Drinking water treatment Flashcards

1
Q

Process for surface water treatment

A

1) screen filter
2) coagulation-flocculation
3) sedimentation
4) filtration
5) disinfection

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2
Q

define coagulation-flocculation

A

causes dissolved and suspended particles to form larger particles.

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3
Q

process of coagulation-flocculation

A

1) add coagulent: aluminum iron
- destabilizes particles to make them sticky
2) flocs form: sticks together to cause groups of particles
3) sedimentation: allows particles to settle due to gravity from weight of particles

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4
Q

what occurs during filtation after coagulation-flocculation

A

1) filters out suspended particles/ microorganisms
2) through filter material: sand
3) overtime biofilm appears on sand: also gets rid of other pathogens

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5
Q

what does CT stand for?

A

The measure disinfectat effectiveness.

C= cocentration of disinfectant

T= time requred to inactivate certain % of microorganisms

The lower CT, the faster/easier/more effective to kill pathogen.

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6
Q

types of disinfectants

A

chlorine, cloramine, chlorine dioxide, ozone, UV light

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7
Q

results of chlorine

A

worst forming DBP.

organic material+chlorine= chlorinated organic compound= bad chemicals

causes cancer causing chemicals

oxidizing agent

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8
Q

what does DBP stand for?

A

Disinfection By Products

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9
Q

Results of chloramine

A

Chlorine+amines

not as effective killing pathogens.

need large quantities(money)

does not form as many DBPs

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10
Q

results of chlorine dioxide

A

need to generate on-site.

relatively effective.

fewer DBP.

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11
Q

Results of Ozone

A

very expensive.

must be generated on site.

no residual

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12
Q

Results of UV light

A

changes shape of DNA, cannot replicate= dead cell

no residual.

very effective.

does not penetrate very far.

algae can grow on lights/poles.

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13
Q

advantages of PCR

A

rapid results.

highly sensitive.

highly specific.

ability to detect non cultureable viruses.

ability to tailor primers for desired application.

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14
Q

limitations of PCR

A

High potential for contamination

Potential for amplification of non-target sequences

Small equivalent sample volume analyzed (0.3 - 3 L)

Quantitation?

Inability to distinguish between infective and non-infective particles

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15
Q

Immunomagnetic Separation

A

Magnet particle + antivirus antibody

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