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Deuterium enrichment and the kinetic isotope effect during ruthenium catalyzed Fischer-Tropsch synthesis.

机译:钌催化费-托合成过程中的氘富集和动力学同位素效应。

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摘要

Fischer Tropsch Synthesis is a highly researched field that is still widely debated today. Research in this field could lead to many different advances, such as alternative fuel sources, explanations of abiogenic hydrocarbons and the formation of organic matter in the solar nebula. Analysis of this synthesis was carried out with a ruthenium catalyst at controlled temperatures and pressures. Two types of experiments were performed: H 2/D2 switching and competitive methods. The products showed that the hydrocarbon production rate was slightly increased when syngas was switched to D2/CO. Also, the H/D ratios of the hydrocarbons produced by the FT reaction using equal amount of H2 and D2 are always less than 1 indicating deuterium enrichment. We also observed that the ratios of [2-alkene]H/[2-alkene]D is about 1.4, indicating a normal isotope effect. However, the ratio of [1-alkene] H/[1-alkene]D was around 0.9, indicating a different pathway for production than 2-olefins. We attempt to explain these experimental facts by the modified alkylidene mechanism.
机译:Fischer Tropsch合成是一个高度研究的领域,今天仍被广泛争论。在这一领域的研究可能会导致许多不同的进展,例如替代燃料来源,对生碳氢化合物的解释以及太阳星云中有机物的形成。用钌催化剂在受控的温度和压力下进行该合成的分析。进行了两种类型的实验:H 2 / D2转换和竞争方法。产物表明,当合成气转换为D2 / CO时,烃的产率略有​​增加。同样,通过使用等量的H2和D2的FT反应生成的烃的H / D比始终小于1,表明氘富集。我们还观察到,[2-烯烃] H / [2-烯烃] D的比率约为1.4,这表明其同位素效应正常。但是,[1-烯烃] H / [1-烯烃] D的比率约为0.9,表明生产途径与2-烯烃不同。我们试图通过修饰的亚烷基机理来解释这些实验事实。

著录项

  • 作者

    Naumovitz, Jennifer.;

  • 作者单位

    Eastern Kentucky University.;

  • 授予单位 Eastern Kentucky University.;
  • 学科 Physical chemistry.
  • 学位 M.S.
  • 年度 2015
  • 页码 137 p.
  • 总页数 137
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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