Related Experiment Video
Updated: Jun 1, 2025

Author Spotlight: Scaling Microalgal Biotechnology for Enhanced Biomethane Production
Published on: March 22, 2024
Methane Bubbled Through Seawater Can be Converted to Methanol With High Efficiency
Xiaowei Song1, Chanbasha Basheer2, Jinheng Xu1
1Department of Chemistry, Stanford University, 380 Roth Way, Stanford, CA, 94305, USA.
This study demonstrates efficient partial oxidation of methane (POM) into methanol using air-methane microbubbles in saltwater with an electric field. The novel method achieves high methanol selectivity, offering potential for methane removal and conversion.
Area of Science:
- Electrochemistry
- Catalysis
- Environmental Science
Background:
- Partial oxidation of methane (POM) is crucial for converting methane into valuable chemicals.
- Traditional POM methods often face challenges with selectivity and efficiency.
- Methane's low solubility in water limits reaction efficiency in aqueous systems.
Purpose of the Study:
- To develop an efficient and selective method for partial oxidation of methane (POM) to methanol.
- To investigate the use of air-methane microbubbles in saltwater under an alternating electric field.
- To explore the synergistic effects of electrochemistry and microbubble dispersion on methane conversion.
Main Methods:
- Formation of air-methane microbubbles (20-40 µm) in 3% NaCl or KCl saltwater.
- Application of an alternating electric field (100 mV) using a copper oxide foam electrode.
- Control of POM process pathways and extent by tuning electric field frequency and amplitude.
Main Results:
- Achieved over 90% selectivity for methanol formation from methane.
- Demonstrated synergistic POM processes driven by Cl- and O2- radical generation.
- Estimated methane to methanol conversion yield of 57% at a rate of 887 µM h-1.
Conclusions:
- The microbubble-enhanced electrochemical method offers precise control over POM.
- This technique shows promise for atmospheric methane removal using seawater.
- Potential for converting concentrated methane sources into value-added methanol.
Related Concept Videos
Oxymercuration-Reduction of Alkenes
Hydroboration-Oxidation of Alkenes
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Radical Substitution: Halogenation of Alkanes and Alkyl Substituents
In the initiation step of the reaction, the chlorine molecule undergoes homolytic cleavage in the presence of light or heat, forming two highly reactive chlorine radicals. Propagation occurs in two...
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more...

