首页> 外文期刊>Catalysis Today >Active sites of sulfided NiMo/Al2O3 catalysts for 4,6-dimethyldibenzothiophene hydrodesulfurization-effects of Ni and Mo components, sulfidation, citric acid and phosphate addition
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Active sites of sulfided NiMo/Al2O3 catalysts for 4,6-dimethyldibenzothiophene hydrodesulfurization-effects of Ni and Mo components, sulfidation, citric acid and phosphate addition

机译:硫化NiMO / Al2O3催化剂的活性位点,用于4,6-二甲基二苯甲酸苯酚肼的Ni和Mo组分,硫化,柠檬酸和磷酸盐添加剂的催化剂

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摘要

The active sites of the sulfided 5.2 wt%Ni9.8 wt%Mo/Al2O3 catalyst for the hydrodesulfurization of 4,6dimethyldibenzothiophene were studied using a high-pressure flow system. The catalysts were prepared by dry sulfidation or after the calcination of four sets of NiMo precursors with and without citric acid and phosphoric acid. The dry sulfidation Wing the precursor of nickel carbonate and molybdenum trioxide with citric acid and phosphate produced the HDS MoO3 is considered a precursor for the hydrogenation activity, and ammonium heptamolybdate is a precursor for the direct desulfurization activity. and the highest number of active sites of the Ni2+MoS2 slab (NiMoS phase) based on the NO and XPS. The sulfidation after calcination using nickel nitrate and ammonium hexamolybdate had the highest HDS rate for the desulfurization, and the number of sites of the MoS2 (Mo4+) slab covered with Ni sulfide (Ni2+). This site was stacked with 3.3 layers and 34 angstrom length for the 2% phosphorus catalyst and widely dispersed as multilayers, and increased when stacked by the phosphate addition and contained highly stacked slabs by the citric acid addition. (C) 2017 Elsevier B.V. All rights reserved.
机译:利用高压流动系统研究了用于4,6dimethyldenzoOphene的加氢脱硫的硫化物5.2wt%Ni9.8wt%Mo / Al 2 O 3催化剂的活性位点。催化剂通过干硫化制备或在煅烧四组NiMO前体之后,没有柠檬酸和磷酸。干硫化翼碳酸镍和三氧化钼与柠檬酸和磷酸盐产生的原制Hds MoO3被认为是氢化活性的前体,七淀粉酸铵是直接脱硫活性的前体。基于NO和XPS的NI2 + MOS2板(NiMOS相)的最高数量的NI2 + MOS2板(NIMOS相)的最高数量。使用硝酸镍和六氨基铵煅烧后煅烧的硫化率最高的脱硫的HDS速率,以及用Ni硫化物(Ni2 +)覆盖的MOS2(MO4 +)板的部位数。该部位用3.3层和34埃长的34埃长,用于2%磷催化剂,广泛分散为多层,并且当通过磷酸盐添加而堆叠时增加,并通过柠檬酸加入包含高堆叠的板坯。 (c)2017 Elsevier B.v.保留所有权利。

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