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Citral hydrogenation over novel niobia and titania supported Au, Ir-Au and Ir catalysts

机译:新型铌和二氧化钛上的柠檬醛加氢负载Au,Ir-Au和Ir催化剂

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The hydrogenation of citral over Au, Ir-Au and Ir catalysts prepared from colloids using as supports TiO2 and Nb2O5 has been studied. The samples were characterized by N2 adsorption at 77 K, transmission electron microscopy and temperature programmed reduction. The reactivity and selectivity differences between the prepared catalysts have been explained considering that the deposition of colloids prepared in basic media at high pressures of hydrogen occurs preferentially as iridium oxide or gold complexes, similarly to classical methods of preparation (wetness impregnation and deposition-precipitation). In this sense, the catalytic behavior of supported colloids is similar to these methods without the reduction process. This was corroborated when the solids were reduced at 773 K, which leads to catalysts active and highly selective to the hydrogenation of the carbonyl bond.
机译:研究了由TiO2和Nb2O5为载体的胶体制备的Au,Ir-Au和Ir催化剂上柠檬醛的加氢反应。样品的特征在于在77 K上的N2吸附,透射电子显微镜和程序升温还原。考虑到制备催化剂之间的反应性和选择性差异,考虑到在碱性介质中在高压氢气下制备的胶体的沉积优先以氧化铱或金络合物的形式发生,这与经典的制备方法(润湿浸渍和沉积沉淀)相似。从这个意义上讲,负载的胶体的催化行为类似于这些方法,没有还原过程。当固体在773 K下还原时,这得到了证实,这导致催化剂具有活性并且对羰基键的氢化具有高度选择性。

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