Related Experiment Video
Updated: Mar 17, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Catalyst design for natural-gas upgrading through oxybromination chemistry
Vladimir Paunović1, Guido Zichittella1, Maximilian Moser1
1Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering, ETH Zurich, Vladimir-Prelog-Weg 1, CH-8093 Zurich, Switzerland.
This study introduces an efficient oxybromination method for functionalizing methane, a key component of natural gas. Vanadium phosphate (VPO) catalysts achieve high selectivity for methyl bromide production under mild conditions.
Area of Science:
- Catalysis
- Chemical Engineering
- Materials Science
Background:
- Natural gas, rich in light alkanes, presents a valuable feedstock for chemicals and fuels.
- Selective C-H bond activation in hydrocarbons remains a significant challenge in catalysis.
Purpose of the Study:
- To develop a novel, one-step oxybromination method for methane functionalization.
- To identify optimal catalyst design strategies for integrating gas-phase alkane bromination and HBr oxidation.
Main Methods:
- Integration of gas-phase alkane bromination with heterogeneous HBr oxidation.
- Screening of various material families for catalytic performance.
- Evaluation of vanadium phosphate (VPO) catalysts for methane oxybromination.
Main Results:
- Vanadium phosphate (VPO) demonstrated superior performance as an oxybromination catalyst.
- Achieved up to 95% selectivity for methyl bromide (CH3Br) production.
- VPO catalysts exhibited stable operation exceeding 100 hours and high activity in HBr oxidation with low side-reaction propensity.
Conclusions:
- The developed oxybromination method offers an attractive route for methane valorization.
- VPO catalysts are highly effective for selective methane to methyl bromide conversion.
- Further research is needed for higher alkanes due to increased reaction complexity.
More Related Videos
Related Concept Videos
Catalysis
Hydroboration-Oxidation of Alkenes
Heterogeneous Catalysis
Radical Anti-Markovnikov Addition to Alkenes: Mechanism
The mechanism starts with chain initiation, which involves two steps. In the first chain initiation step, a weak peroxide bond is homolytically cleaved upon mild heating to form two alkoxy radicals. In the second initiation step, a hydrogen atom is abstracted by the alkoxy...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Radical Substitution: Allylic Bromination

