Struvite crystallisation is a fast and reliable phosphorus removal and recovery process for concentrated waste streams - such as hydrolysed human urine. In order to optimise P-elimination efficiency, it is beneficial to obtain larger particle sizes: they are easier to separate and less prone to wash-out than smaller particles. This paper presents the results of a study on the effect of process parameters on particle size in a single step struvite precipitation. Crystals formed in batch experiments with real hydrolysed urine were shown to have an average size of >90 μm at pH 9 and 20 °C. This is reduced to 45 μm when changing stirrer type. Particle size increases with lower supersaturation. The results showed that under otherwise constant conditions, particle size decreases with lower temperature and has a minimum between pH 9 and 10. Deviating trends are observed at pH <8. Struvite formation in a CSTR (continuously stirred tank reactor) process was shown to be a reliable stable process that does not require any pH control. A method based on conductivity measurement is presented to estimate ionic strength, which is needed for equilibrium calculations.@en

Separating urine from wastewater at the source reduces the costs of extensive wastewater treatment. Recovering the nutrients from urine and reusing them for agricultural purposes adds resource saving to the benefits. Phosphate can be recovered in the form of struvite (magnesium ammonium phosphate). In this paper, the behaviour of pharmaceuticals and heavy metals during the precipitation of struvite in urine is studied. When precipitating struvite in urine spiked with hormones and non-ionic, acidic and basic pharmaceuticals, the hormones and pharmaceuticals remain in solution for more than 98%. For heavy metals, initial experiments were performed to study metal solubility in urine. Solubility is shown to be affected by the chemical conditions of stored and therefore hydrolysed urine. Thermodynamic modelling reveals low or very low equilibrium solute concentrations for cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), nickel (Ni) and lead (Pb). Experiments confirmed Cd, Cu and Pb carbonate and hydroxide precipitation upon metal addition in stored urine with a reaction half-life of ca. 7 days. For all metals considered, the maximum specific metal concentrations per gram phosphate or nitrogen showed to be typically several orders of magnitudes lower in urine than in commercially available fertilizers and manure. Heavy metals in struvite precipitated from normal stored urine could not be detected. Phosphate recovery from urine over struvite precipitation is shown to render a product free from most organic micropollutants and containing only a fraction of the already low amounts of heavy metals in urine.@en

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.@en