Abstract

Synthetic and commercial drinking waters with different composition were studied as reaction media to study the influence of salts in NO3- catalytic reduction using a Pd-Cu catalyst supported on a carbon black. As a general trend, a decrease in NO3- conversion and an increase in NH4+ selectivity were observed for high HCO3- concentration media in mixed salts waters. Literature has commonly ascribed HCO3- effect to competitive adsorption with NO3-. However, in the current work, the mechanism for effect HCO3- is reconsidered basis on HCO2- formation during NO3- catalytic reduction, here reported for the first time. HCO2- formation indicates that hydrogenation of HCO3- occurs in addition to adsorption. Likewise, decomposition of HCO2- on the catalysts surface releases hydrogen leading to increased spill-over and relevant hydrogenation of NO3- to NH4+. The presence of SO42-, Cl- reduces NH4+ selectivity due to competition for active sites and lower HCO2- generation. Furthermore, it was observed that the use of CO2 as buffer also contribute to the hydrogenation of NO3- to NH4+ through HCO2- route.

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