Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractVolatile pheromone signalling in Drosophila    Next AbstractParticles and vegetation: implications for the transfer of particle-bound organic contaminants to vegetation »

Environ Sci Technol


Title:Secondary organic aerosol production from aqueous reactions of atmospheric phenols with an organic triplet excited state
Author(s):Smith JD; Sio V; Yu L; Zhang Q; Anastasio C;
Address:"Department of Land, Air and Water Resources, double daggerAgricultural and Environmental Chemistry Graduate Group, and section signDepartment of Environmental Toxicology, University of California-Davis , 1 Shields Avenue, Davis, California 95616, United States"
Journal Title:Environ Sci Technol
Year:2014
Volume:20140109
Issue:2
Page Number:1049 - 1057
DOI: 10.1021/es4045715
ISSN/ISBN:1520-5851 (Electronic) 0013-936X (Linking)
Abstract:"Condensed-phase chemistry plays a significant role in the formation and evolution of atmospheric organic aerosols. Past studies of the aqueous photoformation of secondary organic aerosol (SOA) have largely focused on hydroxyl radical oxidation, but here we show that triplet excited states of organic compounds ((3)C*) can also be important aqueous oxidants. We studied the aqueous photoreactions of three phenols (phenol, guaiacol, and syringol) with the aromatic carbonyl 3,4-dimethoxybenzaldehyde (DMB); all of these species are emitted by biomass burning. Under simulated sunlight, DMB forms a triplet excited state that rapidly oxidizes phenols to form low-volatility SOA. Rate constants for these reactions are fast and increase with decreasing pH and increasing methoxy substitution of the phenols. Mass yields of aqueous SOA are near 100% for all three phenols. For typical ambient conditions in areas with biomass combustion, the aqueous oxidation of phenols by (3)C* is faster than by hydroxyl radical, although rates depend strongly on pH, oxidant concentrations, and the identity of the phenol. Our results suggest that (3)C* can be the dominant aqueous oxidant of phenols in areas impacted by biomass combustion and that this is a significant pathway for forming SOA"
Keywords:Aerosols/*chemistry Atmosphere/*chemistry Benzaldehydes/chemistry *Electrons Hydrogen-Ion Concentration Hydroxyl Radical/chemistry Kinetics Molecular Weight Organic Chemicals/*chemistry Oxidation-Reduction Phenols/*chemistry Protons Water/*chemistry;
Notes:"MedlineSmith, Jeremy D Sio, Vicky Yu, Lu Zhang, Qi Anastasio, Cort eng Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. 2013/12/25 Environ Sci Technol. 2014 Jan 21; 48(2):1049-57. doi: 10.1021/es4045715. Epub 2014 Jan 9"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024