Related Experiment Video
Updated: Jun 14, 2025

Production of Near-Infrared Sensitive, Core-Shell Vaccine Delivery Platform
Published on: October 20, 2020
HCl Intake via Nanobubbles Induces Redox Radicals for Aqueous Cl2 and H2 Production Without Catalyst and Bias Applied
Ruijuan Zhao1, Lei Li1, Di Wu1
1Molecular Electrochemistry Laboratory, Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Abstract:
Bubbling is a widely used method to enhance gas hydration and dissolution in aqueous solutions. Understanding the bubble-induced interface-rich aqueous system is crucial for elucidating gas-involved solution chemical reactions, yet this area remains underexplored. Here we report the formation of aqueous Cl2 and H2 driven by nanobubbles, achieved by introducing redox-active HCl gas through a gas diffusion electrode without applying bias or loading catalysts. Electron paramagnetic resonance (EPR) revealed that increasing HCl intake elevates the concentration of hydroxyl radical (·OH) and hydrated electrons (e- aq), more than an order of magnitude higher than that of feeding Ar alone. High-resolution mass spectrometry identified spin-trapping agent stabilized radical intermediates, including ·Cl, ClO·, and ·H. Iodometric titration estimated the equivalent Cl2 content at approximately 18 mmol L-1, while gas chromatography verified H2 formation. This study demonstrates that bubbling redox-active gases through aqueous solution can activate water reactivity, leading to the conversion of the gases themselves.
More Related Videos
08:23Chemiluminescence-based Assays for Detection of Nitric Oxide and its Derivatives from Autoxidation and Nitrosated Compounds
Published on: February 16, 2022
05:50Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
Related Concept Videos
Radical Substitution: Allylic Chlorination
Radical Formation: Homolysis
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...
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...
Radical Reactivity: Concentration Effects
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...