Geerts Lisa, Geerts-Claes Hannelore, Skorikov Alexander, Vermeersch Julie, Vanbutsele Gina, Galvita Vladimir, Constales Denis, Chandran C Vinod, Radhakrishnan Sambhu, Seo Jin Won, Breynaert Eric, Bals Sara, Sree Sreeprasanth Pulinthanathu, Martens Johan A
KU Leuven, Center for Surface Chemistry and Catalysis, Celestijnenlaan 200F, 3001 Leuven, Belgium.
University of Antwerp, Electron Microscopy for Materials Science, Groenenborgerlaan 171, 2020 Antwerpen, Belgium.
Nanoscale. 2021 Feb 25;13(7):4221-4232. doi: 10.1039/d0nr08456e.
γ- and δ-alumina are popular catalyst support materials. Using a hydrothermal synthesis method starting from aluminum nitrate and urea in diluted solution, spherical core-shell particles with a uniform particle size of about 1 μm were synthesized. Upon calcination at 1000 °C, the particles adopted a core-shell structure with a γ-alumina core and δ-alumina shell as evidenced by 2D and 3D electron microscopy and 27Al magic angle spinning nuclear magnetic resonance spectroscopy. The spherical alumina particles were loaded with Pt nanoparticles with an average size below 1 nm using the strong electrostatic adsorption method. Electron microscopy and energy dispersive X-ray spectroscopy revealed a homogeneous platinum dispersion over the alumina surface. These platinum loaded alumina spheres were used as a model catalyst for bifunctional catalysis. Physical mixtures of Pt/alumina spheres and spherical zeolite particles are equivalent to catalysts with platinum deposited on the zeolite itself facilitating the investigation of the catalyst components individually. The spherical alumina particles are very convenient supports for obtaining a homogeneous distribution of highly dispersed platinum nanoparticles. Obtaining such a small Pt particle size is challenging on other support materials such as zeolites. The here reported and well-characterized Pt/alumina spheres can be combined with any zeolite and used as a bifunctional model catalyst. This is an interesting strategy for the examination of the acid catalytic function without the interference of the supported platinum metal on the investigated acid material.
γ-氧化铝和δ-氧化铝是常用的催化剂载体材料。采用水热合成法,以硝酸铝和尿素为原料,在稀释溶液中合成了粒径均匀约为1μm的球形核壳颗粒。在1000℃煅烧后,通过二维和三维电子显微镜以及27Al魔角旋转核磁共振光谱证实,颗粒呈现出以γ-氧化铝为核、δ-氧化铝为壳的核壳结构。采用强静电吸附法将平均尺寸低于1nm的铂纳米颗粒负载到球形氧化铝颗粒上。电子显微镜和能量色散X射线光谱显示铂在氧化铝表面均匀分散。这些负载铂的氧化铝球用作双功能催化的模型催化剂。铂/氧化铝球与球形沸石颗粒的物理混合物等同于铂沉积在沸石本身的催化剂,便于分别研究催化剂组分。球形氧化铝颗粒是获得高度分散的铂纳米颗粒均匀分布的非常方便的载体。在其他载体材料如沸石上获得如此小的铂粒径具有挑战性。本文报道并表征良好的铂/氧化铝球可与任何沸石结合,用作双功能模型催化剂。这是一种在不受到负载的铂金属对所研究的酸性材料干扰的情况下研究酸催化功能的有趣策略。