Applied Thermal Engineering 30 (2010) 2180e2186 Contents lists available at ScienceDirect Applied Thermal Engineering journal homepage: www.elsevier.com/locate/apthermeng Thermodynamic simulation and evaluation of sugar refinery evaporators using a steady state modelling approach A.E. Lewis a, *, F. Khodabocus b, V. Dhokun b, M. Khalife c a Crystallization and Precipitation Research Unit, Department of Chemical Engineering, University of Cape Town, Cape Town, South Africa Department of Chemical and Environmental Engineering, University of Mauritius, Reduit, Mauritius c BluESP (Mauritius) Limited, President John Kennedy Street, Port-Louis, Mauritius b a r t i c l e i n f o a b s t r a c t Article history: Received 27 October 2009 Accepted 27 May 2010 Available online 2 June 2010 In a sugar refinery, the juice is concentrated through evaporation, with the objective of concentrating the juice to syrup as rapidly as possible. Because the heat of vaporization of water is relatively high, the evaporation process can be highly energy intensive, and therefore the economical use of steam is important in the refinery. This paper reports on the development of a simulation model for the evaporation sections of two Mauritian sugar refineries. The first objective was to use the simulation model to carry out an energy balance over the evaporators in order to assess the economy of steam usage over the refinery. The second objective was to examine to what extent a fundamental steady state model, based on thermodynamics (not kinetics) was capable of predicting the material and energy flows in two operating sugar refineries and thereby to evaluate the applicability of the modelling framework. The simulation model was validated using historical data as well as data from the plant DCS system. The simulation results generally correlated well with the measured values, except for one of the evaporators on one refinery. Some suggestions were made as to the cause of the discrepancy. On balance, it was found that both refineries are extremely efficient in terms of steam and equipment usage and that there is not much scope for energy optimisation within the present configuration e nor for much spare steam capacity for an additional refinery. It was also shown that steady state process simulation, using thermodynamic models, can generate a very useful representation of a working refinery. Besides being able to use the model to “benchmark” the operation and thus evaluate its performance as a whole as well as across individual units, it could also be used to evaluate refinery performance across refineries, nationally as well as globally. Ó 2010 Elsevier Ltd. All rights reserved. Keywords: Sugar refinery Modelling Simulation Aspen Plus Steam consumption Energy balance 1. Introduction In a raw sugar or white sugar refinery, the juice is initially concentrated through a process of evaporation, during which water is removed from the solution by vaporization. The juice usually enters the evaporator at approximately 12 mass percent sucrose (12 Brix) and is concentrated to about 65 mass percent (65 Brix) in the final evaporator [1]. The objective of the process is to concentrate the thin juice to a syrup as rapidly as possible, at temperatures that will minimise sucrose losses and colour formation, while at the same time minimise steam consumption. Because the heat of vaporisation of water (latent heat) is relatively high (2257 kJ/kg), the evaporation process can be highly energy * Corresponding author. Tel.: þ27 21 650 4091; fax: þ27 21 650 5501. E-mail address: Alison.Lewis@uct.ac.za (A.E. Lewis). 1359-4311/$ e see front matter Ó 2010 Elsevier Ltd. All rights reserved. doi:10.1016/j.applthermaleng.2010.05.031 intensive. The traditional fuel of a sugar cane refinery is the final bagasse discharged by the mill. Steam, generated by burning bagasse under steam boilers, is then used for mechanical purposes (live steam) and subsequently for heating (exhaust steam) [2]. Using steam economically in the sugar factory is as important as generating it efficiently, but far more attention has been paid to the generation step [3]. However, as sugar refineries become more complex; as quality standards become more stringent; and as energy consumption and wastage is of increasing concern, it has become necessary to pay more attention to the efficient and economical use of steam in the refinery itself. An energy balance is also important to be able to investigate the performance and capacity of the system and to compare performance with the original equipment specs. In addition, with the commissioning of sugar refineries to further refine the raw sugar, there will be additional demands for steam as a source of energy for the refineries. A.E. Lewis et al. / Applied Thermal Engineering 30 (2010) 2180e2186 ZVv " 2181 # RT v dV lnZm V T;V;niej The particular focus of this paper is the expansion of two Mauritian sugar factories to include a refining step. The refineries will have additional steam requirements and thus place extra demands on the current steam. For this reason, it is an important exercise to be able ascertain firstly: to what extent the current steam production is optimally used and secondly: if there will be sufficient steam to cope with the extra demands. From a broader and more academic perspective, developing a model of the evaporator section of a sugar refinery has additional benefits. Sugar refineries are by and large run by very experienced operators who have the benefit of many years of plant expertise. However, partly because of this depth of experience, there is often not a very rigorous or fundamental approach to the energy and the material balance on the plant. Developing a model that is based on fundamental principles has two benefits: firstly, in the process of developing the model, the information about how the plant is configured and operated must be established. This is often an illuminating and educative exercise in itself. The second benefit is the ability to “benchmark” the operation against some standard and thus to be able to evaluate its performance as a whole as well as across individual units. Although it is the primary objective of this paper to answer the specific questions about steam usage in the two case study plants, the secondary objective is to see to what extent a fundamental steady state model, based on thermodynamics (not kinetics) is capable of predicting the material and energy flows in two operating sugar refineries and thereby to evaluate the applicability of the modelling framework. Aspen PlusÔ was chosen as the modelling tool, since it has the capacity to generate steady state simulations of a range of process plants. These simulations can then be used to investigate material balance issues such as raw material conservation, product quality optimisation or waste minimisation. They can also be used to explore energy balance issues such as energy analysis and minimisation. Aspen Plus has been widely used as a tool to investigate a range of energy questions, such as evaluation of steam power plants [4] and heat integration [5]. In this case, the software was used for the purposes of energy analysis. A process simulation of the evaporator section of a sugar refinery was developed using Aspen Plus. The simulation was then used to analyse the evaporator sections of two Mauritian sugar refineries with a view to ascertaining the efficiency of the current steam consumption, and to what extent the current steam generation will be able to satisfy the additional steam demands of a refinery. 2. Thermodynamic modelling 2.2. Choice of thermodynamic property methods and models The key thermodynamic property calculation that is performed in order to carry out the thermodynamic modelling is the phase equilibrium calculation. Besides the calculation itself, the phase equilibrium method also determines how other thermodynamic properties, such as enthalpies and molar volumes, are calculated. The basic relationship for every component i in the vapour and liquid phases of a system at equilibrium is: The starting point for the development of the simulation model is to ensure that the correct thermodynamic property methods and models are selected. For these case studies, the most important thermodynamic property is the correct prediction of the elevated boiling point of the sucrose solution as it becomes progressively more concentrated in each evaporator. A number of different Aspen Plus thermodynamic models were tested and the predicted boiling point elevation compared with data obtained from Tressler [6]. It was also necessary to input the data for the Antoine equation vapour pressure prediction and the heat of formation of crystalline sucrose. The relevant data is given in the appendix. The most accurate prediction was obtained using the UNIFAC thermodynamic model with the molecular structure of sucrose specified. The structure of the sugar molecule is depicted in Fig. 1, and the thermodynamic data is tabulated in Table 1. The salt equilibrium constant for sucrose crystallization was obtained from the regression of sucrose solubility data using Aspen Plus DRS. fiv ¼ fil (1) Where: f iv ¼ the fugacity of component i in the vapour phase fil ¼ the fugacity of component i in the liquid phase. For the sugarewater system, the calculation of the fugacities from the phase equilibrium relationship in terms of measurable state variables was carried out using an activity coefficient method. When using an activity coefficient method, the liquid properties are determined from summation of the pure component properties to which a mixing term or an excess term is added. This is important for systems where there is non-ideality present. The vapour phase properties are derived from an equation of state. In the activity coefficient method: fil ¼ xi gi fi;l (2) fiv ¼ fvi yi p (3) lnfvi 1 ¼ RT N vp vni Where R ¼ universal gas constant 8.315 J K1 mol1 T ¼ temperature (K) V ¼ total volume (m3) p ¼ pressure (Nm2) ni ¼ mole number of component i Z ¼ compressibility factor 2.1. Thermodynamic modelling using Aspen PlusTM *,l Where fi ¼ liquid fugacity of pure component i at mixture temperature xi ¼ mole fraction of component i in the liquid phase gi ¼ liquid activity coefficient of component i yi ¼ mole fraction of component i in the vapour phase 4vi ¼ fugacity coefficient and is calculated according to: (4) Fig. 1. Structure of sugar molecule. 2182 A.E. Lewis et al. / Applied Thermal Engineering 30 (2010) 2180e2186 Table 1 Numerical data used for the thermodynamic model. Number of functional groups CH Number of functional groups OH Number of functional groups C Number of functional groups CH2 Number of functional groups CHO (ether) Vapour pressure constants for the Antoine equation 1 2 3 4 5 6 7 8 9 Solid enthalpy of formation at 25 C for crystalline sucrose [8] Constants in the expression for the calculation of Ksp A B C D 5 8 1 3 3 Units: bar and C 56.6050745 12433.0 0 0 6.0186 2.2518E-19 6 460.15 1063 DHs,frm531.9 kcal/gmol 233.53780 5602.2690 42.62540 0.08658790 The UNIFAC (UNIversal Functional Activity Coefficient) model is an activity coefficient model that can be used to describe vapoureliquid equilibria, liquideliquid equilibria and enthalpic behaviour of highly non-ideal systems. The model is a semiempirical one that uses the functional groups present on the molecules that make up the liquid mixture to calculate activity coefficients. The UNIFAC model is one of a group that includes WILSON, NRTL and UNIQUAC, all of which are used to model highly non-ideal systems at low pressures. Fig. 2 shows the comparison between the Boiling Point Elevation as predicted by Aspen Plus and that generated using the experimental data. Since the maximum error is never greater than 1 C, this prediction was deemed sufficiently accurate to model the evaporator section. Since the Aspen Plus prediction of the Boiling Point Elevation was slightly less than that of the experimental data, the Aspen Plus simulation will tend to under predict the Boiling Point Elevation and thus under predict the steam requirement. However, given that the largest deviation between the two curves 3. The sugar refinery evaporator train In both sugar refineries, the evaporator trains consist of a number of vessels, each successive vessel operated at decreasing pressure, thereby counteracting the boiling point elevation effect of the increasing sucrose concentration of the solution. Steam generated in the bagasse-fired boilers is used in the first evaporator to evaporate the clarified juice. The juice is fed to the tube side of each evaporator, with the vapours produced by the boiling juice being collected and fed as the heating medium to boil up the juice in the next evaporator, which is operated at lower temperature and pressure. The steam is fed to the shell side, with the latent heat of the condensing steam used to heat the juice and the condensate being collected and removed from the vessel. This scheme is followed sequentially all the way down the evaporator train. 3.1. Case study 1 In the first refinery, the evaporator train consists of eight vessels, the entire train evaporating approximately 94% of the water, concentrating the juice from 12 Brix to about 70 Brix. The eight evaporators are used in a quintuple evaporator arrangement. The first and second effects are both Kestner type Evaporators; the third effect is three Robert Evaporators in parallel; the fourth effect is a single Robert evaporator and the fifth effect is two Robert Evaporators in parallel. The configuration of the evaporator train for case study 1 is given in Fig. 3, with the measured Brix values for the juice and the temperatures and pressures for the tube sides given on the diagram. 3.2. Case study 2 In the second refinery, the evaporator train consists of ten vessels connected in series, the entire train evaporating approximately 92% of the water, concentrating the juice from 13 Brix to about 67 Brix. The ten evaporators are used in a quintuple evaporator arrangement. The first and second effects both comprise three vessels, the third effect is two columns, and the fourth and fifth are each single evaporating columns. The configuration of the evaporator train for case study 2 is given in Fig. 4, with the measured Brix values for the juice and the temperatures and pressures for the tube sides given on the diagram. 110 108 106 Boiling Point (°C) is 0.78 C (which occurs at 50.4 Brix), the error deriving from this slight deviation will not be significant. Boiling Point Elevation is a colligative property, meaning that it depends only on the number of dissolved particles and not the identity of the particles. The physical significance of the boiling point elevation in sugar crystallization is that, as the sugar solution becomes more concentrated, there is an increase in its boiling point. This means that, with increasing juice concentration, there is a concomitant increase in the requirement of energy in order to effect boiling and thus solvent evaporation. 104 102 100 98 3.3. Modelling of the evaporators at the sugar refineries 96 BP Aspen Plus calculation 94 BP (Tressler Data) 92 90 0 20 40 Brix (°) 60 80 Fig. 2. Boiling point of sucrose solution with increasing concentration in water (experimental data compared to Aspen Plus calculation). The multiple effect evaporator trains at both sugar refineries were simulated using Aspen PlusÔ. The Aspen Plus flowsheet for the evaporator sections is presented in Fig. 5. The shell sides of the evaporators (the steam side) were modelled using condensers, which calculate the duty required to produce a saturated liquid at the specified pressure. This heat duty was then transferred to the tube side of each evaporator in the form of latent heat, as illustrated in Fig. 5. A.E. Lewis et al. / Applied Thermal Engineering 30 (2010) 2180e2186 2183 Fig. 3. Schematic representation of the evaporator configuration for Case Study 1. The tube side of the evaporators (the juice side) were modelled using flash equilibrium vessels, which perform rigorous two-phase (vapoureliquid) phase equilibrium calculations and calculate the compositions and flows of the two outgoing streams based on the specified pressure and the heat duty (from the latent heat). The steam vents were modelled with simple flow splitters. 3.4. Model validation The data used in model validation was that obtained from a combination of the plant DCS (Distributed Control System) and historical recorded data [7]. The tube side (juice) pressure for each evaporator was fixed at the measured or recorded values. The temperature on the tube side of each evaporator was then adjusted by varying the quantity of vapour fed to the shell side such that the calculated temperature of the juice matched the measured value. The Brix of the product syrup was then calculated using the Aspen Plus simulation, assuming that the syrup was at its bubble point and that the overhead steam was saturated. These calculated Brix values were then compared with those measured on the plant. The comparison between calculated and measured values is given in Fig. 6 for both Case Study 1 and for Case Study 2. Fig. 4. Schematic representation of the evaporator configuration for Case Study 2. 2184 A.E. Lewis et al. / Applied Thermal Engineering 30 (2010) 2180e2186 Vent Steam Condenser 3 Condensate Vent Steam Condenser 2 Condensate Vapour out Flash Equilibrium Vessel 1 Vapour out from stage 5 Latent heat Vapour out from stage 4 Condensate Vapour out Condensate out Latent heat Condensate Flash Equilibrium Vessel 3A Steam Condenser 1 Steam in Steam Condenser 4 Latent heat Vent Steam Condenser 0 Vent Vapour out from stage 3 Latent heat Flash Equilibrium Vessel 4 Flash Equilibrium Vessel 3B Flash Equilibrium Vessel 2 Juice4 Juice2 Juice in Flash Equilibrium Vessel 5A Flash Equilibrium Vessel 5B Juice1 Juice5 Flash Equilibrium Vessel 3C Juice3 Fig. 5. Schematic representation of the Aspen Plus flowsheet for Evaporator Train for Case Study 1. The calculated steam consumption necessary to achieve the product Brix values is given in Fig. 7 for Case Study 1 and Fig. 8 for Case Study 2, where t/h refers to metric tonnes. The steam fed to the first evaporator is the only fresh steam fed to the evaporator sections of both plants. The remaining evaporators (two through to five) all use the vapours generated by the boiling juice in the previous evaporator. The theoretically calculated steam requirement according to Rillieux’s First Principle [2], which states that every tonne of steam used should evaporate a tonne of juice, is also given in Fig. 7, Fig. 8 and Fig. 9. Fig. 6. Measured vs calculated product Brix for Case Studies 1 and 2. 4. Discussion 4.1. Brix values 4.1.1. Case study 1 As expected, both the calculated and measured Brix values increase monotonically with evaporator number. The rate of increase of the Brix slows down slightly over Evaporators 4 and 5, indicative of the increase in energy requirements as the sugar solution becomes more concentrated. The point at which this curve begins to level off corresponds with the point at which the slope of Fig. 7. Measured vs calculated steam usage for Case Study 1. A.E. Lewis et al. / Applied Thermal Engineering 30 (2010) 2180e2186 2185 Although the measured and calculated product Brix values are generally in good agreement, the measured Brix from Evaporator 4 is 12.7% higher than the calculated value. This discrepancy arises from the fact that that there is not sufficient vapour produced in Evaporator 3 to satisfy the steam requirement for the juice concentration in Evaporator 4, despite all vapour being used and none vented. The problem originates further upstream, with the steam requirement in Evaporator 3. This will be discussed further below. 4.2. Steam requirements For the steam requirements, in both case studies, the errors in measured vs calculated values are slightly larger than those for the Brix, ranging from 0 to 60.2%. This is partly due to the fact that the Brix measurement is a less sensitive parameter than the steam usage, with the boiling point elevation curve being relatively flat over the entire operating range. 4.3. Steam requirementsecase study 1 Fig. 8. Measured vs calculated steam usage for Case Study 2. the boiling point elevation curve in Fig. 2 suddenly increases. In other words, the sharp increase in boiling point elevation is translated into the flattening off of the Brix curve in Fig. 6. The measured and the calculated product Brix values were generally in good agreement, with errors between 0 and 6.1% for all evaporators in the case study. It is to be expected that the calculated product Brix will be higher than the measured value, as the calculation is based on 100% efficient use of the steam and heat transfer area. In reality, it is likely that the steam usage is not 100% efficient and that there will be some wastage in the evaporators, and thus the measured Brix will not be as high as the theoretical value. 4.1.2. Case study 2 In Case Study 2, the calculated and measured Brix values also increase monotonically with evaporator number. However, the levelling off of the Brix curve with evaporator number is not as apparent as it was for Case Study 1. This is potentially due to the lack of vapour generated in Evaporator 3, which means that the Brix out of Evaporator 3 is lower than expected. If this value had been in the normal range of 52e56 Brix, then the characteristic flattening off of the Brix curve would have been apparent. Fig. 9. Comparison of normalised steam usage for the Case Studies 1 and 2. In Case Study 1, the 124 t/h of steam necessary to achieve the measured temperature and pressure in Evaporator 1 results in a vapour flow rate out of the evaporator of 118 t/h. The ratio of 1 t steam to approximately 1 t vapour correlates with values given in literature [2] also known as Rillieux’s First Principle. For Case Study 1, the agreement between the calculated and measured steam usage is generally good, with the calculated usage being less than the measured value for all of the evaporators, except for Evaporator 4, where it is slightly more. The discrepancy for Evaporator 4 is most likely due to the limit of accuracy in the measurement of the steam flow rate; with a measured steam flow rate of 8.8 t/h and a calculated value of 8 t/h. There would only need to be a 10% error in the measured value for the calculated value to match exactly. The theoretical steam usage in each evaporator was also calculated using Rillieux’s First Principle, with the results correlating well with both the calculated and measured steam usage values. This correlation between steam input and vapour generated is preserved over the whole evaporator train. The relative magnitudes of the three values is also expected, with the theoretical value calculated using Rillieux’s First Principle being the lowest, followed by the value calculated using the thermodynamic model and lastly followed by the measured value being the highest. 4.4. Steam requirementsecase study 2 For Case Study 2, 110 t/h of steam generates 107 t/h of vapour in the first evaporator. The approximately 1 t/h steam to 1 t/h vapour correlation is also preserved over the whole evaporator train. The correlation between measured and calculated steam usage is reasonable for all of the evaporators except for Evaporator 3, where the error is very significant e 45 t/h steam measured compared to 18 t/h predicted by the model. There are two possible causes of this discrepancy: (1) either there is a significant inefficiency in the evaporator, which causes it to use almost double the quantity of steam expected or (2) it is most likely that this is an error in the measured steam consumption, since a simple material balance over the evaporator shows that, where Evaporator 3 to use approximately 45 t/h steam, then the syrup product from the evaporator would be approximately 55 Brix, far more than the measured Brix value out of Evaporator 3. For Case Study 2, the theoretical steam usage in each stage, when calculated using Rillieux’s First Principle, correlates well with both the calculated and the measured values (except for Evaporator 3, which has been previously discussed). 2186 A.E. Lewis et al. / Applied Thermal Engineering 30 (2010) 2180e2186 4.5. Overall steam requirements per tonne of juice treated When evaluating the steam usage per tonne of juice treated, and comparing the two refineries, there are two aspects that are apparent. The first is that Case Study 1 is more slightly efficient than Case Study 2 in terms of steam usage, using 0.92 as opposed to 0.98 tonne steam per tonne juice treated. This could be due to the fact that the refinery in Case Study 1 is 30% larger than the refinery in Case Study 2, and the improved efficiency might be due to an economy of scale. The second aspect that is apparent is that there is not a significant difference between the actual steam usage and the calculated values, which assume 100% efficiency of both steam and equipment. For Case Study 1, Rillieux’s First Principle predicts 0.8 tonne steam per tonne of juice, compared to the actual value of 0.92. For Case Study 2, Rillieux’s First Principle predicts 0.85 tonne steam per tonne of juice, compared to the actual value of 0.98. These differences are relatively small. This indicates that, in fact, both refineries are extremely efficient in terms of steam and equipment usage and that there is not much scope for steam optimisation within the present configuration. The efficiencies were much better than expected, given that much of the equipment is old and many of the control systems date from the 1950s. In practice, it is often the many years of experience of sugar technologists that keep the plants running at high efficiencies, despite the fact that the equipment is not the most modern. However, the implication of this study is that, since the existing steam is being used with such good economy and relatively optimally, there is not much spare capacity for extracting extra steam out of the existing system. Therefore, on commissioning of the new sugar refineries, it is likely that additional steam will need to be generated. 5. Conclusions For product Brix and steam usage, the measured values and those calculated using the Aspen Plus model generally correlated well. The reasonably good agreement extended over the entire evaporator train for both case studies, except for Evaporator 3 in Case Study 2. Some suggestions were made as to the cause of this particular discrepancy. On balance, it was found that both refineries are extremely efficient in terms of steam and equipment usage and that there is not much scope for steam optimisation within the present configuration. The implication is that, since the existing steam is being used with such good economy and relatively optimally, there is not much spare capacity for extracting extra steam out of the existing system. Therefore, on commissioning of the new sugar refineries, it is likely that additional steam will need to be generated. Although the primary objective was to answer the specific questions about steam usage in the two case study plants, the secondary objective was to see to what extent a fundamental steady state model was capable of predicting the material and energy flows in two operating sugar refineries. This is perhaps the more interesting and significant outcome. Acknowledgements Acknowledgements are due to the staff of a number of Sugar Factories and Refineries in Mauritius, for their willing assistance and provision of valuable data and advice. References [1] C.C. Chung (Ed.), Handbook of Sugar Refining: a Manual for the Design and Operation of Sugar Refining Facilities, John Wiley and Sons Inc, 2000. [2] C.G.M. Perk, The Manufacture of Sugar from Sugarcane. Sugar Milling Research Institute, University of Natal, Durban, South Africa, 1973. [3] L. Zheng, E. Furimsky, ASPEN simulation of cogeneration plants. Energy Conversion and Management 44 (2003) 1845e1851. [4] A. Ong’iro, V. Ismet Ugursal, A.M.A. Taweel, G. Lajeunesse, Thermodynamic simulation and evaluation of a steam CHP plant using aspen plus. Applied Thermal Engineering 16 (3) (1996) 263e271. [5] M. Krajnc, A. Kova c-Kralj, P. Glavi c, Heat integration in a speciality product process. Applied Thermal Engineering 26 (8e9) (2006) 881e889. [6] C.J. Tressler, W.I. Zimmerman, C.O. Willits, Boiling-point elevation of sucrose solutions. Journal of Physical Chemistry 45 (8) (1941) 1242e1245. [7] J.N. Carolin, Analysis of the Evaporating Station of FUEL Sugar Factory. University of Mauritius, Réduit, 1995. [8] D.R. Lide, CRC Handbook of Chemistry and Physics, 65th ed. CRC Press, 1984, pg D-280.