fig. 2.2.15B). This is considered to be related to step density subtract as the off angle decrease resulting a decrease of carbon adsorbing site on the surface. For the agreement of relationship between the improvement of doping efficiencies and drop of growth rate, we demand to continue further investigations in the phosphorus-doping mechanism. Through these experiments, nosotros could demonstrate the strategy to obtain highly efficient phosphorus-doping by decision-making the off bending of diamond substrate.

Effigy 2.two.fifteen. The effect of off angles of substrate on (A) phosphorus incorporations and (B) growth rates of phosphorus-doped sparse films.

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