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Modern Engineering Thermodynamics

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

12.8 PSYCHROMETRIC ENTHALPIES<br />

The psychrometric chart also contains enthalpy information that is useful in energy balance calculations. Though<br />

water vapor may be added or removed from the mixture by an air conditioning system, the mass flow rate of<br />

the dry air component is usually constant throughout the system. This makes it convenient to define the<br />

mixture’s specific enthalpy on a per unit mass of dry air basis, rather than on a per unit mass of mixture basis.<br />

Specific enthalpies so constructed are referred to as psychrometric enthalpies, denotedbyh # to distinguish them<br />

from the ordinary form of the specific enthalpy. Thus, the specific psychrometric enthalpy is defined as<br />

h # = H m /m a<br />

whereas the ordinary mixture specific enthalpy is defined as<br />

h m = H m /m m<br />

Note that, since H m = m a h # = m m h m = (m a + m w )h m , we have<br />

Further, since<br />

then,<br />

h # = ð1 + ωÞh m<br />

H m = H a + H w = m a h a + m w h w<br />

H m /m a = h # = h a + ðm w /m a Þh w = h a + ωh w (12.32)<br />

Values of h # are given on the psychrometric charts in Charts D.5 and D.6. 7<br />

EXAMPLE 12.10<br />

Air has a dry bulb temperature of 50.0°C and a relative humidity of 40.0% at a total pressure of 0.101 MPa. Calculate the<br />

value of h # from its definition and compare this value with that found in Chart D.6 for these conditions.<br />

Solution<br />

The basic definition of h # is given by Eq. (12.32) as h # = h a + ωh w , where h a = c p (T DB − T ref ). When the psychrometric Charts D.5<br />

and D.6 were developed, the reference temperature used in the h a ideal gas equation was chosen to be 0°C. From Table C.13b,<br />

we find for air that c p = 1.004 kJ/(kg·K). Then,<br />

h a = ½1:004 kJ=ðkg.KÞŠ½ð50:0 + 273:15 KÞ − ð0 + 273:15 KÞŠ = 50:2kJ=ðkg dry airÞ<br />

Equation (12.26b) gives the humidity ratio ω for this mixture as<br />

<br />

ϕp sat<br />

ω = 0:622<br />

p m − ϕp sat<br />

where, from Table C.1b, p sat = p sat (50.0°C) = 0.01235 MPa. Then,<br />

<br />

<br />

0:400 × 0:01235<br />

ω = 0:622<br />

0:101 − 0:400 × 0:01235<br />

kg water vapor<br />

= 0:0319<br />

kg dry air<br />

Since the water vapor in the mixture is superheated, its specific enthalpy h w is determined from Table C.3b at the temperature<br />

of the mixture and the partial pressure of the water vapor. From Eq. (12.24), we have p w = ϕp sat = 0.400 × 0.01235 = 5.00 ×<br />

10 −3 MPa. Then, from Table C.3b at 50.0°C and 5.00 × 10 −3 MPa, we find that h w = 2593.6 kJ/kg water vapor. Using the definition<br />

of h # given in Eq. (12.32), we now have<br />

<br />

<br />

<br />

h # kJ<br />

= h a + ωh w = 50:2<br />

kg dry air + kg water vapor<br />

kJ<br />

0:0319 × 2593:6<br />

kg dry air<br />

kg water vapor<br />

kJ<br />

= 133<br />

kg dry air<br />

Chart D.6 also gives this value for ω at T DB = 50.0°C and ϕ = 40.0%.<br />

7 Note that h a has a zero reference state at 0°F (not 0 R) in Chart D.6a and 0°C in Chart D.6b with the h w value coming from the<br />

appropriate steam table in each case. Recall that the choice of a reference state is arbitrary, so long as property differences are used in<br />

the calculations.

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