首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Role of Na in the dehydro-aromatization of 1,2-cyclohexanediol to catechol over the Na/Ni/HZSM-5 catalyst
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Role of Na in the dehydro-aromatization of 1,2-cyclohexanediol to catechol over the Na/Ni/HZSM-5 catalyst

机译:Na在Na / Ni / HZSM-5催化剂上对1,2-环己二醇脱氢芳构化为邻苯二酚的作用

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摘要

A series of Na-and/or Ni-modified HZSM-5 catalysts were employed in the dehydro-aromatization of 1,2-cyclohexanediol to catechol. The characterization of catalyst by XRD, N2-physisorption, FT-IR, NH3-TPD, H2-TPD, H2-TPR and FE-SEM showed that the Ni-loading over HZSM-5 zeolite generated the mesopores in the catalyst. The reduction to the Ni/HZSM-5 catalyst favored the formation of mesopores and also decreased largely both the acid property of strong acid sites and interaction between nickel species and HZSM-5 zeolite. The Na-loading to the Ni/HZSM-5 enabled the catalyst to be more easily reduced, and particularly, diminished the Bronsted acid sites, causing more large modifications to the catalyst than what the reduction process had done. The catalytic performance evaluation indicated that catechol could be only generated over the reduced Ni-containing catalysts but not over the pure HZSM-5 and unreduced Ni-containing catalysts. As high as 95.8% selectivity to catechol at 99.9 conversion of 1,2-cyclohexanediol was achieved over the reduced Na/Ni/HZSM-5 catalyst, while much lower selectivity to catechol was obtained, accompanied by the formation of large amounts of byproducts, over the reduced catalysts without the modification by Na. Accordingly, the modifications of Na to the pore structure, acidity and interaction between nickel species and HZSM-5 zeolite were responsible to the high performance of the reduced Na/Ni/HZSM-5 catalyst.
机译:一系列Na和/或Ni改性的HZSM-5催化剂用于1,2-环己二醇脱氢芳构化为邻苯二酚。通过XRD,N2-物理吸附,FT-IR,NH3-TPD,H2-TPD,H2-TPR和FE-SEM对催化剂进行表征,结果表明,HZSM-5分子筛上的Ni负载产生了介孔。 Ni / HZSM-5催化剂的还原有利于中孔的形成,也大大降低了强酸位点的酸性质以及镍物种与HZSM-5沸石之间的相互作用。 Na / Ni / HZSM-5的负载使催化剂更容易还原,特别是减少了布朗斯台德酸位,与还原过程相比,对催化剂的修饰更大。催化性能评估表明,邻苯二酚只能在还原的含Ni催化剂上生成,而不能在纯HZSM-5和未还原的含Ni催化剂上生成。与还原的Na / Ni / HZSM-5催化剂相比,1,2-环己二醇在99.9的转化率下,邻苯二酚的选择性高达95.8%,而邻苯二酚的选择性却低得多,并伴随着大量副产物的形成,在没有被Na改性的还原的催化剂上。因此,Na对孔结构,酸性和镍物质与HZSM-5沸石之间相互作用的改性是还原的Na / Ni / HZSM-5催化剂的高性能的原因。

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