The Phase Rule and Its Applications. Alexander Findlay

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The Phase Rule and Its Applications - Alexander Findlay

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356.8 40° 5.516 200° 1162.5 60° 14.932 250° 2973.4 80° 35.54 270° 4110.1 100° 76.00 364.3° (critical temperature) 14790.4 (194.6 atm.) (critical pressure).

      The pressure is, of course, independent of the relative or absolute volumes of the liquid and vapour; on increasing the volume at constant temperature, a certain amount of the liquid will pass into vapour, and the pressure will regain its former value. If, however, the pressure be permanently maintained at a value different from that corresponding to the temperature employed, then either all the liquid will pass into vapour, or all the vapour will pass into liquid, and we shall have either vapour alone or liquid alone.

      Upper Limit of Vaporization Curve.—On continuing to add heat to water contained in a closed vessel, the pressure of the vapour will gradually increase. Since with increase of pressure the density of the vapour must increase, and since with rise of temperature the density of the liquid must decrease, a point will be reached at which the density of liquid and vapour become identical; the system ceases to be heterogeneous, and passes into one homogeneous phase. The temperature at which this occurs is called the critical temperature. To this temperature there will, of course, correspond a certain definite pressure, called the critical pressure. The curve representing the equilibrium between liquid and vapour must, therefore, end abruptly at the critical point. At temperatures above this point no pressure, however great, can cause the formation of the liquid phase; at temperatures above the critical point the vapour becomes a gas. In the case of water, the critical temperature is 364.3°, and the critical pressure 194.6 atm.; at the point representing these conditions the vapour-pressure curve of water must cease.

      Sublimation Curve of Ice.—Vapour is given off not only by liquid water, but also by solid water, or ice. That this is so is familiar to every one through the fact that ice or snow, even at temperatures below the melting point, gradually disappears in the form of vapour. Even at temperatures considerably lower than 0°, the vapour pressure of ice, although small, is quite appreciable; and it is possible, therefore, to have ice and vapour coexisting in equilibrium. When we inquire into the conditions under which such a system can exist, we see again that we are dealing with a univariant system—one component existing in two phases—and that, therefore, just as in the case of the system water and vapour, there will be for each temperature a certain definite pressure of the vapour, and this pressure will be independent of the relative or absolute amounts of the solid or vapour present, and will depend solely on the temperature. Further, just as in the case of the vapour pressure of water, the condition of equilibrium between ice and water vapour will be represented by a line or curve showing the change of pressure with the temperature. Such a curve, representing the conditions of equilibrium between a solid and its vapour, is called a sublimation curve. At temperatures represented by any point on this curve, the solid (ice) will sublime or pass into vapour without previously fusing. Since ice melts at 0° (vide infra), the sublimation curve must end at that temperature.

      Vapour Pressure of Ice.

Temperature. Pressure in mm. mercury. Temperature. Pressure in mm. mercury.
-50° 0.050 -8° 2.379
-40° 0.121 -6° 2.821
-30° 0.312 -4° 3.334
-20° 0.806 -2° 3.925
-15° 1.279 4.602
-10° 1.999

      Equilibrium between Ice and Water. Curve of Fusion.—There is still another univariant system of the one component water, the existence of which, at definite values of temperature and pressure, the Phase Rule allows us to predict. This is the system solid—liquid. Ice on being heated to a certain temperature melts and passes into the liquid state; and since this system solid—liquid is univariant, there will be for each temperature a certain definite pressure at which ice and water can coexist or be in equilibrium, independently of the amounts of the two phases present. Since now the temperature at which the solid phase is in equilibrium with the liquid phase is known as the melting point or point of fusion of the solid, the curve representing the temperatures and pressures at which the solid and liquid are in equilibrium will represent the change of the melting point with the pressure. Such a curve is called the curve of fusion, or the melting-point curve.

      It was not until the middle of the nineteenth century that this connection between the pressure and the melting point, or the change of the melting point with the pressure, was observed. The first to recognize the existence of such a relationship was James Thomson,[31] who in 1849 showed that from theoretical considerations such a relationship must exist, and predicted that in the case of ice the melting point would be lowered by pressure. This prediction was fully confirmed by his brother, W. Thomson[32] (Lord Kelvin), who found that under a pressure of 8.1 atm. the melting point of ice was -0.059°; under a pressure of 16.8 atm. the melting point was -0.129°.

      The experiments which were first made in this connection were more of a qualitative nature, but in recent years careful measurements of the influence of pressure on the melting point of ice have been made more especially by Tammann,[33] and the results obtained by him are given in the following table and represented graphically in Fig. 2.

      Fusion Pressure of Ice.

Temperature. Pressure in kilogms. per sq. cm.[34] Change of melting point for an increase of pressure of 1 kilogm. per sq. cm.
-0° -2.5° -5° -7.5° -10.0° -12.5° -15.0° -17.5° -20.0° -22.1° 1 336 615 890 1155 1410 1625 1835 2042 2200 0.0074° 0.0090° 0.0091° 0.0094° 0.0100° 0.0116° 0.0119° 0.0121° 0.0133°

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