With the goal of nutrient recovery, full nitrification of human urine is investigated for its stabilization in simple, decentralized reactors. In a first part of this work, undiluted urine was completely nitrified in a laboratory-scale moving-bed biofilm reactor (MBBR), with automated dosage of a KHCO₃ solution keeping the pH at 7.0-7.1. The effluent contained up to 2706 mg-N/L of nitrate; on average > 99% of the total nitrogen. Maintaining low concentrations of ammonium and nitrite (generally below 1 ‰ and 4.7‰ respectively of the influent total ammonia) proved to reduce the risks of dramatic process instabilities due to inhibition with nitrous acid and free ammonia. Although full nitrification by adding a base presents several advantages, for decentralized applications, it is recommended to add alkalinity in a way requiring less expensive and complex material than by dosing a basic solution.
Hoping that calcite (CaCO₃) could be a simple alternative to buffer nitrification, in a second part we studied the dissolution of chalk powder in synthetic urine solutions, both in the presence and absence of phosphate. Experiments and simulations with PHREEQC verified the hypothesis that phosphate may precipitate on the surface of calcite, and thus slow down dissolution. In the absence of phosphate, calcite dissolved rapidly until saturation of the solution. By contrast, with the high phosphate concentrations in stored urine (around 200-250 mg_P/L), calcite dissolution was inhibited by the rapid formation of  amorphous calcium-phosphate (ACP; eventually converting into hydroxyapatite, HAP) directly on the particle’s surface, as was revealed by XRD and REM analysis. To prevent calcite passivation, precipitation of struvite (MgNH₄PO₄•6H₂O) is suggested before the full nitrification reactor.  In real urine, the effect of biofilm growth directly on calcite may be of advantage to compensate possibly too slow calcite dissolution, and should inform further work.