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Microcalorimetric and IR spectroscopic studies of CO adsorption on molybdenum nitride catalysts

机译:氮化钼催化剂上CO吸附的量热法和红外光谱研究

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The adsorption of CO on both nitrided and reduced passivated Mo2N catalysts in either alumina supported or unsupported forms was studied by adsorption microcalorimetry and infrared (IR) spectroscopy. The CO is adsorbed on nitrided Mo2N catalysts on three different surface sites: 4-fold vacancies, Modelta+ ( 0 < δ < 2) and N sites, with differential heats of CO adsorption decreasing in the same order. The presence of the alumina-support affects the energetic distribution of the adsorption sites on the nitrided Mo2N, i.e. weakens the CO adsorption strength on the different sites and changes the fraction of sites adsorbing CO in a specific form, revealing that the alumina supported Mo2N phase shows lower electron density than pure Mo2N. On reduced passivated Mo2N catalysts the CO was found to adsorb mainly on Mo4+ sites, although some slightly different surface Modelta+ d (0 < δ < 2) sites are also detected. The nature, density and distribution of surface sites of reduced passivated Mo2N/gAl(2)O(3) were similar to those on reduced MoO3/gamma-Al2O3. [References: 25]
机译:通过吸附量热法和红外光谱研究了在氧化铝负载或未负载的氮化和还原钝化的Mo2N催化剂上CO的吸附。 CO吸附在氮化的Mo2N催化剂上的三个不同的表面位置:4倍的空位,Modelta +(0 <δ<2)和N位,CO的吸附热差以相同的顺序降低。氧化铝载体的存在会影响氮化的Mo2N上吸附位的能量分布,即削弱不同位置上的CO吸附强度并改变特定形式的吸附CO的位点比例,表明氧化铝负载的Mo2N相显示出比纯Mo2N低的电子密度。在还原的钝化Mo2N催化剂上,虽然还检测到一些表面有些不同的Modelta + d(0 <δ<2)位点,但发现CO主要吸附在Mo4 +位点上。还原钝化的Mo2N / gAl(2)O(3)的性质,密度和表面位置分布与还原的MoO3 /γ-Al2O3相似。 [参考:25]

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