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Modern Engineering Thermodynamics

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68 CHAPTER 3: Thermodynamic Properties<br />

Table 3.3 Triple Point Data for Various Materials<br />

Substance T (R) T (K) p (psia) p (kPa)<br />

Ammonia (NH 3 ) 351.7 195.4 0.89 6.16<br />

Carbon dioxide (CO 2 ) 389.9 216.6 75.98 523.8<br />

Helium-4 (λ point) 3.9 2.17 0.74 5.11<br />

Hydrogen (H 2 ) 24.9 13.84 1.03 7.13<br />

Neon (Ne) 44.2 24.57 6.35 43.77<br />

Nitrogen (N 2 ) 113.7 63.18 1.84 12.67<br />

Oxygen (O 2 ) 97.8 54.36 0.02 0.15<br />

Sulfur dioxide (SO 2 ) 355.9 197.7 0.02 0.17<br />

Water (H 2 O) 491.7 273.16 0.09 0.62<br />

Source: Adapted by permission of the publisher from Zemansky, M. W., Abbott, M. M., Van Ness, H. C., 1975. Basic <strong>Engineering</strong><br />

<strong>Thermodynamics</strong>, second ed. McGraw-Hill, New York.<br />

300,000<br />

100,000<br />

Additional solid<br />

ice phases<br />

VI<br />

VII<br />

50,000<br />

30,000<br />

II<br />

IV<br />

III<br />

V<br />

Compressible liquid<br />

Supercritical fluid<br />

10,000<br />

Pressure (psia)<br />

3203.8<br />

1000<br />

100<br />

10<br />

0.089<br />

0.01<br />

Solid<br />

(Ice (I))<br />

Solid−vapor<br />

equilibrium<br />

Liquid<br />

Liqid−vapor<br />

equilibrium<br />

Triple point<br />

Superheated<br />

vapor<br />

Gas<br />

Critical point<br />

0.002<br />

491.69<br />

Temperature (R)<br />

1165.1<br />

FIGURE 3.8<br />

Phase diagram for water (not drawn to scale).<br />

shows a more complete p-T phase diagram for water including 7 of its 15 known solid phases. Each intersection<br />

of three phase transition lines forms a new triple point.<br />

The vaporization curve for all known substances has a peak at a curious point, known as the critical point. This is<br />

the state at which the densities of the liquid and the vapor phases become equal and, consequently, where the<br />

physical interface between the liquid and the vapor disappears. At or above the critical state, there is no longer any<br />

physical difference between a liquid and a vapor. Substances existing under these conditions are called gases. In<br />

this text, we use the term gas to describe the state of any substance whose temperature is greater than its critical<br />

state temperature. A substance in the vapor phase that does not meet the definition of a gas is called a superheated<br />

vapor (sometimes just vapor). These definitions are illustrated in Figures 3.8 and 3.10. Table 3.4 gives the critical<br />

state temperature, pressure, and specific volume for various common pure substances. A larger critical state data<br />

table is given in Table C.12 of Thermodynamic Tables to accompany <strong>Modern</strong> <strong>Engineering</strong> <strong>Thermodynamics</strong>.<br />

Notice in Table 3.4 that, at 14.7 psia and 70.°F (530. R), ammonia is a vapor (T c > 530. R). Also, it should be clear<br />

from Figure 3.10 that, to liquefy any gas whose pressure is initially less than its critical pressure simply by increasing<br />

its pressure alone, the gas must first be made into a vapor by lowering its temperature below its critical temperature.<br />

Vapor-liquid condensation is shown by process A-B in Figure 3.10. Thus, for example, no matter how high the<br />

applied pressure, hydrogen cannot be liquefied unless its temperature is below 59.9 R (see Table 3.4).

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