首页> 外文期刊>Journal of Catalysis >AN O-18(2) TEMPERATURE-PROGRAMMED ISOTOPE EXCHANGE STUDY OF TRANSITION-METAL-CONTAINING ZSM-5 ZEOLITES USED FOR OXYDEHYDROGENATION OF ETHANE
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AN O-18(2) TEMPERATURE-PROGRAMMED ISOTOPE EXCHANGE STUDY OF TRANSITION-METAL-CONTAINING ZSM-5 ZEOLITES USED FOR OXYDEHYDROGENATION OF ETHANE

机译:用于乙烷加氢加氢的含过渡金属的ZSM-5沸石的O-18(2)温度程序化同位素交换研究

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The oxydehydrogenation of ethane was studied over a number of transition-metal containing ZSM-5 catalysts, e.g., Co-H-ZSM-5, Cu-Na-ZSM-5, Nb-ZSM-5, and V-ZSM-5. It has been shown that the introduction of transition metal cations into ZSM-5 zeolite, either as charge balancing cations (Co2+, Nb5+) or as lattice cation (V5+), enhances the activity and selectivity of the catalysts for the oxydehydrogenation of ethane. The O-18(2) temperature-programmed isotope exchange technique was used to probe the likely active sites on the catalysts. It was demonstrated that the introduction of transition metal cations results in the formation of active sites responsible for the formation of single-step double exchange between gas phase oxygen and lattice oxygen. The activity for formation of single-step double exchange O-16(2) is a good indicator for the activity for oxydehydrogenation of ethane to form ethylene. The introduction of transition metal cations (Cu2+, Co2+, etc.) into ZSM-5 zeolite lowers the temperature required for isotope exchange between gas phase oxygen and lattice oxygen. The temperature required for isotope exchange depends on the cations introduced. The activity for facilitating single-step double exchange between gas phase O-18(2) and lattice oxygen (O-16) and the activity for oxydehydrogenation of ethane to ethylene decrease in the same order: Co-H-ZSM-5 > Cu-Na-ZSM-5 > [V]-ZSM-5 > Nb-ZSM-5 > Na-ZSM-5 similar to H-ZSM-5 similar to Cu-ZSM-5. It appears that the structural defects created by introducing transition metal cations are responsible for the enhanced activity and selectivity for the oxydehydrogenation of ethane. NH3-TPD results show that the presence of strong Bronsted acid sites are undesired for oxydehydrogenation reactions. However, the presence of relatively weaker acid sites is not harmful for the reaction. (C) 1995 Academic Press, Inc. [References: 17]
机译:在许多含过渡金属的ZSM-5催化剂(例如Co-H-ZSM-5,Cu-Na-ZSM-5,Nb-ZSM-5和V-ZSM-5)上研究了乙烷的氧化脱氢。已经表明,将过渡金属阳离子作为电荷平衡阳离子(Co 2+,Nb 5+)或作为晶格阳离子(V 5+)引入ZSM-5沸石中,增强了乙烷的氧脱氢催化剂的活性和选择性。 O-18(2)温度程序化的同位素交换技术用于探测催化剂上可能存在的活性位点。已经证明,过渡金属阳离子的引入导致活性位点的形成,该活性位点负责形成气相氧和晶格氧之间的单步双交换。单步双交换O-16(2)的形成活性是乙烷氧脱氢形成乙烯的活性的良好指示。将过渡金属阳离子(Cu2 +,Co2 +等)引入ZSM-5沸石可降低气相氧和晶格氧之间同位素交换所需的温度。同位素交换所需的温度取决于所引入的阳离子。促进气相O-18(2)与晶格氧(O-16)之间单步双交换的活性和将乙烷氧化脱氢为乙烯的活性依次降低:Co-H-ZSM-5> Cu -Na-ZSM-5> [V] -ZSM-5> Nb-ZSM-5> Na-ZSM-5与H-ZSM-5类似,与Cu-ZSM-5类似。看来,通过引入过渡金属阳离子而产生的结构缺陷是对乙烷的氧化脱氢的增强的活性和选择性的原因。 NH3-TPD结果表明强氧化性酸位点的存在对于氧化脱氢反应是不希望的。然而,相对较弱的酸位的存在对反应无害。 (C)1995 Academic Press,Inc. [参考:17]

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