optimal design of hybrid msfro desalination plant
TRANSCRIPT
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Optimal Design of Hybrid MSF/RO
Desalination Plants
Submitted By:
Abdullah I. Al-Khudhiri
Supervised By:
Prof. Ibrahim S. Al-Mutaz
Examination Committee Members
1- Prof. Ibrahim S. Al-Mutaz 2- Dr. Malik I. Al-Ahmad
3- Dr. Osman A. Hamed
A Thesis submitted in partial fulfillment of the requirements forthe degree of Master of Science in Chemical Engineering
December 2006
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Table of Content
Table of Contents iList of Table v
List of Figures viiNomenclature ixAcknowledgment xiiAbstract xiii
CHAPTER1
Introduction 11-1 Importance of Desalination in Saudi Arabia 1
1-2 Seawater and Drinking Water Properties 3
1-3 The Current Work
CHAPTER 2
5
Major Desalination Technologies 62-1 Reverse Osmosis System (RO) 7
2-2 Multi-Stage Flash (MSF) 9
2-3 Electrodialysis 12
2-4 Vapor Compression 13
2-5 Freezing 15
2-6 Solar Desalination 16
CHAPTER 3
MSF and RO Modeling and Economics 18Multi-Stage Flash (MSF) 19
3-1-1 MSF-Once Through 19
3-1-1-1 Definition and Advantages 19
3-1-1-2 Simplified Model of MSF-Once Through 19
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3-1-1-2-1Temperature Distribution 20
3-1-1-2-2 Energy Balance On Stage i 20
3-1-1-2-3 Stage Material and Salt Balance 21
3-1-1-2-4 Brine Heater and Condensers Heat Transfer Area 233-1-1-2-5 Total Plant Areas 24
3-1-1-3 Water Production Cost Estimation of MSF-OT Plant 24
3-1-2 MSF- Brine Recirculation 27
3-1-2-1 Definition and Advantages 27
3-1-2-2 Simplified Model for MSF- Brine Recirculation 27
3-1-2-2-1 Overall Material Balance 28
3-1-2-2-2 Temperature Distribution 28
3-1-2-2-3 Energy Balance On Stage i 29
3-1-2-2-4 Stage Material and Salt Balance 30
3-1-2-2-5 Brine Heater and Condensers Heat Transfer Area 33
3-1-2-2-6 Total Plant Heat Transfer Areas 35
3-1-2-3 MSF-BR Economics 35
3-2 Reverse Osmosis (RO) 36
3-2-1 Definition and Advantages 36
3-2-2 Simplified Model of RO Design 37
3-2-3 Cost Methodology of RO 38
3-2-3-1 Water Production Cost Estimation of RO Plant 38
3-2-3-1-1 Estimation of the direct capital cost 40
3-2-3-1-2 Estimation of the water production cost 41
3-3 Comparative Study of MSF and RO 43
CHAPTER4 Hybrid MSF/RO Desalination Systems
4-1 Identification of Hybridization System
45
46
4-2 Advantages of hybrid MSF/ RO system 46
4-3 Previous Work 48
4-4 Options for Hybridization System 53
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4-4-1 Simple Hybrid Desalination Plants 53
4-4-1-1 Simplified MSF-OT/RO 53
Design Procedure 53
Cost Methodology 54 4-4-1-2 Simple MSF-BR/RO 56
Design Procedure 56 Cost Methodology 57
4-4-2 Integrated Hybrid Desalination Plants 58
4-4-2-1 Integrated Hybrid MSF-OT/RO 58
4-4-2-1-1 MSF-OT brine as a feed of RO 58
Design Procedure 58 Cost Methodology 59
4-4-2-1-2 RO reject brine as a feed part of MSF-OT 60
Design Procedure 60 Cost Methodology 61
4-4-2-2 Integrated Hybrid MSF-BR/RO 62
4-4-2-2-1 MSF cooling water as a feed of RO 62 Design Procedure 62 Cost Methodology 63
4-4-2-2-2 part of MSF brine and part of cooling water as
feed of RO
64
Design Procedure 64 Cost Methodology 65
4-4-2-2-3 Mixing MSF feed with RO rejected brine 66
Design Procedure 66 Cost Methodology 67
4-4-2-2-4 RO rejected brine is used as MSF feed 68
Design Procedure 68 Cost Methodology 69
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CHAPTER5
5-Results and Discussions70
5-1 Results of Single Type Desalination Plants 71
5-1-1 MSF-Once Through (MSF-OT) 71
5-1-2MSF- Brine Recirculation (MSF-BR) 74
5-1-3 Reverse Osmosis (RO) 77
5-2 Simple Hybrid Desalination Plants 79
5-2-1 MSF-OT/RO 79
5-2-2 MSF-BR/RO 83
5-3 Integrated Hybrid Desalination Plants 87
5-3-1 MSF-OT brine as feed of RO 87
5-3-2 Mixing RO brine reject with MSF feed 91
5-3-3 MSF-BR cooling water as feed of RO 95
5-3-4 Part of MSF Brine and Part of Cooling Water as
feed of RO
99
5-3-5 Mixing MSF-BR feed with RO rejected brine 103
5-3-6 RO rejected brine as MSF-BR feed 107
5-4 Summary of water production and production cost 111
5-5 Discussion 112
CHAPTER6
6-Conclusion and Recommendations 115
6-1 Conclusion 116
6-2 Recommendations 117
Bibliography 118
Appendix AMATLAB Computer Programs for Desalination Plants
122
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List of Tables
Table 1-1 Saudi desalination plants Production 2
Table 1-2 Major constituents of seawater 4
Table 1-3 Drinking Water Standards 4
Table 5-1 MSF-OT Characteristic 71
Table 5-2 MATLAB Result of MSF-OT ( Modeling ) 71
Table 5-3 MATLAB Result of MSF-OT ( Economics ) 71
Table 5-4 MSF-BR Characteristic 74
Table 5-5 MATLAB Result of MSF-BR (Modeling) 74
Table 5-6 MATLAB Result of MSF-BR (Economics) 74
Table 5-7 RO Characteristic 77
Table 5-8 MATLAB Result of RO (Modeling) 77
Table 5-9 MATLAB Result of RO (Economics) 77
Table 5-10 The feed flow rate of simple hybrid MSF-OT / RO 79
Table 5-11 MATLAB Result of Simple Hybrid Desalination
Plants MSF-OT/RO(Modeling)
79
Table 5-12 MATLAB Result of Simple Hybrid DesalinationPlants MSF-OT/RO(Economics)
80
Table 5-13 The feed flow rate of simple hybrid MSF-BR/ RO 83
Table 5-14 MATLAB Result of Simple Hybrid Desalination
Plants MSF-BR/RO(Modeling)
83
Table 5-15 MATLAB Result of Simple Hybrid Desalination
Plants MSF-BR/RO(Economics)
84
Table 5-16 The feed flow rate of integrated hybrid
MSF-OT1/ RO
87
Table 5-17 MATLAB Result of integrated hybrid MSF-OT1/RO
(Modeling)
87
Table 5-18 MATLAB Result of integrated hybrid MSF-OT1/RO
(Economics)
88
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Table 5-19 The feed flow rate of integrated hybrid MSF-OT2/RO
91
Table 5-20 MATLAB Result of integrated hybridMSF-OT2 /RO
(Modeling)
91
Table 5-21 MATLAB Result of integrated hybrid MSF-OT2/RO
(Economics)
92
Table 5-22 The feed flow rate of integrated hybrid MSF-BR1/RO
95
Table 5-23 MATLAB Result of integrated hybrid MSF-BR1/RO
(Modeling)
95
Table 5-24 MATLAB Result of integrated hybridMSF-BR1/RO
(Economics)
96
Table 5-25 The feed flow rate of integrated hybrid MSF-BR2/RO
99
Table 5-26 MATLAB Result of integrated hybridMSF-BR2/RO
(Modeling)
99
Table 5-27 MATLAB Result of integrated hybrid MSF-BR2/RO(Economics)
100
Table 5-28 The feed flow rate of integrated hybrid MSF-BR3/RO
103
Table 5-29 MATLAB Result of integrated hybrid MSF-BR3/RO
(Modeling)
103
Table 5-30 MATLAB Result of integrated hybridMSF-BR3/RO
(Economics)
104
Table 5-31 The feed flow rate of integrated hybrid MSF-BR4/RO
107
Table 5-32 MATLAB Result of integrated hybrid MSF-BR4/RO
(Modeling)
107
Table 5-33 MATLAB Result of integrated hybrid MSF-BR4/RO
(Economics)
108
Table 5-34 Summary of Production & Production Cost 111
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List of Figures
Fig 2-1 Reverse Osmosis System (RO) 7
Fig 2-2 Multi-Stage Flash (MSF) 9
Fig 2-3 Electrodialysis 12
Fig 2-4 Vapor Compression 13
Fig 2-5 Freezing 15
Fig 2-6 Single Basin Solar Still 16
Fig 3-1 MSF-Once Through 19
Fig 3-2 MSF- Brine Recirculation 27
Fig 3-3 Reverse Osmosis RO 36
Fig 3-4: a simplified RO membrane 37
Fig4-1: Simplified MSF-OT/RO Design 53
Fig4-2: Simplified MSF-BR/RO Design 56
Fig4-3: MSF-OT brine as a feed of RO 58
Fig4-4: RO reject brine as a feed part of MSF-OT 60
Fig4-5: MSF cooling water as a feed of RO 62 Fig4-6: part of MSF brine and seawater as feed of RO 64
Fig4-7: Mixing MSF feed with RO rejected brine 66
Fig4-8: rejected brine as MSF feed 68
Fig 5-1: MSF-Once Through 73
Fig 5-2: MSF- Brine Recirculation 76
Fig 5-3: Reverse Osmosis RO 78
Fig 5-4: Simple Hybrid Desalination Plant (MSF-OT/RO) 82
Fig 5-5: Simple Hybrid Desalination Plant ( MSF-BR/RO ) 86
Fig 5-6: MSF-OT brine as feed of RO 90 Fig 5-7: Mixing RO brine reject with MSF feed 94
Fig 5-8: MSF Cooling Water as feed of RO 98 Fig 5-9: Part of MSF Brine and Part of Cooling Water as feed ofRO
102
Fig 5-10:Mixing MSF feed with RO rejected brine 106
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Fig 5-11: RO rejected brine as MSF-BR feed 110
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Nomenclature
MHf Total hybrid seawater feed, Kg/h
Mf MSF feed, Kg/hFf RO feed, Kg/h
AW Pure water permeability, m/sec pa
AS Salt permeability, m/sec
ks Mass transfer coefficient, m/sec
p1 Operating pressure, pa
tcw Feed Temperature, C
nJ nr
Total number of rejection section stages,Total number of recovery section stages,
Tcw Intake seawater Temperature, C
Ts Steam temperature, C
To Top brine temperature, C
Tn Brine temperature in the last stage, C
cp Heat capacity of the liquid streams liquid, kJ/kg oC
Xf Salinity of the intake seawater, ppm
Xb Salinity of the rejected brine, ppm
Mcw Cooling water, Kg/h
Md Product feed (MSF-BR), kg/h
M b The rejected brine flow rate, kg/h
Mr Brine recycle flow rate, kg/h
Ms Steam flow rate, kg/h
Xr Recycled brine concentration, ppm
Ub The overall heat transfer coefficient of brineheater,
Kw/m 2 oC
Ab Brine heater area, m 2
Ur The overall heat transfer coefficient of recoverysection,
kW/m 2 oC
Ar Recovery section Area, m 2
Uj The overall heat transfer coefficient of rejection kW/m 2 oC
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section,
Aj Rejection section Area, m 2
Ac Total condenser area, m 2
PR The performance ratio,A total Total heat transfer area, m
2
cw Salt concentration at membrane wall, kg/m 3
cp permeate Concentration, kg/m 3
Fp Total Product Flow Rate (RO), kg/h
Frj Reject flow rate, kg/h
crj Concentration of reject flow rate kg/m3
Atmod Total membrane area, m 2
MHd Total product of hybrid system (MSF/ RO), kg/h
XHd Concentration of hybrid system (MSF/ RO), ppm
MHb Total BRINE of hybrid system (MSF / RO), kg/h
XHb Concentration of hybrid system, ppm
CDM Direct capital investment, $/year
CIDM Indirect capital investment, $/year
Csteam Steam cost, $/year
Cche Chemical treatment, $/year
C power Power Cost, $/year
Cspar Spares Cost, $/year
Clab Labor Cost $/year
COM The Operation & maintenance Cost $/year
CAM Annual Cost $/yearMS cost_p Production Cost of MSF, $/m
3
Rf Recovery fraction,
cost mem Membrane cost, $/year
cost civil Civil cost estimation, $/year
cost dir Direct capital cost $/year
cost 1 Fixed charges cost, $/year
cost fix Annual fixed charges, $/m3
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cost 2 Electric power cost, $/year
cost ep Annual electric power cost, $/m3
cost 3 chemicals cost, $/year
cost che Annual chemicals cost, $/m3
cost 4 Membrane replacement $/year
cost mem_rep Annual membrane replacement, $/m3
cost 5 Annual labor cost, $/year
cost labor Annual labor cost $/m3
cost RO_total RO plant cost, $/year
RO prod_cost Production Cost of RO, $/m3
Cost H1 Electromechaical equipment cost, $Cost H2 Hybrid civil work cost, $
Cost H3 Hybrid elctrochlorination, $
Cost H4 Hybrid brine disposal cost, $
cost H_total Reference hybrid intake-outfall cost $/year
COST HA annual plant intake-outfall cost, $/year
COST INT_HY Total annual cost of integrated hybrid (MSF/RO), $/year
total cost Water cost of integrated hybrid (MSF/RO), $/m3
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Acknowledgment
Praise and Thanks first and last to almighty Allah
I Would like to thank deeply Prof. Ibrahim Al-mutaz forsuggesting the topic of this thesis and for his suggestions. Prof.Ibrahim Al-mutaz alloys support me and give me great helpthroughout this thesis.Also, I Would like to thank Chemical Engineering Department fortheir cooperation and encouragement.Finally, I Would like to thank my parents and my wife.
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Abstract
This thesis addressed a very important subject in the desalination field. It is
called hybrid desalination. Hybrid desalination systems combining both
thermal and membrane desalination processes in the same site are currently
considered a good economic alternative to either of these two processes when
operated individually. The research work carried out to simulate hybrid
desalination processes is limited.
The main objective of the thesis is to carry out an in-depth and comprehensive
simulation study to determine the optimum design configuration of hybrid
desalination systems combining synergistically multi-stage flash (MSF)
desalination with seawater reverse osmosis (SWRO) process. The impact of
combining MSF and SWRO desalination processes in different hybrid
configurations on water production cost was explored.
Mathematical steady state models which incorporated mass and energy
balances equations were combined with economic relationships to predict the
unit water production cost as a targeted objective function. The simulationmodels developed in this work and the results obtained can be as an
appropriate guide by designers and operators to optimize the design and
operating conditions of hybrid desalination systems.
A total of eleven desalination systems were simulated and analyzed. For
comparison, the first three desalination arrangements include SWRO and MSF
with and without brine recirculation. The fourth and fifth systems considered a
simple hybrid configuration where The MSF and SWRO processes are
operating in parallel forming simple hybrid arrangements. The remaining six
systems include partially or totally integrated SWRO/MSF hybrid desalination
systems.
For each system mass, energy balance and heat capacity equations together
with economic relationships were developed and solved by a using MATLAB
computer programs to estimate the water production cost for a specific
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Chapter 1
Introduction
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1-Introduction
1-1 Importance of Desalination in Saudi ArabiaThe Arabian Gulf countries have about 60% of the total world desalting
capacity. Saudi Arabia has the largest capacity of desalination in the world.
Desalination in Saudi Arabia started in 1907. The first multistage flash plant,
MSF, was built in Doba and Al-Wajh on the Red Sea coast in 1969 with a
capacity of 227.1m 3/day. On the Arabian Gulf, Al-Khobar I was started in
1973 with a capacity of 28,390 m 3/day. All these plants are MSF type. The
first RO seawater desalination plant in Saudi Arabia was constructed in
Jeddah (Jeddah RO-1) in 1978 with a capacity of 12,110m 3/day. Al-Jubail
phase II is considered the world largest desalination plant. It has a design
capacity of about 960,000m 3/day and was on operation in 1983. It comprises
40 MSF units each producing 23,500m 3/day [1].
Most of the Saudi desalination plants are multistage flash type MSF. Saudi
MSF plants capacity are more than 33% of the total world MSF desalting
capacities. Saudi MSF plants accounted for more than 19% of the totalnumbers of MSF units. Reverse Osmosis, RO, has about 17.8% of the total
desalting capacity of plants producing more than 4000 m 3/day [1].
In 2004, there were 25 desalination plants in operation in Saudi Arabia with a
design total capacity of about 2.88 Mm 3/day. Nine of the 25 operated
desalination facilities in Saudi Arabia are dual system plants that generate
about 3,600 MW of electricity per day or 33%of the total power generated in
the country [2].
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Table1-1 Saudi desalination plants Production[2].
Region Plant Water production
(m 3/day)
Al-Jubail 118,447
Al-Jubail 815,185
Al-Jubail RO 78,182Al-Jubail
Total 1,011,814
AlKhobar II 191,780
AlKhobar III 240,800AlKhobarTotal 432,580
AlKhafji AlKhafji 19,682
Total Water production of East Coast 1,464,076
Jeddah II 38,916
Jeddah III 75,987
Jeddah IV 190,555
Jeddah I RO 48,848
Jeddah II RO 48,848
Jeddah
Total 402,154
Shoaibah I 191,780
Shoaibah II 390,909Shoaibah
Total 582,687Yanbu I 94,625
Yanbu II 120,069
Yanbu RO 106,904Yanbu
Total 321,625
Al Shkik Al Shkik I 91,000
Hagl 3,784
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Duba 3,784
AI-Waih 3,611
Urn Lujj 3,784
Rabig 1,978
Aziziah 3,870
AlBirk 1,952
Farasan 1,505
Small Plants
Total 24,268
Total Water production of West Coast 1,421,736
Total SWCC Production 2,885,812
1-2 Seawater and Drinking Water PropertiesSeawater is composed of about 96.57% water and 3.5% dissolved substances
of various elements. Seawater concentration in the Arabian Gulf countries
is considered to be the highest concentrations in the world, 41000-45000 ppm.
Seawater constituents can be divided into the following categories [3]:
Major elements with concentrations of more than 100 ppm, such
as chlorine, sodium, magnesium, sulfur, calcium and potassium.
Minor elements which have concentrations between 1 and 100 ppm.
These include bromine, carbon, boron and fluorine. Traces of all other elements with concentrations below 1 ppm. These
elements have a total concentration below 0.24%.
Three compounds or six elements, represent about 98% of the total mineral
concentration.
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Table1-2 Major constituents of seawater (ppm) [3]Constituent Arabian Gulf Red Sea Normal
SeawaterChloride, Cl 23,000 22,219 18,980
Sodium, Na+
15,850 14,255 10,550:Sulfate, SO 42- 3,200 3,078 2,649Magnesium, Mg 2+ 1,765 742 1,272
Calcium, Ca 2+ 500 225 400Potassium, K + 460 210 380Bicarbonate,
HCO 3 142 146 140
Strontium, Sr 2- 13Bromide, Br 80 72 65Fluoride, F 1Silicon,Si 4 1Iod1de, I
Total dissolvedsalt
45,000 41,000 34,438
Table 1-3 Drinking Water Standards (ppm)[4]Constituent Maximum
ConcentrationOptimumConcentration
Carbon dioxide 20 Carbonates(Na,K) 150 Chlorides 250 250Chlorine 1 Copper 3 Fluorides 1.5 0.5Iron 0.3 Lead 0.1 Magnesium 125 125
Zinc 15 Nitrate 10 NaCl 250 Sulfate 250 250Total DissolvedSalts
550 500
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1-3 The Current WorkThis study will focus on finding the optimum design of hybrid MSF/ RO
desalination plant. Research methodology can be summarized as follows: Review of the existing RO and MSF desalination plants in Saudi
Arabia for:- understanding the general design characteristics of these processes.- exploring the advantages of each process.
Suggestion of applicable design configurations of the hybrid MSF/ROsystems.
Modeling of each proposed design configurations of the hybridMSF/RO systems by solving the governing conservation equations ofmass and energy.
Performing an economic optimization study based on the minimumwater production cost for each proposed hybrid MSF/ROconfigurations.
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Chapter 2Major Desalination
Technologies
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2-Major Desalination Technologies
2-1 Reverse Osmosis System (RO):
Fig 2-1 Reverse Osmosis System (RO) [ 5]
All of the RO cases presented are based on the use of spiral wound membrane.
The brackish water units are operated at 400 psi and the seawater plant is
operated at about 1000 psi. It should be emphasized that feed water quality is
very important to the success of RO. The pretreatment section must be
designed and operated with due regard for the composition of the specific
water being used. For seawater, it is assumed that filtration followed by
treatment with acid and SHMP (sodium hexametaphosphate). Enough acid
should be added to reduce the pH to 6.2-6.4. Additional pretreatment would berequired for waters with high turbidity or a high content of bacteria and
algae[5].
Some of the general considerations in pretreatment for RO are[5]:
Iron and manganese must be removed to around 0.5 ppm or less,
depending on the type of membrane.
The calcium concentration should be 600 ppm or less to prevent scaling
as the concentration increases in the water brine. Injection of SHMP
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permits calcium concentrations up to 900 ppm, but for high calcium
concentrations, other means of water softening may be necessary.
Chlorine addition may be required to kill marine life or control bacterial
action.Bacterial attack can destroy the membranes. Acid addition (usually sulfuric acid) may be required to eliminate
calcium carbonate and magnesium hydroxide deposits and to reduce the
pH to 5.56.5.
Final polishing filters are required to eliminate particulate matter.
The extent of pretreatment is related to the water recovery of the plant, in as
much as the highest recoveries result in the most concentrated waste brines.
Scaling may also increase because the reject brine becomes more concentrated
and the solubility limits of scale-forming compounds such as calcium sulfate
may be exceeded.
Seawater typically is taken from a submerged inlet equipped with coarse
screens to keep out fish and trash. In most cases, concentrated brine from
seawater RO would probably be returned to the sea.
In most RO plants the high pressure brine stream is let down to a lower
pressure through a throttling valve and the energy in the high pressure stream
is not utilized. As the cost of energy rises, it becomes more and more
attractive to recover this energy, especially in large plants. A simple way to
recover some of the energy is to use hydraulic turbines connected to the high
pressure pumps or to an electric generator. A preliminary evaluation indicates
that the additional capital for power recovery is probably not justified for plants under about 10 mgd.
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MSF tubes are subjected to corrosive environments. Suitable materials vary
with the conditions of usage but they include titanium, copper-nickel alloy,
copper-nickel aluminum alloy, and aluminum brass [5].
The actual design depends on specific conditions such as the temperature andcomposition of the feed water, steam pressure available, and the cost of steam
and electricity. An actual seawater MSF plant might consist of 19-30 heat
recovery stages and 2-3 heat rejection stages.
Seawater at about 20C is screened and pumped through the condenser tubes
of the final, or heat rejection stages of the plant. With any seawater feed,
chlorination may be necessary at the source to inhibit biological growth in the
water.
After being heated in the condenser tubes, about 60% of the water is
discharged to the sea (cooling water) and the remainder is feed water for the
plant. Sulfuric acid is metered into the feed water to decompose bicarbonates,
which would otherwise cause fouling of heat transfer surfaces in the unit. The
acidified stream is pumped to a deaerator-decarbonator tower for separation of
carbon dioxide and other dissolved gases such as oxygen and nitrogen. Steam
may be admitted at the bottom of the tower to assist in separation of the gases,
which are vented to a vacuum system. A metered stream of 50% caustic may
be added to the water leaving the deaerator-decarbonator to raise the pH to a
noncorrosive level [5].
The treated seawater is mixed with concentrated brine from the last stage and
the mixture is pumped to the heat recovery section. The brine mixture containsapproximately 30% fresh feed and 70% recirculated brine. It enters the
preheater tubes and flows through the entire heat recovery section, being
preheated by the condensing product water on the outside of the tubes. When
it leaves the preheater, the brine enters a brine heater, where it is heated to its
maximum temperature, about 121C by steam from a boiler or by waste heat
from some other source. The maximum temperature is limited by the scale-
forming properties of the brine and it depends on the kind of pretreatment
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used and the concentration ratio desired. High brine temperatures are desirable
for high efficiencies and minimum cost [5].
The brine heater supplies all of the thermal energy used for vaporizing water
in the plant. From the heater, the brine passes through a flow control valveinto the first and hottest stage of the MSF unit. Because this stage is at a lower
pressure than the brine heater, part of the water in the brine flashes into vapor.
It rises through an entrainment separator and condenses on the outside of the
preheater tubes, transferring its latent heat to the brine inside the tubes. The
remaining brine at the bottom of the stage is cooled by the flashing vapor and
it passes through an orifice or flow control weir into the next stage, where the
pressure is lower and more flashing occurs. The process is repeated until the
brine leaves the last and coldest heat rejection stage at about 32C. Some of
the brine is discharged as blowdown to prevent precipitation of salts; the
remainder is recycled. The distillate that is condensed on the preheater tubes
drops into trays below the tubes and flows from stage to stage through flow
control devices much as the brine does. It is pumped from the last stage to
storage or distribution. It is essential to have a vacuum system to remove the
noncondensible gases from the unit and to maintain the reduced pressures
required. A typical system would be a three stage steam jet ejector system
with a barometric precondenser, an intercondenser, and a final condenser [5].
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2-3 Electrodialysis
Fig 2-3 Electrodialysis [6]
Electrodialysis unit ED comprises a series of alternating cation-permeable (C)
and anion-permeable (A) membranes set between two electrodes with saline
water being fed in between the membranes. As the DC current passes throughthe system the water streams become alternately diluted and concentrated
giving rise to a product and concentrate. The combination of membranes,
spacers, gaskets, electrodes, together with necessary devices for dividing,
directing and collecting the-streams of water is called an electrodialysis stack.
Each pair of membranes sealed around the edges to prevent leakage and
separated by-spacers to provide for water to flow across the membrane surface
is called a cell [7].
ED desalination cell contains two different types of ion-selective -membranes.
One of the membranes is cation-permeable allows the passage of positive ions
(cations) While the other anion-permeable membrane allows the passage of
negative ions (anions). If a direct current is established across a stream of
saline water passing between a pair of those membranes, ions acting as
carriers of electricity will migrate across the stream. The cation-permeable
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membrane will permit positive ions (e.g. Na +) to pass through while repelling
negative ions (e.g. Cl ), and the other membrane allows negative ions to go
through but not positive ions. The membranes act as one-way check valves
thus preventing the reentry of the ions they let through. Hence, the space between the membranes gets desalted while the streams on the electrode sides
become concentrated with the penetrating ions. In practical ED desalting
devices many pairs of membranes are used between a single pair of electrodes,
forming an ED stack. Plastic separators are inserted in the solution
compartment to keep the membranes apart and to promote mixing. The cells
can be stacked either horizontally or vertically. The saline water flow is
divided into many small streams in which most of the current-carrying ions
are trapped in half of these streams and desalted water in the other half. The
amount of electric current requirement varies proportionately to the amount of
dissolved salts to be removed. Increasing the number of pairs of membranes
between the electrodes increases the efficiency of current utilization [7].
2-4 Vapor Compression
Fig 2-4 Vapor Compression [5] The vapor compression (VC) distillation process is generally used for small-
and medium-scale desalting units. The heat for evaporating the water comes
from the compression of vapor rather than the direct exchange of heat from
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steam produced in a boiler. Two primary methods are used, a mechanical
compressor or a steam jet (thermo-vapor-compression).
VC is based on compression of the vapor generated by evaporating water to a
higher pressure, which allows reuse of the vapor for supplying heat for theevaporating process. Compression of the vapor may be carried out by using a
mechanical compressor (the most common way), or by mixing with small
amounts of high pressure steam (Thermal Compression). Feed water is
preheated against brine and the product leaving the system. Heat transfer
usually takes place in the form of a double falling film, which is an effective
heat transfer mechanism.
The latent heat of evaporating and condensing fluids are very equal.
Therefore, the energy required to keep process in operating is only that needed
to offset the boiling point elevation on the evaporating side and provide a
small difference is 4-5 C in order to minimize energy consumption. So that,
high performance ratios are obtained from this process[4].
The mechanical vapor compression (MVC) system is the most attractive as it
is compact and dose not require an external heating source like other systems,
but it does need highly skilled operators and has a higher maintenance cost.
The operation of the system at low temperature ranges from 60-70C, and at
this low temperature the scale and corrosion are reduced. Aluminum gives the
ability to operate at low temperatures [8].
A schematic diagram of a verticaltube design VC Unit as shown above
consisting essentially of a shell and tube evaporator, a vapor compressor, anda heat exchanger for recovering heat from the effluent brine and the distillate.
In operation, a mixture of vapor and liquid ascends through the tubes at high
velocity to provide high heat transfer coefficients. The mixture is discharged
from the top of the tubes and follows a tortuous path, as shown to separate the
vapor from liquid droplets. The vapor flows to the vapor compressor and is
discharged at a higher pressure into the shell side of the evaporator, where it
yields its heat to the brine and it is condensed, forming the product water. An
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efficient heat exchanger is necessary in order to recover heat from the effluent
streams and achieve acceptable economy of operation. Titanium plates are
used in heat exchangers in typical units[ 5].
2-5 Freezing
Fig 2-5 Freezing [5]
Freezing has a number of important technical and economic advantages as a
desalination process. These advantages include low energy consumption,
especially in comparison with distillation, and freedom from corrosion,
scaling, and fouling problems. Most of these advantages stem from the use of
low temperatures. Because scaling does not occur, pretreatment is usually not
necessary [5].The seawater feed passes through a vacuum deaerator and is cooled by
countercurrent flow of product water and reject brine in an aluminum plate
type feed heat exchanger. The stream is further cooled to within -17C of its
freezing point in a refrigerated feed cooler, then it enters the freezer- absorber
unit, which operates under a pressure of about 3.3 mm Hg. A slurry of ice
crystals in brine forms in the bottom of the unit. This vapor pressure 3.3 mm
Hg is less than that of the seawater slurry and thus provides a driving force for
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vaporizing water from it. The slurry of ice crystals in the bottom of the freezer
is pumped to a wash column, where a large portion of the brine is separated
and recycled to the freezer to maintain a concentration of about 20% ice in the
freezer. In a wash column, ice crystals rise to the top, where they are washed by a portion of the product water to remove any adhering brine. Less than 5%
of the melt is lost in washing the ice, although a much larger quantity is
applied to the top of the wash column. Most of the wash water adheres to the
crystals and is recycled between the melter and wash column. When the
washed crystals reach the top of the wash column, they are conveyed into the
melter, which is combined with the generator to eliminate vapor ductwork.
The ice is melted by hot water vapor from the absorbent regenerator. The
product water is used to cool incoming feed in the feed heat exchanger [5].
2-6 Solar Desalination
Fig 2-6 Single Basin Solar Still [9]
Solar energy can be converted to heat at low temperatures by direct absorption
or to heat at high temperatures by absorption after focusing. This heat can be
used directly in desalination processes, so called passive methods. Solar still is
the simplest form of solar desalination. It uses the solar energy directly to heat
saline water up to its evaporation. The vapors formed are condensed and
collected to obtain the product. Water in these stills evaporates at a
temperature below its boiling points. Normally evaporation occurs at 50-60C.
The average still production per day is 3.3-4.1 liter/m2
[10].
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Different solar stills were designed to improve the operating efficiencies.
These designs tried to achieve low heat capacity, low air content, vapor tight
basin and good insulation around the basin. Increasing radiation and using
mltieffect thin film diffusion stills will improve the still performance.Two important problems faced the application of solar energy in desalination.
These are the low efficiency of energy conversion and the inefficient storage
of energy. So most desalination processes are limited in capacity and work
during certain hours in the day time. Solar powered desalination systems do
not differ much from conventional desalination systems. They often consist of
feed water pretreatment, solar collectors, electric power generator, a
distillation or membrane unit with an energy storage subsystem, brine disposal
subsystem and product water storage and delivery subsystem [10].
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Chapter 3MSF and ROModeling and
Economics
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3-1 Multi-Stage Flash (MSF):
3-1-1 MSF-Once Through
Fig 3-1 MSF-Once Through
3-1-1-1 Definition and AdvantagesThe once through system has the following features [11]:
-Simple plant operation with few process control since the brine recirculation
pump is omitted as well as the heat rejection section.
-The brine concentration at the exit of the brine heater is lower if compared
with the brine recirculation design.
-The cost of chemical dosing is higher than for the recirculation system.
3-1-1-2 Simplified Model of MSF-Once Through:
Basic Assumptions:
Constant and equal specific heat for all liquid streams, Cp. Equal temperature drop per stage for the flashing brine.
Equal temperature drop per stage for the feed seawater.
The latent heat of vaporization in each stage is assumed equal to the
average value for the process.
Non-condensable gases have negligible effect on the heat transfer process.
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Effects of the boiling point rise and non-equilibrium losses on the stage
energy balance are negligible; however, their effects are included in the
design of the condenser heat transfer area.
The overall material balance equations is given by:Mf = M d + M b (3-1)
Where M is the mass flow rate and the subscript b, d, and defines the brine,
distillate, and feed. The overall salt balance is given by
Xf Mf = X b M b (3-2)
Where X is the salt concentration. Equation (3-2) assumes that the distillate is
salt free.
3-1-1-2-1Temperature Distribution
The temperature drop per stage, T, is obtained from the relation
T = (T o Tn)/n (3-3)
where n is the number of stages. Therefore, the temperature in the first and
second stages are given by
T1 = To T and T 2 = T1 T
Substituting for T 1 in the T 2 equation gives
T2 = To T T = T o2 T
so the temperature of stage i
Ti = To i T (3-4)
3-1-1-2-2 Energy Balance On Stage i Di-1 Cp T vi-1 + Bi-1 Cp T i-1 Di Cp T vi Bi Cp T i = M f C p (ti-1 ti)
Assuming the temperature difference, T i-1 Tvi-1, is small and has a
negligible effect on the stage energy balance. Thus, the above equation
reduces to
(Di-1 + Bi-1) Cp T i-1 (D i + Bi) Cp T i = Mf C p (ti-1 ti)
Recalling that the sum (D i-1+Bi-1) in each stage is equal to M f , wouldsimplify the above equation to
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Mf Cp T i-1 Mf Cp T i = M f C p (ti-1 ti)
Elimination of the like terms on both sides of the equation gives the pursued
relation, thus,
Ti-1 Ti = ti-1 ti , or generally Ti=ti
The seawater temperature, which leaves the condenser of the first stage, is
then defined by
t1 = Tf + n t
The seawater temperature leaving the condenser of the second stage, t 2, is less
than t 1 by t, so
t2 = t1t
Substituting for t 1 in the above equation gives
t2 = Tf + (n 1) t
So a general equation is obtained for the condenser temperature in stage i
ti = Tf + (n (i 1)) t (3-5)
3-1-1-2-3 Stage Material and Salt BalanceThe amount of flashing vapor formed in each stage obtained by
D1 = y M f
Where
D1 is the amount of flashing vapor formed in the first stage, M f is the feed
seawater flow rate, and y is the specific ratio of sensible heat and latent heat
and is equal toy =Cp T / av (3-6)
Where Cp is the specific heat capacity and av is the average latent heat
calculated at the average temperature
Tav = (To + Tn)/2 (3-7)
The amount of distillate formed in the second stage is equal to
D2 = y (M f D1)
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Comparison of the summations of D 1+D2 and D 1+D2+D3 gives the generalform for the total summation of the distillate formed in all stages, M d, whichis given by
Md = Mf (1 (1 y)n
) (3-9)
Equation (3-9) is used to calculate the distillate flow rate, since the feed flow
rate is always specified in a design problem.
The flow rate of the brine stream leaving stage (i) is given by
==
i
1k k f i DMB (3-10)
The salt concentration in the brine stream leaving stage i is given by
Xi = Mf Xf /Bi (3-11)
The flow rate of the heating steam, Ms, is obtained the energy balanceequation for the brine heater, where
Ms s = Mf Cp (T o t1)
The above equation is arranged to calculate M s
Ms = M f Cp (T o t1) / s (3-12)
3-1-1-2-4 Brine Heater and Condensers Heat Transfer
AreaThe brine heater area is given by
A b = M s s / (U b (LMTD) b ) (3-13)
Where LMTD is given by
(LMTD) b=((Ts To) (T s t1) ) / ln ( (T s T) / (T s t1) ) (3-14)
and U b is given by [12]
U b=1.7194+3.206310 -3Ts+1.597110 -5(Ts)2 1.991810 -7(Ts)3 (3-15)
The heat transfer area for the condenser in each stage is assumed equal.
Therefore, the calculated heat transfer area for the first stage is used to obtain
the total heat transfer area in the plant. The condenser heat transfer area in the
first stage is obtained from
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Ac = M f Cp (t 1 t2)/(Uc (LMTD) c) (3-16)
Where is given by [12]
Uc=1.7194+3.206310 -3Tv1+1.597110-5Tv12 1.991810 -7Tv1
3 (3-17)
Tv1 = T1 BPE 1 NEA 1 (3-18)
and
(LMTD) c =((T v1 t1) (T v1 t2) ) /ln ( (T v1 t1) / (T v1 t2) ) (3-19)
In the above equations (BPE) is the boiling point elevation, (NEA) is the non-
equilibrium allowance, (T v) is the condensing vapor temperature and (U c) is
the condenser overall heat transfer coefficient .BPE can be estimated from the following correlation [13]:
( ) ( )( ) 31 1 1 10 BPE X B X C = + where values of B and C in the correlation for the boiling point elevation are[12]:
( ) ( )22 51 1(6.71 6.34 10 9.74 10 )10 B x T x T = + + 38
( ) ( )23 51 1(22.238 9.59 10 9.42 10 )10C x T x T = + + The non-equilibrium allowance, NEA 1, in the first stage is calculated from the
gate height, GH 1, the height of the brine pool, H 1, the stage width, W, the
stage pressure drop, P 1-P2, and the brine density. For a good approximation
NEA 1= 0.213 oC [14].
3-1-1-2-5 Total Heat Transfer AreasThe total heat transfer in the plant is obtained by summing the heat transfer
area for all condensers and the brine heaterA = A b + n A c (3-20)
3-1-1-3 Water Production Cost Estimation of MSF-OT
PlantThe capital needed to supply the necessary manufacturing and plant facilities
is called the fixed-capital investment, while that necessary for the operation of
the plant is termed the working capital. In other words, we can say The
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Capital investment is the total amount of money needed to supply the
necessary plant and manufacturing facilities plus the amount of money
required as working capital for operation of the facilities. The sum of the
fixed-capital investment and the working capital is known as the total capitalinvestment. The fixed-capital portion may be further subdivided into
manufacturing fixed-capital investment (Direct Costs) and nonmanufacturing
fixed-capital investment (Indirect Costs) . Manufacturing fixed-capital
investment represents the capital necessary for the installed process equipment
with all auxiliaries that are needed for complete process operation. Expenses
for piping, instruments, insulation, foundations, and site preparation are
typical examples of costs included in the manufacturing fixed-capital
investment [15].
Fixed capital required for construction overhead and for all plant components
that are not directly related to the process operation is designated as the
nonmanufacturing fixed-capital investment. The construction overhead cost
consists of field-office and supervision expenses, home-office expenses,
engineering expenses, miscellaneous construction costs, contractors fees, and
contingencies [15].
The approximate formula of MSF, Once-through type can be summarized as
follow [16]:
direct capital investment, C DM is given by
CDM =0.0963 A total / Md0.27 (3-21)
where = has value between 5000-9000
A total = total heat transfer area, m 2
Md = Distillate flow rate, kg/h
Indirect capital investment, C IDM can be expressed
CIDM = 0.1 C DM (3-22)
Steam cost, C steam in $/year is given by
C steam = 8000 M s [(TS 40)/85](0.00415) (3-23)
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Chemical treatment, C che in $/year is obtained from
C che = 8000*(M f /rj) 0.024 (3-24)
where
rj = density of rejection stream, kg/m 3
Power Cost, C power in $/year is expressed as
C power = 8000 (M d/ d)*0.109 (3-25)
Where
d = density of distillate stream, kg/m 3
Spares Cost, C spar in $/year is given by
C spar = 8000 (M d / d )*0.082 (3-26)
Labor Cost, C lab in $/year is given by
C lab =8000(M d / d )*0.1 (3-27)
So, the Operation & maintenance Cost, C OM in $/year is obtained
COM = C steam + C che + C power + C spar + C lab (3-28)
Annual Cost, C AM in $/year is expressed as
CAM = C DM + C IM + COM (3-28)
Then the water production cost is found by dividing the total annual cost by
the total water product.
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3-1-2 Simplified Model of MSF- Brine Recirculation
Fig 3-2 MSF- Brine Recirculation
3-1-2-1 Definition and AdvantagesThe recirculation system has the following characteristics [11]:
Limited make-up flow rate which means small amounts of antiscalant
chemicals to be injected.
The heat rejection section acts as a deaerator and degasifier for the
make up seawater thus help to minimize the corrosion problems in the
evaporator.
Higher concentration of flashing brine compared with the once-through
arrangement.
3-1-2-2 Simplified Model for MSF- Brine RecirculationModel assumptions:
-Constant and equal specific heat for all liquid streams, Cp.
-Equal temperature drop per stage for the flashing brine.
-Equal temperature drop per stage for the feed seawater.
-The latent heat of vaporization in each stage is assumed equal to the average
value for the process.
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-The non-condensable gases have negligible effect on the heat transfer
process.
-Effects of the boiling point rise and non-equilibrium losses on the stage
energy balance are negligible; however, their effects are included in thedesign of the condenser heat transfer area.
-The temperature of the feed seawater leaving the rejection section is equal to
the brine temperature in the last stage.
3-1-2-2-1 Overall Material Balance
The overall material balance equations is given by
Mf = M d + M b (3-29)
where M is the mass flow rate and the subscript b, d, and defines the brine,
distillate, and feed. The overall salt balance is given by
Xf M f = X b M b (3-30)
where X is the salt concentration. Equation (3-30) assumes that the distillate is
salt free. Equations (3-29) and (3-30) can be rearranged to obtain the
expression for the total feed flow rate in terms of the distillate flow rate; this is
Md = M f (1- X f /X b ) (3-31)
Equation (3-31) is used to calculate M d, since the values of X b , X f , and M f
are known.
3-1-2-2-2 Temperature DistributionThe temperature drop per stage, T, is obtained from the relation
T = (T o Tn)/n (3-32)
where n is the number of recovery and rejection stages. Therefore, the
temperature in the first stage is given by
T1 = T o T
As for the second stage temperature it is equal to
T2 = T 1 T
Substituting for T 1 in the above equation gives
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T2 = T o T T = T o 2 T
The same procedure is repeated for subsequent stages and a general
expression is developed for the temperature of stage i
Ti = T o i T (3-33)
3-1-2-2-3 Energy Balance On Stage iAn energy balance on stage i in the heat recovery section gives
Di-1CpT vi-1+ B i-1Cp T i-1 D iCpT vi B iCpT i = M r C p(Tr i-1 T r i)
Assuming the temperature difference, T i-1 T vi-1, is small and has a negligible
effect on the stage energy balance. Thus, the above equation reduces to
(D i-1 + B i-1) Cp T i-1 (D i + B i) Cp T i = Mr C p (Tr i-1 T r i)
Recalling that the sum (D i-1 + B i-1) in each stage is equal to M r , would
simplify the above equation to
Mr Cp T i-1 Mr Cp T i = Mr C p (T r i-1 T r i)
Elimination of the like terms on both sides of the equation gives the pursued
relation, thus,Ti-1 T i = T r i-1 T r i , or Ti= Tri
The seawater temperature, which leaves the condenser of the first stage, is
then defined by
Tr 1= Tn +( n j) T
The seawater temperature leaving the condenser of the second stage, T r 2, is
less than T r 1 by T, so T r 2 = T r 1 T
Substituting for T r 1 in the above equation gives
Tr 2 = T n + (n j) T T
Similar to Equation (3-25), a general equation is obtained for the condenser
temperature in stage i
Tr i = T n + (n j) T (i 1) T (3-34)
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As for the temperature drop of the seawater in the condensers of the heat
rejection section, it is obtained from the stage energy balance. This is
Di-1 Cp T vi-1 +B i-1 Cp T i-1 D i Cp T vi B i Cp T i =(M f +Mcw) C p (Tf j T f j+1)
Assuming the small temperature difference, T i-1Tvi-1, has a negligible effect
on the stage energy balance. Thus, the above equation reduces to
(D i-1 + B i-1) Cp T i-1 (D i + B i) Cp T i = (M f +M cw) C p (T f i-1 T f i)
Recalling that the sum (D i-1+B i-1) in each stage is equal to M r , would simplify
the above equation to
Mr Cp T i-1 M r Cp T i = (M f +M cw) C p (T ji-1 T ji)
Elimination of the like terms on both sides of the equation gives the pursued
relation, thus,
(T ji-1 T ji) = (T i-1 T i) (M r /(M f +M cw) ) , or generally
( T ji) = Ti (M r /(M f +M cw) )
Since the temperature profile is assumed linear, the above relation can also be
obtained from the following simple relation( T ji) = (T n-Tcw) / j
The seawater temperature, which leaves the condenser of the last stage, is then
defined by
T jn = T cw+ (T ji)
This gives the general relation for the seawater temperature in the rejection
sectionT ji = T cw + (n-i+1)( T ji) (3-35)
3-1-2-2-4 Stage Material and Salt BalanceThe amount of flashing vapor formed in each stage obtained by conservation
of energy within the stage, where the latent consumed by the flashing vapor is
set equal to the decrease in the brine sensible heat. This is
D1 = y M r
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where D 1 is the amount of flashing vapor formed in the first stage, M r is the
recycle brine flow rate, and y is the specific ratio of sensible heat and latent
heat and is equal to
y = Cp T/ av (3-36)
where Cp is the specific heat capacity and av is the average latent heat
calculated at the average temperature
Tav = (T o+Tn)/ 2 (3-37)
The amount of distillate formed in the second stage is equal to
D2 = y (M r D 1)
Substituting the value of D 1 in the above equation gives
D2 = y (M r y M r )
Which simplifies to
D2 = M r y (1 y)
The D 3 balance is
D3 = y(M r D 1 D 2)
Substituting for the values of D 1 and D 2 in the above equation gives
D3 = y (M r M r y M r y (1 y) )
Taking M r as a common factor in the above equation gives
D3 = M r y (1 y y + y2
)
This simplifies to
D3= M r y (1 y)2
The balance equations for D 2 and D 3 will reveal the general form for the
formula of D i Accordingly, the resulting general formula for D i is
Di = M r y (1 y)(i 1) (3-38)
The total distillate flow rate is obtained by summing the values of D i for all
stages. The summation is performed in steps in order to obtain a closed form
equation. Therefore, the summation of D 1 and D 2 gives
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D1 + D 2 = M r (y + y (1 y) )
= M r (2 y y2 )
= M r (1 (1 y)2
)
Addition of D 3 to the above gives
D1 + D 2 + D 3 = M r ((2 y y2) + y(1 y)
2 )
This simplifies to
D1 + D 2 + D 3 = M r (2 y y2 + y 2 y
2 + y
3 )
= M r (3 y 3 y2 + y 3 )
= M r (3 y 3 y2 + y 3 )
= M r (1 (1 y)3
)
Comparison of the summations of D 1+D2 and D 1+D2+D3 gives the general
form for the total summation of the distillate formed in all stages, M d, which
is given by
Md = M r (1 (1 y)
n
) (3-39)Equation (3-39) is used to calculate the brine recycle flow rate, since the
distillate flow is calculated.
The salt concentration in the recycle stream, X r , is obtained by performing salt
balance as follows
Xr M r + M b X b = X f M f + (M r M d) Xn
The above balance is arranged toXr = (X f M f + (M r M d) Xn M b X b)/M r
Assuming that X n = X b, simplifies the above equation to
Xr = (X f M f + (M r M d) X b M b X b)/M r
Since M f = M b + M d, then,
Xr = ((X f X b) M f + M r X b)/M r (3-40)
The flow rate of the brine stream leaving stage i is given by
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==
i
1k k r i DMB (3-41)
The salt concentration in the brine stream leaving stage i is given by
i
i
1k k r iBDMX
==
(3-42)
The determination of the cooling water flow rate, M cw required to obtain the
specific cooling water flow rate, M cw,which affects the process economics.
This flow rate is obtained from an overall energy balance around the
desalination plant. The intake seawater temperature, T cw, is used as the
reference temperature in the energy balance. This gives
Ms s = M cw C p (Tn T cw) + M b C p(Tn T cw) + M d C p (Tn Tcw)The above equation is arranged to obtain an expression for M cw
Mcw = (M s s M f C p(Tn T cw))/ (C p (Tn T cw)) (3-43)
3-1-2-2-5 Brine Heater and Condensers Heat Transfer Area
The motive steam provides the brine heater with the necessary energy to
increase the feed seawater temperature from T f 1 to the top brine temperature,To. This requires calculation of the motive steam flow, which is obtained from
the brine heater energy balance
Ms s = M r Cp (T o T f1)
The above equation is arranged to calculate M s
Ms = M r Cp (T o T f1)/ s (3-44)
The brine heater area is given byA b = M s s /(U b (LMTD) b) (3-45)
where LMTD is given by
(LMTD) b=((T s To) (Ts Tf1))/ln((T s To)/(T s Tf1)) (3-46)
and U b is given by [12]
U b=1.7194+3.2063 10-3
Ts+1.5971 10-5
Ts2 1.9918 10
-7Ts
3 (3-47)
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The heat transfer area for the condenser in each stage in the heat recovery
section is assumed equal. The same assumption is made for the condenser heat
transfer area in the heat rejection section. Therefore, the calculated heat
transfer area for the first stage is used to obtain the total heat transfer area inthe heat recovery section. The condenser heat transfer area in the first stage is
obtained from
Ar = M r Cp (T r 1 T r 2)/(U r (LMTD) r ) (3-48)
Where U r [12]
Ur = 1.7194+3.2063 10-3
Tv1+1.5971 10-5
Tv12 1.9918 10
-7Tv1
3 (3-49)
Tv1 = T1 BPE1 NEA 1 (3-50)
and
(LMTD) r =((T v1 Tr 1)
(Tv1 Tr 2))/ln((T v1
Tr 1)/(Tv1 Tr 2)) (3-51)
In the above equations (BPE) is the boiling point elevation, (NEA) is the non-
equilibrium allowance, (T v) is the condensing vapor temperature and (U c) is
the condenser overall heat transfer coefficient.
BPE can be estimated from the following correlation [13]:
( ) ( )( ) 31 1 1 10 BPE X B X C = + where values of B and C in the correlation for the boiling point elevation are:
( ) ( )22 51 1(6.71 6.34 10 9.74 10 )10 B x T x T = + + 38
( ) ( )23 51 1(22.238 9.59 10 9.42 10 )10C x T x T = + +
The non-equilibrium allowance, NEA1
, in the first stage is calculated from the
gate height, GH 1, the height of the brine pool, H 1, the stage width, W, the
stage pressure drop, P 1-P2, and the brine density. For a good approximation in
brine recirculation MSF plant, the non-equilibrium allowance is equal 0.213 oC
for heat recovery section and 1.217 oC heat rejection section [14].
The same procedure is applied to the stages in the heat rejection section,
where the condenser area in rejection stages is given by
A j = (M f + M r ) Cp (T jn T cw)/(U j (LMTD) j) (3-52)
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3-2 Reverse Osmosis (RO)
Fig 3-3 Reverse Osmosis RO
3-2-1 Definition and AdvantagesRO process consists of three main steps: (a) pre-treatment. (b) membrane
passage, and (c) post treatment. In the post-treatment step, product water
passes through a decarbonation system, pH adjustment system. Chlorine
injection to comply with the required quality and use of the product water.
The purpose of the pretreatment step is to avoid any risk of clogging, fouling
or scaling the membrane. Pre-treatment is an important aspect of RO system.
All RO devices required pretreatment to remove the suspended solids,
sealants, foulants, and colloidal matters.
The benefits of RO against MSF can be stated in the following points [11]:
Limited make-up flow rate which means small amounts of antiscalantchemicals to be injected.
The flexibilities in RO in meeting various water and power ratio while
maintaining maximum process efficiency.
Corrosion problems are much less in RO than MSF.
Energy consumption is low in RO than MSF.
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3-2-2 Simplified Model of RO Design
Fig 3-4: a simplified RO membrane
Figure 3-4 shows a simplified spiral wound RO module. The mathematical
formula of this process as follows:
Pure water flux, N w in (kg/m 2.sec) is given by:
Nw= Aw ( P ) (3-57)
While the salt flux, Ns in (kg/m 2.sec) is given by
Ns= A s ( cw cp) (3-58)
Where
Aw = water permeability coefficient, m/sec.pa
As = salt permeability coefficient, m/sec
P = net applied pressure, Pa
= differential osmotic pressure, Pa
cw = salt concentration at membrane wall, kg/m 3
cp = permeate concentration, kg/m 3
The salt flux can be expressed based on the permeate concentration as Ns = N w cp (3-59)
The osmotic pressure of seawater can be expressed as [17]
= (0.6955 + 0.0025 t) 10 8 ( ci/i) (3-60)
where
ci = concentration, kg/m 3
t = temperature, C
The density of seawater, in (kg/m 3) is calculated by the formula [17]
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= 498.4 m + ( 248,400 m 2 + 752.4 m c ) (3-61)
where m is constant and equal to
m=1.0069 2.757 10 -4 t (3-62)
The net applied pressure, P in pa isP = P 2 P 1 (3-63)
where
P2 = operated pressure, Pa
P1 = atmospheric pressure, Pa
The permeate flux, N p in (kg/m 2. sec) is given by
N p = Nw + N s (3-64)
Salt concentration at membrane wall,cw in (kg/m 3)
cw = cp + (cf cp) exp [Nw/ks*1000] (3-65)
where
cf = seawater concentration, kg/m 3
ks = mass transfer coefficient, m/sec
mass transfer coefficient, ks can be calculated by[18]
ks = 1.10110 -4 u b0.5 (3-66)
Where
u b = velocity of brine, m/sec
3-2-3 Cost Methodology of RO
3-2-3-1 Water Production Cost Estimation of RO PlantEstimation of the water product cost depends on the plant capacity, site
characteristics, and design features. Plant capacity specifies sizes for various
process equipment, pumping units, and membrane area. Site characteristics
have a strong effect on the type of pretreatment and postreatment equipment,
and rates of chemicals. The electric power consumption, steam requirement
and chemicals are also design dependant. Water product cost depend on
several design and operational variables which includes [19]:
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Salinity and quality of feed water: Lower feed salinity allows for higher
conversion rates. As a result, the plant can operate with lower specific
power consumption and dosing of antiscalent chemicals. Also, downtime
related to chemical scaling is considerably reduced. Plant capacity: Larger plant capacity reduces the capital cost for unit
product. Although, the increase in the plant capacity implies higher capital.
Site conditions: Installation of new units as an addition to existing sites,
would eliminate cost associated with facilities for feed water intake, brine
disposal, and feed water pretreatment.
Qualified manpower: Availability of qualified operators, engineers, andmanagement would result in higher plant availability, production capacity,
and lower down time caused by trips of devices.
Energy cost: Availability of inexpensive sources for low cost electric
power and heating steam have strong impact on the unit product cost.
Plant life and amortization: Increase in plant life reduces the capital
product cost.
The production cost of desalted water is made up of two major components;
the capital cost and the operating cost. Capital cost covers the direct and the
indirect cost. The direct capital cost covers purchasing cost of various types of
equipment, auxiliary equipment, land cost, construction, and buildings.
Indirect capital costs include the freight and insurance, construction overhead
and contingency. Indirect capital costs are expressed as percentage of the total
direct capital cost. Operating cost covers all expenditure incurred after plantcommissioning and during actual operation. These items include labor,
energy, chemical, spare parts, and miscellaneous.
The most critical parameters in cost evaluation are the fixed charges
(amortization) and the energy cost. Other parameters that have lesser effect on
the unit product cost include the cost of chemicals and labor.
Amortization or fixed charges defines the annual payments that cover the totaldirect and indirect cost. This cost is obtained by multiplying the total direct
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and indirect cost by the amortization factor, which is defined by the following
relation [20]
1)i1(
)i1(i
a n
n
+
+=
where i is the annual interest rate and n is the plant life. Accumulated
experience in the desalination industry indicates that an amortization life of 30
years is adequate. As for the interest rate, its average value is equal 5%,
however, a range of 3-8% should be considered in economics analysis.
The following is a general procedure to estimate the water production cost in
Reverse osmosis plants:
3-2-3-1-1 Estimation of the direct capital costAs mentioned before the direct capital cost consist mainly of membrane
purchase cost (cost_mem), civil work cost (cost_civil) and pumping and
energy recover systems cost (cost_pump). These items can be evaluated as
[16]:
Membrane cost in ($) is given by
cost_mem = cost mem(A mem /Amodule ) (3-67)
where
A mod = area of one module, m 2
A mem = total Area of membrane, m 2
Civil work cost in ($) is obtained fromcost_civil = 2390 Q ref 0.8 (3-68)
where
Q ref = reference RO plant capacity, m 3/day
Pumping and energy recovery system cost in $ is given by
cost_pump = 0.0141 [(Q ref 101.32 P)/R f ] (3-69)
where
R f = recovery fraction
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power cost = 0.04 $/m 3
power consumption = 5 kWh/m 3 as a typical RO power consumption
value.
RO plant availability = 0.90The annual chemicals cost in $/m 3 is approximately give as [20]:
cost_chem = 0.03 $/m 3
The annual membrane replacement cost is normally taken as 10% of the
membrane purchase cost:
cost_mem_rep = 0.10 cost_mem (3-74)
The annual labor cost is approximately equal to 0.05 $/m 3 [19]:
cost_labor = 0.05 $/m 3
Then the water production cost is found by dividing the total annual costs by
the total water product.
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3-3 Comparative Study of MSF & ROThe applications of MSF distillation have been mainly large seawater
desalting plants producing water for municipal, industrial, or power generating
uses mostly on the Middle East.
An important characteristic of MSF plants is that scaling has little effect on
their production capacity. It reduces the thermal efficiency and thus more
energy is required per unit of fresh water, but as long as the required quantity
of water can be flashed through the design temperature range, the design
output can be maintained. MSF plants have therefore been favored where
reliability of water quantity has been of major importance.Comparison of the two design arrangements MSF clearly indicate that the
once-through option is more economical particularly for MSF units of large
capacities due to its simplicity of construction and lower pumping power
requirements.
RO is a recent technology for seawater desa1ting, although it has been
successfully used for many years to purify brackish waters. It reduces the
seawater TDS from approximately 41,000 ppm to less than 1,000 ppm.
Indications are that the RO plant has significantly lower capital and operating
costs than do MSF plants in the same area, even though the MSF plants are
much larger. The plant will be important in assessing the long-term reliability
of large scale RO in comparison with MSF in a difficult application. The
reliability of an RO plant is not so closely related to plant capacity as it is in a
distillation plant, where equipment size increases and design problems tend to
multiply as capacity is increased. Large capacity in an RO plant is obtained by
using a large number of standard units rather than by increasing the unit size.
Reliability can therefore be adequately demonstrated with a small plant. RO
has major advantages over MSF and other distillation processes in terms of
capital and operating costs.
RO also has significantly lower absolute energy requirements per unit of water produced than does MSF, although this may not translate directly into a cost
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benefit if MSF uses a low-cost, degraded steam. A large part of the energy
used for RO is consumed in raising the feed water to operating pressure,
which in a seawater plant may be 800 to 1500 psig.
At low fuel cost MSF will continue to be the optimum choice for largedesalting plants. For moderate capacities, RO offers low water cost. RO would
be the correct selection if fuel costs were increased. In any case an RO/MSF
hybrid plant is worth considering. It gives the lowest possible water cost if it
is associated with a dual plant.
RO plants are operated by electrical power to derive the high-pressure pumps
and other plant auxiliaries, mainly the pretreatment processes. RO power
consumption depends mainly on water recovery and the working pressure.
The following can summarize some of the technical differences between RO
and MSF [11]:
1- Seawater intake in MSF is twice that of RO.
2- Energy consumption per cubic meters in MSF is about three times that
of RO.
3- Volume and area required for MSF are large compared to those required
for RO.
4- Pumping energy in RO is about 25% of that required for MSF. A
possible decrease in pumping consumption in RO might be while using
energy recovery systems.
5- RO has no thermal energy consumption. In 2,750 m 3/d MSF about 8 MW
of thermal energy is consumed. This can be very expensive if not extractedfrom the steam turbine.
6- Heavy foundation and extensive civil work is required by MSF due to its
heavy weight.
The main benefits of RO against MSF are Limiting make-up flow rate which
means small amounts of antiscalant chemicals to be injected, Corrosion
problems are much less in RO than MSF and energy consumption is low in
RO than MSF [11].
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Chapter 4Hybrid
DesalinationSystems
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4-1 Identification of Hybridization SystemHybridization System is a combination of two or more processes in order to
provide a better cost effective product than either alone can provide. In
desalination, there are membrane and thermal (distillation) processes. The
effective integration of membrane / thermal desalination technology is to
reduce the cost of desalination and electrical power consumption. There are
two Possible Options for Hybridization System, Simple Hybridization and
Integrated Hybridization.
In the simple hybrid MSF/ RO desalination process, the seawater RO plant is
combined with either a new or existing dual-purpose MSF plant but theintegrated MSF/RO desalination process is much more advance than simple
hybrid such as:
The RO feed water temperature is optimized and controlled by using
cooling water from the heat-reject section of the MSF plant.
Brine discharged from RO plant is combined with brine recycle in
MSF.
4-2 Advantages of hybrid MSF/ RO systemHybrid RO MSF desalination-power process has the following advantages
[16,21]:
The capital cost of the combined RO/MSF plant can be reduced.
A common seawater intake is used.
Product waters from the RO and MSF plants are blended to obtain
suitable product water quality.
A single-stage RO process can be used.
RO membrane life can be extended by blending the high purity
distillate of the MSF plant with the RO permeate
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MSF plant provides better control of the feed water temperature to
the RO plant by using the warm reject coolant water from the MSF
heat rejection section.
The low-pressure steam from the power plant can be used todeaerate and warm up the feed to the RO plant this minimizes
corrosion hazard by eliminating residual chlorine and dissolved
oxygen.
A common post-treatment plant can handle the combined product
of the two plants.
Electric power production from the MSF plant can be efficientlyutilized in the RO plant, thereby reducing net export power
production.
Blending MSF product with RO product water reduces the
temperature of the MSF product water. RO for high-pressure brine
without energy recovery can be used to cool the MSF product
water.
Preheat RO feed water increases the recovery significantly.
The RO reject brine can be combined with the recycle stream in
the MSF plant.
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Layyah plant, Sharjah, UAE. They found the hybridization of sweater reverse
osmosis (SWRO) and the multi stage flash (MSF) technology was considered
to improve the performance of latter and reduce the cost of the produced
water. Integrating MSF with RO has been implemented recently in Fujairahdesalination plant with a total capacity of 100 MIGD of which 37.5 MIGD are
produced by RO and the balance is produced by MSF.
They studied the data search and collection, technology selection, water
demand, power demand, and fuel availability were all used to come up with
optimum scenarios to reduce cost of power and water generation and to meet
increasing demand of water and power.
Al-Mutaz [21] investigated the Desalination plants required. He found that,
the Desalination plants require significant amounts of energy in the form of
heat and/or electricity (power). This energy can be supplied by nuclear
reactors since nuclear reactors are used mainly for the production of either
heat or power. Coupling desalination plants with nuclear reactors gives many
economical and technical advantages. The hybrid RO MSF desalination plant
coupled to nuclear power plant gives high overall availability factor. He
suggested that, the CANDU PHWR is the appropriate type of nuclear reactor
for coupling with hybrid RO MSF desalination plants. This hybrid system has
potential advantages of a low power demand, improved water quality and
possible lower running cost.
Al-Mutaz et al. [23] reviewed the hybrid plant concept. They found that the
hybrid plant is only useful to bring the salinity of the water produced from RO plants to an acceptable limit. If high pressure membranes(higher than 80 atm)
are developed and become reliable and fuel cost increases, the reverse osmosis
plants would certainly replace the MSF Plants Al-Mutaz and his team
concluded that more efforts should be given to scaling up MSF and RO plants
and for developing high pressure membrane.
Jacques Andrianne and Felix Alardin [24] found that the reduction in cost and
the improved economics of desalination plants are essential elements for the
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development of communities. Energy, capital, and operating costs are key
issues of water desalination economics. The choice will depend on the specific
conditions prevailing on site, such as existing facilities, power and water
demand increase, land availability, raw water quality, quality of water to be produced, ratio between power and water production, ratio between thermal
and membrane desalination.
Essam El-Sayed et al. [25] made a experimental testing of RO performance in
an MSF/RO hybrid model for 1,800 h. The RO feed water temperature
ranging from 24 to 31C. They found a significant increases in the RO product
water flow rate when the data from before and after hybridization were
compared. 42-48% gain in the product water flow rate for RO plant operating
at temperature of 33C, over that operating at 15C. The energy consumption
of RO can be reduced to the level of 5.2 kWh/m 3 using a simple MSF/RO
hybrid arrangement in which the RO plant is fed the preheated seawater
rejected from the MSF heat rejection section.
M. Turek and P. Dydo [26] determined the highly concentrated solutions
cannot be treated by RO as a consequence of a physical limit imposed by their
osmotic pressure value as well as the scaling phenomenon. Scaling
phenomenon can be diminished with partial softening of RO feed with
nanofiltration membranes. They found the integration of NF, RO and MSF
makes it also possible to overcome these limits. The performance of
desalination and concentration in hybrid membrane-thermal systems seems to
be higher than the performance of simple membranes. They determined thethermal methods seem to be more effective than membrane methods in term
of Production of highly concentrated brines.
Neil M. Wade et al.[27] studied the cost of water production .They found the
cost of water produced by RO plant is less sensitive to increase in fuel cost
than MSF plant in dual purpose schemes. At fuel costs above $35 per barrel
there would be substantial cost savings for RO plant compared with
conventional dual purpose plant.
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Also, Al-Mutaz and Alabdula'aly [28] reviewed the issue of water production
cost for RO and MSF in Saudi Arabia. The results indicate that the RO has
lower capital and production costs. At high membrane replacement rate and
low energy cost. MSF offers lower water production cost specially at largecapacity plants.
Van Dijk et al. [29] discussed the influence of design parameters, such as raw
water temperature and total dissolved solids content (TDS), design pressure,
and recovery, on total unit cost for the production of desalinated water from
the Arabian Gulf in Saudi Arabia. They found the total water costs are
influenced significantly by raw water TDS. Also, they found the cost of
seawater RO increase from 1.62 $/m 3 at 35,000 ppm TDS to 2.31 $/m 3 at
44,000 ppm TDS to 3.84 $/m 3 at 55,000 ppm TDS. Operation at a pressure of
900 psi rather than 800 psi will lead to a significant drop in total water costs
down to 2.05 $/m 3 at 44,000 ppm TDS, and to 3.09 $/m 3 at 55,000 ppm TDS.
As the effects of this increased pressure are yet unknown, it is recommended
to study these effects. Total water costs may decrease significantly when
membrane costs are lower.
Braj M. Misra et al. [30] reviewed Hybrid system (MSF/RO). There is
significant reduction in the operation and maintenance (O&M) cost of
desalted water by taking the advantage of producing both process and drinking
quality water, common pretreatment to a considerable extent and possibility of
using reject streams from one plant to the other. Preliminary investigations
also, have been carried out in terms of using ultrafiltration (UF) asapretreatment for RO and nanofiltration (NF) to improve the performance of
MSF and RO. UF will reduce the fouling and scaling of RO giving longer life
of the membrane elements. NF will remove the hardness and scaling
constituent improving the recovery for RO and increasing the top brine
temperature for MSF.
Osman A.Hamed [31] studied the simple and fully integrated hybrid
desalination systems. He found the hybrid desalination systems combining
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with power generation systems are currently considered a good economic
alternative to dual purpose evaporation plants. Hybrid (membrane /thermal
/power) configurations are characterized by flexibility in operation, less
specific energy consumption, low construction cost, high plant availability and better power and water matching.
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4-4 Options for Hybridization System
4-4-1 Simple Hybrid Desalination Plants
4-4-1-1 Simplified MSF-OT/RO
Fig4-1: Simplified MSF-OT/RO Design
Design Procedure
In the simple hybrid multistage flashreverse osmosis (MSF/RO) desalination
power process, a seawater RO plant is combined with either a new or an
existing dual purpose MSF plant in the simplest possible manner. In this case,
the seawater feed is split to two streams. One of them to MSF-OT unit and the
other is to RO unit. RO product water is combined with MSF product water.
The overall material balance equations is given by
MHf = M Hd + M H b (4-1)
Where M is the mass flow rate and the subscript Hb, Hd, and Hf defines the
brine, distillate, and feed.
where
Mass balance for hybrid product
MHd=M d + F p (4-2)
Salt balance
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XHd MHd=c p FP (4-3)
Assuming the product from MSF is salt free.
The overall salt balance is given by
X Hf M Hf = X Hd M Hd + X Hb MHb (4-4)
The mass balance and the energy balance for the MSF-OT will be the same as
the stand alone MSF-OT. The RO also is at the same condition.
Cost MethodologyThe water production cost of Simple Hybrid Desalination Plants equal to the
summation of annual water production cost of MSF section and annual water production cost of RO section and also the total annual plant intake-outfall
cost of hybrid plant divided by the summation of water production of MSF
section and RO section.
The annual Cost of MSF-OT procedure calculation and Annual Cost of RO
procedure calculation will be the same as before.
Annual Cost of MSF-OT, C AM in $/year isCAM = C DM + C IM + C OM
The water production cost of RO is calculated from the total annual cost. The
total annual cost has following major cost items:
- the annual fixed charges,
- the annual electric power cost,
- the annual chemicals cost,
- the annual membrane replacement cost,
- the annual labor cost,
RO_prod_cost = cost_fix + cost_ep + cost_chem + cost_mem_rep +
cost_labor (4-5)
The total annual plant intake-outfall cost of hybrid plant has the following
[11]:
hybrid electromechaical equipment cost
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cost_H1=44000+70*F_ref (4-6) hybrid civil work cost
cost_H2=150000+375*F_ref (4-7)
hybrid elctrochlorinationcost_H3=22000+12000*F_ref (4-8)
hybrid brine disposal cost
cost_H4=25000+10*B_ref (4-9)
Where
F_ref = reference feed flowrate = has value between 200-1000 m 3/h
B_ref= reference blowdown flowrate = has value between 40-1000 m 3/h
The reference hybrid intake-outfall cost:
cost_H_total=cost_H1+cost_H2+cost_H3+cost_H4 (4-10)
the annual plant intake-outfall cost in $/year:
COST_HA=0.0963*(cost_H_total)*(f_ratio 0.9) (4-11)
Then, the total annual cost of SIMPLE HYBRID (MSF-OT/RO)
COST_SIM_HY=(C_AM + cost_RO_total + 1.1*COST_HA) (4-12)
WATER COST OF SIMPLE HYBRID (MSF-OT/RO) in $/m 3
total_cost=(C_AM+cost_RO_total+1.1*COST_HA)/M_Hd1 (4-13)
Where
M_Hd1= the summation of water production of MSF section and RO section
in m 3/year .
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4-4-1-2 Simple MSF-BR/RO
MSF- BR
RO
M Hf
Mf
Frj
Mb
M Hb
Fp
MdM Hd
M cw
Fig4-2: Simple MSF-BR/RO
Design Procedure Same as before, the seawater feed is split to two stream. One is to MSF-BR
unit and the other is to RO unit and RO product water is combined with MSF
product water to become one steam.The overall material balance equations is given by
MHf = M Hd + M H b+M cw (4-14)
Where M is the mass flow rate and the subscript Hb, Hd, and Hf defines the
brine, distillate, and feed.
where
Mass balance for hybrid product
MHd=M d + F p
Salt balance
XHd MHd=c p FP
Assuming the product from MSF is salt free.
The overall salt balance is given by
X Hf M Hf = X Hd M Hd + X Hb MHb+X f Mcw (4-15)
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The mass balance and the energy balance for the MSF-OT will be the same as
the stand alone MSF. The RO also is at the same condition.
Cost MethodologyThe same procedure was used for evaluating the water production cost in
MSF-BR/RO as used in MSF-OT/RO .
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