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Supported mesoporous solid base catalysts for condensation of carboxylic acids

机译:负载的介孔固体碱催化剂,用于羧酸的缩合

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摘要

New mesoporous base catalysts (CM-HMS and CM-MCM-41) were synthesized by generating uniform particles of cerium and manganese oxides (MnO _x/CeO_2) in situ within hexagonal mesoporous silica (HMS) and MCM-41 supports. These catalysts were characterized by N2 adsorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), energy-dispersive X-ray spectrometry (EDX), FTIR, temperature-programmed desorption of CO_2 (CO_2-TPD), and diffuse reflectance UV-visible (UV-vis) spectroscopy. Spectroscopic studies reveal that some particles of MnO_x/CeO_2 are incorporated into the walls of the silica network of HMS and MCM-41, while others are highly dispersed onto the surface of the HMS or MCM-41. The catalytic activity of CM-HMS and CM-MCM-41 for the ketonization of carboxylic acids was confirmed; better utilization of Ce and Mn was observed than in unsupported MnO_x/CeO_2. The citrate-based preparation of MnO_x/CeO_2 catalyst supported on HMS and MCM-41 has not been previously reported in the literature.
机译:通过在六角形介孔二氧化硅(HMS)和MCM-41载体中原位生成铈和锰氧化物(MnO _x / CeO_2)的均匀颗粒,合成了新的介孔碱催化剂(CM-HMS和CM-MCM-41)。这些催化剂的特征在于N2吸附,X射线衍射(XRD),透射电子显微镜(TEM),能量色散X射线光谱法(EDX),FTIR,程序升温的CO_2解吸(CO_2-TPD)和扩散反射率紫外可见(UV-vis)光谱。光谱研究表明,某些MnO_x / CeO_2颗粒被掺入HMS和MCM-41的二氧化硅网络壁中,而另一些则高度分散在HMS或MCM-41的表面上。证实了CM-HMS和CM-MCM-41对羧酸酮化的催化活性。与未负载的MnO_x / CeO_2相比,Ce和Mn的利用率更高。 HMS和MCM-41负载的基于柠檬酸盐的MnO_x / CeO_2催化剂的制备以前尚未在文献中报道。

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