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.
Abstract:
Partial oxidation of methane (POM) is achieved by forming air-methane microbubbles in saltwater to which an alternating electric field is applied using a copper oxide foam electrode. The solubility of methane is increased by putting it in contact with water containing dissolved KCl or NaCl (3%). Being fully dispersed as microbubbles (20-40 µm in diameter), methane reacts more fully with hydroxyl radicals (OH·) at the gas-water interface. The alternating voltage (100 mV) generates two synergistic POM processes dominated by Cl- → Cl· + e- and O2 + e- → O2 -• under positive and negative potentials, respectively. By tuning the frequency and amplitude, the extent and path of the POM process can be precisely controlled so that more than 90% methanol is selectively formed compared to the two byproducts, dichloromethane, and acetic acid. The methane to methanol conversion yield is estimated to be 57% at a rate of approximately 887 µM h-1. This method appears to have potential for removing methane from air using seawater or for converting higher-concentration 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...

