Platinum Resistor
Platinum Resistor
JOHNSON MATTHEY
TECHNOLOGY REVIEW www.technology.matthey.com
temperatures both A and l have to be corrected for have been superseded by the later high precision
thermal expansion effects. It is found below room measurements of Williams and Weaver (15) (0 K–300 K)
temperature that for the level of accuracy given for ρ, and Khellar and Vuillemin (16) (17 K–300 K), with the
thermal expansion corrections are generally negligible latter given only in the form of an equation which was
but at higher temperature the measurements have to evaluated at 17 K and then at 10 K intervals from 20 K
be corrected, especially if they are based entirely on to 270 K. The measurements of Williams and Weaver
the room temperature values for A and l which are were interpolated above 100 K so as to also obtain a
usually measured at 293.15 K, the accepted reference full evaluation at 10 K intervals from 20 K to 270 K.
temperature for length change measurements: The measurements of Schriempf and of Williams and
Weaver agree satisfactorily and were averaged to 10 K
ρ (corrected) = ρ (uncorrected) [(AT / A293.15) × (l293.15 / lT)] (ii)
with the measurements of Williams and Weaver being
extended to 16 K. The measurements of the latter
= ρ (uncorrected) [1 + (lT – l293.15) / l293.15] (iii)
and of Khellar and Vuillemin do not agree below 35 K.
where Equation (iii) can be considered to be a close However the equation of Khellar and Vuillemin showed
approximation of Equation (ii). However since 273.15 K peculiar behaviour below this temperature with derived
is the actual reference temperature then corrected values being 6% higher than those of Williams and
values of ρ(T) should be further corrected for thermal Weaver at 17 K but 31% lower at 20 K. Therefore the
expansion from 293.15 K to 273.15 K. Since this latter measurements were given preference up to 35 K.
correction is usually negligible at the level of accuracy At this temperature and above values from the two sets
given then it is not applied. of measurements were averaged. Overall agreement
In the case of rapid pulse heating to high temperatures, is to within 0.5% between 60 K and 180 K and to within
because of inertia l generally is unaltered and it is A 0.1% above 180 K. The selected values of Matula
that changes. If D is the diameter of the wire then: below 273.15 K are based on a combination of the
measurements of White and Woods and of Laubitz and
ρ (T) = ρ (measured) (DT2 / D293.152) = ρ (measured) (VT / V293.15)
Matsumura and on average the intrinsic values show a
(iv)
bias of 0.02 μΩ cm above the more recently selected
where VT is the volume of the sample at temperature values. Other measurements in the low temperature
T and V293.15 is the volume at 293.15 K. These are region were discussed by Matula.
essentially DT2 and D293.152 respectively since l is In the high temperature region Matula (5) selected
assumed to be unaltered. only the measurements of Laubitz and Matsumura (14)
(90 K–1300 K). After correction for ρ0 = 0.020 μΩ cm
2. Palladium the values were calculated at 50 K intervals from 350 to
1300 K. In the present evaluation these measurements
Palladium has a face-centred cubic structure and were combined with the more recent measurements of
the melting point is a secondary fixed point on the Khellaf et al. (18) (295 K–1700 K) which were given in
International Temperature Scale of 1990 (ITS-90) at the form of an equation which was also evaluated at
1828.0 ± 0.1 K (10). 50 K intervals but over the range 350 K to 1750 K. After
correction of both sets of measurements for thermal
2.1 Solid expansion using the values selected by the present
Electrical resistivity values for solid palladium at author (19) they were fitted to Equation (v) which
273.15 K are given in Table I. The selected value is an has an overall accuracy as a standard deviation of
average of the last three determinations. The ρ0 correction ± 0.13 μΩ cm. The two sets of measurements show
to the measurement of Laubitz and Matsumura (14) a maximum disagreement of 1.0% at 1300 K. The
was suggested by Matula (5) who also appears to have equation was extrapolated to the melting point and
selected this value as the reference value. selected values are given in Table II.
From 71 data sets for solid palladium Matula (5) Measurements of Milošević and Babić (20)
selected only the measurements of Schriempf (17) (250 K–1800 K) were independently corrected for
(1.6 K–10.6 K), White and Woods (13) (10 K–295 K) and thermal expansion. Their equation differs from the
Laubitz and Matsumura (14) (90 K–1300 K). However selected equation sinusoidally by trending from initially
it is considered that the values of White and Woods 0.3% high to 1.7% high at 400 K to 0.9% low at 1400 K
to 0.4% high at 1800 K. Figure 1 shows the deviations Löffler (23) (295 K–1100 K) were corrected from
of the selected values of Matula (which are considered RT/R295 to RT/R273.15 and were also corrected for thermal
as incorporating the measurements of Laubitz and expansion. On this basis the differences reached
Matsumura) and the experimental values of Khellaf a maximum of 4.1% high at 450 K but then showed
et al. and Milošević and Babić from the fitted curve. some scatter varying between 1.0% low at 800 K and
Measurements of Binkele and Brunen (4) (273–1423 K) 1.6% high at 1100 K. Figure 2 shows the deviations of
which were also independently corrected for thermal these three sets of measurements from the fitted curve
expansion, showed systematic biases of 1.3% high for where the resistivity ratios of García and Löffler were
runs 1 and 2 and 1.7% high for run 3. converted to electrical resistivity values for comparison
purposes.
2 2.2 Liquid
Ref. (5) Electrical resistivity values for palladium at the melting
1.5
Ref. (18)
point are given in Table III. In the liquid state neither
Ref. (20)
1 Dupree et al. (24) (1832 K–1924 K) nor Güntherodt
Deviation, %
4
3
Also in the high temperature region there are a
number of other measurements which were published 2
Table III Differences Between the Solid and Liquid Electrical Resistivity of Palladium at the Melting Point
ρS, ρL,
Authors Reference ρL /ρS Notes
μΩ cm μΩ cm
Dupree et al. 24 (48.8) 83.0 1.700 (a)
Güntherodt et al. 25 47.3 78.8 1.666
Seydel and Fischer 26 50.2 79.1 1.576
Khellaf et al. 18 (45.2) 77.3 1.710 (b)
Pottlacher 22 49.6 81.4 1.641
Present assessment – 46.84 81.4 1.738
Notes to Table III
(a) Solid value based on (ρL – ρS)/ ρS = 0.70 ± 0.05
(b) Solid value based on ρL /ρS = 1.71
Equation (vi) with selected values for the electrical Rosso (27) (1000 K–2000 K), Laubitz and van der
resistivity of the liquid and are also given in Table II. Meer (28) (300 K–1500 K), and Flynn and O’Hagan (29)
(273 K–1373 K) and the resistance ratios of Roeser (30)
3. Platinum (73 K–1773 K) and Kraftmakher (31) (1000 K–2000 K)
together with resistivity measurements given by Martin
Platinum has a face-centred cubic structure and the et al. (32) (300 K–1200 K). White fitted all selected
melting point is a secondary fixed point on ITS-90 at values from 100 K to 2000 K to Equation (vii) which
2041.3 ± 0.4 K (10). was extrapolated to the melting point. Differences
between values derived from this equation and the
3.1 Solid tabulated values of White as given in Table IV do not
The resistance ratio of platinum, W T = RT/R 273.15, forms exceed 0.01 μΩ cm. An abridged version of the values
the basis of the International Temperature Scale which for the solid phase as given in Table IV was originally
White (6) extended to 1300 K and calculated values given in Platinum Metals Review by Corti (33).
of intrinsic resistivity using the fixed reference value of For comparison between these measurements
9.82 ± 0.01 μΩ cm at 273.15 K. Above 1300 K White and the selected values as given in Figure 3, the
combined the selected values to this temperature with resistivity ratios of Roeser (30) and Kraftmakher (31)
the electrical resistivity measurements of Righini and were converted to electrical resistivity values and all
Solid
Liquid
(29) were corrected for thermal expansion using values Ref. (22), run 2
1.5
selected by the present author (34). In addition the
measurements of Martin et al. (32) were corrected to 1
correspond to the selected electrical resistivity value at 0.5
273.15 K. Because of their larger deviations values of 0
Righini and Rosso (27) are compared with the selected 300 500 700 900 1100 1300 1500 1700 1900 2100
Temperature, K
values in Figure 4.
Fig. 5. Solid platinum – percentage deviations from selected
curve
0.6
3.2 Liquid
Ref. (30)
0.4 Ref. (31) Electrical resistivity values of platinum at the
Ref. (32) melting point are given in Table V. In the liquid state
0.2 electrical resistivity measurements of Pottlacher (22)
(2042 K–2900 K) were selected as Equation (viii)
Deviation, %
Table V Differences Between the Solid and Liquid Electrical Resistivity of Platinum at the Melting Point
ρS, ρL,
Authors Reference ρL /ρS
μΩ cm μΩ cm
14. M. J. Laubitz and T. Matsumura, Can. J. Phys., 1972, 26. U. Seydel and U. Fischer, J. Phys. F: Met. Phys.,
50, (3), 196 1978, 8, (7), 1397
15. R. K. Williams and F. J. Weaver, Phys. Rev. B, 1982, 27. F. Righini and A. Rosso, High Temp.-High Pressures,
25, (6), 3663 1980, 12, (3), 335
28. M. J. Laubitz and M. P. Van Der Meer, Can. J. Phys.,
16. A. Khellar and J. J. Vuillemin, J. Phys.: Condens.
1966, 44, (12), 66
Matter, 1992, 4, (7), 1757
29. D. R. Flynn and M. E. O’Hagan, J. Res. Natl. Bur.
17. J. T. Schriempf, Phys. Rev. Lett., 1968, 20, (19), 1034 Stand., 1967, C71, (4), 255
18. A. Khellaf, R. M. Emrick and J. J. Vuillemin, J. Phys. F: 30. W. Roeser, “Temperature: Its Measurement and
Met. Phys., 1987, 17, (10), 2081 Control in Science and Industry”, ed. M. S. van Dusen,
Vol. I, Reinhold Publishing Corp, New York, USA,
19. J. W. Arblaster, Platinum Metals Rev., 2012, 56,
1941, p. 1312
(3), 181
31. Ya. A. Kraftmakher, High Temp.-High Pressures,
20. N. Milošević and M. Babić, Int. J. Mater. Res., 2013,
1973, 5, (4), 433
104, (5), 462
32. J. J. Martin, P. H. Sidles and G. C. Danielson, J. Appl.
21. A. P. Miiller and A. Cezairliyan, Int. J. Thermophys.,
Phys., 1967, 38, (8), 3075
1980, 1, (2), 217
33. C. W. Corti, Platinum Metals Rev., 1984, 28, (4), 164
22. G. Pottlacher, “High Temperature Thermophysical
Properties of 22 Pure Metals”, Edition Keiper, Graz, 34. J. W. Arblaster, Platinum Metals Rev., 1997, 41, (1), 12
Austria, 2010, p. 76 35. M. M. Martynyuk and V. I. Tsapkov, Fiz. Metal.
23. E. Y. García and D. G. Löffler, J. Chem. Eng. Data, Metalloved., 1974, 37, (1), 49; translated into English
1985, 30, (3), 304 in Phys. Met. Metallogr., 1974, 37, (1), 40
24. B. C. Dupree, J. B. Van Zytveld and J. E. Enderby, J. 36. G. R. Gathers, J. W. Shaner and W. M. Hodgson, High
Phys. F: Met. Phys., 1975, 5, (11), L200 Temp.-High Pressures, 1979, 11, (5), 529
25. H.-J. Güntherodt, E. Hauser, H. U. Künzi and R. 37. R. S. Hixson and M. A. Winkler, Int. J. Thermophys.,
Müller, Phys. Lett. A., 1975, 54, (4), 291 1993, 14, (3), 409
The Author
John W. Arblaster is interested in the history of science and the evaluation of the thermodynamic and
crystallographic properties of the elements. Now retired, he previously worked as a metallurgical
chemist in a number of commercial laboratories and was involved in the analysis of a wide range
of ferrous and non-ferrous alloys.