Zirconium (Zr) alloys are widely used in nuclear power plants as fuel cladding and are susceptible to hydrogen (H) degradation. For long operational service, Zr-based components can suffer a mechanism known as Delayed Hydride Cracking (DHC) associated to an increase of the crack propagation velocity by the re-orientation and precipitation of Zr hydride. In this process, the H mobility has a great influence. In the present work, the isothermal diffusion of H in Zr-2.5%Nb specimens obtained from a CANDU pressure tube were studied at consecutive temperatures of 300°C, 350°C, 375°C and 400°C. H content and mobility were quantified by in-situ neutron imaging experiments performed on ANTARES, the cold neutron imaging facility of FRM II. The time evolution of the H concentration across the specimen allowed the determination of diffusion coefficients, and an assessment of the limitations of existing models commonly used to describe H diffusion.