Weight Ratio Of Alum Required To Phosphorus Removed

22:1 for 95% removal; 16:1 for 85% removal

ALUM REQUIREMENT TO REMOVE 85% OF A 10 MG/L PHOSPHORUS CONTENT

160 mg/l or 1335 lb per million gal

Wastewater treatment facilities can effectively use metal salts such as alum, ferrous sulfate, and ferric chloride to precipitate phosphorus in wastewater in conventional activated-sludge processes. Alum and ferric chloride are typically added into mixed liquor at the end of the aeration basin. Ferrous sulfate is added toward the front, allowing oxidation of ferrous into ferric ions. The molar ratio of metal ions to phosphorus depends on the required effluent phosphorus concentration and wastewater pH. Typically, the lower the effluent phosphorus concentration, the higher the molar ratio.

Environmental engineers often incorporate chemical precipitation into the design of EBPR processes as a standby or emergency measure to supplement biological processes in overcoming upset situations or augment phosphorus removal beyond the capacity of the biological process in meeting low effluent limits.

Many ionic forms effectively precipitate phosphorus from solution. The most notable are aluminium, calcium, and iron due to their low cost and general availability. Table 7.38.5 shows that all three of these ionic materials

(multivalent metallic cations) form insoluble precipitates with phosphorus. In general, the degree of phosphorus removal by chemical precipitation is a function of the following factors:

• initial phosphorus concentration

• precipitating cation concentration

• concentration of other anions competing with phosphorus for precipitating cations

• wastewater pH

The tendency of aluminum and iron to hydrolyze in aqueous solution creates competition between the hydroxide and phosphate ions for the precipitating metal ions. Thus, the efficiency of phosphorus removal depends on the relative concentrations of these two anions in solution and is consequently pH dependent. A decrease in pH or hydroxide favors phosphate precipitation with metallic cations. When calcium is the precipitant, competition for calcium is predominantly between the phosphate and carbonate anions. As Table 7.38.5 shows, hydroxy-lapatite, Ca10(OH)2(PO4) 6, is the most stable calcium phosphate solid phase.

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