Related Experiment Video
Updated: Jul 10, 2026

Production and Measurement of Organic Particulate Matter in the Harvard Environmental Chamber
Published on: November 18, 2018
Impact of propene on secondary organic aerosol formation from m-xylene
Chen Song1, Kwangsam Na, Bethany Warren
1Bourns College of Engineering-Center for Environmental Research and Technology (CE-CERT), University of California, Riverside, California 92521, USA.
Abstract:
Propene is widely used in smog chamber experiments to increase the hydroxyl radical (OH) level based on the assumption that the formation of secondary organic aerosol (SOA) from parent hydrocarbon is unaffected. A series of m-xylene/NO(x) photooxidation experiments were conducted in the presence of propene in the University of California CE-CERT atmospheric chamber facility. The experimental data are compared with previous m-xylene/N0(x) photooxidation work performed in the same chamber facility in the absence of propene (Song et al. Environ. Sci. Technol. 2005, 39, 3143-3149). The result shows that, for similar initial conditions, experiments with propene have lower reaction rates of m-xylene than those without propene, which indicates that propene reduces OH in the system. Furthermore, experiments with propene showed more than 15% reduction in SOA yield compared to experiments in the absence of propene. Additional experiments of m-xylene/ NO(x) with CO showed similar trends of suppressing OH and SOA formation. These results indicate that SOA from m-xylene/NO(x) photooxidation is strongly dependent on the OH level present, which provides evidence for the critical role of OH in SOA formation from aromatic hydrocarbons.
Related Concept Videos
Radical Substitution: Allylic Bromination
Regioselectivity of Electrophilic Additions-Peroxide Effect
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Autoxidation of Ethers to Peroxides and Hydroperoxides

