•Nitrate photoreduction using ilmenite and oxalic acid is feasible in saline water.•Oxalic acid scavenging in presence of Ca2+ hinders the NO3− reduction.•Acidification with HCl limits CaC2O4 formation and precipitation.•Ea = 9.8 kJ/mol, which is lower than that reported for catalytic hydrogenation. As climate change progresses, there is an increasing interest on the use of non-conventional water sources such as brackish or saline waters. Nowadays, the main threat in Europe detected in these waterbodies is nitrate contamination. Within the multiple available methods studied for nitrate reduction, photocatalysis presents promising results, but this technology has not yet been tested in saline water. This work tackles the elimination of nitrate (NO3− =50 mg/L) in brackish and saline water (sea salt = 5–33 g/L) using ilmenite as photocatalyst and oxalic acid as an environmental-friendly reducing agent. The main challenge when working in saline water is to overcome oxalic acid scavenging by Ca2+ present in the water matrix. This can be solved either working at over stoichiometric concentrations of oxalic acid (≈300% stoich. dose) or acidifying the reaction media. The addition of hydrochloric acid ensures the protonation of oxalic acid, reducing drastically its precipitation as CaC2O4. Working at C2O42− = 180 mg/L, FeTiO3 = 450 mg/L and HCl 37% = 13 mM, 73% total nitrogen (TN) elimination was reached after 420 min. Reaction temperature was also evaluated in the range of 20–80 °C, which allowed to calculate the Ea=9.8 kJ/mol. Finally, the effect of dissolved O2 on the TN reduction was assessed. Overall, photocatalytic nitrate reduction presents itself as a feasible technology regardless of the water salinity. Display omitted