Hvac CH 4-2
Hvac CH 4-2
Hvac CH 4-2
Composition
mass fraction
where mA and mW are the mass of ammonia and water in solution, respectively
mall fraction
where MA (= 17.0 kg/kmol) and MW (= 18.0 kg/kmol) are the molecular weights of
ammonia and water respectively
where x is the liquid phase mole fraction of ammonia, PA and PW are the
saturation pressures of pure ammonia and pure water at that
temperature. ammonia-water solutions also deviate from ideal solution
behavior predicted by Raoult’s law in a negative manner at a given
temperature of the solution the actual vapour pressure will be less than
that predicted by Raoult’s law (activity coefficient is much smaller
than 1.0 For example, at a mass fraction of 0.4 and temperature of
40oC, Raoult’s law predicts a vapour pressure of 6.47 bar, whereas the
measured vapour pressure is 3.029 bar.
Equilibrium temperature-concentration
curve for NH3-H2O at a constant
pressure
Vapour phase:
where y is the vapour phase mole fraction of ammonia and P total is the total pressure.
It should be noted that PA and PW are equal to the partial pressures of ammonia and
water only if they behave as ideal gases. However since ammonia and water vapour
may not approach the ideal gas behavior at all temperatures and pressures, in general
PA and PW are not equal to the partial pressures. Using this method enthalpies of
ammonia-water mixtures in vapour phase have been obtained as functions of
temperature and mass fraction.
For point P
kPa and 1.227 kPa, respectively; and the specific vapour enthalpies of ammonia and
water are 1471.57 kJ/kg and 2519.9 kJ/kg, respectively, find a) the vapour pressure of the
mixture, and b) the specific enthalpy of the mixture.
a) Assume the vapour mixture to behave as a mixture of ideal gases, then the total
pressure of the mixture Pv is given by:
Find the dryness fraction (quality) and specific enthalpy of the two-phase (liquid &
vapour) of ammonia-water mixture using the following data:
Liquid phase mass fraction, ξL = 0.30
Vapour phase mass fraction, ξV = 0.87
Mass fraction of 2-phase mixture, ξ = 0.50
Specific enthalpy of saturated liquid, hL = 340 kJ/kg
Specific enthalpy of saturated vapour, hV = 1640 kJ/kg
The dryness fraction and temperature of the mixture (T 3) have to be obtained by trial-and-error
method by applying mixing rules. The fraction of the vapour in the mixture at 3 is then given
by
The process of mixing of two streams with heat transfer takes place in absorber and
generator of absorption refrigeration systems
Hence the inlet and outlet states, points 1 and 2 are identical on enthalpy-composition
diagram as shown in the figure. However, as there is possibility of vapour generation due to
flashing, the exit condition may be a mixture of saturated liquid and vapour at the outlet
pressure P2 then the exit temperature T2 will be much lower than the inlet temperature T 1.
Taking point 2 as in the two-phase region corresponding to the outlet pressure P 2, one can get
the vapour fraction and exit temperature T 2 by trial-end-error method as discussed earlier.
Two solution streams are mixed in a steady flow device. A heat transfer rate of 24 kW
takes place from the device. Find the exit concentration and enthalpy using the data given
below:
Stream 1: Mass flow rate, m1 = 0.1 kg/s
Concentration, ξ1 = 0.7
Enthalpy, h1 = 110 kJ/kg
Stream 2: Mass flow rate, m2 = 0.3 kg/s
Concentration, ξ2 = 0.4
Enthalpy, h2 = 250 kJ/kg
Generator/desorber
Condenser
Evaporator
Solution pump