Coagulation\Flocculation Flashcards

(50 cards)

1
Q

In drinking water treatment, why is coagulation/flocculation used before sedimentation/filtration for particles <10 µm?

A

To aggregate fine, often negatively charged particles so they can be cost-effectively removed by sedimentation/filtration

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2
Q

T/F — Most suspended particles in raw water carry a positive charge, so they naturally attract each other.

A

False - Many carry a negative charge and repel; coagulants reduce this stability.

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3
Q

Coagulation is the process of ______ colloidal particles to permit particle growth; flocculation is the ______ of these destabilized particles.

A

destabilizing; agglomeration.

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4
Q

Which step directly produces settleable “flocs”?
A) Coagulation
B) Flocculation
C) Disinfection
D) Aeration

A

B) Flocculation

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5
Q

What two opposing forces govern whether colloids stick together?

A

Electrostatic repulsion vs van der Waals attraction.

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6
Q

T/F — Coagulation/flocculation must overcome repulsion so attractive forces or chemical reactions can hold particles together.

A

True

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7
Q

When does van Der Waals cause attraction?

A

At very close distances

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8
Q

What is the “energy barrier” in colloid stability diagrams?

A

The net energy hump from electrostatic repulsion that prevents particles from approaching closely enough for van der Waals attraction to dominate.

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9
Q

What enables particles to aggregate?

A

Reducing the energy barrier

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10
Q

Name the four basic coagulation destabilization mechanisms.

A

Diffuse layer compression, charge neutralization, sweep flocculation, inter-particle bridging.

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11
Q

Which mechanism relies on polymers chemically linking multiple particles?
A) Diffuse layer compression
B) Charge neutralization
C) Sweep flocculation
D) Inter-particle bridging

A

D) Inter-particle bridging

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12
Q

What happens to the electrical double layer when ionic strength increases?

A

It compresses, lowering the energy barrier between particles.

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13
Q

T/F — Higher ionic strength expands the double layer and stabilizes colloids.

A

False - it compresses the double layer and promotes aggregation.

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14
Q

On an energy-vs-distance plot, high ionic strength shifts which curve?
A) Attraction up
B) Repulsion down (net barrier decreases)
C) Both up
D) No change

A

B) Repulsion down, reducing the net energy barrier.

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15
Q

Practically, why does lowering the energy barrier matter?

A

It lets particles approach closely so van der Waals forces can hold them together, enabling floc growth

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16
Q

T/F — In full-scale plants, increasing ionic strength is a common primary method to destabilize colloids.

A

False - it’s generally not practical to add enough ions.

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17
Q

If diffuse layer compression isn’t practical, what mechanisms are typically used?

A

Charge neutralization, sweep flocculation, and polymer bridging.

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18
Q

Define charge neutralization in coagulation.

A

Addition of oppositely charged ions (e.g., Al³⁺, Fe²⁺/Fe³⁺) that adsorb to negatively charged particles to reduce net surface charge to ~0

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19
Q

How do cations behave?

A

Cations adsorb to surface of (-ve) particles

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20
Q

T/F — Overdosing a cationic coagulant can restabilize particles.

A

True - particles can become net positively charged and repel again

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21
Q

What dosing target avoids restabilization?

A

Dose near the zero-charge point—just enough to neutralize particle surface charge, not exceed it.

22
Q

What is “sweep flocculation”?

A

Precipitating hydroxides/carbonates at suitable pH so particles adsorb onto the precipitate en masse (“sweep”), forming large fluffy flocs.

23
Q

Which precipitates commonly form during sweep flocculation?
A) NaCl, KCl
B) Al(OH)₃, Fe(OH)₃, CaCO₃, Mg(OH)₂
C) SiO₂, TiO₂
D) NH₄Cl, NaNO₃

A

B) Al(OH)₃, Fe(OH)₃, CaCO₃, Mg(OH)₂

24
Q

T/F — Polymer bridging relies mainly on electrostatic attraction.

A

False - it’s chemical binding of polymer strands to multiple particles.

25
When would you prefer polymer bridging over metal salts?
When using polymers as primary coagulants/coagulant aids to link particles, especially where charge neutralization alone is insufficient.
26
The two most common coagulant metals in water treatment are: A) Na and K B) Ca and Mg C) Al and Fe D) Cu and Zn
C) Al and Fe.
27
Give common commercial forms of these coagulants.
Alum (Al₂(SO₄)₃·14.3H₂O) and ferric chloride (FeCl₃·6H₂O).
28
Around what pH is alum most effective for charge neutralization?
5.5, where precipitate formation is maximized and dominant species are positively charged.
29
T/F — Sweep flocculation with alum requires low pH near 5.5 to be effective.
False - sweep floc can be effective at higher pH because it doesn’t rely solely on charge neutralization.
30
Name two practical drawbacks of ferric chloride.
Higher cost; handling issues (staining, corrosion).
31
Adding alum produces H⁺ and can lower pH; sufficient ______ buffers this effect.
alkalinity (e.g., HCO₃⁻).
32
If source water lacks alkalinity, what is commonly added? A) Chlorine B) Lime or soda ash C) CO₂ D) Ozone
B) Lime or soda ash
33
List two key purposes of a jar test.
Optimize coagulant/coagulant-aid dose and pH; determine mixing intensity and sequence/timing effects.
34
T/F — Jar testing can evaluate the effect of lag time between rapid mix and flocculation.
True
35
The visual difference in turbidity across jars mainly helps assess: A) Disinfection efficiency B) Coagulant dosage effectiveness C) Pipe roughness D) Chlorine demand
B) Coagulant dosage effectiveness
36
After a jar test, which simple metric often indicates better coagulation?
Lower turbidity in settled samples.
37
T/F — Flocculation uses intense, high-shear mixing.
False - it uses gentle/slow mixing.
38
What two competing processes set floc size during flocculation?
Aggregation (collisions) vs shear-induced breakup
39
Increasing collision frequency generally (before excessive shear) leads to: A) Smaller flocs B) Larger flocs C) No change D) Floc dissolution
B) Larger flocs (until breakup balances growth)
40
T/F — Turbidity typically keeps decreasing indefinitely as you extend flocculation time
False - beyond a point, further time gives no additional floc formation
41
What operational strategy follows from the “plateau” in floc formation vs time?
Use tapered flocculation and avoid overly long, high-G mixing once growth plateaus.
42
What is G in flocculation design?
The mean velocity gradient (s⁻¹), reflecting mixing intensity/shear
43
Why use tapered flocculation (decreasing G in series)? A) To increase shear on big flocs B) To reduce shear on growing flocs and continue net growth C) To neutralize charge D) To disinfect
B) To reduce shear on growing flocs and continue net growth
44
Typical flocculation G range is __ to __ s⁻¹.
20 to 70 s⁻¹
45
How to calculate G.
mean vel. gradient = vel./dist
46
Give the relation between G, power P, viscosity μ, and volume V.
G = (P/(μV))^(1/2)
47
Increasing which parameter decreases G, all else constant? A) P B) μ C) V D) A and B only
C) V (larger volume lowers G for given P, μ)
48
What is the dimensionless design parameter combining intensity and time?
G·t (typical 10⁴ to 10⁵)
49
By roughly what factor should G vary from influent to effluent in tapered flocculation?
By about a factor of 2 (decreasing).
50
Why are variable-speed drives useful in flocculation basins? A) For aesthetics B) To optimize mixing under changing raw water conditions C) To boost chlorine residual D) To increase pH
B) To optimize mixing under changing raw water conditions