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Mesoporous MgO and Ni-MgO prepared by using carboxylic acids

机译:用羧酸制备的介孔MgO和Ni-MgO

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MgO and NiO-MgO with large mesopores were prepared by using the corresponding nitrates and carboxylic acids.Their pore structures were characterized by N_2 adsorption,and reduced Ni-MgO samples were used in the liquid-phase hydrogenation of ketone.The mesopore size of MgO was controllable with the alkyl-chain length of the carboxylic acid inthe range between 13 and 38 nm.The mesopores are located at the MgO interparticles.In the hydrogenation of 4-heptanone to 4-heptanol,the catalytic activity of the Ni-Mgo,which had mesopores at 11 nm,prepared using dodecanoic acid was higher than that of a commercial Raney Ni with mesopores around 4 nm,while the Ni surface of the Ni-MgO was lower than that of a Raney Ni catalyst.At an optimum regulated size of mesopores,the Ni-MgO catalyst would show high catalytic activity satisfying both rapid mass transfer of the reactants and high dispersion of Ni metals on the catalyst surface.
机译:利用相应的硝酸盐和羧酸制备具有大中孔的MgO和NiO-MgO,通过N_2吸附表征其孔结构,并将还原的Ni-MgO样品用于酮的液相加氢中.MgO的中孔尺寸羧酸的烷基链长度在13到38 nm之间是可控的。介孔位于MgO粒子之间。在4-庚酮加氢成4-庚醇中,Ni-Mgo的催化活性十二烷酸制得的中孔在11 nm处高于中孔在4 nm附近的商业阮内Ni,而Ni-MgO的Ni表面低于阮内Ni催化剂。对于中孔,Ni-MgO催化剂将显示出高的催化活性,既满足了反应物的快速传质又满足了镍金属在催化剂表面的高分散性。

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