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Heterogeneous Catalysis01:22

Heterogeneous Catalysis

109
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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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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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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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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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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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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Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation01:28

Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation

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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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Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration02:34

Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration

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The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can significantly influence the rate.
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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
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Selectividad inducida por la mesoestructura en la catálisis de reducción de CO2

Anthony Shoji Hall1, Youngmin Yoon1, Anna Wuttig1

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

Journal of the American Chemical Society
|November 5, 2015
PubMed
Resumen
Este resumen es generado por máquina.

Las películas de ópalo inverso dorado convierten eficientemente el dióxido de carbono (CO2) en monóxido de carbono (CO), suprimiendo la evolución del hidrógeno. La mesostructuración de electrodos optimiza la selectividad de la reducción de CO2.

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Área de la Ciencia:

  • Ciencias de los materiales
  • La electroquímica
  • Catálisis

Sus antecedentes:

  • Se investiga la reducción electroquímica del CO2 mediante películas delgadas de ópalo inverso dorado (Au-IO).
  • Se desea una alta eficiencia y selectividad para la producción de CO sobre la evolución del hidrógeno.
  • La comprensión de los factores que influyen en la selectividad es crucial para el diseño del catalizador.

Objetivo del estudio:

  • Investigar el papel de la mesostructuración en las películas Au-IO para la reducción de CO2.
  • Para determinar el origen de la supresión de la evolución del hidrógeno.
  • Optimizar el diseño de electrodos para una alta selectividad de CO.

Principales métodos:

  • Fabricación de películas delgadas de Au-IO con un grosor poroso variable.
  • Caracterización electroquímica del rendimiento de reducción de CO2.
  • Análisis de los gradientes de difusión y su impacto en las vías de reacción.

Principales resultados:

  • Las películas Au-IO presentan una alta eficiencia y selectividad para la conversión de CO2 en CO.
  • La actividad de la evolución del hidrógeno disminuye significativamente con el aumento del grosor de la película.
  • Los gradientes de difusión dentro de la estructura mesoporosa se identifican como la causa de la supresión del hidrógeno.
  • Se obtiene una selectividad de CO del 99% a un exceso de potencia de 0,4 V con electrodos optimizados.

Conclusiones:

  • La mesostructuración de electrodos es una estrategia eficaz para ajustar la selectividad en la reducción de CO2.
  • Los gradientes de difusión juegan un papel clave en la supresión de la evolución del hidrógeno.
  • Los electrodos Au-IO optimizados ofrecen una vía prometedora para una catálisis eficiente de CO2 a combustibles.