The competition between pathways that lead to adsorbed CO and CO, during the electrochemical oxidation of 1.0 M methanol in 0.1 M HClO4 on two bulk Pt-Ru alloys (10 at.% Ru (X-Ru approximate to 0.1) and 90 at.% Ru (X-Ru approximate to 0.9)) was investigated for temperatures in the range of 25-80 degreesC. On the high Ru content alloy studied (X-Ru approximate to 0.9), the dissociative chemisorption of methanol was inhibited below 70 degreesC; the faradaic current for methanol oxidation was low, and only small quantities of adsorbed CO and CO, were detected with infrared spectroscopy between 0.2-0.8 V (vs. RHE). At 80 degreesC, strong infrared bands from CO2 and adsorbed, atop coordinated CO were observed over the potential ranges of 0.4-0.8 V and 0.2-0.8 V, respectively. The infrared measurements are consistent with the observation that bulk, high Ru content alloy electrodes appear passivated toward methanol oxidation below 70 degreesC. On the low Ru content ahoy studied (X-Ru approximate to 0.1), the methanol surface chemistry was similar to that of pure, polycrystalline Pt, but the electrode was more poison resistant than Pt. For both alloys, the persistence of strong adsorbed CO bands and rapid CO2 production between 0.4-0.8 V suggests CO functions as a reactive species with high steady-state coverages at these potentials.