Even traces of CO in the hydrogen-rich feed gas to proton exchange membrane fuel cells (PEMFC) poison the platinum anode electrode and dramatically decrease the power output. In this work, a variety of catalytic materials consisting of noble metals supported on A zeolites were synthesised, characterised and tested under realistic conditions in the quest of a catalyst for the removal of CO via the CO preferential oxidation (CO-PROX) reaction. Pt, Pd and Ru-based catalysts, prepared by wet impregnation and characterised by XRD and HRTEM, were investigated in a fixed bed reactor, by determining CO conversion and selectivity through the outlet concentrations of CO and O
2. In contrast to supported Pd and Ru catalysts, Pt-catalysts showed complete CO-conversion and a comparatively high selectivity. The 1 % Pt-3A catalyst showed the best performance: it kept the complete CO-conversion in a wide temperature range, showing the highest selectivity for CO oxidation with minimal involvement in side reactions, such as H
2 oxidation and RWGS reaction. Experimental data proved that the RWGS outcome is directly related to the support structure. The rather high temperature (
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260°C) at which complete CO conversion is achieved by the 1 % Pt-3A catalyst enables to locate the CO-PROX unit immediately after the low temperature water-gas shift unit of the fuel processor converting hydrocarbons into hydrogen-rich gas.