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LECTURE #4 & 5

COAGULATION, MIXING, AND


FLOCCULATION
CLOS

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 Discuss the flocculation and coagulation
processes
 Enlist the various coagulants

 Calculate G value for mixing tank

 Describe the sedimentation theory

 Design a clarifier

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Typical water treatment process flow diagram employing coagulation
(chemical mixing) with conventional treatment, direct filtration, or contact
filtration.

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COAGULATION PROCESS

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Involve addition of chemical(s) (Coagulant(s))

 Destabilization of small suspended and colloidal


particulate matter

 Adsorption and/or reaction of portion of the colloidal


and dissolved NOM to particulate

 The creation of flocculent particles that will sweep


through the water to be treated
Enmeshing small suspended, colloidal, and dissolved
materials as they settle.
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COAGULATION PROCESS

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 Alum, ferric chloride, and ferric sulfate
 Hydrolyze rapidly when mixed with water
Form insoluble precipitate
Destabilize particles by neutralizing the charge on fine
particles or
Adsorb on the surface of the particulate

Reduce the repulsive forces

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Surface charge on a particle in water

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ZETA POTENTIAL
• Electrophoresis
– When a charged particle is subjected to an electrical
field between two electrode
A negatively charged particle will migrate toward the
positive electrode

Fig 9-6
ZETA POTENTIAL
The electrical potential between the actual shear
plane and the bulk solution is called Zeta potential
Electrophoretic mobility, (μm/s)/(V/cm), vE/E

Zeta potential, mV
v k2 
o Dynamic viscosity

Z
Permittivity relative to a vacuum o Permittivity in a vacuum

vE= electrophoretic velocity of migrating particle, μm/s


E= electric field at particle , V/cm
K2=constant = 4π to 6π

Empirically, when the absolute value of the zeta potential is reduced below
about 20 mV, rapid flocculation occurs (Kruyt, 1952).
COAGULATION PROCESS

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 Key properties
 Trivalent cation
 Colloidal are negatively charged
 Effectiveness of cations: trivalent>divalent>monovalent

 Non toxic
 For production of potable water

 insoluble in the neutral pH range


 High concentrations of coagulants in treated water are
undesirable
 Aluminum (Al3+) and ferric iron (Fe3+)
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Ex6-2
COAGULATION PRACTICE

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 Stiochiometry of metal ion coagulants

Al 2 (SO 4 )3 .14H 2O  6(HCO3 )  2Al(OH)3 (am)  3SO24  14H 2O  6CO2

Fe2 (SO 4 )3 .9H 2O  6(HCO 3 )  2Fe(OH)3 (am)  3SO 24  9H 2O  6CO2

FeCl3 .7 H 2O  3( HCO3 )  Fe(OH )3 (am)  3Cl   7 H 2O  3CO2

 If natural alkalinity is not sufficient


 NaOH, Ca(OH)2, Na2CO3 (Caustic soda, lime, soda ash)

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COAGULATION PRACTICE

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 NOT possible to predict coagulation performance
 Due to sequence of reactions
 Jar test

 pH and optimum dose

Optimal pH range for alum =5.5-6.5


Adequate coagulation 5 -8

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Ex 6-3, 6-4

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COAGULATION PRACTICE

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 Interactions with other constituents in water
 SO42-, NOM, F-, PO43-

 Typical dosage
 Alum 10 -150 mg/L
 Ferric Sulfate 10 -250 mg/L
 and Ferric Chloride 5-150 mg/L
 Importance of initial mixing with metal salt

 Half of Al3+ hydrolyzed to Al(OH)2+ within 10-5 s


 Coagulation of silica dispersion with Al3+ in order of 10-3s
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EXAMPLE

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A water treatment plant with an average flow of Q=0.044
m3.s-1 treat its water with alum (Al2(SO4)3.14H2O) at a dose
of 25 mg.L-1. Alum coagulation is used to remove particulate
matter, reduce the concentration of organic matter, and
reduce the alkalinity of the water according to the reaction
given below
Al 2 (SO 4 )3 .14H 2O  6(HCO3 )  2Al(OH)3 (am)  3SO24  14H 2O  6CO2
If organic matter concentration is reduced from 8 mg.L-1 to 3
mg.L-1, determine the total mass of alkalinity consumed and
the total mass of dry solids removed.

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IRON

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 With alkalinity

FeCl3 .7 H 2O  3( HCO3 )  Fe(OH )3 (am)  3Cl   7 H 2O  3CO2

 Without alkalinity

FeCl3  3H 2O  Fe(OH )3 (am)  3Cl   3H 

Effective pH range 4-9

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COAGULANT AND FLOCCULANT AIDS

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 Coagulant Aid
 Insoluble particulate materials
 Added to enhance coagulation

 Clay (bentonite, kaolinite)


 Sodium silicate

 Powdered activated carbon

 Added to water that contain low concentration of


particles
 To form nucleating sites

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COAGULANT AND FLOCCULANT AIDS

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 Flocculent aids
 Uncharged and –vely charged organic polymers

 Added after coagulants are added (already


destabilized particles)

 Jar test
 Floc strength
 Size

 Settling rate

 Activated Silica
 Inorganic flocculant aid
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MIXING

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 Mixing (rapid mixing)
 Chemicals are quickly and uniformly dispersed in the
water

 Chemical reaction in coagulation is completed within


0.1 s
 Mixing must be instantaneous and complete as possible

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RAPID MIXING

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 Volume of rapid mixing tank
V= td*Q td= detention time
Volume not more than 8m3
- mixing equipment and geometry constrains
Mixing equipment
electric motor, gear-type speed reducer
turbine or axial-flow impeller

Design liquid depth = 0.5 to 1.1 times of diameter or


width
Impeller diameter = 0.30-0.50 times of tank diameter or
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Portion of influent
flow used to
disperse chemical
into bulk flow

Pumps

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Water to be mixed
with chemicals

Inline static mixer (b)

Water to be mixed
with chemical

Converging section results in


increased fluid velocity
Water to be mixed with
chemical In-line venturi mixture

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EXAMPLE 2

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A water treatment plant is to be turned into
a research facility treating 0.044 m3/s. A
low-turbidity iron coagulation plant has
been proposed with the following design
parameters
Rapid mixing to= 10 s ,
water temperature =18oC
Determine the size of the rapid-mix tank

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SOLUTION

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- Volume of the rapid-mix tank
V= Qxto = 0.044m3/s x 10 s = 0.44 m3
Less then 8 m3 OK

Two tanks are need in case of failure


Two alternate tanks, each with volume 0.44 m3 (because
volume of tank is very small)

Depth-to-dia (or width) ratio = 0.75


Depth = 0.75xdiameter
Volume of cylinder = [pi(dia)2]/4 x depth
0.44 m3=[pi(d)2]/4 0.75 d => d= 0.907
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Surface area = pi x d2/4 = 0.646 m or 0.65 m2
Depth = volume/surface area = 0.44 m3/0.65m2 = 0.68m
SOLUTION

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 Practical problem – not suitable dimensions

Let’s pick a tank with diameter = 1 m


Depth = 0.75
Volume = pi(d)2/4 * depth = pi(1)2/4 *0.75=0.59m3

Detention time = 0.59m3/0.044m3/s = 13.4 s

Detention time within suggested guidelines


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ROOT MEAN SQUARE VELOCITY GRADIENT

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 RMS velocity gradient
G
 Design parameter
 Speed of flocculation is directly proportional to the
velocity gradient
 Simple relation for G
equate with the velocity gradient with power
dissipated per unit volume (P/V)

P
G
Global RMS velocity gradient
(energy input rate, s-1) Power of mixing input to vessel, J/s
V
Dynamic viscosity of water, N.s/m2 Volume of mixing vessel, m3
(Pa.s)
G is widely adopted standard used by engineers for assessing energy input in all mixing 27
processes
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 Recommended G values for
adsorption/destabilization reactions
 G values= 3,000 to 5,000 s -1 and
 detention times =on the order of 0.5 s.

 For sweep coagulation,


 Detention times of 1 to 10 s and
 G values in the range of 600 to 1,000 s s -1 are
recommended (Amirtharajah, 1978).

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P
EXAMPLE G
V
Using Table 6-4 select an in-
line blender for an alum
coagulant. The jar test data

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resemble that shown in Figure
6-11 . The design flow rate is
383 m3 /h, and the design
water temperature is 17oC.
viscosity of the water is 1.081 x10-3 Pa · s at 17o C

Recommended G values for adsorption/destabilization reactions


G values= 3,000 to 5,000 s -1 and
detention times =on the order of 0.5 s.
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SOLUTION
 G values in the range of 3,000 to 5,000 s-1 and detention times on
the order of 0.5 s are recommended for adsorption/destabilization
reactions

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 As a first trial, select model AZ-6,
 reaction chamber diameter of 36 cm (dimension C in Table 6-4 )
 length of 60 cm (dimension D in Table 6-4 ) and
 calculate the volume of the reaction chamber

 Check the detention time , t=V/Q

Close to recommended

 Estimate the value of G assuming that the water power is 80% of


the motor power. From Table 6-4find the motor power is 1,500 W
P = 0.8x 1500W= 1200 W viscosity of the water is 1.081
x10-3 Pa · s at 17o C

P
G 31
This meets the velocity gradient criteria.
V
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Comparison of (a) radial and (b) axial flow mixers with
respect to shape, velocity profiles, and circulation patterns. (Adapted 32
from Oldshue and Trussell, 1991.)
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IMPELLER

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 The power imparted to the liquid in a baffled
tank by an impeller for fully turbulent flow
(Rushton,1952)

P power, W
N p impeller constant (also called power
number)
n rotational speed, revolutions/s
D i impeller diameter, m
r density of liquid, kg/m 3

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V
P
G
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Source: MHW’s Water treatment: Principles and design


FLOCCULATION PROCESS

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 Production of particles by aggregation for
removal in subsequent particle separation
process
Depending on size

 Microflocculation (perikinetic flocculation)


 Random thermal motion of fluid molecules

 Macroflocuulation (orthokinetic flocculation)


 Inducing velocity gradient and mixing in the fluid

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FLOCCULATION

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Schematic illustrating the progression of the particle aggregation
process
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FLOCCULATION PRACTICE

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Vertical-shaft turbine flocculation system

Horizontal paddle wheel flocculation system

Hydraulic flocculation systems


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Source: MHW’s Water treatment: Principles and design


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DESIGN APPROACH

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 Basic Design criteria (mechanical flocculator)

 Velocity gradient G

 Hydraulic detention time, t


 Depend more on downstream process
 Direct filtration - shorter detention time (10-20 min)

 Conventional treatment – 20-30 min

 Longer time for cold climates

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Source: Water and wastewater engineering by Mackenzie


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Source: MHW’s Water treatment: Principles and design


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Source: MHW’s Water treatment: Principles and design


DESIGN OF VERTICAL TURBINE
FLOCCULATOR

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Source: MHW’s Water treatment: Principles and design


SOLUTION

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