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 AbstractThe Endophytic Fungus Cyanodermella asteris Influences Growth of the Nonnatural Host Plant Arabidopsis thaliana    Next AbstractMutations in a gene encoding the alpha subunit of a Saccharomyces cerevisiae G protein indicate a role in mating pheromone signaling »

J Phys Chem A


Title:"Gas-Phase Chlorine Radical Oxidation of Alkanes: Effects of Structural Branching, NO(x), and Relative Humidity Observed during Environmental Chamber Experiments"
Author(s):Jahn LG; Wang DS; Dhulipala SV; Ruiz LH;
Address:"McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, 78712 Texas, United States. Now at Laboratory of Atmospheric Chemistry, Paul Scherrer Institute, 5232 Villigen, Switzerland. Now at Department of Mechanical Engineering, The University of British Columbia, V6T 1Z4 Vancouver, Canada"
Journal Title:J Phys Chem A
Year:2021
Volume:20210812
Issue:33
Page Number:7303 - 7317
DOI: 10.1021/acs.jpca.1c03516
ISSN/ISBN:1520-5215 (Electronic) 1089-5639 (Linking)
Abstract:"Chlorine-initiated oxidation of alkanes has been shown to rapidly form secondary organic aerosol (SOA) at higher yields than OH-alkane reactions. However, the effects of alkane volatile organic compound precursor structure and the reasons for the differences in SOA yield from OH-alkane reactions remain unclear. In this work, we investigated the effects of alkane molecular structure on oxidation by chlorine radical (Cl) and resulting formation of SOA through a series of laboratory chamber experiments, utilizing data from an iodide chemical ionization mass spectrometer and an aerosol chemical speciation monitor. Experiments were conducted with linear, branched, and branched cyclic C(10) alkane precursors under different NO(x) and RH conditions. Observed product fragmentation patterns during the oxidation of branched alkanes demonstrate the abstraction of primary hydrogens by Cl, confirming a key difference between OH- and Cl-initiated oxidation of alkanes and providing a possible explanation for higher SOA production from Cl-initiated oxidation. Low-NO(x) conditions led to higher SOA production. SOA formed from butylcyclohexane under low NO(x) conditions contained higher fractions of organic acids and lower volatility molecules that were less prone to oligomerization relative to decane SOA. Branched alkanes produced less SOA, and branched cycloalkanes produced more SOA than linear n-alkanes, consistent with past work on OH-initiated reactions. Overall, our work provides insights into the differences between Cl- and OH-initiated oxidation of alkanes of different structures and the potential significance of Cl as an atmospheric oxidant"
Keywords:
Notes:"PubMed-not-MEDLINEJahn, Leif G Wang, Dongyu S Dhulipala, Surya Venkatesh Ruiz, Lea Hildebrandt eng 2021/08/13 J Phys Chem A. 2021 Aug 26; 125(33):7303-7317. doi: 10.1021/acs.jpca.1c03516. Epub 2021 Aug 12"

 
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 19-11-2024