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Liquid-phase Hydrogenation of Ketones over Mesoporous Ni-MgO Catalysts Prepared by Using Fatty Acids

机译:通过使用脂肪酸制备的介孔Ni-MgO催化剂对酮的液相氢化

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摘要

MgO and NiO-MgO with large mesopores were prepared by using fatty acids. The pore size of MgO increased with increasing alkyl-chain length of fatty acids. Each fatty acid was coordinated with Mg to form an organic-inorganic complex, and the complex formed lamella mesophase in the precursor heated at 170 deg C. The lamella mesophase, however, collapsed by removing fatty acid during calcination at 400 deg C. The calcined MgO consisted of the aggregates of crystallites, and the mesopores were located at interparticles. Ni-MgO catalyst with large mesopores (NM-b) was prepared by using the mesoporous MgO as a catalyst support. The catalytic activity of NM-b was higher than that of a commercial Raney Ni catalyst in the liquid-phase hydrogenation of 4-heptanone. Since the pore size of NM-10 was larger than that of Raney Ni, the Ni-MgO with large mesopores is probably effective in rapid mass-transfer of the reactants.
机译:通过使用脂肪酸制备具有大型中孔的MgO和NiO-MgO。 MgO的孔径随着脂肪酸的烷基链长度的增加而增加。 每种脂肪酸与Mg配位,形成有机 - 无机络合物,并且在前体中的复合物形成的薄片中间相热在170℃下加热。然而,通过在400℃的煅烧过程中除去脂肪酸在煅烧过程中除去脂肪酸塌陷。煅烧 MgO由微晶的聚集体组成,并且中孔位于晶粒处。 通过使用介孔MgO作为催化剂载体制备具有大型索孔(NM-B)的Ni-MgO催化剂。 NM-B的催化活性高于4-庚酮的液相氢化中的商业阮内Ni催化剂的催化活性。 由于NM-10的孔径大于Raney Ni的孔径,因此具有大的中孔的Ni-MgO可能在反应物的快速传递中有效。

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