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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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Heterogeneous Catalysis

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Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
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Reduction of Alkenes: Catalytic Hydrogenation02:13

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Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
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Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
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Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
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Catalysis02:50

Catalysis

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The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
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用于减少二氧化碳的石墨结合催化剂

Seokjoon Oh1, James R Gallagher2, Jeffrey T Miller2,3

  • 1Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.

Journal of the American Chemical Society
|January 26, 2016
PubMed
概括

新的石墨结合 (GCC-Re) 催化剂有效地将二氧化碳转化为二氧化碳. 这些异质催化剂表现出高活性和稳定性,为二氧化碳减少提供了有前途的途径.

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科学领域:

  • 电化学
  • 材料科学
  • 催化剂

背景情况:

  • 开发高效的二氧化碳电催化剂对于可持续能源至关重要.
  • 不同质的催化剂在分离和可重复使用方面比同质系统具有优势.

研究的目的:

  • 合成和描述新的石墨结合 (GCC-Re) 催化剂.
  • 评估GCC-Re的电催化性能,以减少二氧化碳.
  • 调查催化机制并与分子类型进行比较.

主要方法:

  • 在石墨碳表面上凝结复合物.
  • 用于X射线光电子光谱 (XPS) 和X射线吸收光谱 (XAS) 进行表征.
  • 电化学测量包括循环电压测量和时电压测量.

主要成果:

  • 形成具有定义的协调环境的表面绑定的Re中心.
  • GCC-Re催化剂在减少二氧化碳方面具有高活性 (>50 mA cm(-2)) 和选择性 (>96% 法拉代效率).
  • GCC-Re的转换频率和数量高于可溶类型,Tafel斜率表示一个电子转移机制.

结论:

  • 石墨结合是一种有效的策略,用于制造明确的异质电催化剂.
  • GCC-Re催化剂在减少二氧化碳方面具有高度活性和稳定性.
  • 这种方法可以在易于获得的石墨基上设计可调节的催化剂.