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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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