Kim Da Jeong, Li Yan, Kim Yun Jin, Hur Nam Hwi, Seo Won Seok
Department of Chemistry, Sogang University, Seoul, 121-742, Korea.
Chem Asian J. 2015 Dec;10(12):2755-61. doi: 10.1002/asia.201500773. Epub 2015 Sep 9.
We have developed a highly stable and magnetically recyclable nanocatalyst system for alkene hydrogenation. The materials are composed of mesoporous silica spheres (MSS) embedded with FeCo/graphitic shell (FeCo/GC) magnetic nanoparticles and Pt nanocatalysts (Pt-FeCo/GC@MSS). The Pt-FeCo/GC@MSS have superparamagnetism at room temperature and show type IV isotherm typical for mesoporous silica, thereby ensuring a large enough inner space (surface area of 235.3 m(2) g(-1), pore volume of 0.165 cm(3) g(-1), and pore diameter of 2.8 nm) to undergo catalytic reactions. We have shown that the Pt-FeCo/GC@MSS system readily converts cyclohexene into cyclohexane, which is the only product isolated and Pt-FeCo/GC@MSS can be seperated very quickly by an external magnetic field after the catalytic reaction is finished. We have demonstrated that the recycled Pt-FeCo/GC@MSS can be reused further for the same hydrogenation reaction at least four times without loss in the initial catalytic activity.
我们开发了一种用于烯烃氢化的高度稳定且可磁回收的纳米催化剂体系。该材料由嵌入FeCo/石墨壳(FeCo/GC)磁性纳米颗粒和Pt纳米催化剂(Pt-FeCo/GC@MSS)的介孔二氧化硅球(MSS)组成。Pt-FeCo/GC@MSS在室温下具有超顺磁性,并呈现介孔二氧化硅典型的IV型等温线,从而确保有足够大的内部空间(表面积为235.3 m² g⁻¹,孔体积为0.165 cm³ g⁻¹,孔径为2.8 nm)来进行催化反应。我们已经表明,Pt-FeCo/GC@MSS体系能轻易地将环己烯转化为环己烷,这是唯一分离出的产物,并且在催化反应完成后,Pt-FeCo/GC@MSS可以通过外部磁场非常快速地分离。我们已经证明,回收的Pt-FeCo/GC@MSS可以至少重复用于相同的氢化反应四次而不会损失初始催化活性。