Key Laboratory for Advanced Materials, Research Institute of Industrial Catalysis, East China University of Science and Technology, Shanghai, 200237 China.
Chem Asian J. 2010 May 3;5(5):1178-84. doi: 10.1002/asia.200900628.
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=C double bonds in the aqueous phase under mild reaction conditions (40-90 degrees 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.
镍纳米粒子(NPs)在水相中很好地分散,通过在功能化离子液体 1-(3-氨基丙基)-2,3-二甲基咪唑溴化物的存在下用肼还原镍(II)盐来方便地制备。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)表明功能化离子液体与 Ni(II)和 Ni(0)配合物之间存在弱相互作用。Ni(0)NPs 的面心立方结构通过 X 射线衍射(XRD)表征得到证实。透射电子显微镜(TEM)图像显示,较小的 Ni(0)颗粒(平均直径约为 6-7nm)聚集在一起,形成较大的、黑莓状的颗粒,平均直径约为 35nm。镍纳米粒子作为高效催化剂,在温和的反应条件下(40-90 摄氏度,1.0-3.0MPa)用于 C=C 双键在水相中的选择性加氢,并且镍(0)纳米催化剂在水相中足够稳定,可至少重复使用七次,在随后的重复使用循环中没有明显的催化活性损失。