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Triple point

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For other uses, see Tripoint and Tripoint (disambiguation).

In thermodynamics, the triple point of a substance is the temperature and pressure at which the three phases (gas, liquid, and solid) of that substance coexist in thermodynamic equilibrium.[1] It is that temperature and pressure at which the sublimation curve, fusion curve and the vaporisation curve meet. For example, the triple point of mercury occurs at a temperature of −38.8 °C (−37.8 °F) and a pressure of 0.165 mPa.

In addition to the triple point for solid, liquid, and gas phases, a triple point may involve more than one solid phase, for substances with multiple polymorphs. Helium-4 is a special case that presents a triple point involving two different fluid phases (lambda point).[1]

The triple point of water was used to define the kelvin, the base unit of thermodynamic temperature in the International System of Units (SI).[2] The value of the triple point of water was fixed by definition, rather than measured, but that changed with the 2019 redefinition of SI base units. The triple points of several substances are used to define points in the ITS-90 international temperature scale, ranging from the triple point of hydrogen (13.8033 K) to the triple point of water (273.16 K, 0.01 °C, or 32.018 °F).

The term "triple point" was coined in 1873 by James Thomson, brother of Lord Kelvin.[3]

Triple point of water

Gas–liquid–solid triple point

See also: Properties of water § Triple point
A typical phase diagram. The solid green line applies to most substances; the dashed green line gives the anomalous behavior of water

The single combination of pressure and temperature at which liquid water, solid ice, and water vapor can coexist in a stable equilibrium occurs at exactly 273.1600 K (0.0100 °C; 32.0180 °F) and a partial vapor pressure of 611.657 pascals (6.11657 mbar; 0.00603659 atm).[4][5] At that point, it is possible to change all of the substance to ice, water, or vapor by making arbitrarily small changes in pressure and temperature. Even if the total pressure of a system is well above the triple point of water, provided that the partial pressure of the water vapor is 611.657 pascals, then the system can still be brought to the triple point of water. Strictly speaking, the surfaces separating the different phases should also be perfectly flat, to negate the effects of surface tension.

The gas–liquid–solid triple point of water corresponds to the minimum pressure at which liquid water can exist. At pressures below the triple point (as in outer space), solid ice when heated at constant pressure is converted directly into water vapor in a process known as sublimation. Above the triple point, solid ice when heated at constant pressure first melts to form liquid water, and then evaporates or boils to form vapor at a higher temperature.

For most substances the gas–liquid–solid triple point is also the minimum temperature at which the liquid can exist. For water, however, this is not true because the melting point of ordinary ice decreases as a function of pressure, as shown by the dashed green line in the phase diagram. At temperatures just below the triple point, compression at constant temperature transforms water vapor first to solid and then to liquid (water ice has lower density than liquid water, so increasing pressure leads to a liquefaction).

The triple point pressure of water was used during the Mariner 9 mission to Mars as a reference point to define "sea level". More recent missions use laser altimetry and gravity measurements instead of pressure to define elevation on Mars.[6]

Water boiling at 0°C using a vacuum pump.

High-pressure phases

At high pressures, water has a complex phase diagram with 15 known phases of ice and several triple points, including 10 whose coordinates are shown in the diagram. For example, the triple point at 251 K (−22 °C) and 210 MPa (2070 atm) corresponds to the conditions for the coexistence of ice Ih (ordinary ice), ice III and liquid water, all at equilibrium. There are also triple points for the coexistence of three solid phases, for example ice II, ice V and ice VI at 218 K (−55 °C) and 620 MPa (6120 atm).

For those high-pressure forms of ice which can exist in equilibrium with liquid, the diagram shows that melting points increase with pressure. At temperatures above 273 K (0 °C), increasing the pressure on water vapor results first in liquid water and then a high-pressure form of ice. In the range 251–273 K, ice I is formed first, followed by liquid water and then ice III or ice V, followed by other still denser high-pressure forms.

Phase diagram of water including high-pressure forms ice II, ice III, etc. The pressure axis is logarithmic. For detailed descriptions of these phases, see Ice.
The various triple points of water
Phases in stable equilibrium Pressure Temperature
liquid water, ice Ih, and water vapor 611.657 Pa[7] 273.16 K (0.01 °C)
liquid water, ice Ih, and ice III 209.9 MPa 251 K (−22 °C)
liquid water, ice III, and ice V 350.1 MPa −17.0 °C
liquid water, ice V, and ice VI 632.4 MPa 0.16 °C
ice Ih, Ice II, and ice III 213 MPa −35 °C
ice II, ice III, and ice V 344 MPa −24 °C
ice II, ice V, and ice VI 626 MPa −70 °C

Triple-point cells

Triple-point cells are used in the calibration of thermometers. For exacting work, triple-point cells are typically filled with a highly pure chemical substance such as hydrogen, argon, mercury, or water (depending on the desired temperature). The purity of these substances can be such that only one part in a million is a contaminant, called "six nines" because it is 99.9999% pure. A specific isotopic composition (for water, VSMOW) is used because variations in isotopic composition cause small changes in the triple point. Triple-point cells are so effective at achieving highly precise, reproducible temperatures, that an international calibration standard for thermometers called ITS–90 relies upon triple-point cells of hydrogen, neon, oxygen, argon, mercury, and water for delineating six of its defined temperature points.

Table of triple points

This table lists the gas–liquid–solid triple points of several substances. Unless otherwise noted, the data come from the U.S. National Bureau of Standards (now NIST, National Institute of Standards and Technology).[8]

Substance T [K] (°C) p [kPa]* (atm)
Acetylene 192.4 K (−80.7 °C) 120 kPa (1.2 atm)
Ammonia 195.40 K (−77.75 °C) 6.060 kPa (0.05981 atm)
Argon 83.8058 K (−189.3442 °C) 68.9 kPa (0.680 atm)
Arsenic 1,090 K (820 °C) 3,628 kPa (35.81 atm)
Butane[9] 134.6 K (−138.6 °C) 7×10−4 kPa (6.9×10−6 atm)
Carbon (graphite) 4,765 K (4,492 °C) 10,132 kPa (100.00 atm)
Carbon dioxide 216.55 K (−56.60 °C) 517 kPa (5.10 atm)
Carbon monoxide 68.10 K (−205.05 °C) 15.37 kPa (0.1517 atm)
Chloroform 175.43 K (−97.72 °C)[citation needed] 0.870 kPa (0.00859 atm)[citation needed]
Deuterium 18.63 K (−254.52 °C) 17.1 kPa (0.169 atm)
Ethane 89.89 K (−183.26 °C) 1.1×10−3 kPa (1.1×10−5 atm)
Ethanol[10] 150 K (−123 °C) 4.3×10−7 kPa (4.2×10−9 atm)
Ethylene 104.0 K (−169.2 °C) 0.12 kPa (0.0012 atm)
Formic acid[11] 281.40 K (8.25 °C) 2.2 kPa (0.022 atm)
Helium-4 (lambda point)[12] 2.1768 K (−270.9732 °C) 5.048 kPa (0.04982 atm)
Helium-4 (hcp−bcc−He-II)[13] 1.463 K (−271.687 °C) 26.036 kPa (0.25696 atm)
Helium-4 (bcc−He-I−He-II)[13] 1.762 K (−271.388 °C) 29.725 kPa (0.29336 atm)
Helium-4 (hcp−bcc−He-I)[13] 1.772 K (−271.378 °C) 30.016 kPa (0.29623 atm)
Hexafluoroethane[14] 173.08 K (−100.07 °C) 26.60 kPa (0.2625 atm)
Hydrogen 13.8033 K (−259.3467 °C) 7.04 kPa (0.0695 atm)
Hydrogen chloride 158.96 K (−114.19 °C) 13.9 kPa (0.137 atm)
Iodine[15] 386.65 K (113.50 °C) 12.07 kPa (0.1191 atm)
Isobutane[16] 113.55 K (−159.60 °C) 1.9481×10−5 kPa (1.9226×10−7 atm)
Krypton 115.76 K (−157.39 °C) 74.12 kPa (0.7315 atm)
Mercury 234.3156 K (−38.8344 °C) 1.65×10−7 kPa (1.63×10−9 atm)
Methane 90.68 K (−182.47 °C) 11.7 kPa (0.115 atm)
Neon 24.5561 K (−248.5939 °C) 43.332 kPa (0.42765 atm)
Nitric oxide 109.50 K (−163.65 °C) 21.92 kPa (0.2163 atm)
Nitrogen 63.18 K (−209.97 °C) 12.6 kPa (0.124 atm)
Nitrous oxide 182.34 K (−90.81 °C) 87.85 kPa (0.8670 atm)
Oxygen 54.3584 K (−218.7916 °C) 0.14625 kPa (0.0014434 atm)
Palladium 1,825 K (1,552 °C) 3.5×10−3 kPa (3.5×10−5 atm)
Platinum 2,045 K (1,772 °C) 2×10−4 kPa (2.0×10−6 atm)
Radon 202 K (−71 °C) 70 kPa (0.69 atm)
(mono)Silane[17] 88.48 K (−184.67 °C) 0.019644 kPa (0.00019387 atm)
Sulfur dioxide 197.69 K (−75.46 °C) 1.67 kPa (0.0165 atm)
Titanium 1,941 K (1,668 °C) 5.3×10−3 kPa (5.2×10−5 atm)
Uranium hexafluoride 337.17 K (64.02 °C) 151.7 kPa (1.497 atm)
Water[4][5] 273.16 K (0.01 °C) 0.611657 kPa (0.00603659 atm)
Xenon 161.3 K (−111.8 °C) 81.5 kPa (0.804 atm)
Zinc 692.65 K (419.50 °C) 0.065 kPa (0.00064 atm)

Notes:

  • For comparison, typical atmospheric pressure is 101.325 kPa (1 atm).
  • Before the new definition of SI units, water's triple point, 273.16 K, was an exact number.

See also

References

  1. ^ a b IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (1994) "Triple point". doi:10.1351/goldbook.T06502.
  2. ^ Definition of the kelvin at BIPM.
  3. ^ James Thomson (1873) "A quantitative investigation of certain relations between the gaseous, the liquid, and the solid states of water-substance", Proceedings of the Royal Society, 22 : 27–36. From a footnote on page 28: " … the three curves would meet or cross each other in one point, which I have called the triple point".
  4. ^ a b International Equations for the Pressure along the Melting and along the Sublimation Curve of Ordinary Water Substance. W. Wagner, A. Saul and A. Pruss (1994), J. Phys. Chem. Ref. Data, 23, 515.
  5. ^ a b Murphy, D. M. (2005). "Review of the vapour pressures of ice and supercooled water for atmospheric applications". Quarterly Journal of the Royal Meteorological Society. 131 (608): 1539–1565. Bibcode:2005QJRMS.131.1539M. doi:10.1256/qj.04.94. S2CID 122365938.
  6. ^ Carr, Michael H. (2007). The Surface of Mars. Cambridge University Press. p. 5. ISBN 978-0-521-87201-0.
  7. ^ Murphy, D. M. (2005). "Review of the vapour pressures of ice and supercooled water for atmospheric applications". Quarterly Journal of the Royal Meteorological Society. 131 (608): 1539–1565. Bibcode:2005QJRMS.131.1539M. doi:10.1256/qj.04.94. S2CID 122365938.
  8. ^ Cengel, Yunus A.; Turner, Robert H. (2004). Fundamentals of thermal-fluid sciences. Boston: McGraw-Hill. p. 78. ISBN 0-07-297675-6.
  9. ^ See Butane (data page)
  10. ^ See Ethanol (data page)
  11. ^ See Formic acid (data page)
  12. ^ Donnelly, Russell J.; Barenghi, Carlo F. (1998). "The Observed Properties of Liquid Helium at the Saturated Vapor Pressure". Journal of Physical and Chemical Reference Data. 27 (6): 1217–1274. Bibcode:1998JPCRD..27.1217D. doi:10.1063/1.556028.
  13. ^ a b c Hoffer, J. K.; Gardner, W. R.; Waterfield, C. G.; Phillips, N. E. (April 1976). "Thermodynamic properties of 4He. II. The bcc phase and the P-T and VT phase diagrams below 2 K". Journal of Low Temperature Physics. 23 (1): 63–102. Bibcode:1976JLTP...23...63H. doi:10.1007/BF00117245. S2CID 120473493.
  14. ^ See Hexafluoroethane (data page)
  15. ^ Walas, S. M. (1990). Chemical Process Equipment – Selection and Design. Amsterdam: Elsevier. p. 639. ISBN 0-7506-7510-1.
  16. ^ See Isobutane (data page)
  17. ^ "Silane-Gas Encyclopedia". Gas Encyclopedia. Air Liquide.
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