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

机译:脂肪酸制备介孔Ni-MgO催化剂上酮的液相加氢

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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中孔的MgO和NiO-MgO。 MgO的孔径随脂肪酸烷基链长度的增加而增加。每种脂肪酸与Mg配位形成有机-无机配合物,该配合物在170℃加热的前体中形成层状中间相。但是,层状中间相在400℃的煅烧过程中通过除去脂肪酸而塌陷。 MgO由微晶的聚集体组成,中孔位于粒子间。以介孔MgO为催化剂载体,制备了大中孔Ni-MgO催化剂(NM-b)。在4-庚酮的液相加氢中,NM-b的催化活性高于商业Raney Ni催化剂。由于NM-10的孔径大于阮内镍的孔径,因此具有大的中孔的Ni-MgO可能对反应物的快速传质有效。

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