首页> 外文期刊>Journal of Catalysis >SKELETAL REACTIONS OF N-HEXANE OVER PT-NAY, PT/SIO2, HY, AND MIXED PT/SIO2+HY CATALYSTS
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SKELETAL REACTIONS OF N-HEXANE OVER PT-NAY, PT/SIO2, HY, AND MIXED PT/SIO2+HY CATALYSTS

机译:在Pt-Nay,Pt / SiO 2,Hy和混合Pt / SiO2 + HY催化剂上的N-己烷骨架反应

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The activity and selectivity of three samples of 8% Pt-NaY calcined at 633, 723, and 823 K, respectively, have been probed with n-hexane as the model reactant at 603 K and subatmospheric pressures in a glass closed-loop reactor. These catalysts were compared with 6.3% Pt/SiO2 (EUROPT-1), HY, and a physical mixture of the latter two. The activity of all Pt-NaY catalysts is superior to EUROPT-1 and they deactivate more slowly. The selectivity pattern of all Pt-NaY samples is closer to that characteristic of monofunctional Pt catalysts, as opposed to the pronounced acidic character of pure HY and the mechanical mixtures. The sample calcined at 633 K, which has the highest dispersion and probably contains Pt particles anchored to the support as [Pt-n - H-x](x+) entities, shows the highest aromatization selectivity. The sample precalcined at 823 K with the lowest dispersion has a pronouncedly high skeletal isomerization selectivity. The isomerization pathway may be related to the C-5 cyclic route on metal sites that are more abundant on the larger crystallites of this catalyst and are more easily accessible with its partially collapsed zeolite framework. Characteristic differences between samples in the response of their catalytic performance to changes in hydrogen and hydrocarbon pressure are discussed. (C) 1995 Academic Press, Inc. [References: 40]
机译:在633,723和823K分别煅烧的8%Pt-Nay的三个样品的活性和选择性已被用正己烷探测为玻璃闭环反应器中的603k和亚摩擦压力的模型反应物。将这些催化剂与后两者的6.3%Pt / SiO 2(EUROPT-1),HY和物理混合物进行比较。所有PT-NAY催化剂的活性优于EUROPT-1,它们更慢地停用。所有Pt-NAY样品的选择性模式更接近单官能Pt催化剂的该特征,而不是纯HY和机械混合物的明显酸性特性。在633 k下煅烧的样品,其具有最高的分散体,并且可能含有锚定为载体的Pt颗粒作为[pt-n - h-x](x +)实体,显示出最高的芳族化选择性。在823 k下预先煅烧的样品具有最低分散体具有明显的高骨骼异构化选择性。异构化途径可能与在该催化剂的较大微晶上更丰富的金属位点上的C-5环状途径有关,并且更容易与其部分塌陷的沸石框架一起接近。讨论了它们在催化性能响应中与氢气和烃压力变化的响应的特征差异。 (c)1995年学术出版社,Inc。[参考文献:40]

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