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ZSM-5 STRUCTURED CATALYSTS COATED WITH SILICALITE-1

机译:涂有SILICALITE-1的ZSM-5结构化催化剂

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Alumina beads were coated with ZSM-5 films ranging from 150 nm to 2300 nm in thickness. The ZSM-5 coated alumina beads were subsequently hydrothermally treated in a silicalite-1 synthesis solution in two steps whereupon a dense silicalite-1 film was formed on top of the ZSM-5 film. The materials were tested with two probe reactions and the reactivity was compared before and after coating with silicalite-1. As expected, the para-xylene (pX) isomerization reactivity showed no change for samples with and without the top layer of silicalite-1 for equal amounts of zeolite. Surprisingly, the triisopropylbenzene (TIPB) conversion did not decrease after the silicalite-1 film was introduced. As measured by XPS, the aluminum concentration at the surface of the uncalcined silicalite-1 film surface was lower compared to that at the surface of the calcined ZSM-5 film. However, after calcination the concentration of aluminum was higher at the silicalite-1 film surface than at the ZSM-5 film surface. These results suggest that aluminum migrates from the ZSM-5 film into the silicalite-1 film during calcination and testing which results in an active top layer.
机译:氧化铝珠上涂有厚度范围为150 nm至2300 nm的ZSM-5膜。随后将ZSM-5涂覆的氧化铝珠粒在silicalite-1合成溶液中分两步进行水热处理,随后在ZSM-5膜的顶部形成致密的silicalite-1膜。用两个探针反应测试了该材料,并比较了用silicalite-1涂覆前后的反应性。如预期的那样,对等二甲苯的对二甲苯(pX)异构化反应性没有变化,对于有或没有上硅沸石-1顶层的样品也没有变化。令人惊讶的是,引入silicalite-1膜后三异丙基苯(TIPB)的转化率并未降低。如通过XPS测量的,未煅烧的silicalite-1膜表面的铝浓度低于煅烧的ZSM-5膜的表面的铝浓度。但是,煅烧后,silicalite-1膜表面的铝浓度高于ZSM-5膜表面的铝浓度。这些结果表明,铝在煅烧和测试过程中从ZSM-5膜迁移到silicalite-1膜中,从而形成了活性顶层。

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