CO2の減少とエタンの芳香化のタンデム反応
Elaine Gomez1, Xiaowa Nie1,2, Ji Hoon Lee1
1Department of Chemical Engineering , Columbia University , New York , New York 10027 , United States.
Journal of the American Chemical Society
|October 17, 2019
まとめ
この研究は,エタンと二酸化炭素を改変されたZSM-5触媒を用いて液体芳香質に変換するための新しい1段階プロセスを導入しています. この方法は,触媒の安定性を高め,排出量を削減し,アロマティック生産のための持続可能な経路を提供します.
科学分野:
- カタリシス
- 化学工学
- 材料科学
背景:
- 軽いアルカンの芳香化は,芳香剤の生産のための原料の選択肢を拡大するために不可欠です.
- 簡単に手に入る天然ガスの分子を利用し,二酸化炭素 (CO2) の排出を軽減することは,産業の重要な目標です.
研究 の 目的:
- エタンとCO2から液体アロマティックを生産するための1段階のプロセスを開発する.
- この変換のためのリン (P) とガリウム (Ga) 改変ZSM-5触媒の性能を評価する.
- 計算手法を使って触媒メカニズムを調査する.
主な方法:
- PとGaを改変したZSM-5触媒を873Kと大気圧で実験的に評価.
- 反応経路と触媒の修正を明らかにするための密度関数理論 (DFT) の計算.
主要な成果:
- 改造されたZSM-5触媒は,エタンのCO2補助酸化脱水化と,その後の芳香化のタンデム反応を容易にした.
- P添加は,Ga/ZSM-5触媒の水熱安定性を高め,コック形成を減少させた.
- このプロセスは,未修正の触媒と比較して,より多くの液体アロマティックを産出しました.
結論:
- PとGaで改造されたZSM-5は,エタンとCO2から持続可能な芳香剤の生産のための有望な経路を提供します.
- 触媒の改変により安定性と選択性が向上し,CO2は酸化剤と共反応剤として作用する.
- DFT計算は,触媒メカニズムに関する基本的な洞察を提供します.
関連する概念動画
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
5.6K
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...
5.6K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.8K
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...
3.8K
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
2.2K
The radical dimerization of ketones or aldehydes gives vicinal diols through a pinacol coupling reaction. However, the behavior of titanium metals used for the reaction as a source of electrons is unusual. When the reaction is carried out in the presence of titanium, diols can be isolated at low temperatures. Else titanium further reacts with diols, forming alkenes through the McMurry reaction.
2.2K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
8.9K
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.
8.9K
Reduction of Alkenes: Catalytic Hydrogenation
13.8K
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...
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...
13.8K
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
3.3K
The Cope rearrangement is classified as a [3,3] sigmatropic shift in 1,5-dienes, leading to a more stable, isomeric 1,5-diene. The reaction involves a concerted movement of six electrons, four from two π bonds and two from a σ bond, via an energetically favorable chair-like transition state.
3.3K


