Pure anatase and rutile TiO2 samples were synthesized by thermal treatment of reverse microemulsions and applied as supports for preparing Ru-promoted Co catalysts (0.5 wt% Ru, 10 wt% Co). The catalysts were characterized by ICP-OES, XRD, Raman spectroscopy, N-2 physisorption, H-2-TPR, electron microscopy (FESEM, HAADF-STEM), H-2 chemisorption, XPS, and in situ IR-CO after H-2 reduction and reaction with syngas, and their catalytic performance for Fischer-Tropsch synthesis (FTS) studied at industrial conditions (220 degrees C, 2.0 MPa, H-2/CO = 2). The two catalysts exhibited comparable mean Co particle sizes (5-6 nm) as well as high and alike degrees of cobalt reduction (ca. 90%). The SMSI decoration effect arising during H-2 reduction was much more pronounced for the anatase-supported catalyst resulting in lower cobalt-time yield (CTY) compared to that supported on TiO2-rutile. In situ IR-CO under syngas conversion conditions showed equivalent cobalt surface reconstruction and nature of the surface Co-0 sites for both catalysts in their working state, and revealed a partial reversibility of the SMSI effect during FTS by which a significant fraction of the decorated Co-0 centers in the anatase-based catalyst was uncovered and became available for reaction. The implication of this effect on TOFs is discussed. The C5+ selectivity was higher for the rut(i)le-based catalyst, although a clear impact of the SMSI effect on selectivities was not inferred from our results. (C) 2016 Elsevier B.V. All rights reserved.