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Ionic Liquid Immobilized Nickel(0) Nanoparticles as Stable and Highly Efficient Catalysts for Selective Hydrogenation in the Aqueous Phase

机译:离子液体固定化镍(0)纳米粒子作为稳定且高效的水相中选择性加氢催化剂

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Nickel nanoparticles (NPs) well-dispersed in the aqueous phase were conveniently prepared by reducing nickel(II) salt with hydrazine in the presence of the functionalized ionic liquid 1-(3-aminopropyl)-2,3-dimethylimidazolium bromide. UV/Vis spectroscopy, elemental analysis, thermogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS) show the presence of a weak interaction of the functionalized ionic liquid with Ni~(II) and Ni~(0) complexes. The face-centered cubic structure of the Ni~(0) NPs was confirmed by X-ray diffraction (XRD) characterization. Transmission electron microscopy (TEM) images reveal that smaller Ni~(0) particles of approximately 6-7 nm average diameter assemble to give larger, blackberry-shaped particles with an average diameter of around 35 nm. The Ni NPs were employed as highly efficient catalysts for the selective hydrogenation of C velence C double bonds in the aqueous phase under mild reaction conditions (40-90 deg C at 1.0-3.0 MPa), and the Ni~(0) nanocatalysts in the aqueous phase are stable enough to be reused at least seven times without significant loss of catalytic activity during subsequent reuse cycles.
机译:通过在官能化离子液体1-(3-氨基丙基)-2,3-二甲基咪唑鎓溴化物的存在下用肼还原镍(II)盐可方便地制备在水相中充分分散的镍纳米粒子(NPs)。紫外/可见光谱,元素分析,热重分析(TGA)和X射线光电子能谱(XPS)表明官能化的离子液体与Ni〜(II)和Ni〜(0)配合物之间存在弱相互作用。通过X射线衍射(XRD)表征证实了Ni〜(0)NPs的面心立方结构。透射电子显微镜(TEM)图像显示,平均直径约为6-7 nm的较小Ni〜(0)颗粒会聚集,形成平均直径约为35 nm的较大的黑莓形颗粒。 Ni NPs被用作高效催化剂,用于在温和的反应条件下(1.0-3.0 MPa下40-90摄氏度)在水相中选择性氢化C velence C双键,而Ni〜(0)纳米催化剂被用作高效催化剂。水相足够稳定,可以重复使用至少七次,而在随后的重复使用周期中不会显着降低催化活性。

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