Energy & Fuels · 2017 · 24 citations · 29 references
Natural SciencesChemical EngineeringEnvironmental EngineeringCatalysisInorganic ChemistryReaction EngineeringCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsMetal CatalysisSupported CatalystsCalcinationManganese CatalysisManganese Oxide CatalystsMetal Oxide CatalystsOxidationOxygen Concentration EffectsRemoval EfficiencyTransition Metal Oxides
With the aim of improving the arsine (AsH 3 ) removal efficiency, 5A molecular sieves were modified by the transition metal oxides and used as catalysts. MnO x catalysts supported on 5A molecular sieves (Mn-5A) were prepared by an impregnation method and subsequently tested toward the catalytic oxidation of AsH 3 under micro-oxygen conditions at 150 °C. The effects of the metal oxide types that supported, the impregnate concentration of manganese nitrate, the calcination temperature, the oxygen content, and the fixed bed reaction temperature on the AsH 3 removal efficiency were studied. The optimum catalyst was prepared by a solution impregnation method with a 0.5 mol·L –1 Mn 2+ aqueous solution and subsequently calcined at 500 °C. This catalyst showed the highest activity toward the oxidation of AsH 3 among the samples prepared herein (100% conversion) over a good low-temperature operation window (120–160 °C) and under low oxygen concentration (0–2.0%) conditions. The majority presence of Mn 4+ active species is believed to be one predominant factor accounting for the excellent AsH 3 removal efficiency of this catalyst. The dominant active Mn 4+ species of Mn-5A is found to be a mixture of MnO 2, Mn 3 O 4, and Mn 2 O 3 . BET area analysis coupled with EDS measurement show that after oxidizing AsH 3 with O 2, the resulting As 2 O 5 seems to block the surface of Mn-5A leading to a decrease of the activity. XPS data indicates that the oxidation state of MnO x species on Mn-5A was not affected after reaction. So the main deterioration mechanism of Mn-5A on AsH 3 removal under our reaction condition is mainly due to physical blocking effect. According to the characterizations results, the Mn-5A catalyst possessed a higher number of active sites than the rest of samples and formed active intermediates during reaction, both factors leading the highly efficient removal of AsH 3 under low-temperature micro-oxygen conditions.
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