CHARACTERISTICS
OF WATER
PHYSICAL PROPERTIES:
*DENSITY - 1.0 at 4oC
*Specific Heat - 4.18
Kj/kg at 0oC
*Latent Heat - Fusion
79 kcal/kg
*Latent Heat -
Vaporization 539 kcal/kg
*Viscosity 1.797 mPa.s
at 0oC
*Surface Tension 75.60
dynes/cm
*Osmotic Pressure
p = DCRT
p : Osmotic Pressure in Pa
DC : Difference in Concentration in mol/m3
R : Constant of Ideal gases 8.314 J/mol/K
IMPURITIES OF WATER
*BACTERIA
& VIRUSES
*MICRO-ORGANISMS
*TURBIDITY
*COLOUR
*MINERALIZATION
*METALLIC
*DISSOLVED
GASES
*AMMONIA
*ORGANIC
MATTER
*POLLUTANTS
SOURCES OF WATER FOR INDUSTRIAL APPLICATIONS
*RIVER
*SEA
*PONDS
*LAKES
*IRRIGATION
CANALS
*BOREWELLS
*RECYCLED
WATER
*RESERVOIRS
*RECYCLED
EFFLUENTS
APPLICATIONS OF WATER IN POWER PLANTS
*COOLING
OF CONDENSATE
*AUXILIARY
COOLING
*BOILER
WATER
*ASH
HANDLING WATER
*COAL
DUST SUPPRESSION WATER
*WASHING
*DRINKING
*SANITATION
*FIRE
WATER
*SERVICE
WATER
*HVAC
SYSTEM
MAKE - UP WATER
TREATMENTS
*CLARIFICATION - ALUM, PEs, PAC
*FILTERATION
*ULTRAFILTERATION
*NANOFILTERATION
*REVERSE
OSMOSIS
*ACTIVATED
CHARCOAL
*SOFTENING
- LIME, ION EXCHANGE
*ACID
TREATMENT
*INHIBITORS
*OXYGEN
REMOVAL
*BIOCIDE
ADDITION
*
EFFECT OF CLARIFICATION PROCESS
ON
CORROSION BEHAVIOUR OF COMPONENTS
*
*ALUM
REDUCES pH, INCREASES
SULPHATES
*INCREASED CORROSION
*PAC
- LESS pH REDUCTION,
LESS CORROSION
*POSSIBLE LESS
COST
INCREASED ALUM DOSING
*QUICK
RELIEF FROM PROBLEM
*
*
*EXHAUSTING
MACHINE AND CHEMICALS
*INCREASE
IN IONIC LOAD ON EXCHANGERS
*FREQUENT
BACKWASH OF FILTERS
*CARRYOVER
OF FINE FLOCS OF Al(OH)3
INTO CLARIFIED WATER
*FREQUENT
DESLUDGING OPERATIONS
*DELICATE
PLANT OPERATIONS
*DAMAGE
CONCRETE STRUCTURES
*HIGH
Al CAUSE MENTAL DISORDERS
POLYELECTROLYTE DOSING
*DECREASE
ALUM DOSING EVEN BY 50 %
*WORKS
AT VERY LOW DOSAGES
*REDUCES
SLUDGE VOLUME BY 40 - 50 %
*WORKS
IN WIDE pH RANGE
*LIME
ADDITION CAN BE STOPPED
*NON
CORROSIVE
*NO
INCREASE IN IONIC LOAD ON RESINS
*REDUCTION
IN INDIRECT COST
*NON-TOXICITY
TO HUMANS
*DETRIMENTAL
EFFECT ON RESINS
REVERSE OSMOSIS
PURE
WATER WATER WITH
SALTS
OSMOTIC
PRESSURE = DC x R X t
DC
= CONCENTRATION IN MOL/M3
REVERSE OSMOSIS
*IT
IS A PRESSURE ACTIVATED PROCESS BY WHICH
WATER FROM A HIGHLY CONCENTRATED SOLUTION
PASSES THROUGH SEMI-PERMEABLE MEMBRANE
LEAVING THE SOLUTES BEHIND.
*IT
IS A CROSS-FLOW MEMBRANE PROCESS WHICH
REMOVES ALMOST ALL ORGANIC COMPOUNDS
AND 90 - 99 % OF ALL IONS.
*SOLUTE
PASSAGE CHARACTERISTICS ARE
DETERMINED BY AFFINITY AND SOLUBILITY
PHENOMENA.
*AN
RO UNIT PRECEDING DM FOUND TO REDUCE
PRODUCTION COST OF WATER BY ABOVE 50 %.
MATERIALS OF MEMBRANE
MATERIAL OF MEMBRANE IS CRUCIAL
TO AVOID FOULING :
*POLYSULPHONATE
*POLYACRYLATE
*POLYCARBONATE
*POLYAMIDE
*POLYOLEFIN
*POLYVINYLLIDINE
FLUORIDE
ADVANTAGES OF REVERSE OSMOSIS
*CONTINUOUS
OPERATION
*NO
REGENERATION NEEDED
*CAN HANDLE WIDE RANGE OF TDS (700 - 60,000 ppm)
*LOW
OPERATING COST COMPARED TO DM
*BULK
STORAGE OF CHEMICALS (ACID AND ALKALI)
NOT REQUIRED
*LESS
FLOOR SPACE NEEDED FOR RO PLANT IN
COMPARISON TO DM PLANT
*EASY
OPERATION AND MAINTENANCE
*REDUCED
EFFLUENT QUANTITY AND TREATMENT COST
*COST
OF TREATED WATER IS ALMOST HALF COMPARED
TO DM WATER.
TOPICS TO BE COVERED
*NEED
FOR WATER TREATMENT
*CLARIFLOCULATION
PROCESS
*CHLORINATION
*ALTERNATIVES
TO CHLORINATION WITH SPECIFIC
DISCUSSION ON OZONATION
*REMOVAL
OF COLLOIDAL SILICA AT PRETREATMENT
STAGE
*REVERSE
OSMOSIS
WHY PRETREATMENT
*INCREASING
POLLUTION IN WATER RESOURCES
*INCREASING
STRUCTURES BY REGULATORY BODIES ON USE
OF WATER RESOURCES
*FINE
QUALITY REQUIREMENTS WITH INDUSTRIAL
GROWTH, IN PARTICULAR POWER GENERATION
TECHNOLOGY
*MORE
AWARENESS IN PUBLIC
*ECONOMIC
USE OF DEMINERALISERS/MEMBRANES
BOILER FEED WATER
A PERFECT WATER FOR BOILER FEED
IS ONE WHICH WILL NOT DEPOSIT
ANY SCALE FORMING SUBSTANCES,
WILL NOT CORRODE METAL OF BOILERS AND WILL
NOT RESULT IN
PRIMING OR FOAMING.
COMMON IMPURITIES IN WATER
AND THEIR EFFECTS IF USED FOR BOILER
FEED
*SUSPENDED
SOLIDS : PRIMING, FOAMING, SLUDGE OR
SCALE
*SILICA
: DEPOSITION ESPECIALLY ON TURBINE BLADES
*CARBONATES,
BICARBONATES OF CALCIUM AND
MAGNESIUM : DEPOSITION
*CHLORIDE
AND SULPHATE : SCALE AND CORROSION
*FREE
ACIDS : CORROSION
*CARBONATE
AND BICARBONATE OF SODIUM :
PRIMING, FOAMING, EMBRITTLEMENT
*OXYGEN,
CARBONIC ACID : CORROSION
*OILS,
GREASES : DEPOSITION, FOAMING, PRIMING
*ORGANIC
MATTER : CORROSION, FOAMING, PRIMING,
DEPOSITION
PRE-TREATMENT
TO MAKE WATER FREE FROM ALL
IMPURITIES THAT WILL ADVERSELY EFFECT THE FEED
WATERCHEMISTRY AND FURTHER WATER PURIFICATION PROCESS.
*SUSPENDED
SOLIDS
*ORGANIC
MATTER
*COLLOIDAL
PARTICLES
*NON
REACTIVE SILICA
*COLOUR
AND ODOUR
*EXCESS
DISINFECTANTS
*EXCESSIVE
DISSOLVED IRON
& MANGANESE
CLARIFLOCULATION
REMOVAL OF SUSPENDED SOLIDS BY
*COAGULATION/FLOCULATION
*SETTLING
*SEPARATION
ACHIEVED THROUGH
*RETENTION
TIME
*ADDING
COAGULANT
*ADDING
COAGULANT AID
*CREATING
SUITABLE pH & ENVIRONMENT FOR
PROPER COAGULATION/FLOCULATION/SETTLING.
CHEMICALS USED IN WATER CLARIFLOCULATION
*ALUM/FERROUS
SULPHATE/FERRIC SULPHATE, SODIUM
ALUMINATE, PAC: AS COAGULANT
*ACTIVATED
SILICA, POLY ELECTROLYTES: COAGULANT
AID
*LIME,
SODIUM CARBONATE: pH ADJUSTMENT
*BENTONITE
: FLOC WEIGHTING AGENT
CHANGES IN WATER QUALITY
BY ADDITION OF 1 PPM OF PRETREATMENT
CHEMICALS
*ALUMINIUM
SULPHATE : CHANGE IN ALKALINITY BY
-0.45, SULPHATE BY 0.45
*FERROUS
SULPHATE : CHANGE IN ALKALINITY BY -0.36,
SULPHATE BY 0.36
*FERRIC
SULPHATE : ALKALINITY BY -0.75, SULPHATE BY
0.75
*CHLORINE
: ALKALINITY BY -1.4, CHLORIDE BY 1.4
*HYDRATED
LIME : ALKALINITY BY 1.26, HARDNESS BY
1.26
*SODA
ASH : ALKALINITY BY 0.5
TIPS TO ACHIEVE BETTER CLARIFLOCULATION
*KEEP
RETENTION TIME AS PER YOUR REQUIREMENT OF
WATER QUANTITY
*FOR
ALUM, THE FLOCULATION pH is 5.5 - 7.5
FOR FERRIC ALUM, pH 5.5 - 7.5
FOR NON FERRIC ALUM, pH 5.5 - 6.2
*MAINTAIN
PROPER MIXING RATES AT THE
CLARIFLOCULATORS.
*FOR
EXTREME LOW TURBID WATERS, USE BENTONITE
CLAY OR FUELLERS EARTH ALONGWITH COAGULANT IF
NECESSARY/POSSIBLE GO FOR SLUDGE CIRCULATION
*CLARIFLOCULATION
IMPROVES WITH TEMPERATURES
TIPS TO ACHIEVE BETTER
CLARIFLOCULATION
*MAINTAIN
PROPER SLUDGE BLANKET
*WHEREVER
POSSIBLE/NECESSARY GO FOR COAGULANT
AID INSTEAD OF EXCESS ALUM.
*SODIUM
ALUMINATE, WHICH IS HIGHLY ALKALINE CAN
BE USED ALONGWITH ALUM IN COAGULATION OF LOW
pH WATERS
*USE
PROPER QUANTITY OF WATER DISINFECTANTS FOR
BETTER CLARIFLOCULATION
*GO
FOR BETTER INSTRUMENTATION, IF POSSIBLE ON-
LINE FOR CHECKING AND OPTIMISING PRETREATMENT.
*PURITY
OF LIME AND ITS SHELF LIFE ARE CRUCIAL FOR
PROPER CLARIFLOCULATION
*DO
NOT LOOK PRETREATMENT AND DEMINERALISATION
IN ISOLATION
CHLORINATION PROCESS
*DESTROYING
THE ORGANIC MATTER (BOTH CHEMICAL, BIOLOGICAL) THROUGH OXIDATION USING
CHLORINE.
*Cl2 + H2O HClO
+ HCl (5<pH<10)
*HClO
ClO- + H+ (pH>10)
PROBLEMS WITH CHLORINATION
*CHLORINE
IS A POISONOUS GAS SUPPLIED IN
CYLINDERS/TONNERS
*CHLORINATED
WATERS WITH EXCESS RESIDUAL
CHLORINE ARE HAZARDOUS TO PLANT AND ANIMAL
LIFE
*ASSOCIATED
WITH PROBLEMS LIKE COPPER TUBE
LEAKS, CORROSION OF ASSOCIATED PIPINGS, etc.
*TO
REMOVE EXCESS CHLORINE IN TREATED WATER, WE
HAVE TO USE ACTIVATED CARBON, SODIUM SULPHITE
DOSING RESULTING IN EXCESS O&M COST
PROBLEMS WITH CHLORINATION
*MANGANESE,
IRON, H2S AND ORGANICS WITH
UNSATURATED LINKAGES INCREASE CHLORINE
DEMAND, MICROBIOLOGICAL DISINFECTION WILL BE
EFFECTIVE ONLY AFTER REMOVAL OF THESE IONS.
*EFFECT
OF CHLORINE ON VIRUS IS VERY LITTLE
*PHENOL
IN WATERS REACT WITH CHLORINE TO FORM
CHLOROPHENOLS HAVING BAD ODOR AND TASTE
*CHLORINATION
MAY RESULT IN FORMATION OF TRI
HALO METHANES WHICH ARE TOXIC
*CHLORINATION
INCREASES IONIC LOAD ON FURTHER
TREATMENT SYSTEMS
ALTERNATIVES TO CHLORINATION
*BLEACHING
POWDER DOSING : SOLID, HAVING LESS
AVAILABLE CHLORINE, CAUSING MORE SLUDGE AND
EXCESS LOAD ON ION EXCHANGERS
*SODIUM
HYPOCHLORIDE ADDITION : LIQUID, NOT COST
EFFECTIVE FOR LARGE QUANTITIES OF WATER
*BROMINATION
: SUITABLE FOR WATERS THAT HAVE pH
7.5 OR GREATER AND EXCESS AMMONIA. MOST
COMMONLY USED IS NaBr. EFFECTIVE AT A WIDER pH
RANGE.
*CHLORINE
DIOXIDE ADDITION : SUITABLE WHEN WATER
CONTAINS EXCESS AMINES, EFFECTIVE IN pH RANGE OF
8 - 11.
OZONATION
*GETTING
IMPORTANCE IN EUROPEAN COUNTRIES AS
ALTERNATIVE TO CHLORINE
*PREPARED
AT DOSING SITE BY SILENT ELECTRIC
DISCHARGE OF DRY AIR (WITH DEW POINT<-70oC), OR
DRY OXYGEN (WITH DEW POINT<-60oC)THROUGH SERIES
OF ELECTRODES AND AT A VOLTAGE OF 17.5 KV.
*OZONE
GENERATORS WITH OUTPUT OF EVEN 10 % BY
WEIGHT ARE AVAILABLE
*THERMAL
DESTRUCTION AND CATALYTIC DESTRUCTION
METHODS ARE AVAILABLE FOR DESTROYING EXCESS
OZONE GASES
*
ADVANTAGES OF OZONE
*REMOVAL
OF IRON AND MANGANESE CAN BE
EFFECTIVELY DONE AT NEUTRAL pH. (WITH
*CHLORINATION
pH ABOVE 9 IS NEEDED.
*REMOVAL
OF COLLOIDS AND ORGANICS IS MORE
EFFECTIVE WITH OZONE.
*POLYMERS
AND ORGANIC MACRO MOLECULES IN
WATER GET EASILY BROKEN INTO SMALLER ORGANIC
ACIDS WITH PROPERTIES OF COAGULATANT AIDS. THIS
REDUCES THE FLOCULATING AGENT CONSUMPTION
DURING CLARIFLOCULATION
*RESPONSE
OF OZONE ON ORGANIC CELLS EXCEEDS
CHLORINE BY A FACTOR OF > 10.
ADVANTAGES OF OZONE
*CHLORINE
ATTACKS ENZYMES THAT EFFECT CELL
MULTIPLICATION WHILE OZONE RUPTURE CELL WALL
MAKING IT VERY EFFECTIVE EVEN FOR VIRUS.
*NO
ADDITION OF DISSOLVED SOLIDS AS LOAD TO
FURTHER ION EXCHANGERS
*HEALTH
HAZARDOUS NATURE COMPOUNDS ARE NOT
FORMED
*NOT
HAZARDOUS IN HANDLING
*OZONE
IS EFFECTIVE AT ALL pH
*EFFECTIVE
IN REDUCING FUNGI GROWTH
*OPERATING
COST IS VERY LESS.
PROBLEMS WITH OZONE
*
CAPITAL COST IS VERY HIGH
*
*GAS
IS UNSTABLE
TO BE PREPARED AT SITE ONLY
*
*MAINTENANCE
OF RESIDUALS IS NOT POSSIBLE.
*
CHEMISTRY OF SILICA IN WATER
*REACTIVE
FORM
*
*SILICON
DI OXIDE DISSOLVED IN WATER RESULTING IN
MONOSILICIC ACID
*
*
SiO2 + 2H2O H4SiO4
*
*RESPONDS
TO STANDARD SILICO MOLYBDATE TEST
*
*SUSPENDED
PARTICLE FORM - SAND
CHEMISTRY OF SILICA IN WATER
*COLLOIDAL
SILICA
*INSOLUBLE
& INSEPARABLE
*NON-IONIC
IN THE FORM OF
*SILICON
POLYMERISED WITH SiO2
*SILICON
LOOSELY BOUND WITH ORGANICS
*SILICON
LOOSELY BOUND WITH INORGANICS
*
(Al2O3/CaO)
*CHEMICALLY
NON - REACTIVE
*C(SURFACE
WATER > WELL WATER)
*CONC.
VARIES WITH LOCATION AND SEASON.
WHAT HAPPENS WHEN COLLOIDAL
SILICA ENTERS BOILER?
*RESPOND
TO ALL CHEMICAL TESTS
*
*FORCE
PRESSURE REDUCTIONS, GENERATION
LOSSES.
*
*SEVERE
BLOW DOWNS AND HEAT LOSSES.
*
*LONG
START-UPs.
WHAT HAPPENS IF BOILERS ARE
OPERATED WITH HIGH SILICA
*GETS
CARRIED OVER TO THE TURBINE.
*DEPOSITS
ON VARIOUS STAGES OF TURBINE BLADES
DURING STEAM EXPANSION.
*DEPOSITS
ARE HARD TO REMOVE.
*CAUSE
VIBRATIONS IN THE TURBINE.
*REDUCE
OPERATING EFFICIENCY.
*REQUIRE
TURBINE BLADE WASHING/SHUT DOWN
FOR CLEANING.
INCREASED RETENTION TIME
UPs :
*NO
EXCESS/ NEW CHEMICAL REQUIREMENT.
*EXISTING
MACHINE.
DOWNs :
*REDUCED
OUTPUT.
*NON-UTILISATION
OF PT SYSTEM TO FULL CAPACITY
PRECOAT/POWDEX
PROCESS
UPs :
*EASY
TO OPERATE.
DOWNs :
*OPERATION
COST IS VERY HIGH.
*LESS
SHELF-LIFE OF MATERIALS.
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