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Conventional Surface Water Treatment for Drinking Water

Conventional Surface Water Treatment for Drinking Water. Coagulation / Flocculation. Physical and chemical processes to induce collisions and growth of particles, and to remove some soluble contaminants

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Conventional Surface Water Treatment for Drinking Water

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  1. Conventional Surface Water Treatment for Drinking Water

  2. Coagulation / Flocculation • Physical and chemical processes to induce collisions and growth of particles, and to remove some soluble contaminants • Coagulation: Formally, means making particles “sticky” (rapid mix step); colloquially, also refers to forming new particles that collect dissolved contaminants Flocculation: Causing collisions among sticky particles (slow mix step), to form fewer, larger ones • Suspensions in which most particles remain in the water are “stable,” so coagulation is sometimes referred to as “particle destabilization.”

  3. Particle Removal Regulations • EPA’s surface water treatment rules require systems using surface water or groundwater under the direct influence of surface water to (1) disinfect their water, and (2) filter their water or meet criteria for avoiding filtration so that the following contaminants are controlled at the following levels: • Cryptosporidium 99 percent removal. • Giardia lamblia: 99.9 percent removal/inactivation • Viruses: 99.99 percent removal/inactivation • Turbidity: Turbidity can never exceed 1 nephelometric turbidity unit (NTU), and must not exceed 0.3 NTU in 95 percent of daily samples in any month

  4. Some H+ ions, especially from COOH groups, “jump” to water molecules, leaving the remaining molecule with a negative charge O H O O C C O O O O H H O O C O H C O O H O O O O H O O C O O O O O H O O H Some Properties of Natural Organic Matter (NOM) One Person’s Idea of an NOM Molecule - - - +H3O+ +H2O -

  5. O H O O C C O O O O H H O O C O H C O O H O O O O H O O C O O O O O H O O H Some Properties of Natural Organic Matter (NOM) NOM molecules have a strong affinity for surfaces of natural particles and for polyvalent dissolved ions (Fe3+, Al3+). In most natural waters, the ratio of NOM to particles is large, so particles are substantially coated, and most NOM is dissolved If a little Fe3+ or Al3+ is added, it mostly combines with NOM (both dissolved and on solids). If a lot of Fe3+ or Al3+ is added, it mostly precipitates. - - Fe3+ Fe3+ - -

  6. Coagulation

  7. Coagulation Physics:Particle Stability is Caused Primarily by Electrical Charges on Particle Surfaces • Evidence: Electrophoretic mobility • Origins • Adsorption of dissolved molecules (NOM) • Imperfections/ impurities in solid • Sign and Magnitude • Always negative in natural waters, due to adsorption of NOM molecules that have released H+ • Surface electrical potential typically a few tens of mV • Electrical force between colloidal particles at separations up to a few mm comparable to gravitational force

  8. Particles attract opposite-charged ions, and repel like-charged ions, generating a diffuse layer in which the particle’s charge is neutralized

  9. When the surface potentials are high, the repulsion is strong even at large separations, and particles do not collide When the surface potentials are low, the particles can approach close enough to collide and stick

  10. Like-charged particles experience an electrical repulsion that decreases with distance, and a “Van der Waals” attraction that is even more sensitive to the separation distance.The electrical repulsion can usually be altered; the Van der Waals attraction cannot.

  11. The net effect of the repulsion and attraction is typically a repulsion at large or moderate separation and an attraction at small separation.If approaching particles have enough momentum to bring them to the location of zero net interaction energy, they will spontaneously collide

  12. Reducing the surface potential reduces the magnitude of the energy barrier, and in some cases can eliminate it entirely.

  13. The “zeta potential” is an indicator of the surface electrical potential. When it is zero, the particles have the greatest tendency to collide, and they are therefore easiest to remove.

  14. Coagulation Chemistry • Mechanism 1. Alum [Al2(SO4)3nH2O] and ferric chloride (FeCl3) dissociate to release highly charged ions. • Al2(SO4)3nH2O 2Al3+ + 3SO42-+ nH2O • FeCl3 Fe3+ + 3Cl- • These ions tend to bind either directly to particle surfaces (adsorb) or to NOM on those surfaces. Either way, they reduce the negative charge associated with the particles and reduce repulsion. Ideally, the charge is brought to near zero, and repulsion is almost eliminated.

  15. Coagulation Chemistry • Under some conditions, adsorption of Al and Fe species can overwhelm the charge contributed by adsorbed NOM and cause “restabilization” of the particles. • Mechanism 2. At higher concentrations and pH, solids can precipitate and enmesh the colloids in a “sweep floc”. • Al3+ + 3OH- Al(OH)3(s) • Fe3+ + 3OH- Fe(OH)3(s)

  16. Coagulation Chemistry Mechanism 3. Polymers can induce coagulation by “bridging” between particles

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