Related Experiment Video
Updated: Mar 9, 2026

Non-equilibrium Microwave Plasma for Efficient High Temperature Chemistry
Published on: August 1, 2017
Nonthermal Plasma Chemical Processing of Bromomethane
Aihua Zhang1, Shigeru Futamura1, Toshiaki Yamamoto2
1a National Institute for Resources and Environment , Tsukuba , Ibaraki , Japan.
Abstract:
Nonthermal plasma chemical decomposition of bromomethane (CH3Br) was investigated with a coaxial type packed-bed plasma reactor. It has been demonstrated that plasma chemical processing is an effective approach to decompose CH3Br in a wide concentration range. It has been shown that CH3Br decomposition reactivity depends on reactor operating factors such as background gas, O2 concentration, and humidification. Higher decomposition efficiencies can be obtained in dry N2. However, organic byproducts such as BrCN are concurrently produced under deaerated conditions. Water suppresses CH3Br decomposition and also affects the yields of COx (CO and CO2) and organic byproducts due to the involvement of some active species generated from water. The presence of O2 retards CH3Br decomposition by quenching high-energy electrons, while it suppresses organic byproducts and improves COx yield. The reacted carbons in CH3Br are recovered as COx almost quantitatively in air. Higher CO2 selectivities cannot be achieved by increasing O2 concentration. NOx formation, which is accompanied by CH3Br decomposition, can be effectively suppressed by decreasing O2 concentration down to 2%. Furthermore, reaction mechanisms are discussed by comparing the reactivities of CH3Br and its congeners.
More Related Videos
12:05Preparation of Hydrophobic Metal-Organic Frameworks via Plasma Enhanced Chemical Vapor Deposition of Perfluoroalkanes for the Removal of Ammonia
Published on: October 10, 2013
07:32Reactive Vapor Deposition of Conjugated Polymer Films on Arbitrary Substrates
Published on: January 17, 2018
Related Concept Videos
Radical Substitution: Allylic Bromination
Formation of Halohydrin from Alkenes
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
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...
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
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...