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 AbstractCharacterization of the volatile profile of Antarctic bacteria by using solid-phase microextraction-gas chromatography-mass spectrometry    Next Abstract"Non-Contact, Continuous Sampling of Porous Surfaces for the Detection of Particulate and Adsorbed Organic Contaminations by Low-Temperature Plasma Coupled to Ion Mobility Spectrometer" »

J Phys Chem A


Title:"Aqueous Photochemistry of Secondary Organic Aerosol of alpha-Pinene and alpha-Humulene Oxidized with Ozone, Hydroxyl Radical, and Nitrate Radical"
Author(s):Romonosky DE; Li Y; Shiraiwa M; Laskin A; Laskin J; Nizkorodov SA;
Address:"Department of Chemistry, University of California , Irvine, California 92697, United States. National Institute for Environmental Studies , Tsukuba, Ibaraki 305-8506, Japan"
Journal Title:J Phys Chem A
Year:2017
Volume:20170206
Issue:6
Page Number:1298 - 1309
DOI: 10.1021/acs.jpca.6b10900
ISSN/ISBN:1520-5215 (Electronic) 1089-5639 (Linking)
Abstract:"Formation of secondary organic aerosols (SOA) from biogenic volatile organic compounds (BVOC) occurs via O(3)- and OH-initiated reactions during the day and reactions with NO(3) during the night. We explored the effect of these three oxidation conditions on the molecular composition and aqueous photochemistry of model SOA prepared from two common BVOC. A common monoterpene, alpha-pinene, and sesquiterpene, alpha-humulene, were used to form SOA in a smog chamber via BVOC + O(3), BVOC + NO(3), and BVOC + OH + NO(x) oxidation. Samples of SOA were collected on filters, water-soluble compounds from SOA were extracted in water, and the resulting aqueous solutions were photolyzed to simulate the photochemical aqueous processing of SOA. The extent of change in the molecular level composition of SOA over 4 h of photolysis (approximately equivalent to 64 h of photolysis under ambient conditions) was assessed with high-resolution electrospray ionization mass spectrometry. The analysis revealed significant differences in the molecular composition between SOA formed by the different oxidation pathways. The composition further evolved during photolysis with the most notable change corresponding to the nearly complete removal of nitrogen-containing organic compounds. Hydrolysis of SOA compounds also occurred in parallel with photolysis. The preferential loss of larger SOA compounds during photolysis and hydrolysis made the SOA compounds more volatile on average. This study suggests that aqueous processes may under certain conditions lead to a reduction in the SOA loading as opposed to an increase in SOA loading commonly assumed in the literature"
Keywords:
Notes:"PubMed-not-MEDLINERomonosky, Dian E Li, Ying Shiraiwa, Manabu Laskin, Alexander Laskin, Julia Nizkorodov, Sergey A eng 2017/01/19 J Phys Chem A. 2017 Feb 16; 121(6):1298-1309. doi: 10.1021/acs.jpca.6b10900. Epub 2017 Feb 6"

 
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 29-06-2024