Thermometers development

There are two reference functions IT (T q), one for the range from 13 K to 0.01°C, another for the range 0.01—962°C. The reference functions represent the caUbration of a fictitious thermometer developed from experience in the caUbration of many SPRTs over many years. Below 0.01°C, the reference function is... 

Gabriel Fahrenheit invents an alcohol thermometer (mercury thermometer developed in 1714)... 

For a quartz thermometer, the resonant frequency of a quartz crystal resonator is strongly related to the temperature variation. With high resolution, the temperature change can be directly determined from the frequency change of a quartz crystal thermometer. A quartz thermometer developed for use between -80 and 250°C [85] has a resolution of 0.1 mK. If used at the same temperature, a comparable precision can be achieved. However, with temperature cycling, hysteresis can reduce its repeatability. An accuracy of 0.05°C can be achieved with calibration. Nevertheless the temperature resolution for the quartz resonator is found to be less accurate at lower temperatures Over the temperature range from 4.2 to 400 K, the temperature resolution with the resonant frequency change for a YS cut quartz crystal thermometer drops from 1 kHz/K at 300 K to 80 Hz/K at 4.2 K [86]. 

Torricelli makes the hrst barometer using mercury in a sealed glass tube The Dutch scientist Anton van Feeuwenhoek develops a microscope Isaac Newton invents a reflecting telescope Gabriel Fahrenheit invents an alcohol thermometer (mercury thermometer developed in 1714)... 

Quartz Thermometers. Development of quartz crystal frequency thermometers continues. These devices use the small but highly reproducible variation of the natural vibration frequency of appropriately cut piezoelectric quartz samples. The sensors are compact and useful over a wide cryogenic range (4-400 K) with an accuracy within a few hundredths of a kelvin. There are, however, some problems with hysteresis and aging. 

Girard s reagent P , C5H5NCH2C0NHNH2 C1. In a 1-htre threenecked flask, equipped as in the previous preparation, place 200 ml. of absolute ethyl alcohol, 63 g. (64 -5 ml.) of pure anhydrous pyridine and 98 - 5 g. (84 5 ml.) of ethyl chloroacetate. Heat the mixture under reflux for 2-3 hours until the formation of the quaternary salt is complete acidify a small test-portion with dilute sulphuric acid it should dissolve completely and no odour of ethyl chloroacetate should be apparent. Cool the mixture in ice and salt. Replace the thermometer by a dropping funnel, and add a solution of 40 g. of 100 per cent, hydrazine hydrate in 60 ml. of absolute ethanol all at once. A vigorous exothermic reaction soon develops and is accompanied by vigorous effervescence. The pro duct separates almost immediately. When cold, filter with suction, wash... 

In both of these pieces of apparatus, isothermal operation and optimum membrane area are obtained. Good temperature control is essential not only to provide a value for T in the equations, but also because the capillary attached to a larger reservoir behaves like a thermometer, with the column height varying with temperature fluctuations. The contact area must be maximized to speed up an otherwise slow equilibration process. Various practical strategies for presetting the osmometer to an approximate n value have been developed, and these also accelerate the equilibration process. 

In the late fifteenth century AD mercury was successfully used as a treatment for syphilis. In the late sixteenth century the development of the Patio process for the recovery of silver by amalgamation (see Silverand silveralloys) greatiy increased the consumption of mercury. Usage of mercury increased in 1643 when Torricelli invented the barometer, and again in 1720 when Fahrenheit invented the mercury thermometer. Other scientific and medical appHcations foUowed. Industrial usage after 1900, particularly in electrical appHcations, expanded rapidly, offsetting the sharp decline in its use in amalgamation. 

Microcapsules are used in several film coatings other than carbonless paper. Encapsulated Hquid crystal formulations coated on polyester film are used to produce a variety of display products including thermometers. Polyester film coated with capsules loaded with leuco dyes analogous to those used in carbonless copy paper is used as a means of measuring line and force pressures (79). Encapsulated deodorants that release their core contents as a function of moisture developed because of sweating represent another commercial appHcation. Microcapsules are incorporated in several cosmetic creams, powders, and cleansing products (80). 

A high temperature optical fiber thermometer has beea developed (32,33). It coasists of a sputtered iridium blackbody tip oa a single crystal sapphire laser. Such a device has beea showa to be accurate to within 0.03° C at 1000°C. 

Siace the early 1970s, development work has been reported on thick-film, thin-film, and other resistance elements which are made by deposition rather than wound from wine. Such thermometers might have certain advantages of size, response time, cost, etc. These do not have the stabiUty or iaterchangeabihty of wrought-wke elements. 

Many special-purpose electrical thermometers have been developed, either for use in practical temperature measurement, or as research devices for the study of temperature and temperature scales. Among the latter are thermometers which respond to thermal noise (Johnson noise) and thermometers based on the temperature dependence of the speed of sound. 

Yokagawa Electric Works has developed a thermometer based on the nuclear quadmpole resonance of potassium chlorate, usable over the range from —184 to 125°C. This thermometer makes use of the fundamental properties of the absorption frequency of the Cl nucleus, and its caUbration is itself a constant of nature. 

Control of Dyeing Equipment. Over the years, the dyer and machinery manufacturer have appHed any mechanical or electrical equipment that would enable them, day after day, to produce repeatable dyeings of top quaHty. First, thermometers were installed in dye lines these soon evolved into thermocouples with remote recording. Other improvements were soon developed, such as automatic four-way valves with variable-interval controls, flow controls, pressure recorders, hydrauHc and air pressure sets on roUers, pH controls, etc. 

The ability to measure temperature and temperature differences accurately and reproducibly is essential to the experimental study of thermodynamics. A thermometer constructed with an ideal gas as its working fluid yields temperatures that correspond to the fundamental thermodynamic temperature scale. However, such thermometers are extremely difficult to use, are not amenable to miniaturization, and are very expensive. Therefore, other means to measure temperatures that reproduce the ideal gas or thermodynamic temperature scale (Kelvin) have had to be developed. The international temperature scale represents a method to determine temperatures over a wide range with measuring devices that are easier to use than the ideal gas thermometer. The goal is to make temperature measurements that correspond to the thermodynamic temperature as accurately as possible. 

The international temperature scale is based upon the assignment of temperatures to a relatively small number of fixed points , conditions where three phases, or two phases at a specified pressure, are in equilibrium, and thus are required by the Gibbs phase rule to be at constant temperature. Different types of thermometers (for example, He vapor pressure thermometers, platinum resistance thermometers, platinum/rhodium thermocouples, blackbody radiators) and interpolation equations have been developed to reproduce temperatures between the fixed points and to generate temperature scales that are continuous through the intersections at the fixed points. 

A 250-mL, two-necked, round-bottomed flask equipped with a magnetic stirbar, thermometer, and a reflux condenser fitted with a rubber septum and balloon of argon is charged with a solution of methyltrioxorhenium (MTO) (0.013 g, 0.05 mmol, 0.1% mol equiv) in 100 mL of methanol (Note 1). Urea hydrogen peroxide (UHP) (14.3 g, 152 mmol) is added (Notes 1, 2, 3, 4), the flask is cooled in an ice bath, and dibenzylamine (9.7 mL, 50.7 mmol) is then added dropwise via syringe over 10 min (Notes 1, 5). After completion of the addition, the ice bath is removed and the mixture is stirred at room temperature (Note 6). A white precipitate forms after approximately 5 min (Note 7) and the yellow color disappears within 20 min (Note 8). Another four portions of MTO (0.1% mol equiv, 0.013 g each) are added at 30-min intervals (2.5 hr total reaction time). After each addition, the reaction mixture develops a yellow color, which then disappears only after the last addition does the mixture remain pale yellow (Note 9). The reaction flask is cooled in an ice bath and solid sodium thiosulfate pentahydrate (12.6 g, 50.7 mmol) is added in portions over 20 min in order to destroy excess hydrogen peroxide (Note 10). The cooled solution is stirred for 1 hr further, at which point a KI paper assay indicates that the excess oxidant has been completely consumed. The solution is decanted into a 500-mL flask to remove small amounts of undissolved thiosulfate. The solid is washed with 50 mL of MeOH and the methanol extract is added to the reaction solution which is then concentrated under reduced pressure by rotary evaporation. Dichloromethane (250 mL) is added to the residue and the urea is removed by filtration through cotton and celite. Concentration of the filtrate affords 10.3 g (97%) of the nitrone as a yellow solid (Note 11). 

Reliable micro-scale measurement and control of the temperature are required in developing thermal micro-devices. Available measurement techniques can be largely classified into contact and non-contact groups. While the resistance thermometer, thermocouples, thermodiodes, and thermotransistors measure temperature at specific points in contact with them, infrared thermography, thermochromic liquid crystals (TLC), and temperature-sensitive fluorescent dyes cover the whole temperature field (Yoo 2006). 

Patients should be educated to recognize the signs and symptoms of complications that would require urgent evaluation. Patients and parents of children with SCD should be educated to read a thermometer properly and to seek immediate medical care when a fever develops or signs of infection occur. With acute illnesses, prompt evaluation is important because deterioration may occur rapidly. Fluid status should be monitored to avoid dehydration or overhydration, both of which may worsen complications of SCD. Patients in acute distress should maintain oxygen saturation at 92% or at their baseline. Any supplemental oxygen requirements should be evaluated.6,27... 

The pH (or pI) term of the Nemst equation contains the electrode slope factor as a linear temperature relationship. This means that a pH determination requires the instantaneous input, either manual or automatic, of the prevailing temperature value into the potentiometer. In the manual procedure the temperature compensation knob is previously set on the actual value. In the automatic procedure the adjustment is permanently achieved in direct connection with a temperature probe immersed in the solution close to the indicator electrode the probe usually consists of a Pt or Ni resistance thermometer or a thermistor normally based on an NTC resistor. An interesting development in 1980 was the Orion Model 611 pH meter, in which the pH electrode itself is used to sense the solution temperature (see below). 

In the flask are placed 240 g. (2 moles) of acetophenone and 1 1. of glacial acetic acid. The thermometer is adjusted so that it extends considerably below the surface of the solution, and chlorine is admitted at such a rate that the temperature does not exceed 60° (Note 1). Chlorination is continued until an excess of the halogen has been absorbed. This requires about five hours completion of the reaction is indicated by the development of a yellow color. The reaction mixture is poured over 6 1. of crushed ice in a 2-gal. jar. The mixture is stirred several times (Note 2) and allowed to stand until the ice has melted. The dichloroacetophenone, which separates as a heavy lachrymatory oil, is removed. The yield is 340-370 g. (90-97 per cent of the theoretical amount). This product, containing only a few per cent of water and acetic acid, is pure enough for the preparation of mandelic acid. It may be purified by adding about 100 cc. of benzene, removing the... 

Recently, a superconductive reference device, SRD1000 (Hightech Development Leiden and Kamerling Onnes Laboratory) [29], with ten reference materials (15mK-lK, see Table 8.10) has been developed to enable simplified in situ calibration of interpolating thermometers. An evaluation of SRD1000 prototypes at various laboratories is reported in ref. [30]. 

Over the years, a simpler instrument called interpolating constant volume gas thermometer (ICVGT) has been developed. It differs from traditional CVGT because it is calibrated at a number of temperatures known from independent measurements. 

The noise thermometer is based on the temperature dependence of the mean square noise voltage V2 developed in a thermistor (Nyquist theorem, 1928) ... 

Coulomb blockade thermometry (CBT) is based on the electric conductance characteristics of tunnel junctions. This type of thermometer has been developed at Jyvaskyla University. The basic results are reported in ref. [112],... 

Most of cryogenic sensors have been developed in close connection with detectors and do not find different applications. This is the case of SSG (superheated superconducting granules) others have also independent applications, e.g. Ge thermometers. 

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