techniques for approximating the international temperature ... - BIPM
techniques for approximating the international temperature ... - BIPM techniques for approximating the international temperature ... - BIPM
84 the remaining liquid increases. The large Kapitza resistance is also troublesome. The temperature of the liquid can be many millikelvins higher than that of the walls (15 mK to 1.5 K). This phenomenon can be corrected for (but not reliably) by calculation, and can be reduced by increasing the surface of the bulb/liquid contact up to several hundreds of cm 2 (metal mesh or spirals of copper in the bulb). Furthermore, the viscosity of the return gas induces a pressure gradient in the capillary which can become important below 1 K. Note that if these problems are not under control, the measured temperatures will be discontinuous at the λ-point. For precise measurements, the error due to the Kapitza effect (which can be about 4 mK at 1.5 K) is too important to ignore [Lounasmaa (1974) for temperatures below 1 K; Wilks (1967) for higher temperatures]. It can be calculated, or it can be avoided by using 3 He, which does not become superfluid, instead of 4 He in the temperature range where the two scales overlap; for 4 He one should always use a bulb above the λ -point, and always measure the bath pressure directly below the λ -point. Below the λ -point the refluxing and Kapitza effects can be avoided by measuring the vapour pressure a short distance up the pumping tube [Rusby and Swenson (1980)]. 6.3.8 Other Corrections Other corrections to be considered in pressure measurements include: expansion of the mercury of the manometer and variation of its density with the temperature; the shape of the meniscus; hydrostatic pressure correction (if we measure the temperature of a body immersed in the liquid). The latter can be uncertain but can usually be kept small because the depth of liquid is seldom large. 6.4 Conclusion The vapour pressure thermometer can be used as a thermodynamic thermometer only within the limits of application of the Clausius-Clapeyron equation which result from lack of knowledge of several of the parameters. Otherwise it is an excellent practical thermometer based upon a physical property of a pure substance. Simple and practical, it allows a high measurement precision once the pressure-temperature relationship has been established. The bulb is simple to construct and can be very small. There are not many corrections to apply (a few for impurities possibly, but no dead space corrections as in the gas thermometer). The major inconveniences are its small working range (no pure substance covers a large temperature range) and its nonlinearity of response. The development of new pressure sensors may give renewed interest in vapour pressure thermometers.
7.1 Magnetic Thermometer 85 7. Magnetic Thermometry Magnetic thermometry is based upon measurement of paramagnetic susceptibility. Useful papers concerned with the EPT-76 temperature range are Rusby and Swenson (1980); Cetas and Swenson (1972); van Rijn and Durieux (1972); Cetas (1976); Mangum and Bowers (1978). For an ideal paramagnet the zero-field susceptibility is related to temperature through the Curie law χ = C/T where C is the Curie constant. Although in magnetic thermometry one approximates to this by using dilute paramagnetic salts, it is generally necessary to take account of interactions and other effects and write χ = C/(T + ∆ + γ/T), where ∆ includes first-order dipole-dipole and exchange couplings and also a shape factor, while γ is due primarily to crystal field splitting of the ground state and second-order interaction effects [Hudson (1972)]. The existence of interactions implies a lower limit for the use of any given salt, while the upper limit is set by diminishing sensitivity (dχ/dT is approximately equal to -C/T 2 ). The susceptibility measurement is usually made by the ac mutual inductance method in which the salt sample is situated in a set of coils whose mutual inductance M is balanced against a reference in a Hartshorn bridge or a variant thereof [Hudson (1972)] (SQUlD techniques do not appear to have been applied much above 1 K). The bridge balance X is linearly related to M and hence to χ. The working equation for a magnetic thermometer becomes X = A + B/( T + ∆ + γ/T) (7.1 ) Unless ∆ or γ is obtainable from theory, a minimum of four fixed points is needed to calibrate the thermometer. Salt crystals must be grown carefully from ingredients of high purity. Most of the suitable salts are hydrates and almost all of these are efflorescent, tending to lose water-ofcrystallization if kept at room temperature. This tendency is considerably diminished if the enclosing volume is small and is filled with an inert gas; but it is catastrophically increased if the enclosure is evacuated. Simple refrigeration, however, avoids most such problems. The properties of the most important salts have been widely discussed and tabulated [e.g. Hudson (1972)]. Cerous magnesium nitrate (CMN) is the closest approximation to an ideal paramagnet in common use: γ = 0 and for a sphere ∆ is about 0.3 mK. It is, however, highly anisotropic and its usefulness is limited to temperatures below 3 K because of its low
- Page 54 and 55: 34 Final readings of the thermomete
- Page 56 and 57: 36 temperatures differ (usually) sy
- Page 58 and 59: 38 Fig. 3.4: Cross sectional drawin
- Page 60 and 61: 40 Fig. 3.5: Miniature graphite bla
- Page 62 and 63: 42 4. Germanium Resistance Thermome
- Page 64 and 65: 44 Fig. 4.3: Example of the Π-type
- Page 66 and 67: 46 Fig. 4.4: Differences between dc
- Page 68 and 69: 48 - conversely, p-doped thermomete
- Page 70 and 71: 50 Fig. 4.6: Effect of a radio-freq
- Page 72 and 73: 52 that it will not be subject to m
- Page 74 and 75: ln R n = ∑ i= 0 54 ⎛ ln T - P
- Page 76 and 77: 56 Fig. 5.1: Resistance (Ω) and s
- Page 78 and 79: 58 thermometer wires) caused a more
- Page 80 and 81: 60 6. Vapour Pressure Thermometry*
- Page 82 and 83: 62 transitions, but it could be app
- Page 84 and 85: n ∑ i= 2 64 L x [ Π − k ] P =
- Page 86 and 87: 66 Fig. 6.3: Diagram at constant pr
- Page 88 and 89: 68 Fig. 6.4: Schematic construction
- Page 90 and 91: 70 Fig. 6.6: Use of an evacuated ja
- Page 92 and 93: 72 Following this, the connecting t
- Page 94 and 95: 74 Fig. 6.9: (c) N2, CO, Ar, O2, CH
- Page 96 and 97: 76 the Weber-Schmidt equation [Webe
- Page 98 and 99: 78 Table 6.1: Temperature values (K
- Page 100 and 101: 80 into the bulb (hydrous ferric ox
- Page 102 and 103: 82 Fig. 6.12: Effect on the vapour
- Page 106 and 107: 86 Curie constant (C⊥ is about 0.
- Page 108 and 109: 8.1 General Remarks 88 8. Platinum
- Page 110 and 111: 90 For a group of 45 thermometers h
- Page 112 and 113: 92 More recently, Seifert [(1980),
- Page 114 and 115: 94 For thermometers with W(4.2 K) <
- Page 116 and 117: 96 after 500 h at 1700 °C in air,
- Page 118 and 119: 98 normally extends about 50 cm bac
- Page 120 and 121: 100 inhomogeneities result from the
- Page 122 and 123: 9.5 Approximations to the ITS-90 10
- Page 124 and 125: 104 10. Infrared Radiation Thermome
- Page 126 and 127: 106 almost negligible. The final ac
- Page 128 and 129: 108 11. Carbon Resistance Thermomet
- Page 130 and 131: 110 Fig. 11.1: Resistance-temperatu
- Page 132 and 133: 112 Table 11.1: Typical Time Consta
- Page 134 and 135: 114 calibration after each cool-dow
- Page 136 and 137: 116 12. Carbon-Glass Resistance The
- Page 138 and 139: 118 Fig. 12.1: Resistance-temperatu
- Page 140 and 141: 120 14. Diode Thermometers Diodes c
- Page 142 and 143: 122 2 BT V = E0 − − CT ln ( DT)
- Page 144 and 145: 124 Fig. 15.1: Principal features o
- Page 146 and 147: 126 For a thermometer graduated abo
- Page 148 and 149: 128 rise decreases with time but in
- Page 150 and 151: 130 Fig. 16.1: (a) Fabrication of I
- Page 152 and 153: 132 capillaries of a twin- (or four
84<br />
<strong>the</strong> remaining liquid increases. The large Kapitza resistance is also troublesome. The<br />
<strong>temperature</strong> of <strong>the</strong> liquid can be many millikelvins higher than that of <strong>the</strong> walls (15 mK to 1.5<br />
K). This phenomenon can be corrected <strong>for</strong> (but not reliably) by calculation, and can be<br />
reduced by increasing <strong>the</strong> surface of <strong>the</strong> bulb/liquid contact up to several hundreds of cm 2<br />
(metal mesh or spirals of copper in <strong>the</strong> bulb). Fur<strong>the</strong>rmore, <strong>the</strong> viscosity of <strong>the</strong> return gas<br />
induces a pressure gradient in <strong>the</strong> capillary which can become important below 1 K.<br />
Note that if <strong>the</strong>se problems are not under control, <strong>the</strong> measured <strong>temperature</strong>s will be<br />
discontinuous at <strong>the</strong> λ-point. For precise measurements, <strong>the</strong> error due to <strong>the</strong> Kapitza effect<br />
(which can be about 4 mK at 1.5 K) is too important to ignore [Lounasmaa (1974) <strong>for</strong><br />
<strong>temperature</strong>s below 1 K; Wilks (1967) <strong>for</strong> higher <strong>temperature</strong>s]. It can be calculated, or it can<br />
be avoided by using 3 He, which does not become superfluid, instead of 4 He in <strong>the</strong><br />
<strong>temperature</strong> range where <strong>the</strong> two scales overlap; <strong>for</strong> 4 He one should always use a bulb<br />
above <strong>the</strong> λ -point, and always measure <strong>the</strong> bath pressure directly below <strong>the</strong> λ -point. Below<br />
<strong>the</strong> λ -point <strong>the</strong> refluxing and Kapitza effects can be avoided by measuring <strong>the</strong> vapour<br />
pressure a short distance up <strong>the</strong> pumping tube [Rusby and Swenson (1980)].<br />
6.3.8 O<strong>the</strong>r Corrections<br />
O<strong>the</strong>r corrections to be considered in pressure measurements include: expansion of<br />
<strong>the</strong> mercury of <strong>the</strong> manometer and variation of its density with <strong>the</strong> <strong>temperature</strong>; <strong>the</strong> shape of<br />
<strong>the</strong> meniscus; hydrostatic pressure correction (if we measure <strong>the</strong> <strong>temperature</strong> of a body<br />
immersed in <strong>the</strong> liquid). The latter can be uncertain but can usually be kept small because<br />
<strong>the</strong> depth of liquid is seldom large.<br />
6.4 Conclusion<br />
The vapour pressure <strong>the</strong>rmometer can be used as a <strong>the</strong>rmodynamic <strong>the</strong>rmometer<br />
only within <strong>the</strong> limits of application of <strong>the</strong> Clausius-Clapeyron equation which result from lack<br />
of knowledge of several of <strong>the</strong> parameters. O<strong>the</strong>rwise it is an excellent practical <strong>the</strong>rmometer<br />
based upon a physical property of a pure substance. Simple and practical, it allows a high<br />
measurement precision once <strong>the</strong> pressure-<strong>temperature</strong> relationship has been established.<br />
The bulb is simple to construct and can be very small. There are not many corrections to<br />
apply (a few <strong>for</strong> impurities possibly, but no dead space corrections as in <strong>the</strong> gas<br />
<strong>the</strong>rmometer). The major inconveniences are its small working range (no pure substance<br />
covers a large <strong>temperature</strong> range) and its nonlinearity of response. The development of new<br />
pressure sensors may give renewed interest in vapour pressure <strong>the</strong>rmometers.