The oxidation of HCl to Cl-2 (Deacon process) was studied over RuO2-based catalysts in bulk and supported forms RuO2 (7 wt %) was incorporated onto different TiO2 carriers (rutile anatase and P25) by deposition-precipitation of Ru(OH)(2) followed by calcination RuO2/TiO2-rutile exhibits the highest activity at ambient pressure in a continuous flow fixed-bed reactor Insights into the mechanism of this experimentally demanding reaction on RuO2 and the influence of the TiO2-rutile carrier were gained by studies in the Temporal Analysis of Products (TAP) reactor at 623 K HCl multipulsing in the absence of O-2 leads to chlorination of the catalysts with no detectable gas-phase Cl-2 production The chlorine uptake of RuO2 amounts to 0 16 mmol Cl g(cat)(-1) which enables to estimate that ca 75% of the total surface Ru atoms (coord'natively unsaturated and bridge sites) are chlorinated forming a RuO2-x Cl-x oxychloride RuO2 is also chlorinated by Cl-2 but to a lesser extent compared to HCl The chlorine uptake of fresh RuO2/TiO2-rutile per gram of sample was four times higher than that of fresh RuO2 namely due to chlorination of the high surface area carrier Upon equilibration at ambient pressure under Deacon conditions the TAP-derived chlorine uptake in the supported catalyst experienced a 6-fold decrease with respect to the fresh sample due to permanent chlorination Pulsing of a mixture of O-2 and HCl over the catalysts revealed that both gas-phase Cl-2 evolution and H2O desorption are impeded processes Pump-probe experiments of O-2 and HCl evidenced the tight dependence of the net Cl-2 production on both the oxygen and chlorine coverage In addition a limited contribution of lattice surface species could be detected by the production of small amounts of Cl-2 at very low coverages The equilibration procedure (ambient or TAP conditions) influences the reaction mechanism and the net Cl-2 production giving account of the reaction complexity due to the highly dynamic state of the catalyst surface The Deacon process on RuO2-xClx-based catalysts can be mostly described by a Langmuir-Hmshelwood scheme with a minor 2D Mars-van Krevelen contribution (C) 2010 Elsevier Inc All rights reserved