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首页> 外文期刊>Industrial & Engineering Chemistry Research >Hydrocracking of n-Decane over Zeolite-Supported Metal Sulfide Catalysts. 2. Zeolite Y-Supported Ni and Ni-Mo Sulfides
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Hydrocracking of n-Decane over Zeolite-Supported Metal Sulfide Catalysts. 2. Zeolite Y-Supported Ni and Ni-Mo Sulfides

机译:正癸烷在沸石负载的金属硫化物催化剂上的加氢裂化。 2.沸石Y负载的Ni和Ni-Mo硫化物

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For zeolite Y-supported nickel sulfide catalysts the influence of the metal sulfide dispersion on the hydrocracking properties for n-decane is examined. In order to obtain different nickel sulfide distributions (inside or outside the zeolite structure) and dispersions, the preparation method (impregnation of CaY or ion exchange of NaY), sulfidation procedure (direct sulfidation or sulfidation after drying), and metal loading are varied. A higher nickel sulfide surface (as measured by dynamic oxygen chemisorption) results in a strong increase of the n-decane conversion, but this is not accompanied by an improvement of the catalytic properties toward ideal hydrocracking. Additionally, some zeolite Y-supported Ni—Mo sulfide catalysts (varying in preparation method and sulfidation procedure) are tested for the hydroconversion of n-decane. However, no promoter effect could be observed. The activity of the bimetallic sulfide catalysts is always almost equal to that of the most active monometallic sulfide constituent.
机译:对于沸石Y负载的硫化镍催化剂,研究了金属硫化物分散体对正癸烷的加氢裂化性能的影响。为了获得不同的硫化镍分布(沸石结构的内部或外部)和分散体,制备方法(CaY的浸渍或NaY的离子交换),硫化步骤(干燥后直接硫化或硫化)和金属负载是变化的。较高的硫化镍表面(通过动态氧化学吸附法测得)会导致正癸烷转化率的大幅提高,但这并没有改善对理想加氢裂化的催化性能。另外,测试了某些沸石Y负载的Ni-Mo硫化物催化剂(制备方法和硫化步骤不同)对正癸烷的加氢转化。但是,没有观察到启动子效应。双金属硫化物催化剂的活性总是几乎等于最具活性的单金属硫化物组分的活性。

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