Struvite precipitation thermodynamics in source-separated urine

Journal article (2007)

Authors

Ronteltap Ronteltap Eawag - Swiss Federal Institute of Aquatic Science and Technology, ETH Zürich
Maurer Maurer Eawag - Swiss Federal Institute of Aquatic Science and Technology, ETH Zürich
Gujer Gujer ETH Zürich, Eawag - Swiss Federal Institute of Aquatic Science and Technology
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Wastewater treatment Struvite Enthalpy Urine Activity coefficients Moderate ionic strength
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Published Date

2007-3

Language

English

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Abstract

Struvite (MgNH4PO4·6H2O) precipitation eliminates phosphate efficiently from urine, a small but highly concentrated stream in the total flux of domestic wastewater. Precipitation experiments with hydrolysed urine evaluated the solubility product of struvite. The stored and fully hydrolysed urine had an ionic strength of between 0.33 and 0.56 M and required the estimation of activity coefficients. From our data, we identified the Davies approximation with the two constants A=0.509 and B=0.3 as agreeing best with our laboratory results. The standard solubility product Ks0=f1[NH4+]f 2[Mg2+]f3[PO43-] ([ ]=concentration of the species; fx=corresponding activity coefficient) of struvite in urine was found to be 10-13.26±0.057 at 25 °C and the enthalpy of struvite formation ΔH was 22.6(±1.1) kJ mol-1. The equilibrium calculations required the following dissolved complexes: [MgCO3]aq, [MgHCO3]+, [MgPO4]-, [NH4HPO4]-, and [NaHPO4]- and to a lesser extent [MgSO4]aq and [NH4SO4]-. Organic complexes do not seem to influence the solubility product substantially. For practical purposes, a conditional solubility product Kscond=[Mgaq]·[NH4 ++NH3]·[Portho]=10-7.57 M3 was derived to calculate struvite solubility in urine at 25 °C, pH=9.0 and ionic strength I=0.4 M directly from measured concentrations.