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• Large nanotubular TiO 2 photocatalytic membranes prepared by anodization. • Galvanostatic anodization improves the process over potentiostatic conditions. • Confirmed activity for photocatalytic methanol oxidation and E.coli inactivation. • Hybrid process proved synergism between filtration and photocatalysis. • Nanotubular TiO 2 do not significantly improve activity of nanoparticulate TiO 2. Hybrid photocatalysis/membrane processes constitute promising alternatives for water and wastewater treatment because they combine the efficiencies of filtration membranes technology and the oxidative effect of the photocatalytic process, increasing the lifetime of the membranes. The main challenge of these systems is the incorporation of the titanium dioxide (TiO 2) catalyst without altering the filtration properties of the membrane and the photocatalytic activity of the catalyst. One way to achieve this goal is generating the TiO 2 layer by direct anodization of titanium supports under controlled conditions to form titanium dioxide nanotubes (TiO 2 -NTs). This work reports the development of novel photocatalytic titanium membranes based on the formation of TiO 2 -NT arrays by anodization under both potentiostatic and galvanostatic conditions, and the scaling-up of the most promising systems to operational membrane photoreactors. The results demonstrated that the galvanostatic method displays more controlled tuneability to obtain NTs formation than the potentiostatic method on porous surfaces. However, despite the formation of TiO 2 -NTs structures, the observed photocatalytic activity is lower than that exhibited by TiO 2 nanoparticles deposited directly on the membrane, although in this case the transmembrane pressure is significantly higher, and therefore the operational pumping costs are greater. Synergistic effects of photocatalysis and microfiltration are clearly demonstrated in the application of the hybrid system to the removal of bacteria for water disinfection processes, showing a significant improvement in the inactivation of E. coli bacteria in water with respect to the bare membrane. [ABSTRACT FROM AUTHOR]