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Accepted Manuscript: Applied Thermal Engineering
Accepted Manuscript: Applied Thermal Engineering
Accepted Manuscript: Applied Thermal Engineering
PII: S1359-4311(16)00012-0
DOI: http://dx.doi.org/doi: 10.1016/j.applthermaleng.2015.12.121
Reference: ATE 7535
Please cite this article as: R. Lizarte, J.D. Marcos, COP optimisation of a triple-effect H2O/LiBr
absorption cycle under off-design conditions, Applied Thermal Engineering (2016),
http://dx.doi.org/doi: 10.1016/j.applthermaleng.2015.12.121.
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1 COP optimisation of a triple-effect H2O/LiBr absorption cycle under
2 off-design conditions
5 Madrid, Spain
b
6 Escuela Técnica Superior Ingeniería Industrial, UNED, c/Juan del Rosal 12, 28040
7 Madrid, Spain
10 Highlights
16
17 Abstract
18 It is desirable for absorption chillers to attain the highest COP possible when working
19 under design conditions. If these conditions change during a working day, the control
20 variables must be readjusted in order to attain the optimal COP. This work shows the
22 design and off-design conditions. Computer simulations are conducted for different
23 evaporation and condensation temperatures, considering the same value for the change
24 in solution concentration (Δx) in all generators. These simulations estimate not only the
25 optimum COP as a function of the outlet HTG solution temperature, but also the
26 solution mass-flow rates to be pumped to each generator in order to attain that optimum.
27 For temperatures of 142ºC to 227ºC, the optimal COP ranged from 1.05 to 2.13, and the
28 solution mass flow rates range pumped to LTG, MTG, HTG were 2.1-22.1 kg/h, 2.2-
Page 1 of 31
29 23.8kg/h, and 2.9-44.6 kg/h per kW of cooling capacity, respectively. These results are
32 1. Introduction
33 Triple-effect H2O/LiBr absorption cycles match the guidelines set by the ambitious
34 "2020 climate and energy package", proposed by the EU. The three main goals of this
35 plan are: 1) a 20% reduction in EU greenhouse emissions from 1990 levels, 2) a 20%
36 improvement in the EU’s energy efficiency, and 3) raising the share of EU energy
38 Regarding the first goal, the H2O/LiBr-absorption technology makes use of a working
40 effects, and which entails a decrease in indirect CO2 emissions derived from its low
42 compression [2, 3]. As for the second goal of EU, concerning absorption machines,
43 more effects require higher heat-source temperature, although the machine is more
44 efficient ([4] - [6]). In air-cooled machines, this energy efficiency decreases when the
45 outdoor temperature increases, but operational costs are lower and they constitute a
46 suitable option for regions under water scarcity ([7]-[9]). Concerning the exergy
47 efficiency, Gomri [6] observed that when the evaporation temperature is varied from
48 4ºC to 10ºC and the condenser temperature is increased from 33ºC to 39ºC, the
49 maximum exergy efficiency values of the triple effect cooling system are in the range of
50 17.7-25.2%. Finally, regarding the third EU objective, this technology can be combined
51 with renewable energies. Waste heat has been used for driving absorption chillers, [10-
52 11], as has solar energy [12]-[19]. Eicker [20] compared some parameters of a single-
53 effect absorption chiller fed by vacuum-tube collectors and double- and triple-effect
54 absorption chillers fed by Fresnel collectors. This researcher concluded that higher
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55 primary energy ratio (PER) and lower specific costs (€ per cooling capacity) were
56 achieved by the triple-effect system. Yabase and Makita [21] suggested a solar cooling
57 system coupled with a triple-effect absorption chiller, driven by steam at 230ºC. They
58 achieved a 26% decrease in CO2 emissions in contrast to a solar cooling system coupled
59 with a double-effect machine. Regarding the corrosion that appears in the HTG at high
60 solution temperatures (above 200ºC) [22], research is under way to solve this problem,
62 these working conditions [24]. High solution temperatures provoke also problems
63 related to solution stability. These problems are mitigated by using less reactive
64 corrosion inhibitors such as lithium molybdate (Li2MoO4) and by using more stable
69 heptanol, 2-ethyl-1-hexanol and FC-171 offered the best alternatives for high
70 temperature systems. Currently, there are two models of H2O/LiBr triple effect
71 absorption chillers in the market [27, 28] and they are fed with temperatures up to
72 250ºC. This means that research aimed at avoiding corrosion and maintaining thermal
73 stability is successful.
74 Another way of avoiding this problem is to prevent H2O/LiBr from reaching high
76 Absorption chillers are devices that transfer heat at three temperature levels
79 HTG solution temperature for which the maximum COP is attained. According to the
80 literature, most researchers calculate the maximum COP in terms of the temperature of
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81 the HTG ([32], [6], [5], [33]). Grossman et al. [32] simulated a wide range of
85 1.729 with outlet HTG solution temperature of 218ºC and a 63% solution concentration
86 at the absorber inlet. For the same inlet conditions, the COP increased to 1.825 when the
87 solution mass flows of each generator were not the same. Kaita [34] carried out a
88 simulation analysis of the aforementioned configurations, but the new design included a
89 refrigerant heat exchanger (CHX) to recover heat from the condensed refrigerant
90 leaving the LTG. This configuration improved the COP by 0.03 to 0.05. On the other
91 hand, the concentration of the solution when entering the absorber decreased to 59.5%.
92 Sedigh and Saffari [35], having made a thermodynamic analysis of the DCCA
93 configuration, reported a design point with a COP of 1.7 for an evaporation temperature
94 of 8ºC, absorption and condensation temperatures of 35ºC, and an outlet HTG solution
95 temperature of 180ºC.
96 Marcos et al. [36] used a different criterion to reach the optimal COP for a double-effect
97 cycle. These researchers considered the same variation of solution concentration (Δx)
98 for each generator and calculated the maximum COP depending on Δx. They claimed
99 that this approach maximized the production of refrigerant. Their results were validated
100 experimentally. The criterion followed in [36] has not been applied for triple-effect
103 facilities, the machine works under off-design conditions most of the time. No mass
104 flow rates are available in the literature for optimising the COP under such conditions,
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106 The present work presents the calculation of optimal COPs for a triple-effect parallel-
107 flow absorption chiller under off-design conditions. The most suitable solution mass-
108 flow rates to be pumped to each generator, in order to reach the optimal COPs as the
109 outlet HTG solution temperature changes, are presented. A variable temperature heat-
110 source scenario can arise, for instance, when working with a solar-collector field. To the
111 authors´ knowledge, this is a novel type of analysis in some respects, since there are no
112 previous works that provide the mass flow rates to be pumped to each generator to get
113 the optimal COPs for a triple-effect parallel flow absorption chiller under off-design
114 conditions. Concerning the solution mass flow rates, most researchers obtain the design
115 point by setting a fixed value for the solution mass flow rate to meet the cooling
116 capacity [29], or considering equal solution mass flow rates to be pumped to each
117 generator [32], [34]. However, it is expected that the optimum solution mass flow rates
118 vary with the operating conditions. From a control point of view, the knowledge of
119 optimum mass flow rates is essential to take full advantage of the chiller as
121 A simulation code has been developed for a wide range of Δx, considering the same
122 value of Δx for each generator, as has been done for double-effect systems [36].
123 Different evaporation (5, 8, and 10ºC) and condensation temperatures (30ºC, 35ºC, and
124 40ºC) are considered. The results may be useful to optimise solar-cooling facilities with
127 Fig. 1 depicts a scheme of the triple-effect cycle studied. It is the double-condenser
129 Grossman [32], in which the refrigerant generated leaves the high and medium
130 temperature generators (HTG, MTG) and feeds the medium and low temperature
131 generators (MTG, LTG), respectively. This configuration was chosen because, on the
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132 one hand, it provides the highest COP [32], and on the other hand, from a regulation
133 standpoint, in contrast to the series configuration, it offers the possibility of setting the
134 solution mass-flow rate in each generator (m4, m11, and m17). This ability is essential if
138 The thermodynamic cycle has been modelled as a preliminary step for its simulation.
139 Thermodynamic properties of the H2O/LiBr solution were determined from the
140 correlations developed by Pátek and Klomfar [37]. The properties of liquid water and
141 steam were drawn from Moran and Shapiro [38]. Computer simulations were conducted
142 for te at 5ºC, 8ºC, and 10ºC, and tc at 30ºC, 35ºC, and 40ºC. Regarding Δx, it has been
143 considered that ΔxLTG = ΔxMTG = ΔxHTG. This criterion has been experimentally
144 validated for the COP optimisation of a double-effect absorption cycle, [36]. Therefore,
145 this criterion might be promising for triple effect cycles as well. In order to check it, a
146 scan of Δx in each generator (from 1% to 10%) has been performed with different Δx
147 combinations, never exceeding either the crystallization limit for low pressures, or the
148 maximum limit of the concentration and temperature of the solution of the correlations
149 by Pátek and Klomfar [37]. Fig. 2 shows the result of that scan. It can be observed, that
150 optimal COP values (black dots) are obtained when Δx are equal in each generator.
151 For a fixed te and tc, an optimal COP curve will be displayed. A total of six optimal
152 COP curves will be shown. The absolute maximum of these curves will be the design
153 point in each case. The calculations were made based on the following assumptions:
156 • Heat is not exchanged between the system and surroundings [6], [35].
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158 • Pressure drop in the tubing and components are considered negligible [6], [35].
159 • The refrigerant is saturated vapour at the outlet of the evaporator, and it is
162 • The refrigerant vapour generated in the HTG and MTG is totally condensed. All
163 the evolved heat is transferred to the MTG and LTG, respectively, as the energy
165 • The refrigerant is totally vaporized in the evaporator and totally absorbed into the
167 The computer program has been developed using MATLAB. By iterative simulation of
168 the cycle and by using the operating parameters reported in Table 1, the output
169 parameters determined were: enthalpies, solution and refrigerant mass-flow rates,
170 temperatures, solution concentration entering the absorber, heat-transfer rates in all heat
171 exchangers, and COP. The tolerance for the energy balance is kept within 0.5 %.
173 Principles of mass and species conservation, and first law of Thermodynamics are
175 (1)
176 (2)
177 (3)
178 The effectiveness of a heat exchanger (Eq.4) can be expressed as follows [39]
179 (4)
180 where it is considered that the heat-capacity rates of hot streams, Chot, are lower than
181 those of cold streams, Ccold, in normal operation (C=m·cp). The efficiencies of all heat
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183 Next, the aforementioned balances in all the components are shown:
184 HTG:
185 (5)
186 (6)
187 (7)
188 MTG:
189 (8)
190 (9)
191 (10)
192 (11)
193 M1R:
194 (12)
195 (13)
196 LTG:
197 (14)
198 (15)
199 (16)
200 (17)
201 HHX:
202 (18)
203 (19)
204 MHX:
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205 (20)
206 (21)
207 LHX:
208 (22)
209 (23)
210 ABS:
211 (24)
212 M2R:
213 (25)
214 (26)
215 COND:
216 (27)
217 EVAP
218 (28)
220 (29)
222 (30)
223 (31)
225 The coefficient of performance (COP) and the exergy efficiency of the cycle (ηex) are
226 defined by means of Eqs. (32) and (33), respectively and considering T0=25ºC.
227 (32)
228 (33)
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229 4. Results and discussions
230 Firstly, the results for te= 5ºC and tc= 30ºC, 35ºC, and 40 ºC, are shown in detail.
231 Afterwards, the results for the other values of te and the aforementioned values of tc are
234 Fig. 3 displays the COP and ηex against t18 for tc= 30ºC, 35ºC and 40ºC. The value of Δx
235 is displayed over each point of this curve. As expected, the COP decreased as tc
236 increased for a given t18 [6]. For tc= 30ºC, the COP curve attained an absolute maximum
237 (design point). This value, 1.94, was reached with 179.3ºC and ΔxLTG= ΔxMTG= ΔxHTG =
238 6%. Results for all the points of the cycle concerning to this design point are shown in
240 The highest COP values for tc= 35ºC and 40ºC are 1.78 and 1.6, respectively, and they
241 are achieved with t18= 219.4ºC and 221.8ºC. These are not absolute maximum points,
243 Besides, the effect of tc and t18 on the ηex of the system has been studied. As expected,
244 ηex increases as tc decreases. The highest value obtained is 0.43 and it is attained at
245 t18=155.1ºC and tc= 30ºC. Fig. 3 shows that, as expected [6], for a fixed te, as tc
246 increases, the maximum ηex occurs at a higher t18. It is observed that the maximum
247 values are higher than those obtained in [6]. It is also observed, that t18 ranges from
248 140ºC to 227ºC, so that these kinds of chillers could be driven by medium-temperature
249 collectors. The possibility of feeding a triple-effect absorption chiller with a solar
250 collector field fits with the priorities for solar thermal cooling and refrigeration
252 Fig. 3 also reflects that, as tc decreases, t18 attains a smaller minimum value. That is, for
253 tc= 40ºC, the minimum value for t18 is 195.3ºC, for tc= 35ºC it is 169.4ºC, and for
Page 10 of 31
254 tc=30ºC it is 141.6ºC. Thus, it can be seen, that the lower tc is, the more advantage can
257 The following paragraphs show the solution concentration, mass flow, and heat-transfer
258 rates, and mechanical power for these optimal COP curves.
260 The solution concentration leaving the absorber (x1) is defined once te and ta are fixed.
261 For tc= 30ºC, 35ºC, and 40ºC, x1 is 52.2%, 54.9%, and 57.4%, respectively. The
262 solution concentration returning to the absorber (x8) was maintained below the
265 Fig. 4 shows the solution mass-flow rates distributed to each generator as a function of
266 t18. The mass-flow rate for HTG (m17) is higher than those for MTG (m11) and LTG
267 (m4). It can be seen that, up to a certain value of t18, a minor change in the solution
268 mass-flow rates (m4, m11, m17) can result in dramatic increases in COPs. Subsequently,
269 any increase in the flow rate has little effect. It is also observed that, for a certain t18, the
270 mass-flow rates to be pumped to the generators increases with tc. For instance, for t18=
271 195ºC, if tc= 30ºC, m17= 4.65 kg/h, but if tc= 40ºC, the value of m17 becomes 10-fold the
272 aforementioned value. Therefore, this graph shows the importance of controlling the
273 solution mass-flow rate to be pumped to each generator as t18 and tc change.
274 The total solution mass-flow rate varies with t18 between 9.4 kg/h and 90 kg/h. The
275 solution mass-flow rates required in each generator to reach the highest COP (1.94) are
276 m4= 4.14 kg/h, m11= 4.53 kg/h and m17= 5.97 kg/h, and the refrigerant mass-flow rates
277 generated are m26= 0.43 kg/h, m23= 0.47 kg/h, and m21= 0.62 kg/h.
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279 The ratio md:mr in HTG increases as t18 increases ( Eq. 6). This makes QHTG decrease
280 and COP increase (Eq. 7, 32). In addition, as expected, QHTG decreases as tc decreases
281 (Fig. 5). QLTG is barely influenced by the increment of tc and t18 (Fig. 5). Fig. 6 shows
282 that, for all tc, as t18 increases, the values of QHHX, QMHX, QLHX decrease and become
283 more similar. On the other hand, Wp ranges from 1 W to 8.6 W. Particularly, at the point
284 with the highest COP, the heat-transfer rates in the heat exchangers and the pump power
285 are: QHTG= 0.52 kW, QMTG= 0.39 kW, QLTG= 0.35 kW, QCOND= 0.35 kW, QABS= 1.17
286 kW, QHHX= 0.21 kW, QMHX= 0.25 kW, QLHX= 0.21 kW, and Wp= 1 W. These heat-
287 transfer values are in the same order of magnitude as those reported by Sedigh and
290 The solution concentration leaving the absorber, for tc= 30ºC, 35ºC, and 40ºC, is 50.1%,
291 53%, and 55.7%, respectively. The solution concentration returning the absorber (x 8)
293 Fig. 7 plots COP and ηex against t18 for a new evaporation temperature, te= 8ºC, and for
294 tc= 30ºC, 35ºC, and 40ºC. As expected, for a given t18, COP increases when te increases
295 [6]. For tc= 30ºC and 35ºC, the COP curves show absolute maximum values (design
296 points). These values are 2.05 and 1.87, and they are attained with t18= 162.4ºC and
297 202.6ºC, respectively, and with ΔxLTG = ΔxMTG = ΔxHTG = 6% and 7%, respectively. The
298 maximum COP for tc = 40ºC (1.74) is attained for t18= 227ºC. It is not an absolute
299 maximum, so it is not going to be considered a design point. The maximum value of ηex
301 Comparing Fig. 3 and Fig. 7, it is observed that as te increases, t18 attains a smaller for
302 t18 is 183.9ºC, for tc= 35ºC it is 154.7ºC, and for tc= 30ºC it is 128.7ºC (Fig. 7). Thus, it
303 can be seen that, the higher te is, the more advantage can be taken of a solar collector
304 field.
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305 The total solution mass-flow rate varies with t18 between 7.3 kg/h and 87 kg/h. If tc=
306 30ºC, the solution mass-flow rates required in each generator to reach the highest COP
307 (design point) are m4= 4.08 kg/h, m11= 4.4 kg/h and m17= 5.6 kg/h, and the refrigerant
308 mass flow rates generated are m26= 0.44 kg/h, m23= 0.47 kg/h, and m21= 0.6 kg/h. On
309 the other hand, if tc= 35ºC, the solution mass-flow rates required in each generator to
310 reach the highest COP (design point) are m4= 3.65 kg/h, m11= 3.98 kg/h and m17= 5.41
311 kg/h while the refrigerant mass-flow rates generated are m26= 0.43 kg/h, m23= 0.46 kg/h
312 and m21= 0.63kg/h. It was found that, in both cases, the solution mass-flow rates
315 The solution concentration leaving the absorber, for tc= 30ºC, 35ºC, and 40ºC, is 48.6%,
316 51.8%, and 54.5%, respectively. The solution concentration returning the absorber (x8)
318 Fig. 9 plots COP and ηex against t18 for a new evaporation temperature, te= 10ºC, and for
319 tc= 30ºC, 35ºC, and 40ºC. For tc= 30ºC and 35ºC, the COP curves reach absolute
320 maximums (design points). These values are 2.13 and 1.94, and they are attained with
321 t18= 152.4ºC, 184.5ºC, respectively. In addition, in both cases ΔxLTG = ΔxMTG = ΔxHTG =
322 6%. The maximum COP for tc= 40ºC (1.78) is attained for t18= 213.4ºC. It is not an
323 absolute maximum, and therefore it is not considered a design point. With this new
324 value of te, for tc=30ºC, the minimum value for t18 is 120.2ºC, for tc=35ºC it is 146.6ºC
325 and for tc=40ºC it is 172.7ºC (Fig. 9). The maximum value of ηex is 0.41 and it is
326 attained at t18=133 ºC and tc= 30ºC. Comparing Figs. 3, 7 and 9 it is observed that, as
327 expected [6], for a fixed tc, as te increases, ηex decreases and the maximum ηex occurs at
328 a lower t18. It is also observed that the maximum values are higher than those obtained
329 in [6].
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330 The total solution mass-flow rate varies with t18 between 7.13 kg/h and 85 kg/h. If tc=
331 30ºC, the solution mass-flow rates distributed to each generator to reach the highest
332 COP (design point) are m4= 4.04 kg/h, m11= 4.31 kg/h and m17= 5.35 kg/h (Fig. 10.)
333 while the refrigerant mass flow rates generated are m26= 0.44 kg/h, m23= 0.47 kg/h, and
334 m21= 0.59 kg/h. On the other hand, if tc= 35ºC, the solution mass-flow rates required in
335 each generator to reach the highest COP (design point) are m4= 4.15 kg/h, m11= 4.5
336 kg/h, and m17= 5.95 kg/h (Fig. 10), whereas the refrigerant mass-flow rates generated are
337 m26= 0.43 kg/h, m23= 0.47 kg/h, and m21= 0.62 kg/h.
338 A comparison of Fig. 4, 8 and 10 shows that, for fixed t18 and tc, with the increase of te,
339 the solution mass-flow rates to be pumped to LTG, MTG and HTG decrease. That is,
340 for t18 = 195ºC and tc = 35ºC, if te = 5ºC the solution mass-flow rates pumped are m4 =
341 7.9 kg/h, m11 = 8.9 kg/h and m17= 12.6 kg/h, but if te =10ºC, they are m4 = 4.1 kg/h, m11=
342 4.5 kg/h and m17= 6 kg/h. Finally, it is also observed that, the design points derived from
343 different te and tc reach similar values for mass-flow rates of the solution to be pumped
345 To the authors´ knowledge, there are no experimental works on triple-effect parallel –
346 flow H2O/LiBr absorption chillers, therefore it is not feasible to experimentally validate
347 this model. On the other hand, the comparisons with those research works that use
348 correlations for the H2O/LiBr solution properties previous to those published by Pátek
349 and Klomfar do not apply, since those previous correlations are valid only up to 175ºC,
350 and the temperatures in a triple effect cycle go beyond this value. In order to discuss the
351 improvement of this methodology, a comparison with the results obtained by Sedigh
352 and Saffari [35] has been carried out. They simulated also a parallel-flow configuration
354 Table 2 shows the results obtained in [35] and from the present work for tc= 35ºC and
355 ɛHE=0.7. It can be observed that for values under off-design conditions, the results of the
Page 14 of 31
356 present work achieve an improvement in the COP up to 0.4. This reinforces the
357 necessity of controlling the mass flow rates pumped to each generator in off-design
358 conditions.
359 5. Conclusions
360 COP optimisation of a triple-effect parallel-flow H2O/LiBr absorption chiller has been
361 carried out for a variable-temperature heat source. Computer simulations were
362 conducted for a number of te (5ºC, 8ºC, and 10ºC) and tc (30ºC, 35ºC, and 40ºC), which
363 are the most commonly used values for te and tc in air-conditioning applications. The
364 same Δx in each generator was considered as an inlet condition. Optimal COP curves
365 have been built as a function of the outlet HTG solution temperature (t18) for each te and
366 tc. Design points are provided for each curve. These points are the absolute maxima of
368 Controlling the solution mass flow rates to be pumped to each generator is
369 essential when working with a heat source whose temperature cannot be
370 controlled, as it happens in solar cooling facilities. These results provide the
371 solution mass flow rates to be distributed to each generator to attain the optimal
372 COP when tc, te and tHTG change, in order to take full advantage of an absorption
373 chiller during its performance. The regulation of the mass flow rate can lead to
375 Different design points derived from different te and tc inlet conditions are
376 displayed. To reach those values, the mass-flow rates to be pumped to low,
377 medium, and high temperature generators are on average, 4 kg/h, 4.3 kg/h, and
378 5.7 kg/h, per kW of cooling capacity, respectively. The COP of those design
379 points range from 1.87 (te =8ºC, tc =35ºC) to 2.13 (te=10ºC, tc=30ºC).
380 When te is varied from 5ºC to 10ºC and tc is varied from 30ºC to 40ºC, the
383 te and tc, the optimal COPs reached are between 1.05 and 2.13 and the total
384 solution mass-flow rate pumped to the generators between 7.13 and 90 kg/h, per
386 The change in solution mass-flow rate with t18, tc and te, and its influence on the
387 optimal COP denotes the necessity of controlling the quantity pumped to each
388 generator. Up to a certain value of t18, a control of the solution, mass-flow rates
389 pumped to each generator is essential, due to their effect on the COP value.
390 Subsequently, the mass-flow rates remain constant, attaining similar values.
391 As tc decreases, and te increases, t18 reaches a smaller minimum value. Thus, it
392 can be concluded, that the higher te and the lower tc are, the more advantage can
395 Thus, these results can be useful for optimising the control regulation of future
397 energy.
398 Appendix
399 Acknowledgements
400 This research was funded by the Spanish Ministry of Science and Technology under
402 Nomenclature
Page 16 of 31
408 EVAP evaporator
415 M mixer
425 η efficiency
426 Subscripts
427 a absorption
428 c condensation
429 e evaporation
430 ex exergy
431 p pump
433 i inlet
Page 17 of 31
434 o outlet
435 r refrigerant
436 s solution
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497 http://members.igu.org/html/wgc2003/WGC_pdffiles/10626_1045222692_11599_1.pdf
500 resisting nickel alloy tube used in triple-effect LiBr/H2O absorption chiller. App.
502 [25] R. H. Reiner, W. Del Cul, H. Pérez-Blanco, M.R. Ally, A. Zaltash. Evaluation of
503 the potential performance additives for the advanced lithium bromide chiller. Oak Ridge
505 [26] S. Bennett. The effect of surfactants on steam absorption into lithium bromide
506 solution. M.S. thesis in mechanical engineering, Pennsylvania State University. 1995.
509 on 2015).
Page 20 of 31
510 [29] J.S. Kim, F. Ziegler, H. Lee. Simulation of the compressor-assisted triple-effect
511 H2O/LiBr absorption cooling cycles. App. Therm. Eng.22 (3) (2002) 295-308.
513 absorption cooling cycle using aqueous (lithium, potassium, sodium) nitrate solution as
515 [31] K. E. Herold, R. Radermacher, S.A. Klein. Absorption Chillers and Heat Pumps.
517 [32] G. Grossman, M. Wilk, RC DeVault, R.C. Simulation and performance analysis of
519 [33] S.C. Kaushik, A. Arora. Energy and exergy analysis of single effect and series
520 flow double effect water–lithium bromide absorption refrigeration systems. Int. J.
522 [34] Y. Kaita. Simulation results of triple-effect absorption cycles. Int. J. Refrigeration
526 [36] J.D. Marcos, M. Izquierdo, E. Palacios. New method for COP optimization in
527 water-and air-cooled single and double effect LiBr-water absorption machines. Int. J.
530 thermodynamic properties of LiBr–H2O solutions from 273 to 500 K over full
532 [38] M.J. Moran, H.N Shapiro. Fundamentals of engineering thermodynamics. 5th
534 [39] F.P. Incropera, D.P Dewitt, T.L Bergman, A.S Lavine. Fundamentals of Heat and
535 Mass Transfer, sixth ed. John Wiley & Sons. 2007.
Page 21 of 31
536 [40] Aleksandar Ivancic, Daniel Mugnier, Gerhard Stryi-Hipp, Werner Weiss. Solar
539
Page 22 of 31
540 Table A. Results for the state points of the cycle (te=5ºC, tc=30ºC).
541
point t (ºC) x (%) P (kPa) m (kg/h) h (kJ/kgK)
Page 23 of 31
28 30.0 - 4.4 1.5 125.7
542
543
Page 24 of 31
544
545
546
QHTG
21
HTG
18 17
Weak solution
Strong solution
Refrigarant QHHX
HHX
19 16
22
MTG
QMTG
23 12
20 11
M1s
13 10
QMHX
M1R MHX
24 14 9
QCOND
25
27 LTG
COND M2R
QLTG
26 5
4
28
15 M2s
6 3
QLHX
LHX
7 2
29 8
1
30
EVAP ABS
QEVAP QABS
547
548
549 Fig. 1 - Scheme of the triple-effect parallel-flow absorption cycle.
550
Page 25 of 31
551
552
553 Fig. 2 - Variation of COP and ηex with t18 and ΔxLTG, ΔxMTG, ΔxHTG (te= 5ºC, tc= 30ºC, 35ºC, 40ºC)
554
555
556
557 Fig. 3- Variation of COPopt and ηex with t18 and ΔxLTG, ΔxMTG, ΔxHTG (te= 5ºC, tc= 30ºC, 35ºC, 40ºC).
Page 26 of 31
558
559 Fig. 4 - Solution mass-flow rates as a function of t18 (QEVAP= 1 kW, te= 5ºC, tc= 30ºC, 35ºC, 40ºC)
560
561
562
563 Fig. 5 - Heat-transfer rates for three generators as a function of t18 (QEVAP= 1 kW, te= 5ºC, tc=
564 30ºC, 35ºC, 40ºC)
Page 27 of 31
565
566 Fig. 6 - Heat-transfer rates for three solution heat exchangers as a function of t18 (QEVAP= 1 kW,
567 te= 5ºC, tc= 30ºC, 35ºC, 40ºC).
568
569
570
571 Fig. 7 - Variation of COPopt and ηex with t18 and ΔxLTG, ΔxMTG, ΔxHTG (te= 8 ºC, tc= 30ºC, 35ºC,
572 40ºC).
573
574
575
Page 28 of 31
576
577 Fig. 8 - Solution mass-flow rates as a function of t18 (QEVAP= 1 kW, te= 8ºC, tc= 30ºC, 35ºC, 40
578 ºC).
579
580
581
582
583 Fig. 9 - Variation of COPopt and ηex with t18 and ΔxLTG, ΔxMTG, ΔxHTG (te= 10ºC, tc= 30ºC, 35ºC,
584 40ºC).
585
586
587
Page 29 of 31
588
589 Fig. 10 - Solution mass-flow rates as a function of t18 (QEVAP= 1 kW, te= 10ºC, tc= 30ºC, 35ºC, 40
590 ºC)
591
592
593
Page 30 of 31
594 Table 1. Operating parameters
595
QEVAP (kW) 1
te (ºC) 5, 8,10
εHX 0.8
ηpump 0.6
596
597 Table 2. Comparison of operation conditions
598
THTG(ºC) COP [35] COP [present work]
599
Page 31 of 31