Related Experiment Video
Updated: Aug 22, 2026

Analyzing the Photo-oxidation of 2-propanol at Indoor Air Level Concentrations Using Field Asymmetric Ion Mobility Spectrometry
Published on: June 14, 2018
Photocatalytic oxidation of VX simulant 2-(butylamino)ethanethiol
Alexandre V Vorontsov1, Yi-Chuan Chen, Panagiotis G Smirniotis
1Boreskov Institute of Catalysis, Novosibirsk 630090, Russian Federation, Russia.
Abstract:
Photocatalytic oxidation of 2-(butylamino)ethanethiol (BAET) was undertaken in aqueous suspension of TiO2 Hombikat UV 100 and Degussa P25 under different initial reaction conditions in order to determine the best parameters for the fastest mineralization of the substrate. BAET is considered to be a simulant for the VX chemical warfare agent. The application of ultrasound had only a small positive effect on the BAET photocatalytic degradation. The highest mineralization rate of 0.433 mg/(l min) was found in unbuffered TiO2 Degussa P25 suspension with initial pH value of about 9.4, TiO2 concentration 500 mg/l and the initial BAET concentration 1000 mg/l. Decreasing of the initial solution pH to 6.1 or below stops the mineralization of BAET while increasing of pH to about 11 drastically changed the degradation profile. At this initial pH, the first 100 min of reaction led to only oxidation of sulfur moiety and organic intermediates accumulated in the solution. Thereafter, mineralization of the products started. The main detected volatile product was butyl aldehyde and the main polar one was 2-(butylamino) acetic acid. In the case of TiO2 Hombikat UV 100, conversion of TOC at initial pH 11 exceeded that at initial pH 9.1. For Degussa P25, the starting pH 9.4 was the best for TOC conversion. The results can be used for treatment of water from pollutants with aliphatic nitrogen and sulfur atoms.
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation and Reactions of Sulfides
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is activated by...
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,...
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids

