在低温CO2化中驱动甲醇形成的TiO2支持的Re的双功能性
Nat Phongprueksathat1, Kah Wei Ting2, Shinya Mine2
1Catalysis Engineering, Department of Chemical Engineering, Delft University of Technology, Van der Maasweg 9, Delft 2629 HZ, Netherlands.
概括
在二氧化 (Re/TiO2) 催化剂上具有高度活性的,可在低温下促进二氧化碳化成甲醇. 这项研究揭示了Re/TiO22.
科学领域:
- 催化剂是一种催化剂.
- 材料科学 材料科学 材料科学
- 化学工程是化学工程的重要组成部分.
背景情况:
- 将二氧化碳化成甲醇对于可持续能源至关重要.
- 低温 (<200°C) 催化在热力学上有利,但在动力学上具有挑战性.
- 像Cu/ZnO/Al2O3这样的现有催化剂在低温下表现出局限性.
研究的目的:
- 为了阐明二氧化碳化Re/TiO2催化剂中的活性位点和活性物种.
- 了解低温中甲醇形成的机制.
- 为了比较Re/TiO2与工业催化剂的性能.
主要方法:
- 在现场/操作的X射线吸收光谱学.
- 拉曼光谱法 拉曼光谱法 拉曼光谱法
- 环境压力X射线光电子光谱学 (AP-XPS)
- 分散反射率红外里埃变换光谱学 (DRIFTS)
主要成果:
- 在125-200°C和高压下,Re/TiO2比Cu/ZnO/Al2O3具有更高的活性和甲醇选择性.
- 二氧化碳的激活形成了在阴离子Re物种上的活性形式中间体.
- 金属Re集群促进H2激活并形成化.
- 电离子Re单个原子和金属Re集群共存,推动甲醇的形成.
结论:
- 电离子Re单个原子和金属Re团的协同效应是Re/TiO2在低温高活性的关键.
- 了解活性中间体对于设计高效的二氧化碳转化催化剂至关重要.
- Re/TiO2为低温二氧化碳转化为甲醇提供了一个有希望的替代方案.
更多相关视频
相关概念视频
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
7.8K
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.
7.8K
Reduction of Alkenes: Catalytic Hydrogenation
12.2K
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...
12.2K
Hydroboration-Oxidation of Alkenes
8.4K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
8.4K
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
4.6K
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...
4.6K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.4K
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...
3.4K
Regioselectivity and Stereochemistry of Hydroboration
8.2K
A significant aspect of hydroboration–oxidation is the regio- and stereochemical outcome of the reaction.
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
8.2K


