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Addition of manganese to alumina and its influence on the formation of supported NiMo catalysts for dibenzothiophene hydrodesulfurization application

机译:氧化铝中锰的添加及其对二苯并噻吩加氢脱硫应用负载型NiMo催化剂形成的影响

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The influence of adding manganese to NiMo/Al2O3 hydrodesulfurization (HDS) catalysts was studied by impregnation of manganese acetate at the surface of an Al2O3 support obtained by a sol-gel method. The as-obtained Mn-containing alumina supports were then impregnated with nickel nitrate, Ni(NO3)(2)center dot 6H(2)O, and ammonium heptamolybdate, (NH4)(6)Mo7O24 center dot 4H(2)O, dried at 120 degrees C for 12 h, and finally calcined in air at 400 degrees C for 4 h. The different solids were then sulfided using 10 mol.% H2S in H-2 at 400 degrees C for 4 h and evaluated in the hydrodesulfurization of dibenzothiophene (DBT) at T = 300 degrees C and P = 30 bars H-2. Catalysts were characterized at each step of the preparation: after drying, after calcination, and finally in the sulfided state. Both the pH of the impregnation solution of Ni and Mo precursors and the Mn content (I or 5 mol.% as MnO) strongly influence the nature of the Ni and Mo species formed. In this respect, the pH of the impregnation solution plays a critical role at low Mn content (1 mol.%). While impregnation at pH 7 results in well-dispersed molybdate species easily sulfided into a highly Ni-promoted MoS2 phase, increasing the pH to 9 favors the formation of more polymerized Mo species and the loss of some nickel into a NiMnO spinel, leading after sulfidation to a lower promotion degree and a lower dispersion. At higher Mn content (5 mol.%), whatever the pH of impregnation, the formation of MoO3 clusters and the loss of Ni into a NiMnO spinel phase leads to deleted HDS activity after sulfidation. Finally, our results also demonstrate a strong positive influence of manganese on the intrinsic activity of the NiMoS phase if conditions of preparation are optimized. (C) 2016 Elsevier Inc. All rights reserved.
机译:通过在溶胶-凝胶法制得的Al2O3载体表面浸渍乙酸锰,研究了向NiMo / Al2O3加氢脱硫(HDS)催化剂中添加锰的影响。然后将所得的含锰氧化铝载体浸入硝酸镍,Ni(NO3)(2)中心点6H(2)O和七钼酸铵(NH4)(6)Mo7O24中心点4H(2)O,在120摄氏度下干燥12小时,最后在400摄氏度的空气中煅烧4小时。然后将不同的固体在400°C的H-2中使用10 mol%的H2S硫化4 h,并在T = 300°C和P = 30 bar H-2的条件下对二苯并噻吩(DBT)进行加氢脱硫。在制备的每个步骤中对催化剂进行表征:干燥后,煅烧后以及最终呈硫化态。 Ni和Mo前体的浸渍溶液的pH值和Mn含量(I或5mol。%,以MnO计)都强烈影响所形成的Ni和Mo物质的性质。在这方面,在低Mn含量(1mol。%)下,浸渍溶液的pH起关键作用。虽然在pH 7浸渍会导致分散良好的钼酸盐物种容易被硫化成高度Ni促进的MoS2相,但将pH值提高到9则有利于形成更多聚合的Mo物种,并使一些镍损失成NiMnO尖晶石,这在硫化之后导致达到较低的推广度和较低的分散度。在较高的Mn含量(5摩尔%)下,无论浸渍的pH值如何,MoO3团簇的形成和Ni损失成NiMnO尖晶石相都会导致硫化后HDS活性降低。最后,我们的研究结果还表明,如果优化制备条件,锰对NiMoS相的内在活性具有很强的积极影响。 (C)2016 Elsevier Inc.保留所有权利。

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