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IEA Solar Heating and Cooling Programm - NachhaltigWirtschaften.at

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<strong>IEA</strong> SHC Task 38 <strong>Solar</strong> Air Conditioning <strong>and</strong> Refriger<strong>at</strong>ion Subtask C2-A, November 9, 2009<br />

From Figure 1 the steady-st<strong>at</strong>e internal he<strong>at</strong> flows of the vessels are as follows.<br />

Evapor<strong>at</strong>or: Q = m&<br />

⋅ ( h − )<br />

& (1)<br />

E, int v 10<br />

h8<br />

Condenser: Q = m&<br />

⋅ ( h − )<br />

& (2)<br />

C, int v 7<br />

h8<br />

Q& = & & & &<br />

(3)<br />

,<br />

m ⋅ h − m ⋅ h + m − m ⋅ h<br />

Absorber: A int v 10 sol,<br />

w 1<br />

(<br />

sol,<br />

w v<br />

)<br />

5<br />

Q& = & & & &<br />

(4)<br />

,<br />

m ⋅ h + m − m ⋅ h − m ⋅ h<br />

Gener<strong>at</strong>or: G int v 7<br />

(<br />

sol,<br />

w v<br />

)<br />

4 sol,<br />

w 3<br />

In equ<strong>at</strong>ions (1) to (4),<br />

& is the mass flow of the diluted solution <strong>and</strong> m&<br />

v<br />

is the mass flow<br />

m<br />

sol , w<br />

of the refrigerant w<strong>at</strong>er vapour which is of equal value <strong>at</strong> st<strong>at</strong>e points 7 <strong>and</strong> 10 in Figure 1.<br />

Equ<strong>at</strong>ions (1) to (4) are based on the calcul<strong>at</strong>ion of internal enthalpies for LiBr/w<strong>at</strong>er solution<br />

<strong>and</strong> refrigerant vapour which requires sound knowledge of these properties. For<br />

comput<strong>at</strong>ional purposes this means th<strong>at</strong> a property d<strong>at</strong>abase of both LiBr/w<strong>at</strong>er <strong>and</strong> w<strong>at</strong>er<br />

vapour has to be implemented into the simul<strong>at</strong>ion model <strong>and</strong> usually requires timeconsuming<br />

iter<strong>at</strong>ions.<br />

The main aim of the model presented is to account for the dynamics. Therefore, no detailed<br />

steady-st<strong>at</strong>e simul<strong>at</strong>ion with all st<strong>at</strong>e points was performed but a simpler approach was taken<br />

which considers the most important physical properties only. This may be refined l<strong>at</strong>er on but<br />

is not intended to be the focus of this work. This kind of refinement will not change the basic<br />

findings of this report. So, to keep the model fast, equ<strong>at</strong>ions (1) to (4) can be simplified using<br />

the l<strong>at</strong>ent he<strong>at</strong> of evapor<strong>at</strong>ion <strong>and</strong> sorption, r <strong>and</strong> l, as shown in equ<strong>at</strong>ions (6) to (9). This<br />

approach has been proposed by Ziegler [4] to avoid a detailed enthalpy calcul<strong>at</strong>ion for each<br />

st<strong>at</strong>e point. Please note th<strong>at</strong> the l<strong>at</strong>ent he<strong>at</strong> is taken <strong>at</strong> condenser pressure. The dependency<br />

of l<strong>at</strong>ent he<strong>at</strong> on temper<strong>at</strong>ure is tre<strong>at</strong>ed according to Plank’s rule [4].<br />

Moreover, not all internal temper<strong>at</strong>ures in Figure 1 are being calcul<strong>at</strong>ed in the model.<br />

Instead, each vessel is being modelled using external <strong>and</strong> internal mean temper<strong>at</strong>ures of the<br />

respective fluids (he<strong>at</strong> carrier <strong>and</strong> working fluid) as well as a mean vessel temper<strong>at</strong>ure.<br />

External mean he<strong>at</strong> carrier temper<strong>at</strong>ures ϑX<br />

are being calcul<strong>at</strong>ed using the arithmetic mean<br />

temper<strong>at</strong>ure of inlet <strong>and</strong> outlet temper<strong>at</strong>ure. Internal mean temper<strong>at</strong>ures<br />

page 64<br />

T X are assumed to<br />

be the mean of the equilibrium temper<strong>at</strong>ures of strong <strong>and</strong> weak solution <strong>and</strong> of the

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