Main group catalysis for H2 purification based on liquid organic hydrogen carriers
Taiki Hashimoto1, Takahiro Asada1, Sensuke Ogoshi1
1Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.
Science Advances
|October 26, 2022
Summary
This study shows N-heterocyclic compounds, known as liquid organic hydrogen carriers (LOHCs), can purify and store hydrogen gas (H2) from mixtures with CO and CO2. This bypasses costly traditional purification methods.
Area of Science:
- Energy storage and conversion
- Chemical engineering
- Materials science
Background:
- Molecular hydrogen (H2) is a key energy carrier, but its production often involves energy-intensive purification steps to remove contaminants like CO and CO2.
- Current methods for H2 purification increase production costs and environmental impact.
- Liquid organic hydrogen carriers (LOHCs) are established for H2 storage and release via dehydrogenation.
Purpose of the Study:
- To investigate the potential of N-heterocyclic compounds as liquid organic hydrogen carriers (LOHCs) for simultaneous H2 purification and storage.
- To develop a cost-effective and environmentally friendly alternative to conventional H2 purification processes.
- To demonstrate the separation of H2 from a complex gaseous mixture containing CO and CO2.
Main Methods:
- Utilizing N-heterocyclic compounds as LOHCs to capture H2 from a gaseous mixture.
- Simultaneously storing the purified H2 within the LOHC structure.
- Analyzing the composition of the gaseous mixture before and after the H2 separation process.
- Evaluating the feasibility of subsequent H2 release through dehydrogenation.
Main Results:
- Demonstrated successful separation of H2 from a mixture containing excess CO and CO2, along with CH4.
- Showcased the capacity of LOHCs to store purified H2.
- Indicated that LOHCs can effectively remove CO and CO2 contaminants from crude H2 streams.
- Confirmed the potential for H2 recovery via dehydrogenation from the H2-loaded LOHCs.
Conclusions:
- N-heterocyclic compounds acting as LOHCs offer a viable dual-functionality for H2 purification and storage.
- This approach presents a promising strategy to reduce the cost and environmental footprint of H2 production.
- LOHCs can be integrated into H2 production pathways to handle crude H2 streams, complementing their established storage applications.
Related Concept Videos
Reduction of Alkenes: Catalytic Hydrogenation
12.4K
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...
12.4K
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
Catalysis
27.3K
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.
27.3K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
8.0K
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.
8.0K
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
4.8K
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...
4.8K
Alcohols from Carbonyl Compounds: Reduction
10.6K
Reduction is a simple strategy to convert a carbonyl group to a hydroxyl group. The three major pathways to reduce carbonyls to alcohols are catalytic hydrogenation, hydride reduction, and borane reduction.
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
10.6K


