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首页> 外文期刊>Energy & fuels >4,6-Dimethyldibenzothiophene Hydrodesulfurization on Nickel-Modified USY-Supported NiMoS Catalysts: Effects of Modification Method
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4,6-Dimethyldibenzothiophene Hydrodesulfurization on Nickel-Modified USY-Supported NiMoS Catalysts: Effects of Modification Method

机译:镍改性的USY负载NiMoS催化剂上的4,6-二甲基二苯并噻吩加氢脱硫:改性方法的影响

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摘要

The effects of the method of modifying USY zeolite with nickel on the hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DMDBT) have been investigated. USY zeolites were modified with a small amount of Ni by three different methods, namely, the in situ synthesis method, the ion-exchange method, and the impregnation method, and the resulting Ni-modified USY zeolites were used as supports for NiMo sulfide catalysts. We found that the Ni modification method affects the textural properties, the acidity of the Ni-modified USY zeolites, the Ni-Mo-S active-phase morphology, the dispersion of the active metals, the structure of the Ni-Mo-S active phase, the sulfidation degree of the active metals, the 4,6-DMDBT HDS reaction rate constant, the turnover frequency, and the selectivity of the 4,6-DMDBT HDS pathways. Although the impregnation modification method was found to promote the dispersion of active metals most strongly and the ion-exchange modification method was found to enhance the sulfidation degrees of both Ni and Mo the most strongly, these changes did not enhance the catalyst activity the most significantly. Rather, the best catalytic activity was observed over the NiMo/USNiY catalyst (prepared by the in situ synthesis method), which was closely related to the proportion of NiMoS structures in the Ni-Mo-S active phase. Among the three investigated modification methods, the in situ synthesis method was found to be the most suitable for the purpose of preparing highly active HDS catalysts for 4,6-DMDBT.
机译:研究了镍修饰USY沸石的方法对4,6-二甲基二苯并噻吩(4,6-DMDBT)的加氢脱硫(HDS)的影响。 USY沸石通过原位合成法,离子交换法和浸渍法三种不同的方法用少量的Ni改性,然后将所得的Ni改性USY沸石用作NiMo硫化物催化剂的载体。 。我们发现,Ni改性方法会影响组织性能,Ni改性USY沸石的酸度,Ni-Mo-S活性相形态,活性金属的分散性,Ni-Mo-S活性剂的结构相,活性金属的硫化程度,4,6-DMDBT HDS反应速率常数,周转频率和4,6-DMDBT HDS途径的选择性。尽管发现浸渍改性方法最有效地促进了活性金属的分散,并且发现离子交换改性方法最有效地增强了镍和钼的硫化程度,但这些变化并未最明显地提高催化剂活性。 。相反,在NiMo / USNiY催化剂(通过原位合成方法制备)上观察到了最佳的催化活性,这与Ni-Mo-S活性相中NiMoS结构的比例密切相关。在三种研究的改性方法中,发现原位合成方法最适合用于制备用于4,6-DMDBT的高活性HDS催化剂。

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  • 来源
    《Energy & fuels》 |2017年第7期|7445-7455|共11页
  • 作者单位

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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