Sonochemical formation of methyl hydroperoxide in polar aprotic solvents and its effect on single-walled carbon nanotube dispersion stability
Related Experiment Video
Updated: Jun 17, 2026

Grafting Multiwalled Carbon Nanotubes with Polystyrene to Enable Self-Assembly and Anisotropic Patchiness
Published on: April 1, 2018
Michael W Forney1, Jordan C Poler
1Department of Chemistry, University of North Carolina at Charlotte, 9201 University City Boulevard, Charlotte, North Carolina 28223-001, USA.
Abstract:
Ultrasonication is a common method for dispersing nanoparticles and colloids. We have found that, under certain conditions, unintended sonochemical reactions can be initiated by the incident ultrasonic energy, yielding unwanted byproducts. In this work, we determined that methyl hydroperoxide can be produced by an autoxidation chain reaction when ultrasonicating polar aprotic solvents containing methyl groups. Methyl radicals were detected during ultrasonication by their interaction with lucigenin, which emits sonochemiluminescence. A colorimetric triiodide test was used to confirm the presence of a hydroperoxide. The concentration of methyl hydroperoxide as a function of the ultrasonication time was measured by titration with NaOH. When above the critical coagulation concentration, this sonochemical byproduct collapses the electrical double layer, disrupting the dispersion stability and lowering the dispersion limits. This is significant when developing ultrasonication processes for dispersion of nanoparticles and colloids. There are no other examples of sonochemically initiated solvent autoxidation destabilizing single-walled carbon nanotube dispersions reported in the literature.
More Related Videos
08:59Dry Oxidation and Vacuum Annealing Treatments for Tuning the Wetting Properties of Carbon Nanotube Arrays
Published on: April 15, 2013
09:12Functionalization of Single-walled Carbon Nanotubes with Thermo-reversible Block Copolymers and Characterization by Small-angle Neutron Scattering
Published on: June 1, 2016
Related Concept Videos
Regioselectivity of Electrophilic Additions-Peroxide Effect
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Radical Anti-Markovnikov Addition to Alkenes: Overview
Hydroboration-Oxidation of Alkenes
Nucleophilic Substitution Reactions
In 1896, the German chemist Paul Walden discovered that he could interconvert pure enantiomeric (+) and (-) malic acids through a series of reactions. This conversion suggested the involvement of optical inversion during the substitution reaction. Further, in 1930, Sir Christopher Ingold described for the first time two different forms of nucleophilic substitution reactions, which are known as SN1 (nucleophilic substitution unimolecular) and SN2 (nucleophilic substitution...
Formation of Halohydrin from Alkenes