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PVP-stabilized mono- and bimetallic Ru nanoparticles for selective ring opening

机译:PVP稳定的单金属和双金属RU纳米颗粒,用于选择性环开口

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Selective ring opening of naphthenic molecules in oil upgrading should result in no loss in molecular weight. Benzocyclopentane (indan) ring opening was studied under hydrogen atmospheric pressure at 609 K over poly-(vinylpyrrolidone)-stabilized Ru, Ir and Pd monometallic and Ru-lr and Ru-Pd bimetallic nanocatalysts prepared by simultaneous reductions. The particle size (mostly within 2 nm) and their monodispersity were confirmed by transmission electron microscopy, while X-ray photoelectron spectroscopy indicated the bimetallics' alloy structure. Pd catalysts displayed the lowest activity in the ring opening; Ru showed the highest formation of undesired o-xylene and lights. Monometallic Ir displayed the highest activity and selectivity toward 2-ethyltoluene and n-propylbenzene. In bimetallic structures, higher Ir content led to improved catalytic performance. Next to the monometallic Ir catalyst, the newly developed Ru1lr4/γ-Al2O3 catalyst (with 1 :4 molar ratio of Ru to Ir) displayed superior single cleavage selectivity as well as lower cracking activity compared to industrial Pt-lr catalysts at a comparable indan conversion. The study can pave the way in the development of Pt-free Ru-containing catalysts with narrow size distributions for selective ring opening, especially taking into consideration a possibility of their higher S-resistance as compared to the Pt catalysts.
机译:在油升级中开放型开环的选择性环开口应不会导致分子量损失。通过同时减少,通过同时减少,在聚 - (乙烯基吡咯烷酮)的氢气压力下,在609 K(乙烯基吡咯烷酮)的氢气压力下,在609 K(乙烯基吡咯烷酮)的氢气压力下研究了苯佐糖环烷(INDAN)环。通过透射电子显微镜证实了粒径(主要是在2 nm之内)及其单分散性,而X射线光电子光谱法表示双金属的合金结构。 PD催化剂在环开口中表现出最低的活性。 RU显示出不希望的O-二甲苯和灯的最高形成。单金属IR表现出对2-乙基甲苯和N-丙烯苯的最高活性和选择性。在双金属结构中,较高的IR含量会改善催化性能。在单一金属IR催化剂旁边,新开发的RU1LR4/γ-Al2O3催化剂(RU与IR的1:4摩尔比)显示出优异的单裂解选择性以及与可比较的IndAN的工业PT-LR催化剂相比,较低的开裂活性转换。这项研究可以为具有较窄的尺寸分布的含无PT RU的催化剂的发展铺平道路,以选择性环开口,尤其是考虑到与PT催化剂相比,其可能具有更高的S耐性。

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