Triple point

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] For example, the triple point ofmercury occurs at a temperature of −38.83440 °C and a
pressure of 0.2 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
ferent fluid phases (lambda point).[1]
multiple polymorphs. Helium-4 is a special case that presents a triple point involving two dif

The triple point of water is 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 is fixed by definition, rather than measured. 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 byJames Thomson, brother of Lord Kelvin.[3]

Contents
Triple point of water
Gas–liquid–solid triple point
High pressure phases
Triple point cells
Table of triple points
See also
References

Triple point of water

Gas–liquid–solid triple point

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 273.16 K (0.01 °C; 32.02 °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 dotted 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 aliquefaction).
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]

High pressure phases

At high pressures, water has a complex phase diagram with 15
known phases of ice and several triple points including ten 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 exampleice II, ice V
and ice VI at 218 K (−55 °C) and 620 MPa (6120 atm).
A typical phase diagram. The solid green line applies to
For those high-pressure forms of ice which can exist in most substances; the dotted green line gives the
equilibrium with liquid, the diagram shows that melting points anomalous behavior of water
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, seeIce.

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. When it is a water-based cell, a
special isotopic composition called VSMOW is used because it is very pure and produces temperatures that are more comparable from lab
to lab. Triple point cells are so effective at achieving highly precise, reproducible temperatures, 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).[7]
 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) 6.076 kPa (0.05997 atm)
Argon 83.81 K (−189.34 °C) 68.9 kPa (0.680 atm)
Arsenic 1,090 K (820 °C) 3,628 kPa (35.81 atm)

Butane[8] 134.6 K (−138.6 °C) 7 × 10−4 kPa

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[9] 175.43 K (−97.72 °C) 0.870 kPa (0.00859 atm)

Deuterium 18.63 K (−254.52 °C) 17.1 kPa (0.169 atm)

Ethane 89.89 K (−183.26 °C) 8 × 10−4 kPa

Ethanol[10] 150 K (−123 °C) 4.3 × 10−7 kPa

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)

2.1768 K
Helium-4 (lambda point)[12] 5.048 kPa (0.04982 atm)
(−270.9732 °C)

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-
1.762 K (−271.388 °C) 29.725 kPa (0.29336 atm)
II)[13]

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 13.84 K (−259.31 °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

Krypton 115.76 K (−157.39 °C) 74.12 kPa (0.7315 atm)

Mercury 234.2 K (−39.0 °C) 1.65 × 10−7 kPa

Methane 90.68 K (−182.47 °C) 11.7 kPa (0.115 atm)
Neon 24.57 K (−248.58 °C) 43.2 kPa (0.426 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 54.36 K (−218.79 °C) 0.152 kPa (0.00150 atm)

Palladium 1,825 K (1,552 °C) 3.5 × 10−3 kPa

Platinum 2,045 K (1,772 °C) 2.0 × 10−4 kPa

Radon 202 K (−71 °C) 70 kPa (0.69 atm)

(mono)Silane[17] 88.48 K (−184.67 °C) 0.00019644 bar (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

Uranium hexafluoride 337.17 K (64.02 °C) 151.7 kPa (1.497 atm)

[4][5]
 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)

* Note: for comparison, typical atmospheric pressure is 101.325 kPa (1 atm).

See also
Critical point (thermodynamics)
Gibbs' phase rule

References
1. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (1994)
"Triple point (http://goldbook.iupac.org/T06502.html)".
2. Definition of the kelvin (http://www1.bipm.org/en/si/base_units/)at BIPM
3. James Thomson (1873)"A quantitative investigation of certain relations between the gaseous, the liquid, and the solid
states of water-substance,"(https://babel.hathitrust.org/cgi/pt?id=hvd.32044106377062;view=1up;seq=47) 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 thetriple point."
4. International Equations for the Pressure along the Melting and along the Sublimation Curve of Ordinaryater
W Substance
(https://www.nist.gov/srd/upload/jpcrd477.pdf) W. Wagner, A. Saul and A. Pruss (1994), J. Phys. Chem. Ref. Data,23,
515.
5. Murphy, D. M. (2005). "Review of the vapourpressures of ice and supercooled water for atmospheric applications".
Quarterly Journal of the Royal Meteorological Society. 131 (608): 1539–1565. Bibcode:2005QJRMS.131.1539M(http://ad
sabs.harvard.edu/abs/2005QJRMS.131.1539M) . doi:10.1256/qj.04.94 (https://doi.org/10.1256%2Fqj.04.94).
6. Carr, Michael H. (2007). The Surface of Mars. Cambridge University Press. p. 5.ISBN 0-521-87201-4.
7. Cengel, Yunus A.; Turner, Robert H. (2004). Fundamentals of thermal-fluid sciences. Boston: McGraw-Hill. p. 78.ISBN 0-
07-297675-6.
8. See Butane (data page)
9. See Chloroform (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 Heliumat the Saturated Vapor
Pressure". Journal of Physical and Chemical Reference Data . 27 (6): 1217–1274. Bibcode:1998JPCRD..27.1217D(http://
adsabs.harvard.edu/abs/1998JPCRD..27.1217D) . doi:10.1063/1.556028 (https://doi.org/10.1063%2F1.556028).
13. Hoffer, J. K.; Gardner, W. R.; Waterfield, C. G.; Phillips, N. E. (April 1976). "Thermodynamic properties of4He. 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 (http://adsabs.harvard.edu/abs/1976JL TP...23...63H). doi:10.1007/BF00117245 (https://doi.o
rg/10.1007%2FBF00117245).
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"(https://encyclopedia.airliquide.com/silane). Gas Encyclopedia. Air Liquide. Retrieved 10 June
2018.

Retrieved from "https://en.wikipedia.org/w/index.php?title=T

riple_point&oldid=839098503"

This page was last edited on 1 May 2018, at 07:14.

Text is available under theCreative Commons Attribution-ShareAlike License ; additional terms may apply. By using this site,
you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of theWikimedia Foundation, Inc., a
non-profit organization.