環境条件下でCO2の水素化のためのコバルトベースの触媒
Matthew S Jeletic1, Michael T Mock, Aaron M Appel
1Fundamental and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.
Journal of the American Chemical Society
|July 23, 2013
まとめ
研究者は,二酸化炭素 (CO2) をフォーマット燃料に変換するための新しいコバルト触媒を開発しました. この触媒は,室温と低圧で効率的に動作し,貴金属触媒の持続可能な代替品を提供します.
科学分野:
- カタリシス カタリシス カタリシス
- グリーン・ケミストリー (Green Chemistry)
- 材料科学 材料科学とは
背景:
- 大気中のCO2濃度の上昇は,効率的な炭素変換技術を必要とします.
- 現在のCO2変換触媒は,しばしば高価な貴金属に依存し,厳しい条件 (高温/高圧) を要求します.
- 分子触媒は有望ですが,効率とコストの限界に直面しています.
研究 の 目的:
- CO2変換のための費用対効果の高い,効率的な分子触媒を設計し,合成する.
- 合理的な触媒設計のために基本的な熱力学特性を活用する.
- 新しい触媒システムを使用して,CO2とH2からフォーマットを生成します.
主な方法:
- 水素性 (ΔGH(-)) と酸性 (pKa) の原則によるコバルトベースの触媒システムの設計.
- コバルト複合物Co ((dmpe) 2Hの合成で,dmpeは1,2-bis ((dimethylphosphino) ethaneである.
- 圧力と室温の変動下でCO2の水素化のための触媒活性を試験する.
主要な成果:
- コバルト触媒Co(dmpe) 2Hは,CO2の水素化を催化して,高効率で形成することを示した.
- 室温で 3400 h−1 と 1 atm (1:1 CO2:H2) の周回頻度を達成しました.
- 74,000 h−1 の有意に高い回転頻度は,20 atm で観察されました.
結論:
- 基本的な熱力学的性質は,効率的で選択的な触媒の設計に価値があります.
- 開発されたコバルト触媒は,CO2変換のための有望で費用対効果の高い代替案を提供します.
- この研究は,CO2から持続可能な燃料生産のための触媒の分野を前進させています.
さらに関連する動画
関連する概念動画
Reduction of Alkenes: Catalytic Hydrogenation
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 surface of...
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 surface of...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
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...
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...
Catalysis
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.
Catalysis
Catalysis influences the rate of chemical reactions by providing an alternative reaction pathway with lower activation energy. A catalyst speeds up a reaction, but it is not consumed during the process. The fundamental principle of catalysis is the ability of a catalyst to alter the reaction mechanism, often introducing a more efficient pathway than the uncatalyzed process.In a catalyzed reaction, the catalyst participates directly in the reaction mechanism. It interacts with reactants to form...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
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...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
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.
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.


