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Modern Engineering Thermodynamics

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418 CHAPTER 12: Mixtures of Gases and Vapors<br />

CRITICAL THINKING<br />

On page 77 of the July/August 1993 issue of Family Handyman magazine, a helpful hint is given on how to determine the<br />

amount of propane remaining a cook stove tank. According to this magazine you just “Pour a cup of hot water over the<br />

outside of the tank. A condensation line will appear on the tank surface at the level of the remaining propane.”<br />

Since the formation of a “condensation line” requires reducing the liquid-vapor interface inside the tank to a temperature<br />

below the dew point temperature, can you explain how this test works? Are there any conditions under which this test<br />

would not work? (Hint: Look at the thermodynamics of the propane’s evaporation and condensation processes that result<br />

from the heating by the hot water and the subsequent cooling by the local atmosphere.)<br />

this mixture are treated as ideal gases (even though we say water vapor and not water gas). This particular mixture<br />

of ideal gases is important because of its meteorological and environmental comfort implications.<br />

To begin this discussion, we define two new composition measures for the amount of water vapor present in the<br />

mixture. Both measures are a type of humidity, as is shown. 5<br />

1. The relative humidity ϕ is the ratio of the actual partial pressure of the water vapor present in the mixture to<br />

the saturation pressure of the water vapor at the temperature of the mixture, or<br />

Relative humidity = ϕ = p w<br />

p sat<br />

(12.24)<br />

The value of p sat can be found in Table C.1 in Thermodynamic Tables to accompany <strong>Modern</strong> <strong>Engineering</strong> <strong>Thermodynamics</strong><br />

at the temperature of the mixture. Since 0 ≤ ϕ ≤ 1, the relative humidity is normally reported as a<br />

percentage. This is the common meteorological humidity measure.<br />

2. The humidity ratio ω is the ratio of the mass of water vapor present in the mixture divided by the mass of dry<br />

air present in the mixture, or<br />

Humidity ratio ω = m w<br />

m a<br />

(12.25)<br />

where m m = m a + m w , and p m = p a + p w = atmospheric pressure. Assuming ideal gas behavior for both the<br />

air and water vapor, we can write m w = p w V m / ðR w T m Þ and m a = p a V m / ðR a T m Þ, then<br />

ω = p wR a<br />

p a R w<br />

= p wM w<br />

p a M a<br />

= 18:016p w<br />

= 0:622 p <br />

w<br />

= 0:622<br />

28:97p a p a<br />

p w<br />

p m − p w<br />

<br />

(12.26a)<br />

Dew point<br />

temperature<br />

isotherm<br />

From Eq. (12.24), we find that p w = ϕp sat , and substituting this into Eq. (12.26a)<br />

provides a formula that relates the two humidity measures:<br />

ω = 0:622ϕ p <br />

sat<br />

ϕp sat<br />

= 0:622<br />

p a p m − p w<br />

(12.26b)<br />

T<br />

p w<br />

Atmospheric<br />

temperature<br />

isotherm<br />

A colorful term from the meteorological profession is the dew point temperature<br />

T DP , which is the temperature at which liquid water (dew) condenses<br />

out of the atmosphere at constant atmospheric pressure (and consequently at<br />

constant water vapor partial pressure):<br />

ω<br />

FIGURE 12.1<br />

The partial pressure and dew point temperature of<br />

a mixture of water vapor and dry air.<br />

T DP = T sat ðevaluated at p w Þ (12.27)<br />

If the partial pressure of the water vapor (p w ) is known, then the dew point<br />

temperature can be found in Table C.2. Figure 12.1 illustrates these concepts<br />

on a pressure-specific volume schematic.<br />

5 Since neither of these two humidity measures corresponds to any of the four composition measures previously discussed, this brings<br />

the number of composition measures used in this chapter to six.

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