Related Experiment Video
Updated: Jul 20, 2026

Free Radicals in Chemical Biology: from Chemical Behavior to Biomarker Development
Published on: April 15, 2013
Degradation of MTBE in dilute aqueous solution by gamma radiolysis
Ling-Ling Hsieh1, Yi-Liang Lin, Chien-Hou Wu
1Department of Atomic Science, Nation Tsing Hua University, Hsinchu 300, Taiwan, ROC.
Abstract:
The radiolytic degradation of methyl tert-butyl ether (MTBE) in air-equilibrated dilute solution was investigated. Complete degradation of MTBE can be achieved within 5 min of irradiation at 59.7 Gy/min. The observed first-order degradation rate constant, called dose constant, increased from 0.04 to 0.56 Gy(-1) as the concentration of MTBE decreased from 92500 to 19 microg/L. Tert-butyl formate, tert-butyl alcohol, acetone and methyl acetate were found to be the primary intermediates of the degradation reaction with yields of 47%, 11%, 6.4% and 9.1%, respectively. The degradation of MTBE or its intermediates was also found to depend on the concentrations of benzene and cupric ion. The study shows that the removal of MTBE can be significantly decreased with increasing concentration of benzene. Little affects were observed with the presence of cupric ions, while the degradation of TBF was apparently reduced. These results indicate that gamma radiolysis can be a potentially effective treatment for the removal of MTBE in contaminated water systems.
More Related Videos
05:46Identification of Pharmaceuticals in The Aquatic Environment Using HPLC-ESI-Q-TOF-MS and Elimination of Erythromycin Through Photo-Induced Degradation
Published on: August 1, 2018
08:30A Complete Method for Evaluating the Performance of Photocatalysts for the Degradation of Antibiotics in Environmental Remediation
Published on: October 6, 2022
Related Concept Videos
Radical Formation: Elimination
Radical Oxidation of Allylic and Benzylic Alcohols
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...